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1
A mutation in sigma-1 receptor causes juvenile amyotrophic lateral sclerosis
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Artigo
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A mutation in sigma-1 receptor causes juvenile amyotrophic lateral sclerosis

Al-Saif, Amr ; Al-Mohanna, Futwan ; Bohlega, Saeed

Annals of neurology, 2011-12, Vol.70 (6), p.913-919 [Periódico revisado por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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2
Riboflavin Has Neuroprotective Potential: Focus on Parkinson's Disease and Migraine
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Artigo
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Riboflavin Has Neuroprotective Potential: Focus on Parkinson's Disease and Migraine

Marashly, Eyad T ; Bohlega, Saeed A

Frontiers in neurology, 2017, Vol.8, p.333-333 [Periódico revisado por pares]

Switzerland: Frontiers Media S.A

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3
Loss of ERLIN2 function leads to juvenile primary lateral sclerosis
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Artigo
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Loss of ERLIN2 function leads to juvenile primary lateral sclerosis

Al-Saif, Amr ; Bohlega, Saeed ; Al-Mohanna, Futwan

Annals of neurology, 2012-10, Vol.72 (4), p.510-516 [Periódico revisado por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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4
Diagnosis and management of Neuro-Behçet’s disease: international consensus recommendations
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Artigo
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Diagnosis and management of Neuro-Behçet’s disease: international consensus recommendations

Kalra, Seema ; Silman, Alan ; Akman-Demir, Gulsen ; Bohlega, Saeed ; Borhani-Haghighi, Afshin ; Constantinescu, Cris S ; Houman, Habib ; Mahr, Alfred ; Salvarani, Carlos ; Sfikakis, Petros P ; Siva, Aksel ; Al-Araji, Adnan

Journal of neurology, 2014-09, Vol.261 (9), p.1662-1676 [Periódico revisado por pares]

Berlin/Heidelberg: Springer Berlin Heidelberg

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5
Multiple sclerosis in the Arabian Gulf countries: a consensus statement
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Artigo
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Multiple sclerosis in the Arabian Gulf countries: a consensus statement

Bohlega, Saeed ; Inshasi, Jihad ; Al Tahan, Abdel Rahman ; Madani, Abu Bakr ; Qahtani, Hussien ; Rieckmann, Peter

Journal of neurology, 2013-12, Vol.260 (12), p.2959-2963 [Periódico revisado por pares]

Berlin/Heidelberg: Springer Berlin Heidelberg

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6
Defining spasticity: a new approach considering current movement disorders terminology and botulinum toxin therapy
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Artigo
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Defining spasticity: a new approach considering current movement disorders terminology and botulinum toxin therapy

Dressler, Dirk ; Bhidayasiri, Roongroj ; Bohlega, Saeed ; Chana, Pedro ; Chien, Hsin Fen ; Chung, Tae Mo ; Colosimo, Carlo ; Ebke, Markus ; Fedoroff, Klemens ; Frank, Bernd ; Kaji, Ryuji ; Kanovsky, Petr ; Koçer, Serdar ; 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 Adib

Journal of neurology, 2018-04, Vol.265 (4), p.856-862 [Periódico revisado por pares]

Berlin/Heidelberg: Springer Berlin Heidelberg

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7
Levodopa-Carbidopa Intestinal Gel Infusion Therapy in Advanced Parkinson's Disease: Single Middle Eastern Center Experience
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Artigo
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Levodopa-Carbidopa Intestinal Gel Infusion Therapy in Advanced Parkinson's Disease: Single Middle Eastern Center Experience

Bohlega, Saeed ; Abou Al-Shaar, Hussam ; Alkhairallah, Thamer ; Al-Ajlan, Fahad ; Hasan, Nael ; Alkahtani, Khalid

European neurology, 2016-01, Vol.74 (5-6), p.227-236 [Periódico revisado por pares]

Basel, Switzerland

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8
Botulinum toxin therapy for treatment of spasticity in multiple sclerosis: review and recommendations of the IAB-Interdisciplinary Working Group for Movement Disorders task force
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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 force

Dressler, 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 Adib

Journal of neurology, 2017-01, Vol.264 (1), p.112-120 [Periódico revisado por pares]

Berlin/Heidelberg: Springer Berlin Heidelberg

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9
Mutations in C2orf37, Encoding a Nucleolar Protein, Cause Hypogonadism, Alopecia, Diabetes Mellitus, Mental Retardation, and Extrapyramidal Syndrome
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Artigo
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Mutations in C2orf37, Encoding a Nucleolar Protein, Cause Hypogonadism, Alopecia, Diabetes Mellitus, Mental Retardation, and Extrapyramidal Syndrome

Alazami, 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, 2008-12-12, Vol.83 (6), p.684-691 [Periódico revisado por pares]

United States: Elsevier Inc

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10
Phenotypic comparison of individuals with homozygous or heterozygous mutation of NOTCH3 in a large CADASIL family
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Artigo
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Phenotypic comparison of individuals with homozygous or heterozygous mutation of NOTCH3 in a large CADASIL family

Al-Shaar, Hussam Abou ; Qadi, Najeeb ; Ahmed, Mohammed ; Meyer, Brian F ; Bohlega, Saeed

Journal of the neurological sciences, 2015, Vol.367, p.239-243 [Periódico revisado por pares]

Netherlands: Elsevier B.V

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