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    Publisher: Academic Journals Inc., USA
   
  American Journal of Biochemistry and Molecular Biology is a peer-reviewed international journal dedicated to provide an active forum to the global scientific community for publishing and disseminating high quality research work in the field of biochemistry and molecular biology. Scope of the journal includes: General biochemistry, pathobiochemistry, molecular and cellular biology, molecular medicine, experimental methodologies and the diagnosis, therapy and monitoring of human disease, Host pathogen interaction, molecular detection of pathogen, current advancements in diagnostic techniques, structure, function, and regulation of biologically active molecules, cell signalling, cell cycle, gene structure and expression, gene editing, biochemical mechanisms, protein biosynthesis, protein folding and protein modelling.
  Editor-in-Chief:  Ashok K. Munjal
 
 
9. Aalaei-Andabili, S.H., M. Fabbri, N. Rezaei, 2013. Reciprocal effects of toll like receptors (TLRs) and microRNAs (MiRs) on biological processes in human health and diseases: A systematic review. Immunotherapy, 5: 1127-1142.
9. Mirghorbani, M., G.S. Van and N. Rezaei, 2013. Myeloid-derived suppressor cells in glioma. Expert Rev. Neurother., 13: 1395-1406.
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Aalaei-Andabili, S.H. and N. Rezaei, 2016. MicroRNAs (MiRs) precisely regulate immune system development and function in immunosenescence process. Int. Rev. Immunol., 35: 57-66.
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Aalaei-andabili, S.H and N. Rezaei, 2013. Toll like receptor (TLR)-induced differential expression of microRNAs (MiRs) and immune response against infection: A systematic review. J. Infect., 67: 251-264.
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Abbasi, F., S. Soltani, A. Saghazadeh, E. Soltaninejad and A. Rezaei et al., 2017. PTPN22 single-nucleotide polymorphisms in Iranian patients with type 1 diabetes mellitus. Immunol. Invest., 46: 409-418.
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Abdollahzade, S., A. Aghamohammadi, H. Soheili, M. Salehi Sadaghiani, H. Abolhassani and N. Rezaei, 2011. The clinical immunological and long-term follow-up of pediatric patients with common variable immunodeficiency. Tehran Univ. Med. J., 68: 600-610.
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Abolhassani, H., A. Aghamohammadi, S. Pourjabbar, M.S. Sadaghiani, S. Nikayin, A. Rabiee and N. Rezaei, 2013. Psychiatric aspects of primary immunodeficiency diseases: the parental study. Iran. J. Allergy Asthma Immunol., 12: 176-181.
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Abolhassani, H., B. Gharib, S. Shahinpour, S.N. Masoom and A. Havaei et al., 2015. Autoimmunity in patients with selective IgA deficiency. J. Investig. Allergol. Clin. Immunol., 25: 112-119.
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Abolhassani, H., B. Mirminachi, M. Daryabeigi, Z. Agharahimi, A. Aghamohammadi, A. Rabbani and N. Rezaei, 2014. Evaluation of physicians' awareness of pediatric diseases in iran. Iran. J. Pediatr., 24: 87-92.
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Abolhassani, H., B.T. Sagvand, T. Shokuhfar, B. Mirminachi, N. Rezaei and A. Aghamohammadi, 2013. A review on guidelines for management and treatment of common variable immunodeficiency. Exp. Rev. Clin. Immunol., 9: 561-575.
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Abolhassani, H., D. Amirkashani, N. Parvaneh, P. Mohammadinejad and B. Gharib et al., 2013. Autoimmune phenotype in patients with common variable immunodeficiency. J. Investig. Allergol. Clin. Immunol., 23: 323-329.
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Abolhassani, H., E.S. Edwards, A. Ikinciogullari, H. Jing and S. Borte et al., 2017. Combined immunodeficiency and Epstein-Barr virus-induced B cell malignancy in humans with inherited CD70 deficiency. J. Exp. Med., 214: 91-106.
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Abolhassani, H., F. Akbari, B. Mirminachi, S. Bazregari, E. Hedayat, N. Rezaei and A. Aghamohammadi, 2014. Morbidity and mortality of iranian patients with hyper igm syndrome: a clinical analysis. Iran. J. Immunol., 11: 123-133.
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Abolhassani, H., M. Vitali, V. Lougaris, S. Giliani and N. Parvaneh et al., 2016. Cohort of Iranian patients with congenital agammaglobulinemia: Mutation analysis and novel gene defects. Exp. Rev. Clin. Immunol., 12: 479-486.
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Abolhassani, H., M.H. Asgardoon, N. Rezaei, L. Hammarstrom and A. Aghamohammadi, 2015. Different brands of intravenous immunoglobulin for primary immunodeficiencies: How to choose the best option for the patient? Exp. Rev. Clin. Immunol., 11: 1229-1243.
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Abolhassani, H., N. Abolhassani, P. Mohammadinejad, B. Mirminachi, L. Hammarstrom and A. Aghamohammadi, 2015. Important differences in the diagnostic spectrum of primary immunodeficiency in adults versus children. Expert Rev. Clin. Immunol., 11: 289-302.
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Abolhassani, H., N. Parvaneh, N. Rezaei, L. Hammarstrom and A. Aghamohammadi, 2014. Genetic defects in b-cell development and their clinical consequences.. J. Invest. Allergol Clin. Immunol., 24: 6-22.
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Abolhassani, H., N. Wang, A. Aghamohammadi, N. Rezaei and Y.N. Lee, 2014. A hypomorphic recombination-activating gene 1 (RAG1) mutation resulting in a phenotype resembling common variable immunodeficiency. Iran. J. Allergy Clin. Immunol., 134: 1375-1380.
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Abolhassani, H., T. Cheraghi, N. Rezaei, A. Aghamohammadi and L. Hammarstrom, 2014. Common variable immunodeficiency or late-onset combined immunodeficiency: A new hypomorphic JAK3 patient and review of the literature. J. Invest. Allergol. Clin. Immunol., 25: 218-220.
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Aflatounian, M., H. Smith, F. Farahani, A.T. Naeem and A. Straatman-Iwanowska et al., 2016. Novel VIPAS39 mutation in a syndromic patient with arthrogryposis, renal tubular dysfunction and intrahepatic cholestasis. Eur. J. Med. Genet., 59: 237-239.
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Aghamohammadi, A., A. Bahrami, S. Mamishi, B. Mohammadi, H. Abolhassani, N. Parvaneh and N. Rezaei, 2011. Impact of delayed diagnosis in children with primary antibody deficiencies. J. Microbiol. Immunol Infect., 44: 229-234.
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Aghamohammadi, A., A. Farhoudi, M. Moin, Z. Pourpak and N. Rezaei et al., 2003. Adverse effects of intravenous immunoglobulin therapy in patients with antibody deficiency. Iran. J. Allergy Asthma. Immunol., 2: 121-126.
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Aghamohammadi, A., A. Farhoudi, M. Moin, Z. Pourpak and N. Rezaeiet al., 2002. 20-year survey of infectious complications in 64 patients with common variable immunodeficiency. Med. J. IR. Iran, 16: 123-128.
