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Articles by A Rousseau
Total Records ( 2 ) for A Rousseau
  F Denoyelle , M Daval , N Leboulanger , A Rousseau , G Roger , N Loundon , I Rouillon and E. N. Garabedian
 

Objectives  To study children who had undergone stapedectomy at an age younger than 16 years to determine the causes (particularly frequency of congenital anomalies vs otosclerosis) and to analyze the functional results over the short-term, 1-year, and long-term postsurgery time course.

Design  Ten-year retrospective study covering 1998 to 2008.

Setting  Pediatric tertiary care centers.

Patients  A total of 33 patients (35 ears) underwent stapes surgery from October 1998 to October 2008.

Main Outcome Measure  Sex, age, preoperative and postoperative audiometric test results, associated anomalies, type of surgery (stapedotomy or partial stapedectomy), method of stapes surgery, and complications.

Results  The median age of patients at surgery was 13.4 years, ranging from 3.3 to 15.9 years. The major cause, which was found in 25 of 35 ears (71%), was nonprogressive conductive hearing loss due to congenital stapes fixation. The second most common cause, which was found in 6 of 35 ears (17%), was otosclerosis with progressive conductive or mixed hearing loss. Three ears presented posttraumatic stapes luxation (1 child aged 3.3 years at surgery). In 1 ear, the cause was osteogenesis imperfecta. Twenty-two ears were treated via the drill or laser-assisted small fenestra technique, and 13 ears were treated by a partial removal of the footplate covered by fascia. Early functional results were good, with a median postoperative air-bone gap of 9.8 dB, and 94% of the results were considered good or very good. There was no significant difference between early, 1-year, and longer-term audiometric results.

Conclusions  Congenital fixation is the major indication for stapedectomy in children younger than 16 years. Functional results are good and remain stable over time.

  S El Hallani , B Boisselier , F Peglion , A Rousseau , C Colin , A Idbaih , Y Marie , K Mokhtari , J. L Thomas , A Eichmann , J. Y Delattre , A. J Maniotis and M. Sanson
 

Glioblastoma is one of the most angiogenic human tumours and endothelial proliferation is a hallmark of the disease. A better understanding of glioblastoma vasculature is needed to optimize anti-angiogenic therapy that has shown a high but transient efficacy. We analysed human glioblastoma tissues and found non-endothelial cell-lined blood vessels that were formed by tumour cells (vasculogenic mimicry of the tubular type). We hypothesized that CD133+ glioblastoma cells presenting stem-cell properties may express pro-vascular molecules allowing them to form blood vessels de novo. We demonstrated in vitro that glioblastoma stem-like cells were capable of vasculogenesis and endothelium-associated genes expression. Moreover, a fraction of these glioblastoma stem-like cells could transdifferentiate into vascular smooth muscle-like cells. We describe here a new mechanism of alternative glioblastoma vascularization and open a new perspective for the antivascular treatment strategy.

 
 
 
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