New findings in a global approach to dissect the whole phenotype of PLA2G6 gene mutations von Salih, Mustafa A, Mundwiller, Emeline, Khan, Arif O, AlDrees, Abdulmajeed, Elmalik, Salah A, Hassan, Hamdy H, Al-Owain, Mohammed, Alkhalidi, Hisham M S, Katona, Istvan, Kabiraj, Mohammad M, Chrast, Roman, Kentab, Amal Y, Alzaidan, Hamad, Rodenburg, Richard J, Bosley, Thomas M, Weis, Joachim, Koenig, Michel, Stevanin, Giovanni, Azzedine, Hamid

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SLC25A22 is a novel gene for migrating partial seizures in infancy von Poduri, Annapurna, Heinzen, Erin L., Chitsazzadeh, Vida, Lasorsa, Francesco Massimo, Elhosary, P. Christina, LaCoursiere, Christopher M., Martin, Emilie, Yuskaitis, Christopher J., Hill, Robert Sean, Atabay, Kutay Deniz, Barry, Brenda, Partlow, Jennifer N., Bashiri, Fahad A., Zeidan, Radwan M., Elmalik, Salah A., Kabiraj, Mohammad M. U., Kothare, Sanjeev, Stödberg, Tommy, McTague, Amy, Kurian, Manju A., Scheffer, Ingrid E., Barkovich, A. James, Palmieri, Ferdinando, Salih, Mustafa A., Walsh, Christopher A.

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Clinical and molecular genetic findings in COLQ-mutant congenital myasthenic syndromes von Mihaylova, Violeta, Müller, Juliane S., Vilchez, Juan J., Salih, Mustafa A., Kabiraj, Mohammad M., D’Amico, Adele, Bertini, Enrico, Wölfle, Joachim, Schreiner, Felix, Kurlemann, Gerhard, Rasic, Vedrana Milic, Siskova, Dana, Colomer, Jaume, Herczegfalvi, Agnes, Fabriciova, Katarina, Weschke, Bernhard, Scola, Rosana, Hoellen, Friederike, Schara, Ulrike, Abicht, Angela, Lochmüller, Hanns

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Hyperekplexia, microcephaly and simplified gyral pattern caused by novel ASNS mutations, case report von Seidahmed, Mohammed Zain, Salih, Mustafa A, Abdulbasit, Omer B, Samadi, Abdulmohsen, Al Hussien, Khalid, Miqdad, Abeer M, Biary, Maha S, Alazami, Anas M, Alorainy, Ibrahim A, Kabiraj, Mohammad M, Shaheen, Ranad, Alkuraya, Fowzan S

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C19orf12 mutation leads to a pallido-pyramidal syndrome von Kruer, Michael C., Salih, Mustafa A., Mooney, Catherine, Alzahrani, Jawahir, Elmalik, Salah A., Kabiraj, Mohammad M., Khan, Arif O., Paudel, Reema, Houlden, Henry, Azzedine, Hamid, Alkuraya, Fowzan

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Alteration of Fatty-Acid-Metabolizing Enzymes Affects Mitochondrial Form and Function in Hereditary Spastic Paraplegia von Tesson, Christelle, Nawara, Magdalena, Salih, Mustafa A.M., Rossignol, Rodrigue, Zaki, Maha S., Al Balwi, Mohammed, Schule, Rebecca, Mignot, Cyril, Obre, Emilie, Bouhouche, Ahmed, Santorelli, Filippo M., Durand, Christelle M., Oteyza, Andrés Caballero, El-Hachimi, Khalid H., Al Drees, Abdulmajeed, Bouslam, Naima, Lamari, Foudil, Elmalik, Salah A., Kabiraj, Mohammad M., Seidahmed, Mohammed Z., Esteves, Typhaine, Gaussen, Marion, Monin, Marie-Lorraine, Gyapay, Gabor, Lechner, Doris, Gonzalez, Michael, Depienne, Christel, Mochel, Fanny, Lavie, Julie, Schols, Ludger, Lacombe, Didier, Yahyaoui, Mohamed, Al Abdulkareem, Ibrahim, Zuchner, Stephan, Yamashita, Atsushi, Benomar, Ali, Goizet, Cyril, Durr, Alexandra, Gleeson, Joseph G., Darios, Frederic, Brice, Alexis, Stevanin, Giovanni

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Rundataxin, a novel protein with RUN and diacylglycerol binding domains, is mutant in a new recessive ataxia von Assoum, Mirna, Salih, Mustafa A., Drouot, Nathalie, H'Mida-Ben Brahim, Dorra, Lagier-Tourenne, Clotilde, AlDrees, Abdulmajeed, Elmalik, Salah A., Ahmed, Taha S., Seidahmed, Mohammad Z., Kabiraj, Mohammad M., Koenig, Michel