Aghamohammadi, A., A. Farhoudi, M. Nikzad, M. Moin and Pourpaket al ., 2004. Adverse reactions of intravenous immunoglobulin therapy in patients with primary immunodeficiencies. Ann. Allergy Asthma Immunol., 92: 60-64.
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Aghamohammadi, A., A. Montazeri, H. Abolhassani, S. Saroukhani and S. Pourjabbar, 2011. Health-related quality of life in primary antibody deficiency. Iran J. Allergy Asthma Immunol. 10: 47-51.
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Aghamohammadi, A., F. Jalali, A. Farhoudi, Z. Pourpak and N. Rezaei et al., 2001. Ear, nose and throat manifestations in patients with antibody deficiencies. Acta Med. Iran., 39: 164-168.
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Aghamohammadi, A., H. Abolhassani, A.H. Latif, F. Tabassomi and T. Shokuhfar et al., 2014. Long-term evaluation of a historical cohort of Iranian common variable immunodeficiency patients. Expert Rev. Clin. Immunol., 10: 1405-1417.
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Aghamohammadi, A., H. Abolhassani, J. Puchalka, N. Greif-Kohistani, S. Zoghi, C. Klein and N. Rezaei, 2017. Preference of genetic diagnosis of CXCR4 mutation compared with clinical diagnosis of WHIM syndrome. J. Clin. Immunol., 37: 282-286.
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Aghamohammadi, A., M. Mahmoodi, N. Rezaei, Z. Safari, D. Heidarnasab, K. Divsalar and M.A. Mohagheghi, 2011. The assessment of antibody response following immunization with polysaccharide vaccine in patients with chronic kidney disease. Tehran Univ. Med. J., 69: 92-98.
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Aghamohammadi, A., M. Moein, A. Farhondi, Z. Puurpak and M. Movahedi et al., 2000. The clinical spectrum of respiratory diseases in patients with primary antibody deficiency. Iran. J. Allergy Asthma Immunol., 1: 135-140.
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Aghamohammadi, A., M. Moein, A. Farhoudi, Z. Pourpak and N. Rezaei et al., 2002. Primary immunodeficiency in Iran: First report of the national registry in children and adults J. Clin. Immunol., 22: 375-380.
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Aghamohammadi, A., M. Moin, A. Farhoudi, N. Rezaei and Z. Pourpaket al., 2004. Efficacy of intravenous immunoglobulin in prevention of pneumonia in patients with agammaglobulinemia. FEMS Immunol. Med. Microbiol., 40: 113-118.
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Aghamohammadi, A., M. Moin, A. Farhoudi, Z. Pourpak and N. Rezaei et al ., 2002. The spectrum of primary immunodeficiency in Iran. Acta Med. Iran, 40: 165-170.
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Aghamohammadi, A., P. Mohammadinejad, H. Abolhassani, B. Mirminachi and M. Movahedi et al., 2014. Primary immunodeficiency disorders in Iran: update and new insights from the third report of the national registry. J. Clin. Immunol., 34: 478-490.
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Aghamohammadi, A., Z.G. Moghaddam, H. Abolhassani, Z. Hallaji and H. Mortazavi et al., 2014. Investigation of underlying primary immunodeficiencies in patients with severe atopic dermatitis. Allergologia et Immunopathologia, 42: 336-341.
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Ahmadi-Nejad, Z., M. Rasouli-Nejad, M. Mahmoudi and N. Rezaei, 2003. The survey of liver complications in patients with brucellosis in imam hospital during 1995 to 2001. J. Faculty Med., 61: 144-152.
Al-Herz. W., H. Aldhekri, M.R. Barbouche and N. Rezaei, 2014. Consanguinity and primary immunodeficiencies. Hum. Heredity, 77: 138-143.
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Alahgholi-Hajibehzad, M., P. Kasapoglu, R. Jafari and N. Rezaei, 2015. The role of T regulatory cells in immunopathogenesis of myasthenia gravis: Implications for therapeutics. Expert Rev. Clin. Immunol., 11: 859-870.
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Alipour, S., S. Zoghi, N. Khalili, A. Hirbod-Mobarakeh, L.A. Emens and N. Rezaei, 2016. Specific immunotherapy in ovarian cancer: A systematic review. Immunotherapy, 8: 1193-1204.
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Alizadeh, M., L.G. Hashtroodi, Z. Chavoshzadeh and N. Rezaei, 2016. Effect of air pollution in frequency of hospitalizations in asthmatic children. Acta Medica Iranica, 54: 542-546.
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Alkhairy, O.K., H. Abolhassani, N. Rezaei, M. Fang and K.K. Andersen et al., 2016. Spectrum of phenotypes associated with mutations in LRBA. J. Clin. Immunol., 36: 33-45.
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Alkhairy, O.K., N. Rezaei, R.R. Graham, H. Abolhassani and S. Borte et al., 2015. RAC2 loss-of-function mutation in 2 siblings with characteristics of common variable immunodeficiency. J. Allergy Clin. Immunol., 135: 1380-1384.
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Alkhairy, O.K., R. Perez-Becker, G.J. Driessen, H. Abolhassani and J. van Montfrans et al., 2015. Novel mutations in TNFRSF7/CD27: Clinical, immunologic and genetic characterization of human CD27 deficiency. J. Allergy Clin. Immunol., 136: 703-712.
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Ameli, S., M. Zenker, A. Zare-Shahabadi, E.S. Taher, A. Madani, M. Monajemzadeh and N. Rezaei, 2013. Novel nphs1 gene mutation in an iranian patient with congenital nephrotic syndrome of the finnish type. Nefrologia (Madrid), 33: 747-749.
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Amirzargar, A., F. Shahram, E. Nikoopour, N. Rezaei, K. Saeedfar, N. Ziaei and F. Davatchi, 2010. Proinflammatory cytokine gene polymorphisms in Behcet`s disease. Eur. Cytokine Netw., 21: 292-296.
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Amirzargar, A.A., A. Yalda, M. Hajabolbaghi, F. Khosravi and H. Jabbariet al., 2004. The association of HLA-DRB, DQA1, DQB1 alleles and haplotypes frequency in Iranian patients with pulmonary tuberculosis Int. J. Tuberc. Lung. Dis., 8: 1017-1021.
PubMed  |  
Andalib, M.M., M.M. Malekzadeh, Z. Agharahimi, M. Daryabeigi and B. Yaghmaei et al., 2015. Evaluation of educational environment for medical students of a tertiary pediatric hospital in Tehran, using DREEM questionnaire. Iran. J. Pediatrics, Vol. 25. 10.5812/ijp.2362.
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Arshi, S., A. Bahrami, M. Faranoush, A. Mehrvar and N. Rezaei, 2014. Non-Hodgkin's lymphoma in a patient with leucocyte adhesion deficiency. Allergologia et Immunopathologia, 42: 379-380.
