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1
A mutation in sigma-1 receptor causes juvenile amyotrophic lateral sclerosis
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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
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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3
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, 2016-08, Vol.367, p.239-243 [Periódico revisado por pares]

Netherlands: Elsevier B.V

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4
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]

Berlin: Springer

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5
Miyoshi myopathy in Saudi Arabia: clinical, electrophysiological, histopathological and radiological features
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Artigo
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Miyoshi myopathy in Saudi Arabia: clinical, electrophysiological, histopathological and radiological features

Cupler, Edward J ; Bohlega, Saeed ; Hessler, Richard ; McLean, Donald ; Stigsby, Bent ; Ahmad, Javed

Neuromuscular disorders : NMD, 1998-06, Vol.8 (5), p.321-326 [Periódico revisado por pares]

England: Elsevier B.V

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6
Neurodegenerative Huntington-like disorder
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Artigo
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Neurodegenerative Huntington-like disorder

Bohlega, Saeed ; Al-Tahan, Abdulrahman ; Kambouris, Marios ; Divakaran, Madai

Movement disorders, 2001-05, Vol.16 (3), p.533-534 [Periódico revisado por pares]

New York: John Wiley & Sons, Inc

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7
T313M PINK1 Mutation in an Extended Highly Consanguineous Saudi Family With Early-Onset Parkinson Disease
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Artigo
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T313M PINK1 Mutation in an Extended Highly Consanguineous Saudi Family With Early-Onset Parkinson Disease

Chishti, Muhammad A ; Bohlega, Saeed ; Ahmed, Maqbool ; Loualich, Arslan ; Carroll, Pamela ; Sato, Christine ; St George-Hyslop, Peter ; Westaway, David ; Rogaeva, Ekaterina

Archives of neurology (Chicago), 2006-10, Vol.63 (10), p.1483-1485

Chicago, IL: American Medical Association

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8
Subacute sclerosing panencephalitis: evaluation with CT and MR
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Artigo
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Subacute sclerosing panencephalitis: evaluation with CT and MR

Brismar, J ; Gascon, GG ; von Steyern, KV ; Bohlega, S

American journal of neuroradiology : AJNR, 1996-04, Vol.17 (4), p.761-772 [Periódico revisado por pares]

Oak Brook, IL: Am Soc Neuroradiology

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9
Impact of the first Gulf war on multiple sclerosis risk in Kuwait: a quasi-experimental study
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Artigo
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Impact of the first Gulf war on multiple sclerosis risk in Kuwait: a quasi-experimental study

Akhtar, Saeed ; Al-Hashel, Jasem Y ; Alroughani, Raed

BMC neurology, 2023-07, Vol.23 (1), p.259-259, Article 259 [Periódico revisado por pares]

England: BioMed Central Ltd

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