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Material Type: Artigo
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Accelerating Novel Candidate Gene Discovery in Neurogenetic Disorders via Whole-Exome Sequencing of Prescreened Multiplex Consanguineous FamiliesAlazami, Anas M. ; Patel, Nisha ; Shamseldin, Hanan E. ; Anazi, Shamsa ; Al-Dosari, Mohammed S. ; Alzahrani, Fatema ; Hijazi, Hadia ; Alshammari, Muneera ; Aldahmesh, Mohammed A. ; Salih, Mustafa A. ; Faqeih, Eissa ; Alhashem, Amal ; Bashiri, Fahad A. ; Al-Owain, Mohammed ; Kentab, Amal Y. ; Sogaty, Sameera ; Al Tala, Saeed ; Temsah, Mohamad-Hani ; Tulbah, Maha ; Aljelaify, Rasha F. ; Alshahwan, Saad A. ; Seidahmed, Mohammed Zain ; Alhadid, Adnan A. ; Aldhalaan, Hesham ; AlQallaf, Fatema ; Kurdi, Wesam ; Alfadhel, Majid ; Babay, Zainab ; Alsogheer, Mohammad ; Kaya, Namik ; Al-Hassnan, Zuhair N. ; Abdel-Salam, Ghada M.H. ; Al-Sannaa, Nouriya ; Al Mutairi, Fuad ; El Khashab, Heba Y. ; Bohlega, Saeed ; Jia, Xiaofei ; Nguyen, Henry C. ; Hammami, Rakad ; Adly, Nouran ; Mohamed, Jawahir Y. ; Abdulwahab, Firdous ; Ibrahim, Niema ; Naim, Ewa A. ; Al-Younes, Banan ; Meyer, Brian F. ; Hashem, Mais ; Shaheen, Ranad ; Xiong, Yong ; Abouelhoda, Mohamed ; Aldeeri, Abdulrahman A. ; Monies, Dorota M. ; Alkuraya, Fowzan S.Cell reports (Cambridge), 2015-01, Vol.10 (2), p.148-161 [Periódico revisado por pares]United States: Elsevier IncTexto completo disponível |
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Material Type: Artigo
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Adherence to Disease-Modifying Drugs in Patients with Multiple Sclerosis: A Consensus Statement from the Middle East MS Advisory GroupYamout, Bassem I. ; Dahdaleh, Maurice ; Jumah, Mohammed Ali Al ; Al-Shammri, Suhail ; Sharoqi, Isa Al ; Al-Tahan, Abdel Rahman ; Bohlega, Saeed ; Deleu, Dirk ; Inshasi, Jihad ; Khalifa, Ahmad ; Szólics, MiklosInternational journal of neuroscience, 2010-04, Vol.120 (4), p.273-279 [Periódico revisado por pares]England: Informa UK LtdTexto completo disponível |
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Material Type: Artigo
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Autosomal Recessive Juvenile Parkinsonism Maps to 6q25.2-q27 in Four Ethnic Groups: Detailed Genetic Mapping of the Linked RegionJones, Alison C. ; Yamamura, Yasuhiro ; Almasy, Laura ; Bohlega, Saeed ; Elibol, Bülent ; Hubble, Jean ; Kuzuhara, Shigeki ; Uchida, Masao ; Yanagi, Tsutomu ; Weeks, Daniel E. ; Nygaard, Torbjoern G.American journal of human genetics, 1998-07, Vol.63 (1), p.80-87 [Periódico revisado por pares]Chicago, IL: Elsevier IncTexto completo disponível |
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Material Type: Artigo
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Autosomal-recessive syndrome with alopecia, hypogonadism, progressive extra-pyramidal disorder, white matter disease, sensory neural deafness, diabetes mellitus, and low IGF1Al-Semari, Abdulaziz ; Bohlega, SaeedAmerican journal of medical genetics. Part A, 2007-01, Vol.143A (2), p.149-160 [Periódico revisado por pares]Hoboken: Wiley Subscription Services, Inc., A Wiley CompanyTexto completo disponível |
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Material Type: Artigo
