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Acta Neurologica Belgica
|
March 1, 1989
[Refsum's disease. Ophthalmologic symptomatology dominated by tight bilateral miosis]
L Defebvre, M Blondel, S Dhellemmes-Defoort, et al.
Journal Francais D'Ophtalmologie
|
March 3, 1999
[Retinal pigment anomalies associated with Fabry's disease]
D Jourdel, S Defoort-Dhellemmes, P Labalette, et al.
Bulletin Des Societes D'Ophtalmologie De France
|
March 1, 1975
[New nondissociative methods for measuring the field of fusion]
M Woillez, J C Hache, M J Besnard, et al.
Revue D'Oto-Neuro-Ophtalmologie
|
July 1, 1984
[Isolated infarction of the pedunculoquadrigeminal artery and malformation of Willis' circle]
F Dubois, M Rousseaux, J L Salomez, et al.
Journal Francais D'Ophtalmologie
|
May 25, 1999
[Simplified electroretinography protocol and diagnosis of retinal dystrophies in children]
S D Dhellemmes, F Vincent, C Arndt, et al.
Acta Neurologica Belgica
|
August 1, 1986
[Fisher's one-and-one half syndrome. Involvement of the 6th cranial nerve nucleus and association with paralytic pontine exotropia]
M Blondel, S Defoort, B Bouchez, et al.
Journal Francais D'Ophtalmologie
|
January 1, 1997
[Eye disorders in children and adolescents]
F Mouriaux, S Defoort-Dhellemmes, F Kochman, et al.
Current Eye Research
|
July 25, 1998
Altered rep-1 expression due to substitution at position +3 of the IVS13 splice-donor site of the choroideremia (CHM) gene
L Beaufrère, S Rieu, J C Hache, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
June 5, 1998
Do visual-evoked potentials and spatiotemporal contrast sensitivity help to distinguish idiopathic Parkinson's disease and multiple system atrophy?
I Delalande, J C Hache, G Forzy, et al.
Genetic Counseling (Geneva, Switzerland)
|
January 23, 1999
Length variations of the poly(T) tract at the exon 3 splice acceptor site of the choroideremia gene
L Beaufrère, S Rieu, J C Hache, et al.
Page
of 15
Search research articles
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Showing results (101-110 of 145) with videos related to
Sort By:
Page
of 15
Acta Neurologica Belgica
|
March 1, 1989
[Refsum's disease. Ophthalmologic symptomatology dominated by tight bilateral miosis]
L Defebvre, M Blondel, S Dhellemmes-Defoort, et al.
Journal Francais D'Ophtalmologie
|
March 3, 1999
[Retinal pigment anomalies associated with Fabry's disease]
D Jourdel, S Defoort-Dhellemmes, P Labalette, et al.
Bulletin Des Societes D'Ophtalmologie De France
|
March 1, 1975
[New nondissociative methods for measuring the field of fusion]
M Woillez, J C Hache, M J Besnard, et al.
Revue D'Oto-Neuro-Ophtalmologie
|
July 1, 1984
[Isolated infarction of the pedunculoquadrigeminal artery and malformation of Willis' circle]
F Dubois, M Rousseaux, J L Salomez, et al.
Journal Francais D'Ophtalmologie
|
May 25, 1999
[Simplified electroretinography protocol and diagnosis of retinal dystrophies in children]
S D Dhellemmes, F Vincent, C Arndt, et al.
Acta Neurologica Belgica
|
August 1, 1986
[Fisher's one-and-one half syndrome. Involvement of the 6th cranial nerve nucleus and association with paralytic pontine exotropia]
M Blondel, S Defoort, B Bouchez, et al.
Journal Francais D'Ophtalmologie
|
January 1, 1997
[Eye disorders in children and adolescents]
F Mouriaux, S Defoort-Dhellemmes, F Kochman, et al.
Current Eye Research
|
July 25, 1998
Altered rep-1 expression due to substitution at position +3 of the IVS13 splice-donor site of the choroideremia (CHM) gene
L Beaufrère, S Rieu, J C Hache, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
June 5, 1998
Do visual-evoked potentials and spatiotemporal contrast sensitivity help to distinguish idiopathic Parkinson's disease and multiple system atrophy?
I Delalande, J C Hache, G Forzy, et al.
Genetic Counseling (Geneva, Switzerland)
|
January 23, 1999
Length variations of the poly(T) tract at the exon 3 splice acceptor site of the choroideremia gene
L Beaufrère, S Rieu, J C Hache, et al.
Page
of 15