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Arshi, S., M. Nabavi, M.H. Bemanian, R. Shakeri and B. Taghvaei et al., 2016. Phenotyping and follow up of forty-seven Iranian patients with common variable immunodeficiency. Allergologia et Immunopathologia, 44: 226-231.
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Aryan, Z and N. Rezaei, 2013. Comment on 'allergy and acute leukaemia in children with down syndrome: a population study. report from the mexican inter institutional group for the identification of the causes of childhood leukaemia (migiccl)'-is increased surveillance by hypersensitive immune system a reality or myth? Br. J. Cancer, 109: 1386-1388.
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Aryan, Z. and N. Rezaei, 2015. Toll-like receptors as targets for allergen immunotherapy. Curr. Opin. Allergy Clin. Immunol., 15: 568-574.
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Aryan, Z., A. Aghamohammadi and N. Rezaei, 2016. Toward the stratification and personalization of common variable immunodeficiency treatment. Expert Opin. Orphan Drugs, 4: 823-830.
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Aryan, Z., E. Comapalati, G.W. Canonica and N. Rezaei, 2013. Allergen-specific immunotherapy in asthmatic children: from the basis to clinical applications. Expert. Rev. Vaccines, 12: 639-659.
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Aryan, Z., N. Rezaei and C.A. Camargo Jr., 2017. Vitamin D status, aeroallergen sensitization and allergic rhinitis: A systematic review and meta-analysis. Int. Rev. Immunol., 36: 41-53.
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Aryan, Z., S.T. Holgate, D. Radzioch and N. Rezaei, 2014. A new era of targeting the ancient gatekeepers of the immune system: toll-like agonists in the treatment of allergic rhinitis and asthma. Int. Arch. Allergy Immunol., 164: 46-63.
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Ashrafi, M.R., D. Amirkashani, A. Hirbod-Mobarakeh, B. Yaghmaei, A. Tavassoli, F. Manafi and N. Rezaei, 2013. Acute disseminated encephalomyelitis mimicking acute meningoencephalitis. Acta Clin. Croat., 52: 523-528.
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Ashtiani, M.T.H., S. Mamishi, A. Masoomi, N. Nasiri, M. Hosseini, B. Nikmanesh and N. Rezaei, 2013. Antimicrobial susceptibility associated with bloodstream infections in children: a referral hospital-based study. Braz. J. Infect. Dis., 17: 497-499.
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Aslani, S., M. Mahmoudi, A. Salmaninejad, S. Poursani, V. Ziaee and N. Rezaei, 2017. Lack of association between STAT4 single nucleotide polymorphisms and Iranian juvenile rheumatoid arthritis patients. Fetal Pediatr. Pathol., (In Press). 10.1080/15513815.2016.1253809.
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Assari, R., Y. Aghighi, V. Ziaee, M. Sadr and A. Rezaei et al., 2016. Interleukin-4 cytokine single nucleotide polymorphisms in Kawasaki disease: A case-control study and a review of knowledge. Int. J. Rheumatic Dis., (In Press). 10.1111/1756-185X.12968.
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Assari, R., Y. Aghighi, V. Ziaee, M. Sadr and F. Rahmani et al., 2016. Pro-inflammatory cytokine single nucleotide polymorphisms in Kawasaki disease. Int. J. Rheumatic Dis., (In Press). 10.1111/1756-185X.12911.
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Ataee, P., M. Najafi, M. Gharagozlou, M. Aflatounian and M. Mahmoudi et al., 2014. Effect of supplementary zinc on body mass index, pulmonary function and hospitalization in children with cystic fibrosis. Turk. J. Pediatr., 56: 127-132.
PubMed  |  Direct Link  |  
Ataeinia, B., A. Montazeri, M. Tavakol, G. Azizi and F. Kiaee et al., 2017. Measurement of health-related quality of life in primary antibody-deficient patients. Immunol. Invest., 46: 329-340.
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Atarod, L., A. Raissi, A. Aghamohammadi, A. Farhoudi and A. Khodadad et al ., 2003. The review of gastrointestinal disorders in patients with primary antibody immunodeficiencies during the 10-year period (1990-2000) in children's medical center. Iran J. Allergy Asthma. Immunol., 2: 75-79.
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Avitzur, Y., C. Guo, L.A. Mastropaolo, E. Bahrami and H. Chen et al., 2014. Mutations in tetratricopeptide repeat domain 7A result in a severe form of very early onset inflammatory bowel disease. Gastroenterol., 146: 1028-1039.
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Aydin, S.E., S.S. Kilic, C. Aytekin, A. Kumar and O. Porras et al., 2015. DOCK8 Deficiency: Clinical and immunological phenotype and treatment options - a review of 136 patients. J. Clin. Immunol., 35: 189-198.
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Ayenehdeh, J.M., B. Niknam, S.M. Hashemi, H. Rahavi, N. Rezaei, M. Soleimani and N. Tajik, 2017. Introducing a new experimental islet transplantation model using biomimetic hydrogel and a simple high yield islet isolation technique. Iran. Biomed. J., 21: 218-227.
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Azimi, M., A. Aghamohammadi, H.D. Ochs and N. Rezaei, 2016. Soluble molecules in intravenous immunoglobulin: Benefits and limitations. Exp. Rev. Clin. Immunol., 12: 99-101.
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Azizi, G., A. Ghanavatinejad, H. Abolhassani, R. Yazdani, N. Rezaei, A. Mirshafiey and A. Aghamohammadi, 2016. Autoimmunity in primary T-cell immunodeficiencies. Expert Rev. Clin. Immunol., 12: 989-1006.
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Azizi, G., H. Abolhassani, M.H. Asgardoon, J. Rahnavard and R. Yazdani et al., 2016. The use of immunoglobulin therapy in primary immunodeficiency diseases. Endocrine Metab. Immune Disord.-Drug Targets, 16: 80-88.
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Azizi, G., H. Abolhassani, M.H. Asgardoon, S. Shaghaghi and B. Negahdari et al., 2016. Managing patients with side effects and adverse events to immunoglobulin therapy. Expert Rev. Clin. Pharmacol., 9: 91-102.
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Azizi, G., H. Abolhassani, M.H. Asgardoon, T. Alinia and R. Yazdani et al., 2017. Autoimmunity in common variable immunodeficiency: Epidemiology, pathophysiology and management. Expert Rev. Clin. Immunol., 13: 101-115.
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Azizi, G., M. Ahmadi, H. Abolhassani, R. Yazdani and H. Mohammadi et al., 2016. Autoimmunity in primary antibody deficiencies. Int. Arch. Allergy Immunol., 171: 180-193.
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Azizi, G., N. Rezaei, F. Kiaee, N. Tavakolinia, R. Yazdani, A. Mirshafiey and A. Aghamohammadi, 2016. T-cell abnormalities in common variable immunodeficiency. J. Invest. Allergol. Clin. Immunol., 26: 233-243.
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Bahrami, T., S. Soltani, K. Moazzami, M.S. Yekaninejad and A. Salmaninejad et al., 2017. Association of PTPN22 gene polymorphisms with susceptibility to juvenile idiopathic arthritis in Iranian population. Fetal Pediatr. Pathol., 36: 42-48.
