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	1.	Electrodiagnosis in neuromuscular disorders. [electronic resource] by Kabiraj, Mohammad M Producer: 20130129 In: Neurosciences (Riyadh, Saudi Arabia) vol. 17 Availability: No items available. Save to lists Add to cart (remove)
	2.	Evoked and event related potentials in chronic respiratory failure. [electronic resource] by 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 Producer: 20130828 In: Neurosciences (Riyadh, Saudi Arabia) vol. 7 Availability: No items available. Save to lists Add to cart (remove)
	3.	C19orf12 mutation leads to a pallido-pyramidal syndrome. [electronic resource] by 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 Producer: 20140624 In: Gene vol. 537 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Rundataxin, a novel protein with RUN and diacylglycerol binding domains, is mutant in a new recessive ataxia. [electronic resource] by 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 Producer: 20101007 In: Brain : a journal of neurology vol. 133 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Hyperekplexia, microcephaly and simplified gyral pattern caused by novel ASNS mutations, case report. [electronic resource] by 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 Producer: 20161213 In: BMC neurology vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Stroke in Saudi children. Epidemiology, clinical features and risk factors. [electronic resource] by 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 Producer: 20060525 In: Saudi medical journal vol. 27 Suppl 1 Availability: No items available. Save to lists Add to cart (remove)
	7.	Clinical and molecular genetic findings in COLQ-mutant congenital myasthenic syndromes. [electronic resource] by 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 Producer: 20080501 In: Brain : a journal of neurology vol. 131 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	New findings in a global approach to dissect the whole phenotype of PLA2G6 gene mutations. [electronic resource] by 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 Producer: 20140624 In: PloS one vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	SLC25A22 is a novel gene for migrating partial seizures in infancy. [electronic resource] by 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 Producer: 20140318 In: Annals of neurology vol. 74 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Alteration of fatty-acid-metabolizing enzymes affects mitochondrial form and function in hereditary spastic paraplegia. [electronic resource] by 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 Producer: 20130214 In: American journal of human genetics vol. 91 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)