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Science Alert
 
    Publisher: Asian Network for Scientific Information
   
  Journal of Applied Sciences seeks to promote and disseminate the knowledge by publishing original research findings, review articles and short communications in the broad field of applied sciences. Scope of the journal includes: Biology, chemistry, physics, environmental, business and economics, finance, mathematics and statistics, geology, engineering, computer science, social sciences, natural and technological sciences, linguistics, medicine and architecture, food science, environmental science, agricultural engineering. Journal of Applied Sciences now accepting new submissions. Submit your best paper via online submission system.
  Editor-in-Chief:  Gazi Mahabubul Alam
 
 
Abdalla, A., H. Al-Marsafawy, M.M. Abou El-Khair, M.E. El-Regal and M.M. Al-Haggar, 2004. Hepatopulmonary syndrome in children with cirrhosis: Echocardiographic findings. Benha Med. J., 21: 515-516.
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Abdallah, A.F., A.M. Bakr, M. El-Haggar and T. Amer, 1999. Renal hemodynamic changes in children with liver cirrhosis. Pediatr. Nephrol., 13: 854-858.
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Abdel-Razik, N., M. Al-Haggar, H. Al-Marsafawy, H. Abdel-Hadi and R. Al-Baz, 2007. Impact of long-term iron supplementation in breast-fed infants. Ind. J. Pediatr., 74: 739-745.
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Al‐Haggar, M., N. Salem, Y. Wahba, N. Ahmad and L. Jonard et al., 2014. Novel homozygous SLC29A3 mutations among two unrelated Egyptian families with spectral features of H‐syndrome. Pediatr. Diabetes, (In Press). 10.1111/pedi.12160.
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Al-Haggar, M., 2012. Fanconi-Bickel syndrome as an example of marked allelic heterogeneity. World J. Nephrol., 1: 63-68.
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Al-Haggar, M., 2013. Cystinosis as a lysosomal storage disease with multiple mutant alleles: Phenotypic-genotypic correlations. World J. Nephrol., 2: 94-102.
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Al-Haggar, M., 2013. Evolving molecular methods for detection of mutations. Gene Technol., Vol. 2. 10.4172/2329-6682.1000e104.
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Al-Haggar, M., 2014. SNPs as co-morbid factors for drug abuse and ischemic heart disease. Gene Technol., Vol. 3. 10.4172/2329-6682.1000107.
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Al-Haggar, M., A. Bakr, T. Tajima, K. Fujieda and A. Hammad et al., 2009. Familial hypomagnesemia with hypercalciuria and nephrocalcinosis: unusual clinical associations and novel claudin16 mutation in an Egyptian family. Clin. Exp. Nephrol., 13: 288-294.
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Al-Haggar, M., A. Madej-Pilarczyk, L. Kozlowski, J.M. Bujnicki and S. Yahia et al., 2012. A novel homozygous p.Arg527Leu LMNA mutation in two unrelated Egyptian families causes overlapping mandibuloacral dysplasia and progeria syndrome. Eur. J. Hum. Genet., 20: 1134-1140.
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Al-Haggar, M., A. Settin, M. Gouida, R. Al-Baz and R. Abu Alkasem et al., 2005. Case report: Early diagnosis of Hodgkin`s disease based on Flow Cytometry parameters. Br. Med. J. Middle East, 12: 14-15.
Al-Haggar, M., A. Shams, A. Madej-Pilarczyk, T. Barakat and M. Puzianowska-Kuznicka, 2013. Ultrastrutural skin changes in Egyptian mandibuloacral dysplasia patients with p.Arg527Leu LMNA mutation and in their asymptomatic heterozygotic mothers. J. Clin. Pathol., 66: 1000-1004.
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Al-Haggar, M., A. Taranta, A. El-Hawary, A. Al-Said, A.A. Shaban and Y. Wahba, 2012. Novel truncating mutation in the CTNS gene in an Egyptian family with cases of infantile nephropathic cystinosis and congenital heart malformations. Middle East J. Med. Genet., 1: 71-75.
Al-Haggar, M., A. Taranta, P. Bencivenga, N. Ahmad, H.A. Hadid and Y. Wahba, 2013. Recent experience in an Egyptian medical center: Strategies for the clinical and genetic diagnoses of nephropathic cystinosis. Br. J. Med. Med. Res., 3: 1918-1928.
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Al-Haggar, M., C.R. Largiader, D. Abdel-Hady, T. Barakat, J.M. Nuoffer and A.A. Al-Refaei, 2014. Partial expression of ornithine transcarbamylase deficiency in an Egyptian female carrier. Int. J. Gynaecol. Obstetr., 124: 174-175.
