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New findings in a global approach to dissect the whole phenotype of PLA2G6 gene mutations.
Salih MA, Mundwiller E, Khan AO, AlDrees A, Elmalik SA, Hassan HH, Al-Owain M, Alkhalidi HM, Katona I, Kabiraj MM, Chrast R, Kentab AY, Alzaidan H, Rodenburg RJ, Bosley TM, Weis J, Koenig M, Stevanin G, Azzedine H. Salih MA, et al. Among authors: hassan hh. PLoS One. 2013 Oct 9;8(10):e76831. doi: 10.1371/journal.pone.0076831. eCollection 2013. PLoS One. 2013. PMID: 24130795 Free PMC article.
Cerebral Iron Accumulation Is Not a Major Feature of FA2H/SPG35.
Marelli C, Salih MA, Nguyen K, Mallaret M, Leboucq N, Hassan HH, Drouot N, Labauge P, Koenig M. Marelli C, et al. Among authors: hassan hh. Mov Disord Clin Pract. 2015 Feb 18;2(1):56-60. doi: 10.1002/mdc3.12118. eCollection 2015 Mar. Mov Disord Clin Pract. 2015. PMID: 30713878 Free PMC article.
Stroke in Saudi children. Epidemiology, clinical features and risk factors.
Salih MA, Abdel-Gader AG, Al-Jarallah AA, Kentab AY, Alorainy IA, Hassan HH, Bahakim HM, Kurbaan KM, Zahraa JN, Al-Nasser MN, Nasir AA, Khoja WA, Kabiraj MM. Salih MA, et al. Among authors: hassan hh. Saudi Med J. 2006 Mar;27 Suppl 1:S12-20. Saudi Med J. 2006. PMID: 16532126
Stroke due to mitochondrial disorders in Saudi children.
Salih MA, Abdel-Gader AG, Zahraa JN, Al-Rayess MM, Alorainy IA, Hassan HH, Ruitenbeek W, Zeviani M. Salih MA, et al. Among authors: hassan hh. Saudi Med J. 2006 Mar;27 Suppl 1:S81-90. Saudi Med J. 2006. PMID: 16532135
75 results