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B Pelosse

Showing results (41-50 of 44) with videos related to

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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|September 3, 1999
[Severe constriction of the visual field associated with vigabatrin discovered by thorough examination of a 17-year old girl]A Roubergue, B Pelosse, D Doummar, et al.
Journal Francais D'Ophtalmologie|June 20, 2008
[Recurrent visual loss in Leber hereditary optic neuropathy: a case report]M Momtchilova, B Pelosse, M Saliba, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|November 3, 2004
[Management of acute visual loss in children]D Doummar, B Roussat, B Pelosse, et al.
Journal of Medical Genetics|August 2, 2005
RPGR is mutated in patients with a complex X linked phenotype combining primary ciliary dyskinesia and retinitis pigmentosaA Moore, E Escudier, G Roger, et al.
Pageof 5

Showing results (41-50 of 44) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 44 results.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|September 3, 1999
[Severe constriction of the visual field associated with vigabatrin discovered by thorough examination of a 17-year old girl]A Roubergue, B Pelosse, D Doummar, et al.
Journal Francais D'Ophtalmologie|June 20, 2008
[Recurrent visual loss in Leber hereditary optic neuropathy: a case report]M Momtchilova, B Pelosse, M Saliba, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|November 3, 2004
[Management of acute visual loss in children]D Doummar, B Roussat, B Pelosse, et al.
Journal of Medical Genetics|August 2, 2005
RPGR is mutated in patients with a complex X linked phenotype combining primary ciliary dyskinesia and retinitis pigmentosaA Moore, E Escudier, G Roger, et al.
Pageof 5