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Bahramsoltani, R., H.R. Sodagari, M.H. Farzaei, A.H. Abdolghaffari, M. Gooshe and N. Rezaei, 2016. The preventive and therapeutic potential of natural polyphenols on influenza. Expert Rev. Anti-Infective Ther., 14: 57-80.
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Barkhordari, E., A.A. Amirzargar, N. Ebrahimi-Daryani, M. Mahmoudi and B. Ansaripour et al., 2011. Lack of association between interleukin 12 C(-1188)A polymorphism and irritable bowel syndrome. Avicenna J. Med. Biotechnol., 3: 45-48.
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Bashashati, M., N. Rezaei, A. Shafieyoun, D.P. McKernan and L. Chang et al., 2014. Cytokine imbalance in irritable bowel syndrome: a systematic review and meta-analysis. Neurogastroenterology Motil., 26: 1036-1048.
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Bazvand, F., S. Shams, M.B. Esfahani, L. Koochakzadeh, M. Monajemzadeh, M.T. Haghi Ashtiani and N. Rezaei, 2011. Total antioxidant status in patients with major β-thalassemia. Iran J. Pediatr. 21: 159-165.
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Behniafard, N., M. Gharagozlou, S. Sotoudeh, E. Farhadi and M. Khaledi et al., 2014. Association of single nucleotide polymorphisms of interleukin-1 family with atopic dermatitis. Allergologia et Immunopathologia, 42: 212-215.
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Belkadi, A., V. Pedergnana, A. Cobat, Y. Itan and Q.B. Vincent et al., 2016. Whole-exome sequencing to analyze population structure, parental inbreeding and familial linkage. Proc. Nat. Acad. Sci., 113: 6713-6718.
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Bidoki, A.Z., S. Harsini, M. Sadr, S. Soltani, M. Mohammadzadeh, S. Najafi and N. Rezaei, 2016. NLRP3 gene polymorphisms in Iranian patients with recurrent aphthous stomatitis. J. Oral Pathol. Med., 45: 136-140.
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Boztug, K., P.M. Jarvinen, E. Salzer, T. Racek and S. Monch et al., 2014. JAGN1 deficiency causes aberrant myeloid cell homeostasis and congenital neutropenia. Nat. Genet., 46: 1021-1027.
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Canessa, C., F. Romano, F. Lippi, L. Bianchi, S. Kashef, N. Rezaei and C. Azzari, 2013. Bcgitis and vaccine-derived poliovirus infection in a patient with a novel deletion in RAG1 binding site. Int. J. Immunopathol. Pharmacol., 26: 511-515.
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Cheraghi, T., A. Aghamohammadi, B. Mirminachi, T. Keihanian and E. Hedayat et al., 2014. Prediction of the evolution of common variable immunodeficiency: HLA typing for patients with selective IgA deficiency. J. Investig. Allergol. Clin. Immunol., 24: 192-211.
PubMed  |  Direct Link  |  
Daryani, N.E., F.N. Varzaneh, M. Hedayat, M. Taher and E. Farhadi et al., 2014. Interleukin-23 receptor single nucleotide polymorphisms in ulcerative colitis. A study in Iranian populations. Clin. Res. Hepatol. Gastroenterol., 38: 360-365.
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Daryani, N.E., M. Sadr, S. Moossavi, S. Shahkarami, S. Soltani, E. Farhadi and N. Rezaei, 2014. Significance of IL -1RA polymorphism in iranian patients with inflammatory bowel disease. Digestive Dis. Sci., 60: 1389-1395.
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Ebadi, M., A. Aghamohammadi, N. Rezaei, 2015. Primary immunodeficiencies: a decade of shifting paradigms, the current status and the emergence of cutting-edge therapies and diagnostics. Expert Rev. Clin. Immunol., 11: 117-139.
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Emami, S., V. Ziaee, A. Rezaei, M. Sadr, M. Maddah, A.A. Amirzargar and N. Rezaei, 2016. IL23R gene polymorphism with juvenile idiopathic arthritis and its association with serum IL-17A. Int. J. Rheumatic Dis., 19: 1189-1196.
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Eskian, M., M. Khorasanizadeh, F. Kraeber-Bodere and N. Rezaei, 2016. Radioimmunotherapy in non-Hodgkin lymphoma: Prediction and assessment of response. Crit. Rev. Oncol./Hematol., 107: 182-189.
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Esmaeilzadeh, H., M. Nabavi, A.A. Amirzargar, Z. Aryan and S. Arshi et al., 2015. HLA-DRB and HLA-DQ genetic variability in patients with aspirin-exacerbated respiratory disease. Am. J. Rhinol. Allergy, 29: e63-e69.
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Esmaeilzadeh, H., M.H. Bemanian, M. Nabavi, S. Arshi and M. Fallahpour et al., 2015. Novel patient with late-onset familial hemophagocytic lymphohistiocytosis with stxbp2 mutations presenting with autoimmune hepatitis, neurological manifestations and infections associated with hypogammaglobulinemia. J. Clin. Immunol., 35: 22-25.
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Fadakar, K., S. Dadkhahfar, A. Esmaeili and N. Rezaei, 2014. The role of toll-like receptors (TLRs) in stroke. Rev. Neurosci., 25: 699-712.
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Fallahi, G., A. Aghamohammadi, A. Khodadad, M. Hashemi, P. Mohammadinejad, H. Asgarian-Omran, and N. Rezaei, 2014. Evaluation of antibody response to polysaccharide vaccine and switched memory b cells in pediatric patients with inflammatory bowel disease. Gut liver, 8: 24-28.
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Fallahi, G., F. Motamed, A. Yousefi, A. Shafieyoun, M. Najafi, A. Khodadad and N. Rezaei, 2013. The effect of probiotics on fecal calprotectin in patients with cystic fibrosis. Turk. J. Pediatr., 55: 475-478.
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Fallahi, G.H., M. Sabbaghian, M. Khalili, N. Parvaneh, M. Zenker and N. Rezaei, 2011. Novel UBR1 gene mutation in a patient with typical phenotype of Johanson-Blizzard syndrome. Eur. J. Pediatr., 170: 233-235.
PubMed  |  
Fallahi, G.H., N. Rezaei and N. Sadjadei, 2013. Bloody diarrhea as a presentation manifestation of familial mediterranean fever in a patient with compound heterozygote mutations of the MEFV gene. Gut liver, 7: 497-499.
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Fallahi, G.H., S. Latifi, M. Mahmoudi, D. Kushki, M.T.H. Ashtiani, A. Morteza and N. Rezaei, 2016. Growth status and its relationship with serum lipids and albumin in children with cystic fibrosis. Acta Med. Iran., 54: 276-279.
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Farahmand, F., K. Soleimani, M. Hashemi, A. Shafieyoun, N. Rezaei and A. Yousefi, 2013. Familial congenital hepatic fibrosis: report of a family with three affected children. Acta Med. Iran., 51: 655-656.
