Resultados da busca - Liena Elsayed

Involvement of ADGRV1 Gene in Familial Forms of Genetic Generalized Epilepsy por Maha Dahawi, Maha Dahawi, Mohamed S. Elmagzoub, Mohamed S. Elmagzoub, Elhami A. Ahmed, Elhami A. Ahmed, Sara Baldassari, Guillaume Achaz, Guillaume Achaz, Guillaume Achaz, Fatima A. Elmugadam, Wasma A. Abdelgadir, Stéphanie Baulac, Julien Buratti, Omer Abdalla, Sahar Gamil, Maha Alzubeir, Maha Alzubeir, Rayan Abubaker, Eric Noé, Eric Noé, Liena Elsayed, Liena Elsayed, Ammar E. Ahmed, Ammar E. Ahmed, Eric Leguern, Eric Leguern

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A heterozygous mutation in the CCDC88C gene likely causes early-onset pure hereditary spastic paraplegia: a case report por Ashraf Yahia, Zhefan Stephen Chen, Ammar E. Ahmed, Sara Emad, Rawaa Adil, Rayan Abubaker, Shaimaa Omer M. A. Taha, Mustafa A. Salih, Liena Elsayed, Ho Yin Edwin Chan, Giovanni Stevanin

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Intra-familial phenotypic heterogeneity in a Sudanese family with DARS2-related leukoencephalopathy, brainstem and spinal cord involvement and lactate elevation: a case report por Ashraf Yahia, Liena Elsayed, Arwa Babai, Mustafa A. Salih, Sarah Misbah El-Sadig, Mutaz Amin, Mahmoud Koko, Rayan Abubakr, Razaz Idris, Shaimaa Omer M.A. Taha, Salah A. Elmalik, Alexis Brice, Ammar Eltahir Ahmed, Giovanni Stevanin

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Genetic heterogeneity in familial forms of genetic generalized epilepsy: from mono- to oligogenism por Maha Dahawi, Jean-Madeleine de Sainte Agathe, Mohamed S. Elmagzoub, Elhami A. Ahmed, Julien Buratti, Thomas Courtin, Eric Noé, Julie Bogoin, Bruno Copin, Fatima A. Elmugadam, Wasma A. Abdelgadir, Ahmed K. M. A. Ahmed, Mohamed A. Daldoum, Rayan Mamoon Ibrahim Altayeb, Mohamed Bashir, Leena Mohamed Khalid, Sahar Gamil, Sara Baldassari, Liena Elsayed, Boris Keren, Gregory Nuel, Ammar E. Ahmed, Eric Leguern

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