Rupture post traumatique de la membrane de Bruch: à propos d'un cas

by Sanaa Ahbeddou, Jinane Ahmimeche, Nazih Tzili, Fadoua Alami, Ramzia Sebbah, Hamza Elorch, Amina Berraho
Published 2015-08-01

Novel mutation in the TGFBI gene in a Moroccan family with atypical corneal dystrophy: a case report

by Yahya Benbouchta, Imane Cherkaoui Jaouad, Habiba Tazi, Hamza Elorch, Mouna Ouhenach, Abdelali Zrhidri, Khalid Sadki, Abdelaziz Sefiani, Jaber Lyahyai, Amina Berraho
Published 2021-01-01

Dacryoadenite tuberculeuse bilatérale: à propos d'un cas

by Bekkay Rezzoug, Nazih Tzili, Hassan Ali, Oubaida Elyamouni, Mahfoud El Khaoua, Hamza Elorch, Redouane El Hlimi, Abdallah El Hassan, Amina Berraho
Published 2015-01-01

Homozygous frameshift mutations in FAT1 cause a syndrome characterized by colobomatous-microphthalmia, ptosis, nephropathy and syndactyly

by Najim Lahrouchi, Aman George, Ilham Ratbi, Ronen Schneider, Siham C. Elalaoui, Shahida Moosa, Sanita Bharti, Ruchi Sharma, Mones Abu-Asab, Felix Onojafe, Najlae Adadi, Elisabeth M. Lodder, Fatima-Zahra Laarabi, Yassine Lamsyah, Hamza Elorch, Imane Chebbar, Alex V. Postma, Vassilios Lougaris, Alessandro Plebani, Janine Altmueller, Henriette Kyrieleis, Vardiella Meiner, Helen McNeill, Kapil Bharti, Stanislas Lyonnet, Bernd Wollnik, Alexandra Henrion-Caude, Amina Berraho, Friedhelm Hildebrandt, Connie R. Bezzina, Brian P. Brooks, Abdelaziz Sefiani
Published 2019-03-01