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1 |
Material Type: Artigo
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Parkinson's Disease in Saudi Patients: A Genetic StudyAl-Mubarak, Bashayer R ; Bohlega, Saeed A ; Alkhairallah, Thamer S ; Magrashi, Amna I ; AlTurki, Maha I ; Khalil, Dania S ; AlAbdulaziz, Basma S ; Abou Al-Shaar, Hussam ; Mustafa, Abeer E ; Alyemni, Eman A ; Alsaffar, Bashayer A ; Tahir, Asma I ; Al Tassan, Nada A Cookson, Mark R.PloS one, 2015-08, Vol.10 (8), p.e0135950-e0135950 [Periódico revisado por pares]United States: Public Library of ScienceTexto completo disponível |
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Material Type: Artigo
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Nine Hereditary Movement Disorders First Described in Asia: Their History and EvolutionJagota, Priya ; Ugawa, Yoshikazu ; Aldaajani, Zakiyah ; Ibrahim, Norlinah Mohamed ; Ishiura, Hiroyuki ; Nomura, Yoshiko ; Tsuji, Shoji ; Diesta, Cid ; Hattori, Nobutaka ; Onodera, Osamu ; Bohlega, Saeed ; Al-Din, Amir ; Lim, Shen-Yang ; Lee, Jee-Young ; Jeon, Beomseok ; Pal, Pramod Kumar ; Shang, Huifang ; Fujioka, Shinsuke ; Kukkle, Prashanth Lingappa ; Phokaewvarangkul, Onanong ; Lin, Chin-Hsien ; Shambetova, Cholpon ; Bhidayasiri, RoongrojJournal Of Movement Disorders, 2023, 16(3), , pp.231-247 [Periódico revisado por pares]The Korean Movement Disorder SocietyTexto completo disponível |
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Material Type: Artigo
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Clinical and molecular characterization of ataxia with oculomotor apraxia patients in Saudi ArabiaBohlega, Saeed A ; Shinwari, Jameela M ; Al Sharif, Latifa J ; Khalil, Dania S ; Alkhairallah, Thamer S ; Al Tassan, Nada ABMC medical genetics, 2011-02, Vol.12 (1), p.27-27, Article 27 [Periódico revisado por pares]England: BioMed Central LtdTexto completo disponível |
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Material Type: Artigo
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Mutation of fibulin-1 causes a novel syndrome involving the central nervous system and connective tissuesBohlega, Saeed ; Al-Ajlan, Huda ; Al-Saif, AmrEuropean journal of human genetics : EJHG, 2014-05, Vol.22 (5), p.640-643 [Periódico revisado por pares]England: Nature Publishing GroupTexto completo disponível |
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Material Type: Artigo
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Miyoshi myopathy in Saudi Arabia: clinical, electrophysiological, histopathological and radiological featuresCupler, Edward J ; Bohlega, Saeed ; Hessler, Richard ; McLean, Donald ; Stigsby, Bent ; Ahmad, JavedNeuromuscular disorders : NMD, 1998-06, Vol.8 (5), p.321-326 [Periódico revisado por pares]England: Elsevier B.VTexto completo disponível |
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Material Type: Dataset
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Additional file 4: of Identification of a novel genetic locus underlying tremor and dystoniaMonies, Dorota ; Al-Shaar, Hussam ; Goljan, Ewa ; Banan Al-Younes ; Al-Breacan, Muna ; Al-Saif, Maher ; Wakil, Salma ; Meyer, Brian ; Khabar, Khalid ; Bohlega, SaeedFigshare 2017Texto completo disponível |
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Material Type: Dataset
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Additional file 3: of Identification of a novel genetic locus underlying tremor and dystoniaMonies, Dorota ; Al-Shaar, Hussam ; Goljan, Ewa ; Banan Al-Younes ; Al-Breacan, Muna ; Al-Saif, Maher ; Wakil, Salma ; Meyer, Brian ; Khabar, Khalid ; Bohlega, SaeedFigshare 2017Texto completo disponível |
8 |
Material Type: Dataset
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Additional file 2: of Identification of a novel genetic locus underlying tremor and dystoniaMonies, Dorota ; Al-Shaar, Hussam ; Goljan, Ewa ; Banan Al-Younes ; Al-Breacan, Muna ; Al-Saif, Maher ; Wakil, Salma ; Meyer, Brian ; Khabar, Khalid ; Bohlega, SaeedFigshare 2017Texto completo disponível |
9 |
Material Type: Dataset
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Additional file 2: of A first-line diagnostic assay for limb-girdle muscular dystrophy and other myopathiesMonies, Dorota ; Hindi Alhindi ; Almuhaizea, Mohamed ; Abouelhoda, Mohamed ; Alazami, Anas ; Goljan, Ewa ; Banan Alyounes ; Dyala Jaroudi ; Abdulelah AlIssa ; Alabdulrahman, Khalid ; Subhani, Shazia ; El-Kalioby, Mohamed ; Faquih, Tariq ; Wakil, Salma ; Altassan, Nada ; Meyer, Brian ; Bohlega, SaeedFigshare 2016Texto completo disponível |
10 |
Material Type: Artigo
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The role of the PLA2G6 gene in neurodegenerative diseasesDeng, Xinyue ; Yuan, Lamei ; Jankovic, Joseph ; Deng, HaoAgeing research reviews, 2023-08, Vol.89, p.101957-101957, Article 101957 [Periódico revisado por pares]England: Elsevier B.VTexto completo disponível |