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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
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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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]

Darmstadt: Steinkopff Verlag

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5
Truncating ARL6IP1 variant as the genetic cause of fatal complicated hereditary spastic paraplegia
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Artigo
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Truncating ARL6IP1 variant as the genetic cause of fatal complicated hereditary spastic paraplegia

Wakil, Salma M ; Alhissi, Safa ; Al Dossari, Haya ; Alqahtani, Ayesha ; Shibin, Sherin ; Melaiki, Brahim T ; Finsterer, Josef ; Al-Hashem, Amal ; Bohlega, Saeed ; Alazami, Anas M

BMC medical genetics, 2019-07-04, Vol.20 (1), p.119-119 [Periódico revisado por pares]

England: BioMed Central Ltd

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6
Ultrasound-guided botulinum toxin A injection in the treatment of belly dancer's dyskinesia
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Artigo
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Ultrasound-guided botulinum toxin A injection in the treatment of belly dancer's dyskinesia

Alshubaili, Asmahan ; Abou-Al-Shaar, Hussam ; Santhamoorthy, Ponnusamy ; Attia, Hosam ; Bohlega, Saeed

BMC neurology, 2016-11-17, Vol.16 (1), p.226-226 [Periódico revisado por pares]

England: BioMed Central Ltd

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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
Mutations in NHLRC1 cause progressive myoclonus epilepsy
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Mutations in NHLRC1 cause progressive myoclonus epilepsy

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

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

London: Nature Publishing Group

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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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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
A missense mutation in PIK3R5 gene in a family with ataxia and oculomotor apraxia
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A missense mutation in PIK3R5 gene in a family with ataxia and oculomotor apraxia

Al Tassan, Nada ; Khalil, Dania ; Shinwari, Jameela ; Al Sharif, Latifa ; Bavi, Prashant ; Abduljaleel, Zainularifeen ; Abu Dhaim, Nada ; Magrashi, Amna ; Bobis, Steve ; Ahmed, Hala ; AlAhmed, Samaher ; Bohlega, Saeed

Human mutation, 2012-02, Vol.33 (2), p.351-354 [Periódico revisado por pares]

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

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