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Farahmand, F., M. Khalili, L. Shahbaznejad, A. Hirbod-Mobarakeh, M.N. Sani, A. Khodadad and N. Rezaei, 2013. Clinical presentation of cystic fibrosis at the time of diagnosis: a multicenter study in a region without newborn screening. Turk. J. Gastroenterol., 24: 541-545.
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Farhadi, E., S. Nemati, A.A. Amirzargar, A. H. Mobarakeh and M. Nabavi et al., 2014. AICDA single nucleotide polymorphism in common variable immunodeficiency and selective IgA deficiency. Allergologia et Immunopathologia, 42: 422-426.
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Farhoudi, A., Z. Chavoshzadeh, Z. Pourpak, M. Izadyar and M. Gharagozlouet al., 2003. Report of six cases of Chediak-Higashi Syndrome with regard to clinical and laboratory finding. Iran J. Allergy Asthma Immunol., 2: 189-192.
PubMed  |  
Farrokhi, S., N. Abbasirad, A. Movahed, H.A. Khazaei, M. Pishjoo and N. Rezaei, 2017. TLR9-based immunotherapy for the treatment of allergic diseases. Immunotherapy, 9: 339-346.
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Farrokhi, S., T. Mousavi, S. Arshi, A. Varasteh, N. Rezaei and A. Salekmoghadam, 2011. Co-administration of Chenopodium album allergens and CpG oligodeoxy-nucleotides effects on peripheral blood mononuclear cells of patients with allergic rhinitis treated with intranasal corticosteroids and antihistamines. Iran J. Allergy Asthma Immunol., 10: 101-110.
PubMed  |  
Farrokhi, S., T. Mousavi, S. Arshi, N. Javahertarash and A. Varasteh et al., 2010. Effect of treatment with intranasal corticosteroid and oral antihistamine on cytokine profiles of peripheral blood mononuclear cells of patients with allergic rhinitis sensitive to Chenopodium album. Iran J. Allergy Asthma Immunol., 9: 225-230.
PubMed  |  
Farzaei, M.H., R. Bahramsoltani, A.H. Abdolghaffari, H.R. Sodagari, S.A. Esfahani and N. Rezaei, 2016. A mechanistic review on plant-derived natural compounds as dietary supplements for prevention of inflammatory bowel disease. Exp. Rev. Gastroenterol. Hepatol., 10: 745-758.
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Farzaei, M.H.F., F. Farzaei, M. Gooshe, Z. Abbasabadi, N. Rezaei and A.H. Abdolghaffari, 2015. Potentially effective natural drugs in treatment for the most common rheumatic disorder: Osteoarthritis. Rheumatology Int., 35: 799-814.
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Fathi, S.M., M. Tavakol, N. Rezaei, M. Movahedi and A. Aghamohammadi et al., 2016. Impact of IgE-mediated food allergy on parental quality of life in Iranian patients. Iran. J. Allergy Asthma Immunol., 15: 372-380.
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Fazel, A., S. Kashef, S. Aleyasin, S. Harsini and Z. Karamizadeh et al., 2017. Novel AICDA mutation in a case of autosomal recessive hyper-IgM syndrome, growth hormone deficiency and autoimmunity. Allergologia Immunopathologia, 45: 82-86.
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Gamez-Diaz, L., D. August, P. Stepensky, S. Revel-Vilk and M.G. Seidel et al., 2016. The extended phenotype of LPS-responsive beige-like anchor protein (LRBA) deficiency. J. Allergy Clin. Immunol., 137: 223-230.
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Ghanadan, A., A. Saghazadeh, I. Jahanzad and N. Rezaei, 2015. Clinical aspects of indirect immunofluorescence for autoimmune diseases. Expert Rev. Clin. Immunol., 11: 597-616.
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Ghanadan, A., A. Saghazadeh, M. Daneshpazhooh and N. Rezaei, 2015. Direct immunofluorescence for immunobullous and other skin diseases. Expert Rev. Clin. Immunol., 11: 589-596.
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Gharagozlou, M., E. Farhadi, M. Khaledi, N. Behniafard, S. Sotoudeh, R. Salari and N. Rezaei, 2013. Association between the interleukin 6 genotype at position-174 and atopic dermatitis. J. Investig. Allergol. Clin. Immunol., 23: 89-93.
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Gharagozlou, M., N. Behniafard, A.A. Amirargar, S. Hosseinverdi and S. Sotoudeh et al., 2015. Association between single nucleotide polymorphisms of the interleukin-4 gene and atopic dermatitis. Acta Dermatovenerol. Croatica, Vol. 23. .
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Ghazi, B.M., R. Imamzadehgan, A. Aghamohammadi, R.D. Davari and N. Rezaei, 2003. Frequency of allergic rhinitis in school-age children (7-18 years) in Tehran. Iran. J. Allergy Asthma Immunol., 2: 181-184.
PubMed  |  
Gholami, K., E. Laali, H. Abolhassani, A. Ahmadvand and N. Mohebbi et al., 2017. Costs of hospital admission on primary immunodeficiency diseases. Iran. J. Public Health, 46: 342-350.
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Givtaj, N., M. Daylami, H.R. Alaie, N. Rezaei and M. Khodarahmi, 2004.. Survey of fontan and total cavopulmonary connection in patients with single ventricle. Iran Heart J., 5: 23-29.
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Gooshe, M., A.R. Aleyasin, A.H. Abdolghaffari and N. Rezaei, 2014. Toll like receptors: a new hope on the horizon to treat multiple sclerosis. Expert Rev. Clin. Immunol., 10: 1277-1279.
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Gooshe, M., M.H. Abdolghaffari, M.E. Gambuzza and N. Rezaei, 2014. The role of Toll-like receptors in multiple sclerosis and possible targeting for therapeutic purposes. Rev. Neurosci., 25: 713-739.
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Hadi, N., S. Kashef, M. Moazzen, M. Shamoon Pour and N. Rezaei, 2011. Survey of Mycoplasma pneumoniae in Iranian children with acute lower respiratory tract infections. Braz. J. Infect Dis., 15: 97-101.
PubMed  |  Direct Link  |  
Hanaei, S., S. Abdollahzade, A. Khoshnevisan, C.K. Kepler and N. Rezaei, 2015. Genetic aspects of intervertebral disc degeneration. Rev. Neurosci., 26: 581-606.
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Harsini, S., M. Beigy, M. Akhavan-Sabbagh and N. Rezaei, 2014. Toll-like receptors in lymphoid malignancies: double-edged sword. Crit. Rev. Oncol/Hematol., 89: 262-283.
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Harsini, S., V. Ziaee, F. Tahghighi, M. Mahmoudi and A. Rezaei et al., 2016. Association of interleukin-2 and interferon-γ single nucleotide polymorphisms with Juvenile systemic lupus erythematosus. Allergologia Immunopathologia, 44: 422-426.
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Harsini, S., V. Ziaee, M. Maddah, A. Rezaei and M. Sadr et al., 2015. Interleukin 10 and transforming growth factor beta 1 gene polymorphisms in juvenile idiopathic arthritis. Bratislavske Lekarske Listy, 117: 258-262.
