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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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Cladribine Tablets and Relapsing–Remitting Multiple Sclerosis: A Pragmatic, Narrative Review of What Physicians Need to KnowAlJumah, Mohamed ; Alkhawajah, Mona Marwan ; Qureshi, Shireen ; Al-Thubaiti, Ibtisam ; Ayoub, Omar ; Bohlega, Saeed A. ; Bushnag, Areej ; Cupler, Edward ; Daif, Abdulkader ; El Boghdady, Ahmed ; Hassan, Ahmed ; Al Malik, Yaser ; Saeedi, Jameelah ; Al-Shamrany, Fawzia ; Shosha, Eslam ; Rieckmann, PeterNeurology and therapy, 2020-06, Vol.9 (1), p.11-23 [Periódico revisado por pares]Cheshire: Springer HealthcareTexto 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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Clinical, Neurophysiological, Radiological, Pathological, and Genetic Features of Dysferlinopathy in Saudi ArabiaAlharbi, Norah ; Matar, Rawan ; Cupler, Edward ; Al-Hindi, Hindi ; Murad, Hatem ; Alhomud, Iftteah ; Monies, Dorota ; Alshehri, Ali ; Alyahya, Mossaed ; Meyer, Brian ; Bohlega, SaeedFrontiers in neuroscience, 2022-02, Vol.16, p.815556-815556 [Periódico revisado por pares]Switzerland: Frontiers Research FoundationTexto 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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Immune Reconstitution Therapy or Continuous Immunosuppression for the Management of Active Relapsing–Remitting Multiple Sclerosis Patients? A Narrative ReviewAlSharoqi, Isa Ahmed ; Aljumah, Mohamed ; Bohlega, Saeed ; Boz, Cavit ; Daif, Abdelkader ; El-Koussa, Salam ; Inshasi, Jihad ; Kurtuncu, Murat ; Müller, Thomas ; Retief, Chris ; Sahraian, Mohammad Ali ; Shaygannejad, Vahid ; Slassi, Ilham ; Taha, Karim ; Zakaria, Magd ; Sørensen, Per SoelbergNeurology and therapy, 2020-06, Vol.9 (1), p.55-66 [Periódico revisado por pares]Cheshire: Springer HealthcareTexto 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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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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Family Planning for People with Multiple Sclerosis in Saudi Arabia: an Expert ConsensusAl Jumah, Mohammed ; Al Malik, Yaser ; AlKhawajah, Nuha M. ; Saeedi, Jameelah ; AlThubaiti, Ibtisam ; Bohlega, Saeed ; Bunyan, Reem F. ; Cupler, Edward J. ; ElBoghdady, Ahmed ; Hassan, Ahmed ; Ali, Eman Nassim ; Clerico, Marinella Calabrese, Pasquale ; Pasquale CalabreseMultiple sclerosis international, 2021-02, Vol.2021, p.6667006-8 [Periódico revisado por pares]Egypt: HindawiTexto completo disponível |
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Material Type: Artigo
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Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophyBrown, Robert H ; Liu, Jing ; Aoki, Masashi ; Illa, Isabel ; Wu, Chenyan ; Fardeau, Michel ; Angelini, Corrado ; Serrano, Carmen ; Urtizberea, J. Andoni ; Hentati, Faycal ; Hamida, Mongi Ben ; Bohlega, Saeed ; Culper, Edward J ; Amato, Anthony A ; Bossie, Karen ; Oeltjen, Joshua ; Bejaoui, Khemissa ; McKenna-Yasek, Diane ; Hosler, Betsy A ; Schurr, Erwin ; Arahata, Kiichi ; de Jong, Pieter JNature genetics, 1998-09, Vol.20 (1), p.31-36 [Periódico revisado por pares]London: Nature Publishing GroupTexto completo disponível |