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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 pigmentosa
A Moore, E Escudier, G Roger, et al.
Page
of 5
Search research articles
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Showing results (41-50 of 44) with videos related to
Sort By:
Page
of 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 pigmentosa
A Moore, E Escudier, G Roger, et al.
Page
of 5