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Riboflavin Has Neuroprotective Potential: Focus on Parkinson's Disease and Migraine
Riboflavin Has Neuroprotective Potential: Focus on Parkinson's Disease and Migraine
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Riboflavin Has Neuroprotective Potential: Focus on Parkinson's Disease and Migraine

Marashly, Eyad T ; Bohlega, Saeed A

Frontiers in neurology, 2017-07, Vol.8, p.333-333 [Periódico revisado por pares]

Switzerland: Frontiers Media S.A

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2
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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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
Cladribine Tablets and Relapsing–Remitting Multiple Sclerosis: A Pragmatic, Narrative Review of What Physicians Need to Know
Cladribine Tablets and Relapsing–Remitting Multiple Sclerosis: A Pragmatic, Narrative Review of What Physicians Need to Know
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Cladribine Tablets and Relapsing–Remitting Multiple Sclerosis: A Pragmatic, Narrative Review of What Physicians Need to Know

AlJumah, Mohamed ; Alkhawajah, Mona Marwan ; Qureshi, Shireen ; Al-Thubaiti, Ibtisam ; Ayoub, Omar ; Bohlega, Saeed A. ; Bushnag, Areej ; Cupler, Edward ; Daif, Abdulkader ; El Boghdady, Ahmed ; Hassan, Ahmed ; Al Malik, Yaser ; Saeedi, Jameelah ; Al-Shamrany, Fawzia ; Shosha, Eslam ; Rieckmann, Peter

Neurology and therapy, 2020-06, Vol.9 (1), p.11-23 [Periódico revisado por pares]

Cheshire: Springer Healthcare

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5
Clinical heterogeneity of PLA2G6-related Parkinsonism: analysis of two Saudi families
Clinical heterogeneity of PLA2G6-related Parkinsonism: analysis of two Saudi families
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Clinical heterogeneity of PLA2G6-related Parkinsonism: analysis of two Saudi families

Bohlega, Saeed A ; Al-Mubarak, Bashayer R ; Alyemni, Eman A ; Abouelhoda, Mohamed ; Monies, Dorota ; Mustafa, Abeer E ; Khalil, Dania S ; Al Haibi, Sara ; Abou Al-Shaar, Hussam ; Faquih, Tariq ; El-Kalioby, Mohamed ; Tahir, Asma I ; Al Tassan, Nada A

BMC research notes, 2016-06, Vol.9 (1), p.295-295, Article 295 [Periódico revisado por pares]

England: BioMed Central Ltd

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6
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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7
Exome Sequencing: Mutilating Sensory Neuropathy with Spastic Paraplegia due to a Mutation in FAM134B Gene
Exome Sequencing: Mutilating Sensory Neuropathy with Spastic Paraplegia due to a Mutation in FAM134B Gene
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Exome Sequencing: Mutilating Sensory Neuropathy with Spastic Paraplegia due to a Mutation in FAM134B Gene

Wakil, Salma M. ; Monies, Dorota ; Hagos, Samya ; Al-Ajlan, Fahad ; Finsterer, Josef ; Al Qahtani, Aisha ; Ramzan, Khushnooda ; Al Humaidy, Rawan ; Al-Muhaizea, Mohamed A. ; Meyer, Brian ; Bohlega, Saeed A. Paracchini, Silvia

Case reports in genetics, 2018, Vol.2018, p.9468049-5 [Periódico revisado por pares]

United States: Hindawi

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8
Future of Management of Multiple Sclerosis in the Middle East: A Consensus View from Specialists in Ten Countries
Future of Management of Multiple Sclerosis in the Middle East: A Consensus View from Specialists in Ten Countries
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Future of Management of Multiple Sclerosis in the Middle East: A Consensus View from Specialists in Ten Countries

Aljumah, Mohammed ; Alroughani, Raed ; Alsharoqi, I. ; Bohlega, Saeed A. ; Dahdaleh, Maurice ; Deleu, Dirk ; Esmat, Khaled ; Khalifa, Ahmad ; Sahraian, Mohammad A. ; Szólics, Miklós ; AlTahan, Abdulrahman ; Yamout, Bassem I. ; Rieckmann, Peter ; Daif, Abdulkader Bruck, Wolfgang ; Wolfgang Bruck

Multiple Sclerosis International, 2013-01, Vol.2013, p.952321-6 [Periódico revisado por pares]

Egypt: Hindawi Limiteds

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9
LGMD1D myopathy with cytoplasmic and nuclear inclusions in a Saudi family due to DNAJB6 mutation
LGMD1D myopathy with cytoplasmic and nuclear inclusions in a Saudi family due to DNAJB6 mutation
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LGMD1D myopathy with cytoplasmic and nuclear inclusions in a Saudi family due to DNAJB6 mutation

Bohlega, Saeed A ; Alfawaz, Sarah ; Abou-Al-Shaar, Hussam ; Al-Hindi, Hindi N ; Murad, Hatem N ; Bohlega, Mohamed S ; Meyer, Brian F ; Monies, Dorota

Acta myologica, 2018-09, Vol.37 (3), p.221-226 [Periódico revisado por pares]

Italy: Pacini Editore srl

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10
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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