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Hekmat, M., M. Foroughi, H.R. Taghipour, S.A. Hasantash, M. Monfaredet al., 2004. Metastatic sarcoma invasion through pulmonary vein to left atrium; an unusual way of metastasis. Iran Heart J., 5: 53-60.
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Hirbod-Mobarakeh, A., A. Aghamohammadi and N. Rezaei, 2014. Immunoglobulin class switch recombination deficiency type 1 or CD40 ligand deficiency: from bedside to bench and back again. Expert Rev. Clin. Immunol., 10: 91-105.
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Hirbod-Mobarakeh, A., H.A. Gordan, Z. Zahiri, M. Mirshahvalad, S. Hosseinverdi, B.I. Rini and N. Rezaei, 2016. Specific immunotherapy in renal cancer: A systematic review. Therapeut. Adv. Urol., 9: 45-58.
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Hirbod-Mobarakeh, A., M. Mirghorbani, F. Hajiju, M. Marvi, K. Bashiri and N. Rezaei, 2016. Myeloid-derived suppressor cells in gastrointestinal cancers: A systematic review. J. Gastroenterol. Hepatol., 31: 1246-1256.
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Horvath, Z., N. Rezaei, I. Reisli, I. Tuzankina, N. Otarbayev, P. Popandopulo and L. Marodi, 2013. The spread of the j project. J. Clin. Immunol., 33: 1037-1042.
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Hosseinverdi, S., H. Hashemi, A. Aghamohammadi, H.D. Ochs and N. Rezaei, 2014. Ocular involvement in primary immunodeficiency diseases. J. Clin. Immunol., 34: 23-28.
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Jalilian, R., N. Rezaei, 2013. Genetics of mondini malformation. Acta Med. Iran., 51: 345-346.
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Jandaghi, A.B., S. Daliri, M. Kikkawa, M. Khaledi and N. Soleimanifar et al., 2013. The discovery of a Persian family with a form of Birt-Hogg-Dube syndrome lacking the typical cutaneous stigmata of the syndrome. Clin. Imaging, 37: 111-115.
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Jessen, B., S.F. Bode, S. Ammann, S. Chakravorty and G. Davies et al., 2013. The risk of hemophagocytic lymphohistiocytosis in hermansky-pudlak syndrome type 2. Blood, 121: 2943-2951.
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Kashef, S., M. Moghtaderi, M. Borzouee and N. Rezaei, 2011. Giant aneurysm of thoracic and proximal abdominal aorta in a patient with common variable immunodeficiency. Iran J. Allergy Asthma Immunol., 10: 133-137.
PubMed  |  
Kasraianfard, A., K.D. Watt, L. Lindberg, S. Alexopoulos and N. Rezaei, 2016. HBIG remains significant in the era of new potent nucleoside analogues for prophylaxis against hepatitis B recurrence after liver transplantation. Int. Rev. Immunol., 35: 312-324.
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Khaledi, M., A. Fotouhi, E. Farhadi, B. Mahdaviani and S. Sotoudeh et al., 2014. Filaggrin single nucleotide polymorphisms in atopic dermatitis. Acta Dermatovenerol Croat, 22: 200-204.
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Khalili, A., A. Plebani, M. Vitali, H. Abolhassani and V. Lougaris et al., 2014. Autosomal recessive agammaglobulinemia: a novel non-sense mutation in CD79a. J. Clin. Immunol., 34: 138-141.
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Khanbabaee, G., A. Omidian, F. Imanzadeh, F. Adibeshgh, M. Ashayeripanah and N. Rezaei, 2014. Serum level of zinc in asthmatic patients: A case-control study. Allergol. Immunopathol., 42: 19-21.
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Khanbabaee, G., M.H. Yeganeh, S.A. Tabatabaei, A. Khatami, S. Bazrafshan and N. Rezaei, 2010. Langerhans cell histiocytosis with pulmonary involvement and unilateral pneumothorax. Turk. J. Pediatr., 52: 638-641.
PubMed  |  
Khanbabaee, G., S.A. Tabatabaei, F. Rahimpoor, A. Khatami, F. Jadali, J. Ghoroobi and N. Rezaei, 2012. Congenital pulmonary airway malformation. Bratisl. Lek. Listy, 114: 587-589.
PubMed  |  
Khazaei, H.A., A. Aghamohammadi, N. Rezaei, B. Nikbin and M.A. Khosraviet al ., 2004. Major histocompatibility complex class I and II antigens frequencies in Baloch ethnic group living in the south-east region of Iran. Transplant Proc., 36: 1302-1304.
PubMed  |  
Khazaei, H.A., B. Teymuri, A. Nakhaei, M. Mohammadi, M. Noura, A. Khazaei and N. Rezaei, 2013. Association of haptoglobin phenotypes with clinical features of preterm labor disease. Acta Med. Iran., 51: 554-559.
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Khazaei, H.A., B. Teymuri, A. Nakhaei, M. Mohammadi, M. Noura, A. Khazaei and N. Rezaei, 2014. Evaluation of haptoglobin phenotypes in association with clinical features of patients suffered from preterm labor disease. Acta Med. Iran., 52: 106-110.
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Khazaei, H.A., S.R. Hashemi, A. Aghamohammadi, F. Farhoudi and N. Rezaei, 2003. Common allergens in patients with allergic disorders in Zahedan. Tabib-e-Shargh, 4: 149-154.
Khazaei, H.A., S.R. Hashemi, A. Aghamohammadi, F. Farhoudi and N. Rezaei, 2003. The study of type 1 allergy prevalence among people of South-East of Iran by skin prick test using common allergens. Iran J. Allergy Asthma Immunol., 2: 165-168.
PubMed  |  
Khodadad, A., E. Elahi, S.S.B. Hassani, P. Rouhani, B. Sadeghi and N. Rezaei, 2015. Frequency of genotype with ΔF508 mutation in CFTR gene among Iranian cystic fibrosis patients with pancreatic insufficiency. Iran. J. Pediatrics, Vol. 25. 10.5812/ijp.3419.
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Khodadad, A., M. Aflatoonian, R. Jalilian, N. Babaei and F. Motamed et al., 2016. Comparison of oral midazolam with intravenous midazolam for sedation children during upper gastrointestinal endoscopy. Acta Medica Iranica, 54: 576-582.
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Khorasanizadeh, M., M. Eskian, A.H. Assa'ad, C.A. Jr. Camargo and N. Rezaei, 2016. Efficacy and safety of benralizumab, a monoclonal antibody against IL-5Rα, in uncontrolled eosinophilic asthma. Int. Rev. Immunol., 35: 294-311.
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Kiani-Amin, M., M.M. Daneshi, P. Ayazi, S. Mohammadian and N. Rezaei, 2011. Serum immunoglobulin levels in splenectomized and non splenectomized patients with major beta thalassemia. Iran J. Pediatr., 21: 95-98.
