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A mutation in sigma-1 receptor causes juvenile amyotrophic lateral sclerosis
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
Loss of ERLIN2 function leads to juvenile primary lateral sclerosis
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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
Parkinson's Disease in Saudi Patients: A Genetic Study
Parkinson's Disease in Saudi Patients: A Genetic Study
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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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4
Clinical and pathological heterogeneity of a congenital disorder of glycosylation manifesting as a myasthenic/myopathic syndrome
Clinical and pathological heterogeneity of a congenital disorder of glycosylation manifesting as a myasthenic/myopathic syndrome
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Clinical and pathological heterogeneity of a congenital disorder of glycosylation manifesting as a myasthenic/myopathic syndrome

Monies, Dorota M ; Al-Hindi, Hindi N ; Al-Muhaizea, Mohamed A ; Jaroudi, Dyala J ; Al-Younes, Banan ; Naim, Ewa A ; Wakil, Salma M ; Meyer, Brian F ; Bohlega, Saeed

Neuromuscular disorders : NMD, 2014-04, Vol.24 (4), p.353-359 [Periódico revisado por pares]

England: Elsevier B.V

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5
Multiple sclerosis in the Arabian Gulf countries: a consensus statement
Multiple sclerosis in the Arabian Gulf countries: a consensus statement
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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
Functional clinical outcomes in multiple sclerosis: Current status and future prospects
Functional clinical outcomes in multiple sclerosis: Current status and future prospects
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Functional clinical outcomes in multiple sclerosis: Current status and future prospects

Karabudak, Rana ; Dahdaleh, Maurice ; Aljumah, Mohammed ; Alroughani, Raed ; Alsharoqi, I. Ahmed ; AlTahan, Abdulrahman M ; Bohlega, Saeed A ; Daif, Abdulkader ; Deleu, Dirk ; Amous, Amer ; Inshasi, Jihad S ; Rieckmann, Peter ; Sahraian, Mohammed A ; Yamout, Bassem I

Multiple sclerosis and related disorders, 2015-05, Vol.4 (3), p.192-201

Netherlands: Elsevier B.V

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7
Phenotypic comparison of individuals with homozygous or heterozygous mutation of NOTCH3 in a large CADASIL family
Phenotypic comparison of individuals with homozygous or heterozygous mutation of NOTCH3 in a large CADASIL family
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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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8
Chorea-acanthocytosis: Clinical and genetic findings in three families from the Arabian peninsula
Chorea-acanthocytosis: Clinical and genetic findings in three families from the Arabian peninsula
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Chorea-acanthocytosis: Clinical and genetic findings in three families from the Arabian peninsula

Bohlega, Saeed ; Al-Jishi, Adel ; Dobson-Stone, Carol ; Rampoldi, Luca ; Saha, Parthasarathi ; Murad, Hatem ; Kareem, Abid ; Roberts, George ; Monaco, Anthony P.

Movement disorders, 2003-04, Vol.18 (4), p.403-407 [Periódico revisado por pares]

New York: Wiley Subscription Services, Inc., A Wiley Company

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9
Botulinum toxin therapy for treatment of spasticity in multiple sclerosis: review and recommendations of the IAB-Interdisciplinary Working Group for Movement Disorders task force
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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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, Vol.264 (1), p.112-120 [Periódico revisado por pares]

Berlin/Heidelberg: Springer Berlin Heidelberg

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10
Strategies for treatment of dystonia
Strategies for treatment of dystonia
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Strategies for treatment of dystonia

Dressler, Dirk ; Altenmueller, Eckart ; Bhidayasiri, Roongroj ; Bohlega, Saeed ; Chana, Pedro ; Chung, Tae Mo ; Frucht, Steven ; Garcia-Ruiz, Pedro J. ; Kaelin, Alain ; Kaji, Ryuji ; Kanovsky, Petr ; Laskawi, Rainer ; Micheli, Federico ; Orlova, Olga ; Relja, Maja ; Rosales, Raymond ; Slawek, Jaroslaw ; Timerbaeva, Sofia ; Warner, Thomas T. ; Saberi, Fereshte Adib

Journal of Neural Transmission, 2016-03, Vol.123 (3), p.251-258 [Periódico revisado por pares]

Vienna: Springer Vienna

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