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Material Type: Artigo
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Autosomal recessive ADCY5-Related dystonia and myoclonus: Expanding the genetic spectrum of ADCY5-Related movement disordersBohlega, Saeed A. ; Abou-Al-Shaar, Hussam ; AlDakheel, Amaal ; Alajlan, Huda ; Bohlega, Balsam S. ; Meyer, Brian F. ; Monies, Dorota ; Cupler, Edward J. ; Al-Saif, Amr M.Parkinsonism & related disorders, 2019-07, Vol.64, p.145-149 [Periódico revisado por pares]England: Elsevier LtdTexto completo disponível |
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2 |
Material Type: Artigo
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Clinical, neurophysiological, radiological, pathological, and genetic feature of Dysferlinopathy in Saudi ArabiaAlharbi, Norah ; Bohlega, Saeed ; Alhindi, Hindi ; Matar, RawanJournal of the neurological sciences, 2023-12, Vol.455, p.122521, Article 122521 [Periódico revisado por pares]Texto completo disponível |
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3 |
Material Type: Artigo
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Clinical and pathological heterogeneity of a congenital disorder of glycosylation manifesting as a myasthenic/myopathic syndromeMonies, Dorota M ; Al-Hindi, Hindi N ; Al-Muhaizea, Mohamed A ; Jaroudi, Dyala J ; Al-Younes, Banan ; Naim, Ewa A ; Wakil, Salma M ; Meyer, Brian F ; Bohlega, SaeedNeuromuscular disorders : NMD, 2014-04, Vol.24 (4), p.353-359 [Periódico revisado por pares]England: Elsevier B.VTexto completo disponível |
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4 |
Material Type: Artigo
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Patterns of neurological manifestations in Woodhouse-Sakati SyndromeBohlega, Saeed ; Abusrair, Ali H. ; Al-Ajlan, Fahad S. ; Alharbi, Norah ; Al-Semari, Abdulaziz ; Bohlega, Balsam ; Abualsaud, Dalya ; Alkuraya, FowzanParkinsonism & related disorders, 2019-12, Vol.69, p.99-103 [Periódico revisado por pares]England: Elsevier LtdTexto completo disponível |
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5 |
Material Type: Artigo
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Functional clinical outcomes in multiple sclerosis: Current status and future prospectsKarabudak, Rana ; Dahdaleh, Maurice ; Aljumah, Mohammed ; Alroughani, Raed ; Alsharoqi, I. Ahmed ; AlTahan, Abdulrahman M ; Bohlega, Saeed A ; Daif, Abdulkader ; Deleu, Dirk ; Amous, Amer ; Inshasi, Jihad S ; Rieckmann, Peter ; Sahraian, Mohammed A ; Yamout, Bassem IMultiple sclerosis and related disorders, 2015-05, Vol.4 (3), p.192-201Netherlands: Elsevier B.VTexto completo disponível |
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Material Type: Artigo
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MENACTRIMS practice guideline for COVID-19 vaccination in patients with multiple sclerosisYamout, Bassem I ; Zakaria, Magd ; Inshasi, Jihad ; Al-Jumah, Mohammad ; Zeineddine, Maya ; Dahdaleh, Maurice ; Bohlega, Saeed ; Gouider, Riadh ; Alroughani, RaedMultiple sclerosis and related disorders, 2021-11, Vol.56, p.103225-103225, Article 103225Netherlands: Elsevier B.VTexto completo disponível |
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Material Type: Artigo
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Real World Effectiveness of Oral Cladribine in Multiple Sclerosis Treatment, Report from a Single Saudi CenterBohlega, Saeed ; Alkhawajah, Mona ; Sulague, Norah ; Alfugham, NoraMultiple sclerosis and related disorders, 2023-12, Vol.80, p.105298, Article 105298Texto completo disponível |
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8 |
Material Type: Artigo
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A novel splice site mutation in ERLIN2 causes hereditary spastic paraplegia in a Saudi familyWakil, Salma M ; Bohlega, Saeed ; Hagos, Samya ; Baz, Batoul ; Al Dossari, Haya ; Ramzan, Khushnooda ; Al-Hassnan, Zuhair NEuropean journal of medical genetics, 2013-01, Vol.56 (1), p.43-45 [Periódico revisado por pares]Netherlands: Elsevier Masson SASTexto completo disponível |
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9 |
Material Type: Artigo
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Phenotypic comparison of individuals with homozygous or heterozygous mutation of NOTCH3 in a large CADASIL familyAl-Shaar, Hussam Abou ; Qadi, Najeeb ; Ahmed, Mohammed ; Meyer, Brian F ; Bohlega, SaeedJournal of the neurological sciences, 2016-08, Vol.367, p.239-243 [Periódico revisado por pares]Netherlands: Elsevier B.VTexto completo disponível |
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10 |
Material Type: Artigo
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Economic Evaluation of Cladribine Tablets in Patients With High Disease Activity–Relapsing-Remitting Multiple Sclerosis in the Kingdom of Saudi ArabiaBohlega, Saeed ; Elboghdady, Ahmed ; Al-Johani, Awatef ; Mahajan, Koshu ; Mughari, Majdoline Khalil ; Al-Saqa’aby, Mai ; Mohamed, Omneya ; Alarieh, Rola ; Al Malik, YaserValue in health regional issues, 2021-09, Vol.25, p.189-195 [Periódico revisado por pares]United States: Elsevier IncTexto completo disponível |