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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
Ataxia and Hypogonadotropic Hypogonadism with Intrafamilial Variability Caused by RNF216 Mutation
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Artigo
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Ataxia and Hypogonadotropic Hypogonadism with Intrafamilial Variability Caused by RNF216 Mutation

Alqwaifly, Mohammed ; Bohlega, Saeed

Neurology international, 2016-06-15, Vol.8 (2), p.6444-6444 [Periódico revisado por pares]

Italy: MDPI AG

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5
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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6
Cladribine Tablets and Relapsing–Remitting Multiple Sclerosis: A Pragmatic, Narrative Review of What Physicians Need to Know
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Artigo
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Cladribine Tablets and Relapsing–Remitting Multiple Sclerosis: A Pragmatic, Narrative Review of What Physicians Need to Know

AlJumah, Mohamed ; Alkhawajah, Mona Marwan ; Qureshi, Shireen ; Al-Thubaiti, Ibtisam ; Ayoub, Omar ; Bohlega, Saeed A ; Bushnag, Areej ; Cupler, Edward ; Daif, Abdulkader ; El Boghdady, Ahmed ; Hassan, Ahmed ; Al Malik, Yaser ; Saeedi, Jameelah ; Al-Shamrany, Fawzia ; Shosha, Eslam ; Rieckmann, Peter

Neurology and therapy, 2020-06, Vol.9 (1), p.11-23 [Periódico revisado por pares]

Cheshire: Springer Healthcare

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7
Patterns of neurological manifestations in Woodhouse-Sakati Syndrome
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Artigo
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Patterns of neurological manifestations in Woodhouse-Sakati Syndrome

Bohlega, Saeed ; Abusrair, Ali H ; Al-Ajlan, Fahad S ; Alharbi, Norah ; Al-Semari, Abdulaziz ; Bohlega, Balsam ; Abualsaud, Dalya ; Alkuraya, Fowzan

Parkinsonism & related disorders, 2019-12, Vol.69, p.99-103 [Periódico revisado por pares]

England: Elsevier Ltd

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8
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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9
Neurological complications in liver transplantation
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Artigo
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Neurological complications in liver transplantation

Ghaus, Naveed ; Bohlega, Saeed ; Rezeig, Mohammed

Journal of neurology, 2001-12, Vol.248 (12), p.1042-1048 [Periódico revisado por pares]

Darmstadt: Steinkopff Verlag

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10
Novel mutation of the notch3 gene in arabic family with CADASIL
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Artigo
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Novel mutation of the notch3 gene in arabic family with CADASIL

Bohlega, Saeed

Neurology international, 2011-07-05, Vol.3 (2), p.e6-e6 [Periódico revisado por pares]

Italy: MDPI AG

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