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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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Tremor in Parkinson’s Disease: From Pathophysiology to Advanced TherapiesAbusrair, Ali H. ; Elsekaily, Walaa ; Bohlega, SaeedTremor and other hyperkinetic movements (New York, N.Y.), 2022-09, Vol.12 (1) [Periódico revisado por pares]Texto completo disponível |
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Material Type: Artigo
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Age-Period-Cohort Modeling of Multiple Sclerosis Incidence Rates in Kuwait: 1980–2014Akhtar, Saeed ; Al-Abkal, Jarrah ; Al-Hashel, Jasem Y. ; Alroughani, RaedNeuroepidemiology, 2017-12, Vol.49 (3-4), p.152-159 [Periódico revisado por pares]Basel, Switzerland: S. Karger AGTexto completo disponível |
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Material Type: Artigo
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Joinpoint Regression Analysis of Trends in Multiple Sclerosis Incidence in Kuwait: 1980–2019Akhtar, Saeed ; Al-Abkal, Jarrah ; Alroughani, RaedNeuroepidemiology, 2020-12, Vol.54 (6), p.472-481 [Periódico revisado por pares]Basel, Switzerland: S. Karger AGTexto completo disponível |
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Material Type: Artigo
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Impact of the first Gulf war on multiple sclerosis risk in Kuwait: a quasi-experimental studyAkhtar, Saeed ; Al-Hashel, Jasem Y ; Alroughani, RaedBMC neurology, 2023-07, Vol.23 (1), p.259-259, Article 259 [Periódico revisado por pares]England: BioMed Central LtdTexto completo disponível |
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Material Type: Artigo
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Clinical patterns of neurological involvement in Behçet's disease : evaluation of 200 patientsAKMAN-DEMIR, G ; SERDAROGLU, P ; TASCI, BBrain (London, England : 1878), 1999-11, Vol.122 (11), p.2171-2181 [Periódico revisado por pares]Oxford: Oxford University PressTexto completo disponível |
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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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Material Type: Artigo
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Diagnostic implications of pitfalls in causal variant identification based on 4577 molecularly characterized familiesAlAbdi, Lama ; Maddirevula, Sateesh ; Shamseldin, Hanan E. ; Khouj, Ebtissal ; Helaby, Rana ; Hamid, Halima ; Almulhim, Aisha ; Hashem, Mais O. ; Abdulwahab, Firdous ; Abouyousef, Omar ; Alqahtani, Mashael ; Altuwaijri, Norah ; Jaafar, Amal ; Alshidi, Tarfa ; Alzahrani, Fatema ; Al-Sagheir, Afaf I. ; Mansour, Ahmad M. ; Alawaji, Ali ; Aldhilan, Amal ; Alhashem, Amal ; Alhemidan, Amal ; Nabil, Amira ; Khan, Arif O. ; Aljohar, Aziza ; Alsaleem, Badr ; Tabarki, Brahim ; Lourenco, Charles Marques ; Faqeih, Eissa ; AlShail, Essam ; Almesaifri, Fatima ; Mutairi, Fuad Al ; Alzaidan, Hamad ; Morsy, Heba ; Alshihry, Hind ; Alkuraya, Hisham ; Girisha, Katta Mohan ; Al-Fayez, Khawla ; Al-Rubeaan, Khalid ; kraoua, Lilia ; Alnemer, Maha ; Tulbah, Maha ; Zaki, Maha S. ; Alfadhel, Majid ; Abouelhoda, Mohammed ; Nezarati, Marjan M. ; Al-Qattan, Mohammad ; Shboul, Mohammad ; Abanemai, Mohammed ; Al-Muhaizea, Mohammad A. ; Al-owain, Mohammed ; Bafaqeeh, Mohammed Sameer ; Alshammari, Muneera ; Abukhalid, Musaad ; Alsahan, Nada ; Derar, Nada ; Meriki, Neama ; Bohlega, Saeed A. ; Tala, Saeed Al ; Alhassan, Saad ; Wali, Sami ; Mohamed, Sarar ; Coskun, Serdar ; Saadeh, Sermin ; Tkemaladze, Tinatin ; Kurdi, Wesam ; Alhumaidi, Zainab Ahmed ; Rahbeeni, Zuhair ; Alkuraya, Fowzan S.Nature communications, 2023-08, Vol.14 (1), p.5269-5269, Article 5269 [Periódico revisado por pares]London: Nature Publishing GroupTexto completo disponível |
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Material Type: Artigo
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Knowledge and barriers to screening for colorectal cancer among individuals aged 40 years or older visiting primary healthcare clinics in Al-Khobar, Eastern ProvinceAlabdulkader, Assim M ; Mustafa, Tajammal ; Almutailiq, Danah A ; Al-Maghrabi, Razan A ; Alzanadi, Rabab H ; Almohsen, Danyah S ; Alkaltham, Nourah KIndian Journal of Community and Family Medicine, 2024-01, Vol.31 (1), p.25-35 [Periódico revisado por pares]India: Medknow Publications and Media Pvt. LtdTexto completo disponível |
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Material Type: Artigo
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Mutations in C2orf37, Encoding a Nucleolar Protein, Cause Hypogonadism, Alopecia, Diabetes Mellitus, Mental Retardation, and Extrapyramidal SyndromeAlazami, Anas M. ; Al-Saif, Amr ; Al-Semari, Abdulaziz ; Bohlega, Saeed ; Zlitni, Soumaya ; Alzahrani, Fatema ; Bavi, Prashant ; Kaya, Namik ; Colak, Dilek ; Khalak, Hanif ; Baltus, Andy ; Peterlin, Borut ; Danda, Sumita ; Bhatia, Kailash P. ; Schneider, Susanne A. ; Sakati, Nadia ; Walsh, Christopher A. ; Al-Mohanna, Futwan ; Meyer, Brian ; Alkuraya, Fowzan S.American journal of human genetics, 2008-12, Vol.83 (6), p.684-691 [Periódico revisado por pares]United States: Elsevier IncTexto completo disponível |