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21
Immune Reconstitution Therapy or Continuous Immunosuppression for the Management of Active Relapsing–Remitting Multiple Sclerosis Patients? A Narrative Review
Immune Reconstitution Therapy or Continuous Immunosuppression for the Management of Active Relapsing–Remitting Multiple Sclerosis Patients? A Narrative Review
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Immune Reconstitution Therapy or Continuous Immunosuppression for the Management of Active Relapsing–Remitting Multiple Sclerosis Patients? A Narrative Review

AlSharoqi, Isa Ahmed ; Aljumah, Mohamed ; Bohlega, Saeed ; Boz, Cavit ; Daif, Abdelkader ; El-Koussa, Salam ; Inshasi, Jihad ; Kurtuncu, Murat ; Müller, Thomas ; Retief, Chris ; Sahraian, Mohammad Ali ; Shaygannejad, Vahid ; Slassi, Ilham ; Taha, Karim ; Zakaria, Magd ; Sørensen, Per Soelberg

Neurology and therapy, 2020-06, Vol.9 (1), p.55-66 [Periódico revisado por pares]

Cheshire: Springer Healthcare

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22
Multimodal Evoked Potential Profiles in Woodhouse-Sakati Syndrome
Multimodal Evoked Potential Profiles in Woodhouse-Sakati Syndrome
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Multimodal Evoked Potential Profiles in Woodhouse-Sakati Syndrome

Abusrair, Ali ; AlHamoud, Iftetah ; Bohlega, Saeed

Journal of clinical neurophysiology, 2022-09, Vol.Publish Ahead of Print (6), p.504-509 [Periódico revisado por pares]

United States

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23
Intervening to reduce the risk of future disability from multiple sclerosis: are we there yet?
Intervening to reduce the risk of future disability from multiple sclerosis: are we there yet?
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Intervening to reduce the risk of future disability from multiple sclerosis: are we there yet?

Dahdaleh, Maurice ; Alroughani, Raed ; Aljumah, Mohammed ; AlTahan, Abdulrahman ; Alsharoqi, Issa ; Bohlega, Saeed A ; Daif, Abdulkader ; Deleu, Dirk ; Inshasi, Jihad ; Karabudak, Rana ; Sahraian, Mohammed A. ; Taha, Karim ; Yammout, Bassem I. ; Zakaria, Magd

International journal of neuroscience, 2017-10, Vol.127 (10), p.944-951 [Periódico revisado por pares]

England: Taylor & Francis

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24
A first-line diagnostic assay for limb-girdle muscular dystrophy and other myopathies
A first-line diagnostic assay for limb-girdle muscular dystrophy and other myopathies
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A first-line diagnostic assay for limb-girdle muscular dystrophy and other myopathies

Monies, Dorota ; Alhindi, Hindi N ; Almuhaizea, Mohamed A ; Abouelhoda, Mohamed ; Alazami, Anas M ; Goljan, Ewa ; Alyounes, Banan ; Jaroudi, Dyala ; AlIssa, Abdulelah ; Alabdulrahman, Khalid ; Subhani, Shazia ; El-Kalioby, Mohamed ; Faquih, Tariq ; Wakil, Salma M ; Altassan, Nada A ; Meyer, Brian F ; Bohlega, Saeed

Human genomics, 2016-09, Vol.10 (1), p.32-32, Article 32 [Periódico revisado por pares]

England: BioMed Central

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25
Expanding the genotype-phenotype landscape of PDE10A-associated movement disorders (S42.004)
Expanding the genotype-phenotype landscape of PDE10A-associated movement disorders (S42.004)
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Expanding the genotype-phenotype landscape of PDE10A-associated movement disorders (S42.004)

Bohlega, Saeed ; Al-Qahtani, Zainah ; Guzmán-Vega, Francisco J. ; Ramakrishnan, Reshmi ; Abusrair, Ali ; Aldosari, Haya ; AlDakheel, Amaal ; Al-Qahtani, Salma ; Monies, Dorota ; Arold, Stefan

Neurology, 2023-04, Vol.100 (17_supplement_2) [Periódico revisado por pares]

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26
Cerebrotendinous xanthomatosis: A candidate for ACMG list of secondary findings?
Cerebrotendinous xanthomatosis: A candidate for ACMG list of secondary findings?
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Cerebrotendinous xanthomatosis: A candidate for ACMG list of secondary findings?

Khouj, Ebtissal ; Bohlega, Saeed ; Alkuraya, Fowzan S.

Clinical genetics, 2023-01, Vol.103 (1), p.125-126 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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27
Clinical and molecular characterization of ataxia with oculomotor apraxia patients in Saudi Arabia
Clinical and molecular characterization of ataxia with oculomotor apraxia patients in Saudi Arabia
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Clinical and molecular characterization of ataxia with oculomotor apraxia patients in Saudi Arabia

Bohlega, Saeed A ; Shinwari, Jameela M ; Al Sharif, Latifa J ; Khalil, Dania S ; Alkhairallah, Thamer S ; Al Tassan, Nada A

BMC medical genetics, 2011-02, Vol.12 (1), p.27-27, Article 27 [Periódico revisado por pares]

England: BioMed Central Ltd

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28
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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29
Family Planning for People with Multiple Sclerosis in Saudi Arabia: an Expert Consensus
Family Planning for People with Multiple Sclerosis in Saudi Arabia: an Expert Consensus
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Family Planning for People with Multiple Sclerosis in Saudi Arabia: an Expert Consensus

Al Jumah, Mohammed ; Al Malik, Yaser ; AlKhawajah, Nuha M. ; Saeedi, Jameelah ; AlThubaiti, Ibtisam ; Bohlega, Saeed ; Bunyan, Reem F. ; Cupler, Edward J. ; ElBoghdady, Ahmed ; Hassan, Ahmed ; Ali, Eman Nassim ; Clerico, Marinella Calabrese, Pasquale ; Pasquale Calabrese

Multiple sclerosis international, 2021-02, Vol.2021, p.6667006-8 [Periódico revisado por pares]

Egypt: Hindawi

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30
Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy
Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy
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Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy

Brown, Robert H ; Liu, Jing ; Aoki, Masashi ; Illa, Isabel ; Wu, Chenyan ; Fardeau, Michel ; Angelini, Corrado ; Serrano, Carmen ; Urtizberea, J. Andoni ; Hentati, Faycal ; Hamida, Mongi Ben ; Bohlega, Saeed ; Culper, Edward J ; Amato, Anthony A ; Bossie, Karen ; Oeltjen, Joshua ; Bejaoui, Khemissa ; McKenna-Yasek, Diane ; Hosler, Betsy A ; Schurr, Erwin ; Arahata, Kiichi ; de Jong, Pieter J

Nature genetics, 1998-09, Vol.20 (1), p.31-36 [Periódico revisado por pares]

London: Nature Publishing Group

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