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Al-Haggar, M., H. Al-Marsafawy, N. Abdel-Razek, R. Al-Baz and A.H. Mostafa, 2006. Acute painful crises of sickle cell disease in Egyptian children: Predictors of severity for a preventive strategy. Int. J. Hematol., 83: 224-228.
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Al-Haggar, M., M. Al-Aiouty, M. Ragab and S. Yehia, 2006. Neurophysiologic evaluation of peripheral nerve function in uremic egyptian children. J. Pediat. Neurol., 4: 89-95.
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Al-Haggar, M., M. Ragab, M. Awad and R. Al-Baz, 2006. Soluble adhesion molecules in juvenile idiopathic arthritis: Relation to activity and clinical subtype. J. Med. Sci., 6: 474-479.
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Al-Haggar, M., N. Ahmad, S. Yahia, A. Shams and B. Hasaneen et al., 2013. Sporadic fibrodysplasia ossificans progressiva in an Egyptian infant with c.617G > A mutation in ACVR1 gene: A case report and review of literature. Case Rep. Genet., 10.1155/2013/834605.
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Al-Haggar, M., N. Yahia and H. Ghanem, 2006. High dairy calcium intake in pubertal girls: Relation to weight gain and bone mineral status. J. Medical Sci., 6: 631-635.
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Al-Haggar, M., O. Sakamoto, A. Shaltout, A. Al-Hawari, Y. Wahba and D. Abdel-Hadi, 2012. Mutation analysis of the GLUT2 gene in three unrelated Egyptian families with Fanconi-Bickel syndrome: Revisited gene atlas for renumbering. Clin. Exp. Nephrol., 16: 604-610.
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Al-Haggar, M., O. Sakamoto, A. Shaltout, A. El-Hawary, Y. Wahba and D. Abdel-Hadi, 2011. Fanconi Bickel syndrome: Novel mutations in GLUT 2 gene causing a distinguished form of renal tubular acidosis in two unrelated Egyptian families. Case Rep. Nephrol. 10.1155/2011/754369.
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Al-Haggar, M., R. El-Baz, H. Youseff, N. Othman and R. Ali, 2006. Overview on attention deficit hyperactivity disorder among children from Delta regions of Egypt (A 10 years-study). J. Pediatric Neurol., 4: 15-18.
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Al-Haggar, M., S. Yahia, D. Abdel-Hadi, F. Grill and A. Al Kaissi, 2010. Sirenomelia (symelia apus) with Potteri's syndrome in connection with gestational diabetes mellitus: A case report and literature review. Afr. Health Sci., 10: 395-399.
Al-Haggar, M., S. Yahia, K. Damjanovich, N. Ahmad, I. Hamada and P. Bayrak-Toydemir, 2011. p. R672C mutation of MYH3 gene in an Egyptian infant presented with Freeman-Sheldon syndrome. Indian J. Pediatr., 78: 103-105.
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Al-Haggar, M., Z. Al-Morsy, S. Yahia, N. Chalaby, A. Ragab and A. Mesbah, 2008. Correlation of thyroid and growth hormones to chromosomal instability in egyptian fanconi anemia patients. Ind. J. Pediatr., 75: 679-684.
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Al-Haggar, M., Z. Al-Naggar and M. Abdel-Salam, 2006. Biofeedback and cognitive behavioral therapy for Egyptian adolescents suffering from chronic fatigue syndrome. J. Pediatr. Neurol., 4: 161-169.
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Al-Haggar, M.M.S., B.A. Khair-Allaha, M.M. Islam and S.A. Mohamed, 2013. Bioinformatics in high throughput sequencing: Application in evolving genetic diseases. J. Data Mining Genomics Proteomics, Vol. 4. 0.4172/2153-0602.1000131.
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Al-Haggar, M.S., A.A. Settin, M. Ragab, M. Al-Shahat and H. Abdel-Hadi et al., 2006. Segregation analysis of p53, c-myc and DNA ploidy using flow cytometry among Egyptian families with childhood leukemia. J. Medical Sci., 6: 906-914.
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Al-Haggar, M.S., S. Yahia, D. Abdel-Hady, A. Al-Saied, R. Al-Kenawy and R. Abo-El-Kasem, 2014. Phenotype-genotype updates from familial Mediterranean fever database registry of Mansoura University Children' Hospital, Mansoura, Egypt. Indian J. Hum. Genet., 20: 43-50.
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Al-Tonbary, Y., M. Al-Haggar, O. Salama, M. Abul-Kheir, A. El-Alfy and M. Hafez, 2012. Platelet count and serum thrombopoietin level as predictors for morbidity and/or mortality in thrombocytopenic neonates. Hematology, 17: 341-345.
