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Journal Francais D'Ophtalmologie
|
May 29, 2019
[Ocular manifestations in Ehlers-Danlos Syndromes: Clinical study of 21 patients]
S Perez-Roustit, D-T Nguyen, O Xerri, et al.
Journal Francais D'Ophtalmologie
|
April 11, 2021
[Implementation of a new gene therapy in ophthalmology: Regulatory and organizational issues]
A Daruich, R Boinet, C Falcou, et al.
Ophthalmic Genetics
|
September 13, 2022
Foveal hypoplasia in parents of patients with albinism
R Lejoyeux, A-S Alonso, J Lafolie, et al.
AJNR. American Journal of Neuroradiology
|
August 21, 2020
Focal Areas of High Signal Intensity in Children with Neurofibromatosis Type 1: Expected Evolution on MRI
S Calvez, R Levy, R Calvez, et al.
Annales De Dermatologie Et De Venereologie
|
July 4, 2021
Development and co-construction of a therapeutic patient education program for albinism
H Dufresne, A de Longcamp, S Compain, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
July 18, 2020
Multidisciplinary consensus recommendations from a European network for the diagnosis and practical management of patients with incontinentia pigmenti
C Bodemer, A Diociaiuti, S Hadj-Rabia, et al.
Orphanet Journal of Rare Diseases
|
September 23, 2020
Management of ocular involvement in the acute phase of Stevens-Johnson syndrome and toxic epidermal necrolysis: french national audit of practices, literature review, and consensus agreement
D Thorel, S Ingen-Housz-Oro, G Royer, et al.
Revue Neurologique
|
July 16, 2025
Criteria for the use of plasmapheresesis in optic neuritis: A practice review from French expert centers
A Gaulier, V Touitou, M-B Rougier, et al.
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Search research articles
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Showing results (11-20 of 18) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 18 results.
Journal Francais D'Ophtalmologie
|
May 29, 2019
[Ocular manifestations in Ehlers-Danlos Syndromes: Clinical study of 21 patients]
S Perez-Roustit, D-T Nguyen, O Xerri, et al.
Journal Francais D'Ophtalmologie
|
April 11, 2021
[Implementation of a new gene therapy in ophthalmology: Regulatory and organizational issues]
A Daruich, R Boinet, C Falcou, et al.
Ophthalmic Genetics
|
September 13, 2022
Foveal hypoplasia in parents of patients with albinism
R Lejoyeux, A-S Alonso, J Lafolie, et al.
AJNR. American Journal of Neuroradiology
|
August 21, 2020
Focal Areas of High Signal Intensity in Children with Neurofibromatosis Type 1: Expected Evolution on MRI
S Calvez, R Levy, R Calvez, et al.
Annales De Dermatologie Et De Venereologie
|
July 4, 2021
Development and co-construction of a therapeutic patient education program for albinism
H Dufresne, A de Longcamp, S Compain, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
July 18, 2020
Multidisciplinary consensus recommendations from a European network for the diagnosis and practical management of patients with incontinentia pigmenti
C Bodemer, A Diociaiuti, S Hadj-Rabia, et al.
Orphanet Journal of Rare Diseases
|
September 23, 2020
Management of ocular involvement in the acute phase of Stevens-Johnson syndrome and toxic epidermal necrolysis: french national audit of practices, literature review, and consensus agreement
D Thorel, S Ingen-Housz-Oro, G Royer, et al.
Revue Neurologique
|
July 16, 2025
Criteria for the use of plasmapheresesis in optic neuritis: A practice review from French expert centers
A Gaulier, V Touitou, M-B Rougier, et al.
Page
of 2