Publications by authors named "H Elorch"

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Novel mutation in the TGFBI gene in a Moroccan family with atypical corneal dystrophy: a case report.
Yahya Benbouchta, Imane Cherkaoui Jaouad, Habiba Tazi, Hamza Elorch, Mouna Ouhenach

BMC Med Genomics· January 2021

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Homozygous frameshift mutations in FAT1 cause a syndrome characterized by colobomatous-microphthalmia, ptosis, nephropathy and syndactyly.
Najim Lahrouchi, Aman George, Ilham Ratbi, Ronen Schneider, Siham C Elalaoui, Hamza Elorch

Nat Commun· March 2019

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Moth-eaten appearance of the iris in Fuchs heterochromic iridocyclitis.
A Kouisbahi, S Mouine, H Elorch, F Ibrahimi, W Bengarai

J Fr Ophtalmol· December 2018

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Bilateral persistent pupillary membrane in an adult patient: A case report.
A Kouisbahi, H Elorch, S Mouine, K Amhoud, F Ibrahimi

J Fr Ophtalmol· November 2018

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[Orbital metallic foreign body: Case report].
M Elyadari, H Bouchama, S Harchali, S Elmerrouni, M Zarrouki, H Elorch

J Fr Ophtalmol· May 2018

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