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Biosimilars: opinion of an expert panel in the Middle EastBohlega, S. ; Al-Shammri, S. ; Sharoqi, I. Al ; Dahdaleh, M. ; Gebeily, S. ; Inshasi, J. ; Khalifa, A. ; Pakdaman, H. ; Szólics, M. ; Yamout, B.Current medical research and opinion, 2008-10, Vol.24 (10), p.2897-2903 [Periódico revisado por pares]England: Informa UK LtdTexto completo disponível |
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Material Type: Artigo
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Botulinum toxin therapy for treatment of spasticity in multiple sclerosis: review and recommendations of the IAB-Interdisciplinary Working Group for Movement Disorders task forceDressler, Dirk ; Bhidayasiri, Roongroj ; Bohlega, Saeed ; Chahidi, Abderrahmane ; Chung, Tae Mo ; Ebke, Markus ; Jacinto, L. Jorge ; Kaji, Ryuji ; Koçer, Serdar ; Kanovsky, Petr ; Micheli, Federico ; Orlova, Olga ; Paus, Sebastian ; Pirtosek, Zvezdan ; Relja, Maja ; Rosales, Raymond L. ; Sagástegui-Rodríguez, José Alberto ; Schoenle, Paul W. ; Shahidi, Gholam Ali ; Timerbaeva, Sofia ; Walter, Uwe ; Saberi, Fereshte AdibJournal of neurology, 2017, Vol.264 (1), p.112-120 [Periódico revisado por pares]Berlin/Heidelberg: Springer Berlin HeidelbergTexto completo disponível |
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Material Type: Artigo
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CADASIL in Arabs: clinical and genetic findingsBohlega, Saeed ; Al Shubili, Asmahan ; Edris, Abdulrahman ; Alreshaid, Abdulrahman ; Alkhairallah, Thamer ; AlSous, M Walid ; Farah, Samir ; Abu-Amero, Khaled KBMC medical genetics, 2007-11, Vol.8 (1), p.67-67, Article 67 [Periódico revisado por pares]England: BioMed Central LtdTexto completo disponível |
8 |
Material Type: Artigo
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Characteristics of multiple sclerosis in the Middle East with special reference to the applicability of international guidelines to the regionAl Tahan, Abdulrahman M. ; Alsharoqi, Isa ; Bohlega, Saeed A. ; Dahdaleh, Maurice ; Daif, Abdulkader ; Deleu, Dirk ; Esmat, Khaled ; Giampaolo, Dominic ; Freedman, Mark S. ; Gwilt, Michael ; Hosny, Hassan ; Inshasi, Jihad S. ; Aljumah, Mohammed ; Khalifa, Ahmad ; Pakdaman, Hossein ; Szólics, Miklós ; Yamout, Bassem I. ; Sahraian, Mohammed A. ; Zakaria, Magd F.International journal of neuroscience, 2014-09, Vol.124 (9), p.635-641 [Periódico revisado por pares]England: Informa HealthcareTexto completo disponível |
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Material Type: Artigo
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Chorea-acanthocytosis: Clinical and genetic findings in three families from the Arabian peninsulaBohlega, Saeed ; Al-Jishi, Adel ; Dobson-Stone, Carol ; Rampoldi, Luca ; Saha, Parthasarathi ; Murad, Hatem ; Kareem, Abid ; Roberts, George ; Monaco, Anthony P.Movement disorders, 2003-04, Vol.18 (4), p.403-407 [Periódico revisado por pares]New York: Wiley Subscription Services, Inc., A Wiley CompanyTexto completo disponível |
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Material Type: Artigo
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Clinical and genetic features of anoctaminopathy in Saudi ArabiaBohlega, Saeed ; Monies, Dorothy M ; Abulaban, Ahmad A ; Murad, Hatem N ; Alhindi, Hindi N ; Meyer, Brian FNeurosciences (Riyadh, Saudi Arabia), 2015-04, Vol.20 (2), p.173-177 [Periódico revisado por pares]Saudi Arabia: Riyadh : Armed Forces HospitalTexto completo disponível |