Exploration of Risk Factors for Type 2 Diabetes among Arabs in Israel

por Sharkia, Rajech, Sheikh-Muhammad, Ahmad, Mahajnah, Muhammad, Khatib, Mohammad, Zalan, Abdelnaser
Publicado 2019

Sanfilippo type A: new clinical manifestations and neuro-imaging findings in patients from the same family in Israel: a case report

por Sharkia, Rajech, Mahajnah, Muhammad, Zalan, Abdelnaser, Sourlis, Chrysovalantis, Bauer, Peter, Schöls, Ludger
Publicado 2014

Parental mosaicism in another case of Dravet syndrome caused by a novel SCN1A deletion: a case report

por Sharkia, Rajech, Hengel, Holger, Schöls, Ludger, Athamna, Muhammad, Bauer, Peter, Mahajnah, Muhammad
Publicado 2016

Novel homozygous large deletion including the 5′ part of the SPATA7 gene in a consanguineous Israeli Muslim Arab family

por Mayer, Anja-Kathrin, Mahajnah, Muhammad, Zobor, Ditta, Bonin, Michael, Sharkia, Rajech, Wissinger, Bernd
Publicado 2015

Clinical Characteristics of Autism Spectrum Disorder in Israel: Impact of Ethnic and Social Diversities

por Mahajnah, Muhammad, Sharkia, Rajech, Shalabe, Haitham, Terkel-Dawer, Ruth, Akawi, Ashraf, Zelnik, Nathanel
Publicado 2015

Gene and Protein Expression in Subjects With a Nystagmus-Associated AHR Mutation

por Borovok, Natalia, Weiss, Celeste, Sharkia, Rajech, Reichenstein, Michal, Wissinger, Bernd, Azem, Abdussalam, Mahajnah, Muhammad
Publicado 2020

PTRH2 Gene Variants: Recent Review of the Phenotypic Features and Their Bioinformatics Analysis

por Sharkia, Rajech, Jain, Sahil, Mahajnah, Muhammad, Habib, Clair, Azem, Abdussalam, Al-Shareef, Wasif, Zalan, Abdelnaser
Publicado 2023

CLN8 Gene Compound Heterozygous Variants: A New Case and Protein Bioinformatics Analyses

por Sharkia, Rajech, Zalan, Abdelnaser, Zahalka, Hazar, Kessel, Amit, Asaly, Ayman, Al-Shareef, Wasif, Mahajnah, Muhammad
Publicado 2022

High CCL2 Levels Detected in CSF of Patients with Pediatric Pseudotumor Cerebri Syndrome

por Genizi, Jacob, Berger, Lotan, Mahajnah, Muhammad, Shlonsky, Yulia, Golan-Shany, Orit, Romem, Azriel, Halevy, Ayelet, Nathan, Keren, Sharkia, Rajech, Zalan, Abdelnaser, Kessel, Aharon, Cohen, Rony
Publicado 2023

CNTNAP1 mutations cause CNS hypomyelination and neuropathy with or without arthrogryposis

por Hengel, Holger, Magee, Alex, Mahanjah, Muhammad, Vallat, Jean-Michel, Ouvrier, Robert, Abu-Rashid, Mohammad, Mahamid, Jamal, Schüle, Rebecca, Schulze, Martin, Krägeloh-Mann, Ingeborg, Bauer, Peter, Züchner, Stephan, Sharkia, Rajech, Schöls, Ludger
Publicado 2017

First-line exome sequencing in Palestinian and Israeli Arabs with neurological disorders is efficient and facilitates disease gene discovery

por Hengel, Holger, Buchert, Rebecca, Sturm, Marc, Haack, Tobias B., Schelling, Yvonne, Mahajnah, Muhammad, Sharkia, Rajech, Azem, Abdussalam, Balousha, Ghassan, Ghanem, Zaid, Falana, Mohammed, Balousha, Osama, Ayesh, Suhail, Keimer, Reinhard, Deigendesch, Werner, Zaidan, Jimmy, Marzouqa, Hiyam, Bauer, Peter, Schöls, Ludger
Publicado 2020

Correction to: First-line exome sequencing in Palestinian and Israeli Arabs with neurological disorders is efficient and facilitates disease gene discovery

por Hengel, Holger, Buchert, Rebecca, Sturm, Marc, Haack, Tobias B., Schelling, Yvonne, Mahajnah, Muhammad, Sharkia, Rajech, Azem, Abdussalam, Balousha, Ghassan, Ghanem, Zaid, Falana, Mohammed, Balousha, Osama, Ayesh, Suhail, Keimer, Reinhard, Deigendesch, Werner, Zaidan, Jimmy, Marzouqa, Hiyam, Bauer, Peter, Schöls, Ludger
Publicado 2021