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Al-Tonbary, Y., M. Al-Haggar, R. EL-Ashry, S. EL-Dakroory, H. Azzam and A. Fouda, 2009. Vitamin E and N-acetylcysteine as antioxidant adjuvant therapy in children with acute lymphoblastic leukemia. Adv. Hematol., 10.1155/2009/689639.
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Bakr, A., M. Al-Haggar, R. Eid, Y. Wahba and P. Coucke et al., 2014. Focal segmental glomerulosclerosis in a child with marfan syndrome and novel fibrillin gene mutation. Pediatr. Nephrol., 29: 1825-1825.
El-Sayyad, H.I., M.M. Al-Haggar, H.A. El-Ghawet and I.H. Bakr, 2014. Effect of maternal diabetes and hypercholesterolemia on fetal liver of albino Wistar rats. Nutrition, 30: 326-336.
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El-Sayyad, H.I., M.S. Al-Haggar, H.A. El-Ghawet and I.H. Bakr, 2012. Cardiomyopathy and angiogenesis defects of Wistar rat fetuses of diabetic and hypercholesterolemic mothers. Nutrition, 28: e33-e43.
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Nezar, M., A. Abd El-Baky, O. Soliman, A. Hammad and M. Al-Haggar, 2009. Endothelin-1 and leptin as markers of intrauterine growth restriction. Indian J. Pediatr., 76: 485-488.
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Settin, A., M. Al-Haggar, M. Gouida, R. Al-Baz and R. Abu Alkasem et al., 2006. Diagnostic significance of flow cytometric analysis of dna ploidy and apoptosis in children with lymphadenopathy. Haema, 9: 240-246.
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Settin, A., M. Al-Haggar, M. Neamatallah, A. Al- Said and M. Hafez, 2006. Detection of beta-thalassemia mutations using primer-specific amplification compared to reversed dot blot hybridization technique in egyptian cases. Haema, 9: 401-409.
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Settin, A., M. Al-Haggar, R. Al-Baz, H. Yousof and N. Osman, 2006. Screening for G6PD mediterranean mutation among Egyptian neonates with high or prolonged jaundice. Haema, 9: 83-90.
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Settin, A., M. Al-Haggar, R. Al-Baz, M. Al-Aiouty and M. Hafez, 2005. Screening of mentally handicapped Egyptian children for fragile X Syndrome using clinical, cytogenetic and molecular approaches. J. Pediatr. Neurol., 3: 217-225.
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Settin, A., M. Al-Haggar, T. Al-Dosoky, R. Al-Baz, N. Abdelrazik, M. Fouda, S. Aref and Y. Al-Tonbary, 2007. Prognostic cytogenetic markers in childhood acute lymphoblastic leukemia. Indian J. Pediatr., 74: 255-263.
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Settin, A., M. Al-Haggar, T. El-Dosokey, R. Al-Baz and N. Abdelrazik et al., 2006. Prognostic cytogenetic markers in childhood acute lymphoblastic leukemias, Cases from Mansoura, Egypt. Haematology, 11: 341-349.
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Settin, A., M. Al-Haggar, T. El-Dosokey, R. Al-Baz and N. Abdelrazik et al., 2007. Prognostic cytogenetic markers in childhood acute lymphoblastic leukemias, Cases from Mansoura, Egypt. Hematology, 12: 103-111.
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Settin, A., T. Al-Dosokey, M. Al-Haggar, M. Al-Bendary and M. Ezz et al., 2006. Increased risk of liver cirrhosis among Egyptian carriers of S and/or Z mutant alleles of Alpha1 anti-trypsin gene. Arab J. Gastroenterol., 7: 14-18.
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Settin, A., T. Al-Dosokey, M. Al-Haggar, M. El-Bendary and M. Ezz et al., 2006. C282Y and H63D haemochromatosis alleles in Egyptian patients with cirrhosis. Arab J. Gastroenterol., 7: 59-63.
Settin, A.A., M.S. Al-Haggar, H. El Marsafawy, A.A. Alkader and R.A. El Baz et al., 2006. Genetic analysis of rheumatic fever among Egyptian families: Consanguinity pattern, segregation analysis and blood group association. J. Medical Sci., 6: 359-366.
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Zedan, M., A. Bakr, B. Shouman, H. Zaghloul and M. Al-Haggar, 2014. Single nucleotide polymorphism of IL4C-590T and IL4RA 175V and immunological parameters in Egyptian asthmatics with different clinical phenotypes. J. Allergy Ther., Vol. 5. 10.4172/2155-6121.1000189.
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