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Material Type: Artigo
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Riboflavin Has Neuroprotective Potential: Focus on Parkinson's Disease and MigraineMarashly, Eyad T ; Bohlega, Saeed AFrontiers in neurology, 2017-07, Vol.8, p.333-333 [Periódico revisado por pares]Switzerland: Frontiers Media S.ATexto completo disponível |
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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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Integrated Analysis of Whole Exome Sequencing and Copy Number Evaluation in Parkinson's DiseaseYemni, Eman Al ; Monies, Dorota ; Alkhairallah, Thamer ; Bohlega, Saeed ; Abouelhoda, Mohamed ; Magrashi, Amna ; Mustafa, Abeer ; AlAbdulaziz, Basma ; Alhamed, Mohamed ; Baz, Batoul ; Goljan, Ewa ; Albar, Renad ; Jabaan, Amjad ; Faquih, Tariq ; Subhani, Shazia ; Ali, Wafa ; Shinwari, Jameela ; Al-Mubarak, Bashayer ; Al-Tassan, NadaScientific reports, 2019-03, Vol.9 (1), p.3344-3344, Article 3344 [Periódico revisado por pares]England: Nature Publishing GroupTexto completo disponível |
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Material Type: Artigo
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Novel mutation of the notch3 gene in arabic family with CADASILBohlega, SaeedNeurology international, 2011-07, Vol.3 (2), p.e6-e6 [Periódico revisado por pares]Italy: MDPI AGTexto completo disponível |
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Material Type: Artigo
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Truncating ARL6IP1 variant as the genetic cause of fatal complicated hereditary spastic paraplegiaWakil, Salma M ; Alhissi, Safa ; Al Dossari, Haya ; Alqahtani, Ayesha ; Shibin, Sherin ; Melaiki, Brahim T ; Finsterer, Josef ; Al-Hashem, Amal ; Bohlega, Saeed ; Alazami, Anas MBMC medical genetics, 2019-07, Vol.20 (1), p.119-119, Article 119 [Periódico revisado por pares]England: BioMed Central LtdTexto completo disponível |
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Material Type: Artigo
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Hypogonadism, alopecia and neurological manifestations: evolving syndromes from an old association. (P4.9-060)Abusrair, Ali ; Bohlega, SaeedNeurology, 2019-04, Vol.92 (15_supplement) [Periódico revisado por pares]Texto completo disponível |
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Material Type: Artigo
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Multimodal Evoked Potential Profiles in Woodhouse-Sakati SyndromeAbusrair, Ali ; AlHamoud, Iftetah ; Bohlega, SaeedJournal of clinical neurophysiology, 2022-09, Vol.Publish Ahead of Print (6), p.504-509 [Periódico revisado por pares]United StatesTexto completo disponível |
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Material Type: Artigo
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Expanding the genotype-phenotype landscape of PDE10A-associated movement disorders (S42.004)Bohlega, Saeed ; Al-Qahtani, Zainah ; Guzmán-Vega, Francisco J. ; Ramakrishnan, Reshmi ; Abusrair, Ali ; Aldosari, Haya ; AlDakheel, Amaal ; Al-Qahtani, Salma ; Monies, Dorota ; Arold, StefanNeurology, 2023-04, Vol.100 (17_supplement_2) [Periódico revisado por pares]Texto completo disponível |
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Material Type: Artigo
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A first-line diagnostic assay for limb-girdle muscular dystrophy and other myopathiesMonies, Dorota ; Alhindi, Hindi N ; Almuhaizea, Mohamed A ; Abouelhoda, Mohamed ; Alazami, Anas M ; Goljan, Ewa ; Alyounes, Banan ; Jaroudi, Dyala ; AlIssa, Abdulelah ; Alabdulrahman, Khalid ; Subhani, Shazia ; El-Kalioby, Mohamed ; Faquih, Tariq ; Wakil, Salma M ; Altassan, Nada A ; Meyer, Brian F ; Bohlega, SaeedHuman genomics, 2016-09, Vol.10 (1), p.32-32, Article 32 [Periódico revisado por pares]England: BioMed CentralTexto 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 |