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Refinado por: Base de dados/Biblioteca: ClinicalKey remover
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1
Autosomal recessive ADCY5-Related dystonia and myoclonus: Expanding the genetic spectrum of ADCY5-Related movement disorders
Autosomal recessive ADCY5-Related dystonia and myoclonus: Expanding the genetic spectrum of ADCY5-Related movement disorders
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Autosomal recessive ADCY5-Related dystonia and myoclonus: Expanding the genetic spectrum of ADCY5-Related movement disorders

Bohlega, Saeed A. ; Abou-Al-Shaar, Hussam ; AlDakheel, Amaal ; Alajlan, Huda ; Bohlega, Balsam S. ; Meyer, Brian F. ; Monies, Dorota ; Cupler, Edward J. ; Al-Saif, Amr M.

Parkinsonism & related disorders, 2019-07, Vol.64, p.145-149 [Periódico revisado por pares]

England: Elsevier Ltd

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2
Clinical, neurophysiological, radiological, pathological, and genetic feature of Dysferlinopathy in Saudi Arabia
Clinical, neurophysiological, radiological, pathological, and genetic feature of Dysferlinopathy in Saudi Arabia
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Clinical, neurophysiological, radiological, pathological, and genetic feature of Dysferlinopathy in Saudi Arabia

Alharbi, Norah ; Bohlega, Saeed ; Alhindi, Hindi ; Matar, Rawan

Journal of the neurological sciences, 2023-12, Vol.455, p.122521, Article 122521 [Periódico revisado por pares]

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3
Patterns of neurological manifestations in Woodhouse-Sakati Syndrome
Patterns of neurological manifestations in Woodhouse-Sakati Syndrome
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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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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
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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6
MENACTRIMS practice guideline for COVID-19 vaccination in patients with multiple sclerosis
MENACTRIMS practice guideline for COVID-19 vaccination in patients with multiple sclerosis
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MENACTRIMS practice guideline for COVID-19 vaccination in patients with multiple sclerosis

Yamout, Bassem I ; Zakaria, Magd ; Inshasi, Jihad ; Al-Jumah, Mohammad ; Zeineddine, Maya ; Dahdaleh, Maurice ; Bohlega, Saeed ; Gouider, Riadh ; Alroughani, Raed

Multiple sclerosis and related disorders, 2021-11, Vol.56, p.103225-103225, Article 103225

Netherlands: Elsevier B.V

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7
Real World Effectiveness of Oral Cladribine in Multiple Sclerosis Treatment, Report from a Single Saudi Center
Real World Effectiveness of Oral Cladribine in Multiple Sclerosis Treatment, Report from a Single Saudi Center
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Real World Effectiveness of Oral Cladribine in Multiple Sclerosis Treatment, Report from a Single Saudi Center

Bohlega, Saeed ; Alkhawajah, Mona ; Sulague, Norah ; Alfugham, Nora

Multiple sclerosis and related disorders, 2023-12, Vol.80, p.105298, Article 105298

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8
A novel splice site mutation in ERLIN2 causes hereditary spastic paraplegia in a Saudi family
A novel splice site mutation in ERLIN2 causes hereditary spastic paraplegia in a Saudi family
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A novel splice site mutation in ERLIN2 causes hereditary spastic paraplegia in a Saudi family

Wakil, Salma M ; Bohlega, Saeed ; Hagos, Samya ; Baz, Batoul ; Al Dossari, Haya ; Ramzan, Khushnooda ; Al-Hassnan, Zuhair N

European journal of medical genetics, 2013-01, Vol.56 (1), p.43-45 [Periódico revisado por pares]

Netherlands: Elsevier Masson SAS

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9
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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10
Epidemiology of MS
Epidemiology of MS
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Epidemiology of MS

Bohlega, Saeed

Multiple sclerosis and related disorders, 2014-11, Vol.3 (6), p.766-767

Elsevier B.V

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