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Correction: New Findings in a Global Approach to Dissect the Whole Phenotype of PLA2G6 Gene Mutations von Salih, Mustafa A., Mundwiller, Emeline, Khan, Arif O., AlDrees, Abdulmajeed, Elmalik, Salah A., Hassan, Hamdy H., Al-Owain, Mohammed, Alkhalidi, Hisham M. S., Katona, Istvan, Kabiraj, Mohammad M., Chrast, Roman, Kentab, Amal Y., Alzaidan, Hamad, Rodenburg, Richard J., Bosley, Thomas M., Weis, Joachim, Koenig, Michel, Stevanin, Giovanni, Azzedine, Hamid

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Stroke in Saudi children. Epidemiology, clinical features and risk factors von Salih, Mustafa A, Abdel-Gader, Abdel-Galil M, Al-Jarallah, Ahmed A, Kentab, Amal Y, Alorainy, Ibrahim A, Hassan, Hamdy H, Bahakim, Hassan M, Kurbaan, Khadija M, Zahraa, Jihad N, Al-Nasser, Mohammed N, Nasir, Ali A, Khoja, Waleed A, Kabiraj, Mohammad M

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Electrodiagnosis in neuromuscular disorders von Kabiraj, Mohammad M

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C19orf12 mutation leads to Karak pallido-pyramidal syndrome von Kruer, Michael C., Salih, Mustafa A., Mooney, Catherine, Alzahrani, Jawahir, Elmalik, Salah A., Kabiraj, Mohammad M., Khan, Arif O., Paudel, Reema, Houlden, Henry, Azzedine, Hamid, Alkuraya, Fowzan

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New Findings in a Global Approach to Dissect the Whole Phenotype of PLA2G6 Gene Mutations: e76831 von Salih, Mustafa A, Mundwiller, Emeline, Khan, Arif O, AlDrees, Abdulmajeed, Elmalik, Salah A, Hassan, Hamdy H, Al-Owain, Mohammed, Alkhalidi, Hisham MS, Katona, Istvan, Kabiraj, Mohammad M

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Correction: New Findings in a Global Approach to Dissect the Whole Phenotype of Gene Mutations von Mustafa A. Salih, Emeline Mundwiller, Arif O. Khan, Abdulmajeed AlDrees, Salah A. Elmalik, Hamdy H. Hassan, Mohammed Al-Owain, Hisham M. S. Alkhalidi, Istvan Katona, Mohammad M. Kabiraj, Roman Chrast, Amal Y. Kentab, Hamad Alzaidan, Richard J. Rodenburg, Thomas M. Bosley, Joachim Weis, Michel Koenig, Giovanni Stevanin, Hamid Azzedine

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Stroke in saudi children : Epidemiology, clinical features and risk factors: Childhood stroke von SALIH, Mustafa A, ABDEL-GADER, Abdel-Galil M, NASIR, Ali A, KHOJA, Waleed A, KABIRAJ, Mohammad M, AL-JARALLAH, Ahmed A, KENTAB, Amal Y, ALORAINY, Ibrahim A, HASSAN, Hamdy H, BAHAKIM, Hassan M, KURBAAN, Khadija M, ZAHRAA, Jihad N, AL-NASSER, Mohammed N

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Evoked and event related potentials in chronic respiratory failure von Al-Tahan, Abdulrahman M, Hussain, Ashraf H, Kabiraj, Mohammad M, Al-Mobeireek, Abdullah F, Bahammam, Ahmed S, Al-Majed, Sulaiman A, Al-Moallem, Mansour A

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Postictal cerebral hemiatrophy: Hemiconvulsion-hemiplegia-epilepsy syndrome von Salih, Mustafah AM, Kabiraj, Mohammad M., Al-Jarallah, Ahmed I., Palkar, Vijay A.

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Postictal hemiatrophy: Hemiconvulsion-hemiplegia-epilepsy syndrome von Salih, Mustafah Am, Kabiraj, Mohammad M., Al-Jarallah, Ahmed I., Palkar, Vijay A.

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Can cytotoxic drugs ameliorate subacute sclerosing panencephalitis? von Al Rajeh, Saad M., Uddin Kabiraj, Mohammad M., Ibrahim Al-Fawaz, Ibrahim M., Daif, Mohammad Abdulkader, Jarallah, Ahmed I.

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Genetic and biological characterization of Newcastle disease viruses circulating in Bangladesh during 2010-2017: further genetic diversification of class II genotype XIII in Southc... von Nooruzzaman, Mohammed, Mumu, Tanjin Tamanna, Kabiraj, Congriev Kumar, Hasnat, Azmary, Rahman, Md Mijanur, Chowdhury, Emdadul Haque, Dimitrov, Kiril M, Islam, Mohammad Rafiqul

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Pseudoathetosis Including Lingual Pseudoathetosis: Successful Treatment with Pregabalin (P6.053) von Biary, Nabil, Khoja, Waleed Ahmed, Malik, Aisha Mohsin, Kabiraj, Mohammad

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