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Koochakzadeh, L., M.H. Khosravi, B. Pourakbari, S. Hosseinverdi, A. Aghamohammadi and N. Rezaei, 2014. Immune response following immunization with dtp/td and mmr vaccines in children treated for acute lymphoblastic leukemia. Pediatr. Hematol. Oncol., 31: 656-663.
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Koochakzadeh, L., S. Hosseinverdi, M. Hedayat, F. Farahani and A. Tofighi et al., 2015. Study of immunodeficiency in pediatric patients with lymphoma. Allergol. Immunopathol., 43: 568-570.
Larki, P., S. Khoshbakht and N. Rezaei, 2014. Genetics of neoplasia: inherited monogenic defects associated with cancers. Acta Med. Iran., 52: 91-92.
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Lashgary, Z., A. Khodadadi, Y. Singh, S.M. Houshmand and F. Mahjoubi et al., 2011. Y chromosome diversity among the Iranian religious groups: A reservoir of genetic variation. Ann. Hum. Biol., 38: 364-371.
PubMed  |  
Maddah, M., S. Harsini, A. Rezaei, M. Sadr and S. Zoghi et al., 2016. Association of Interleukin-2, but not Interferon-Gamma, single nucleotide polymorphisms with juvenile idiopathic arthritis. Allergologia et Immunopathologia, 44: 303-306.
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Maddah, M., S. Harsini, V. Ziaee, M. Moradinejad and F. Tahghighi et al., 2016. Association of tumour necrosis factor-alpha G/A -238 and G/A -308 single nucleotide polymorphisms with juvenile idiopathic arthritis. Int. J. Immunogenet., 43: 391-396.
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Mahdaviani, S.A., P. Mehrian, A. Najafi, S. Khalilzadeh and S. Eslampanah et al., 2014. Pulmonary computed tomography scan findings in chronic granulomatous disease. Allergologia et Immunopathologia, 42: 444-448.
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Mahdaviani, S.A., S.A. Mohajerani, N. Rezaei, J.L. Casanova, S.D. Mansouri and A.A. Velayati, 2013. Pulmonary manifestations of chronic granulomatous disease. Expert. Rev. Clin. Immunol., 9: 153-160.
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Mahmoodi, M., S. Soleyman-Jahi, K. Zendehdel, H. Mozdarani and C. Azimi et al., 2017. Chromosomal aberrations, sister chromatid exchanges, and micronuclei in lymphocytes of oncology department personnel handling anti-neoplastic drugs. Drug Chem. Toxicol., 40: 235-240.
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Mahmoudi, M., A. Rezaiemanesh, A. Salmaninejad, S. Harsini and S. Poursani et al., 2015. PDCD1 single nucleotide genes polymorphisms confer susceptibility to juvenile-onset systemic lupus erythematosus. Autoimmunity, 48: 488-493.
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Mahmoudi, M., F. Tahghighi, V. Ziaee, S. Harsini and A. Rezaei et al., 2014. Interleukin-4 single nucleotide polymorphisms in juvenile systemic lupus erythematosus. Int. J. Immunogenet., 41: 512-517.
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Mahmoudi, M., M. Hedayat, A. Aghamohammadi and N. Rezaei, 2013. Soluble cd26 and cd30 levels in patients with common variable immunodeficiency. J. Investig. Allergol. Clin. Immunol., 23: 120-124.
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Mahmoudi, M.J., A.A. Saboor-Yaraghi, F. Zabetian-Targhi, F. Siassi and A.H. Zarnani et al., 2016. Vitamin A decreases cytotoxicity of oxidized low-density lipoprotein in patients with atherosclerosis. Immunol. Invest., 45: 52-62.
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Mahmoudi, M.J., E. Nematipour, S. Moradmand, M. Gharouni and M. Mahmoudiet al., 2004. Assessment of cardiac risk factors in medical students of Tehran University. Acta Med. Iran., 42: 402-410.
Mahmoudi, M.J., M. Hedayat, M. Taghvaei, E. Nematipour and E. Farhadi et al., 2014. Association of interleukin-4 gene polymorphisms with ischemic heart failure. Cardiol. J., 21: 24-28.
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Mahmoudi, M.J., M. Mahmoudi, F. Siassi, F. Shokri and M.R. Eshraghian et al., 2011. Lymphocyte cytotoxicity of oxLDL in patients with atherosclerosis. Iran J. Immunol., 8: 27-33.
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Mahmoudi, M.J., M. Taghvaei, S. Harsini, A.A. Amirzargar and M. Hedayat et al., 2016. Association of interleukin-1 gene cluster and interleukin-1 receptor polymorphisms with febrile seizures. Bratislavske Lekarske Listy, 117: 367-370.
PubMed  |  Direct Link  |  
Mahmoudi, M.J., N. Rezaei and M. Mahmoudi, 2013. Serum ox-LDL level and severity of stenosis in coronary arteries. Acta Med. Iranica, 51: 512-512.
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Mahne, S.B., S.A. Mahdaviani and N. Rezaei, 2014. Role of the immune cells, mediators and cytokines in pathogenesis of asthma: a review article. Tehran Univ. Med. J., 72: 273-285.
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Mahneh, S.B., M. Movahedi, M.A. Bahar, A. Rezaei, M. Sadr, A. Hirbod-Mobarakeh and N. Rezaei, 2016. IL9 single nucleotide polymorphism and serum levels of interleukin 9 in children with asthma. Pediatr. Allergy Immunol. Pulmonol., 29: 34-37.
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Mahneh, S.B., M. Movahedi, Z. Aryan, M.A. Bahar and A. Rezaei et al., 2015. Serum IL-33 is elevated in children with asthma and is associated with disease severity. Int. Arch. Allergy Immunol., 168: 193-196.
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Mahneh, S.B., M. Movahedi, Z. Aryan, M.A. Bahar and A. Rezaei et al., 2015. Serum IL-33 is elevated in children with asthma and is associated with disease severity. Int. Arch. Allergy Immunol., 168: 193-196.
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Majdzadeh, R. and N. Rezaei, 2016. The knowledge without border. Arch. Iran. Med., 19: 307-307.
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Majnoon, M.T., S. Mamishi, K. Moazzami, L. Shahbaznejad, M. Izadyar, F. Sabouni and N. Rezaei, 2014. Spectrum of bone marrow failures of myeloid series: new report of neutropenic patients from a referral pediatric center in iran. Pediatr. Hematol. Oncol., 31: 109-116.
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Marciano, B.E., C.Y. Huang, G. Joshi, N. Rezaei and B.C. Carvalho et al., 2014. BCG vaccination in patients with severe combined immunodeficiency: complications, risks, and vaccination policies. J. Allergy Clin. Immunol., 133: 1134-1141.
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Masoud, S., G. Rajabi, F. Delavari and N. Rezaei, 2017. Evaluating awareness of pediatricians and general practitioners on transformation of the health system in Iran. Acta Medica Iranica, 55: 49-52.
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Matin, N., O. Tabatabaie, P. Mohammadinejad and N. Rezaei, 2015. Therapeutic targeting of Toll-like receptors in cutaneous disorders. Expert Opin. Ther. Targets, 19: 1651-1663.
