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1
Mutational spectrum of the CHAC gene in patients with chorea-acanthocytosis
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Artigo
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Mutational spectrum of the CHAC gene in patients with chorea-acanthocytosis

Dobson-Stone, C ; Danek, A ; Rampoldi, L ; Hardie, R J ; Chalmers, R M ; Wood, N W ; Bohlega, S ; Dotti, M T ; Federico, A ; Shizuka, M ; Tanaka, M ; Watanabe, M ; Ikeda, Y ; Brin, M ; Goldfarb, L G ; Karp, B I ; Mohiddin, S ; Fananapazir, L ; Storch, A ; Fryer, A E ; Maddison, P ; Sibon, I ; Trevisol-Bittencourt, P C ; Singer, C ; Caballero, I R ; Aasly, J O ; Schmierer, K ; Dengler, R ; Hiersemenzel, L-P ; Zeviani, M ; Meiner, V ; Lossos, A ; Johnson, S ; Mercado, F C ; Sorrentino, G ; Dupré, N ; Rouleau, G A ; Volkmann, J ; Arpa, J ; Lees, A ; Geraud, G ; Chouinard, S ; Németh, A ; Monaco, A P

European journal of human genetics : EJHG, 2002-11, Vol.10 (11), p.773-781 [Periódico revisado por pares]

England: Nature Publishing Group

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2
Mutations in NHLRC1 cause progressive myoclonus epilepsy
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Artigo
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Mutations in NHLRC1 cause progressive myoclonus epilepsy

Minassian, Berge A ; Scherer, Stephen W ; Chan, Elayne M ; Young, Edwin J ; Ianzano, Leonarda ; Munteanu, Iulia ; Zhao, Xiaochu ; Christopoulos, Constantine C ; Avanzini, Giuliano ; Elia, Maurizio ; Ackerley, Cameron A ; Jovic, Nebojsa J ; Bohlega, Saeed ; Andermann, Eva ; Rouleau, Guy A ; Delgado-Escueta, Antonio V

Nature genetics, 2003-10, Vol.35 (2), p.125-127 [Periódico revisado por pares]

London: Nature Publishing Group

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3
CADASIL in Arabs: clinical and genetic findings
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Artigo
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CADASIL in Arabs: clinical and genetic findings

Bohlega, Saeed ; Al Shubili, Asmahan ; Edris, Abdulrahman ; Alreshaid, Abdulrahman ; Alkhairallah, Thamer ; AlSous, M Walid ; Farah, Samir ; Abu-Amero, Khaled K

BMC medical genetics, 2007-11, Vol.8 (1), p.67-67, Article 67 [Periódico revisado por pares]

England: BioMed Central Ltd

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4
Adherence to Disease-Modifying Drugs in Patients with Multiple Sclerosis: A Consensus Statement from the Middle East MS Advisory Group
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Artigo
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Adherence to Disease-Modifying Drugs in Patients with Multiple Sclerosis: A Consensus Statement from the Middle East MS Advisory Group

Yamout, 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, Miklos

International journal of neuroscience, 2010-04, Vol.120 (4), p.273-279 [Periódico revisado por pares]

England: Informa UK Ltd

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5
Clinical and molecular characterization of ataxia with oculomotor apraxia patients in Saudi Arabia
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Artigo
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Clinical and molecular characterization of ataxia with oculomotor apraxia patients in Saudi Arabia

Bohlega, Saeed A ; Shinwari, Jameela M ; Al Sharif, Latifa J ; Khalil, Dania S ; Alkhairallah, Thamer S ; Al Tassan, Nada A

BMC medical genetics, 2011-02, Vol.12 (1), p.27-27, Article 27 [Periódico revisado por pares]

England: BioMed Central Ltd

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6
Will New Injection Devices for Interferon Beta-1a s.c. Affect Treatment Adherence in Patients With Multiple Sclerosis? An Expert Opinion in the Middle East
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Artigo
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Will New Injection Devices for Interferon Beta-1a s.c. Affect Treatment Adherence in Patients With Multiple Sclerosis? An Expert Opinion in the Middle East

Deleu, Dirk ; Alsharoqi, Issa ; Jumah, Mohammed Ali Al ; Tahan, Abdel Rahman Al ; Bohlega, Saeed ; Dahdaleh, Maurice ; Inshasi, Jihad ; Khalifa, Ahmad ; Szólics, Miklos ; Yamout, Bassem I.

International journal of neuroscience, 2011-03, Vol.121 (4), p.171-175 [Periódico revisado por pares]

Informa Healthcare

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7
Natalizumab treatment for multiple sclerosis: Middle East and North Africa regional recommendations for patient selection and monitoring
Material Type:
Artigo
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Natalizumab treatment for multiple sclerosis: Middle East and North Africa regional recommendations for patient selection and monitoring

Alroughani, Raed A ; Aref, Hany M ; Bohlega, Saeed A ; Dahdaleh, Maurice P ; Feki, Imed ; Al Jumah, Mohammed A ; Al-Kawi, Muhammad Z ; Koussa, Salam F ; Sahraian, Mohamad A ; Alsharoqi, Isa A ; Yamout, Bassem I

BMC neurology, 2014-02, Vol.14 (1), p.27-27, Article 27 [Periódico revisado por pares]

England: BioMed Central

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8
Mutation of fibulin-1 causes a novel syndrome involving the central nervous system and connective tissues
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Artigo
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Mutation of fibulin-1 causes a novel syndrome involving the central nervous system and connective tissues

Bohlega, Saeed ; Al-Ajlan, Huda ; Al-Saif, Amr

European journal of human genetics : EJHG, 2014-05, Vol.22 (5), p.640-643 [Periódico revisado por pares]

England: Nature Publishing Group

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9
Characteristics of multiple sclerosis in the Middle East with special reference to the applicability of international guidelines to the region
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Artigo
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Characteristics of multiple sclerosis in the Middle East with special reference to the applicability of international guidelines to the region

Al 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 Healthcare

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10
Parkinson's Disease in Saudi Patients: A Genetic Study
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Artigo
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Parkinson's Disease in Saudi Patients: A Genetic Study

Al-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 Science

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