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Mir Saeid Ghazi, B., A. Aghamohammadi, A. Kouhi, A. Farhoudi and M. Moin et al ., 2004. Mortality in primary immunodeficient patients, registered in Iranian primary immunodeficiency registry. Iran. J. Allergy Asthma Immunol., 3: 31-35.
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Mohammadinejad, P., B. Ataeinia, K. Kaynejad, A. Zeinoddini and B. Sadeghi et al., 2015. Antibiotic resistance in patients with primary immunodeficiency disorders versus immunocompetent patients. Exp. Rev. Clin. Immunol., 11: 1163-1172.
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Mohammadinejad, P., B. Mirminachi, B. Sadeghi, M. Movahedi and M. Gharagozlou et al., 2014. Distribution of primary immunodeficiency disorders diagnosed in a tertiary referral center, Tehran, Iran (2006-2013). Iran. J. Immunol., 11: 282-291.
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Mohammadinejad, P., S. Pourhamdi, H. Abolhassani, B. Mirminachi and A. Havaei et al., 2014. Primary antibody deficiency in a tertiary referral hospital: A 30-year experiment. J. Invest. Allergol. Clin. Immunol., 25: 416-425.
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Mohammadzadeh, I., B. Moazzami, J. Ghaffari, A. Aghamohammadi and N. Rezaei, 2017. Primary immunodeficiency diseases in Northern Iran. Allergologia Immunopathologia, 45: 244-250.
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Mohammadzadeh, I., L. Shahbaznejad, N. Wang, E. Farhadi, A. Aghamohammadi, L. Hammarstrom and N. Rezaei, 2012. A novel CD40 ligand mutation in a patient with pneumonia, neutropenia, and hyperimmunoglobulin m phenotype. J. Investig. Allergol. Clin. Immunol., 23: 50-51.
PubMed  |  
Mohammadzadeh, I., M. Khaledi and N. Rezaei, 2013. Stevens-johnson syndrome: report on a case with a strange complaint of allergy to bus. Acta Clin. Croat., 52: 391-394.
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Moin, M., A. Aghamohammadi, A. Farhoudi and Z. Pourpaket al ., 2004. X-linked agammaglobulinemia: A survey of 33 Iranian patients. Immunol Invest., 33: 81-93.
PubMed  |  
Monajemzadeh, M., R. Shahsiah, M. Vasei, P. Tanzifi, N. Rezaei, M. Najafi and M. Eghbali, 2013. Alpha 1 antitrypsin deficiency in infants with neonatal cholestasis. Iran. J. Pediat., 23: 501-507.
Monajemzadeh, M., S. Sarmadi, M. Moeini, M. Vasei, N. Rezaei, A. Abbasi and M. Eghbali, 2013. Contributory role of viral infection in congenital tumour development. Ecancermedicalscience, 48: 1-9.
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Moossavi, S and N. Rezaei, 2013. Toll-like receptor signalling and their therapeutic targeting in colorectal cancer. Int. Immunopharmacol., 16: 199-209.
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Moossavi, S., H. Zhang, J. Sun and N. Rezaei, 2013. Host-microbiota interaction and intestinal stem cells in chronic inflammation and colorectal cancer. Expert. Rev. Clin. Immunol., 9: 409-422.
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Moqadam, I.F., S. Najafi, M. Mohammadzadeh, A.Z. Bidoki and H. Yousefi et al., 2016. Lack of association between Interleukin-12 gene polymorphisms and recurrent Aphthous stomatitis. Avicenna J. Med. Biotechnol., 8: 200-201.
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Mortazavi, H., A.A. Amirzargar, N. Esmaili, H. Toofan, A.H. Ehsani, S.H. Hosseini and N. Rezaei, 2013. Association of human leukocyte antigen class I antigens in Iranian patients with pemphigus vulgaris. J. Dermatol., 40: 244-248.
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Mortazavi, H., F. Babaeijandaghi, M. Akbarzadeh, N. Rezaei, A.A. Amirzargar, M. Daneshpazhooh and Z. Hallaji, 2013. The influence of systemic therapy on the serum levels of IL-6 and IL-8 in pemphigus vulgaris. J. Eur. Acad. Dermatol. Venereol., 27: 387-390.
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Rostami, P., E. Mahmoudi, A. Sotoudeh, M. Nakhaeimoghadam, I. Lurkin, E.C. Zwarthoff and N. Rezaei, 2013. Epidermal nevus in association with some uncommon manifestations. Acta Dermatovenerol. Croat., 21: 268-270.
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Sani, M.N., M. Ahmadi, P. Roohani and N. Rezaei, 2015. Early onset hepatocellular disease in an infant with zellweger syndrome. Acta Med. Iran., 53: 656-658.
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Shabani, M., K.E. Nichols and N. Rezaei, 2016. Primary immunodeficiencies associated with EBV-induced lymphoproliferative disorders. Crit. Rev. Oncol./Hematol., 108: 109-127.
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Shamsian, B.S., M. Kajizadi, N. Rezaei, N. Ghojehvand, R. Azma, M. Rouzrokh and M.T. Arzanian, 2013. Primary intrarenal neuroblastoma with hypertension and disseminated intravascular coagulation. Case Rep. Oncol. Med., 10.1155/2013/684939.
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Shayanfar, N., L. Bahari, Z. Safaie-Naraghi, Z.K. Kamyab, E. Gheytanchi and N. Rezaei, 2015. Negative HER2/neu amplification using immunohistochemistry and chromogenic in situ hybridization techniques in skin melanoma cases. Asia Pac. J. Cancer Prev., 16: 421-425.
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Shoaran, M., A. Khodadad, F. Mahjoub, M.A. Kiani and N. Rezaei, 2013. Immunoproliferative small intestinal disease presented with ascites and edema. Acta Clin. Croat., 52: 387-390.
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Shoaran, M., M. Najafi, R. Jalilian and N. Rezaei, 2012. Granulomatous hepatitis as a rare complication of bacillus calmette-guerin vaccination. Ann. Saudi Med., 33: 627-629.
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Shokri, S., M. Nabavi, T. Hirschmugl, A. Aghamohammadi and S. Arshi et al., 2016. LPS-responsive beige-like anchor gene mutation associated with possible bronchiolitis obliterans organizing pneumonia associated with hypogammaglobulinemia and normal IgM phenotype and low number of B cells. Acta Medica Iranica, 54: 620-623.
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Sodagari, H.R., M.H. Farzaei, R. Bahramsoltani, A.H. Abdolghaffari, M. Mahmoudi and N. Rezaei, 2014. Dietary anthocyanins as a complementary medicinal approach for management of inflammatory bowel disease. Expert Rev. Gastroenterol. Hepatol., 9: 807-820.
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Sodagari, H.R., R. Bahramsoltani, M.H. Farzaei, A.H. Abdolghaffari, N. Rezaei and A.W. Taylor-Robinson, 2016. Tea polyphenols as natural products for potential future management of HIV infection-an overview. J. Nat. Remedies, 16: 60-72.
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