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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 [Peer Reviewed Journal]

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

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2
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 [Peer Reviewed Journal]

Switzerland: Frontiers Media S.A

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3
Ataxia and Hypogonadotropic Hypogonadism with Intrafamilial Variability Caused by RNF216 Mutation
Ataxia and Hypogonadotropic Hypogonadism with Intrafamilial Variability Caused by RNF216 Mutation
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Ataxia and Hypogonadotropic Hypogonadism with Intrafamilial Variability Caused by RNF216 Mutation

Alqwaifly, Mohammed ; Bohlega, Saeed

Neurology international, 2016-06, Vol.8 (2), p.6444-6444 [Peer Reviewed Journal]

Italy: MDPI AG

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4
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 [Peer Reviewed Journal]

England: Elsevier Ltd

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5
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 [Peer Reviewed Journal]

Cheshire: Springer Healthcare

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6
Mitochondrial Neurogastrointestinal Encephalomyopathy Syndrome Treated with Stem Cell Transplant: A Case Series and Literature Review
Mitochondrial Neurogastrointestinal Encephalomyopathy Syndrome Treated with Stem Cell Transplant: A Case Series and Literature Review
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Mitochondrial Neurogastrointestinal Encephalomyopathy Syndrome Treated with Stem Cell Transplant: A Case Series and Literature Review

Hanbali, Amr ; Rasheed, Walid ; Peedikayil, Musthafa Chalikandy ; Boholega, Saeed ; Alzahrani, Hazza A Haberal,Mehmet

Experimental and clinical transplantation, 2018-12, Vol.16 (6), p.773-778 [Peer Reviewed Journal]

Turkey: Başkent Üniversitesi

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7
The ALS-linked E102Q mutation in Sigma receptor-1 leads to ER stress-mediated defects in protein homeostasis and dysregulation of RNA-binding proteins
The ALS-linked E102Q mutation in Sigma receptor-1 leads to ER stress-mediated defects in protein homeostasis and dysregulation of RNA-binding proteins
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The ALS-linked E102Q mutation in Sigma receptor-1 leads to ER stress-mediated defects in protein homeostasis and dysregulation of RNA-binding proteins

Dreser, Alice ; Vollrath, Jan Tilmann ; Sechi, Antonio ; Johann, Sonja ; Roos, Andreas ; Yamoah, Alfred ; Katona, Istvan ; Bohlega, Saeed ; Wiemuth, Dominik ; Tian, Yuemin ; Schmidt, Axel ; Vervoorts, Jörg ; Dohmen, Marc ; Beyer, Cordian ; Anink, Jasper ; Aronica, Eleonora ; Troost, Dirk ; Weis, Joachim ; Goswami, Anand

Cell death and differentiation, 2017-10, Vol.24 (10), p.1655-1671 [Peer Reviewed Journal]

England: Nature Publishing Group

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8
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 [Peer Reviewed Journal]

United States: Public Library of Science

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9
Consensus guidelines for botulinum toxin therapy: general algorithms and dosing tables for dystonia and spasticity
Consensus guidelines for botulinum toxin therapy: general algorithms and dosing tables for dystonia and spasticity
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Consensus guidelines for botulinum toxin therapy: general algorithms and dosing tables for dystonia and spasticity

Dressler, Dirk ; Altavista, Maria Concetta ; Altenmueller, Eckart ; Bhidayasiri, Roongroj ; Bohlega, Saeed ; Chana, Pedro ; Chung, Tae Mo ; Colosimo, Carlo ; Fheodoroff, Klemens ; Garcia-Ruiz, Pedro J. ; Jeon, Beomseok ; Jin, Lingjing ; Kanovsky, Petr ; Milanov, Ivan ; Micheli, Federico ; Orlova, Olga ; Pandey, Sanjay ; Pirtosek, Zvezdan ; Relja, Maja ; Rosales, Raymond ; Sagástegui-Rodríguez, José Alberto ; Shahidi, Gholam Ali ; Timerbaeva, Sofia ; Wan, Xinhua ; Walter, Uwe ; Saberi, Fereshte Adib

Journal of Neural Transmission, 2021-03, Vol.128 (3), p.321-335 [Peer Reviewed Journal]

Vienna: Springer Vienna

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10
Novel mutation of the notch3 gene in arabic family with CADASIL
Novel mutation of the notch3 gene in arabic family with CADASIL
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Novel mutation of the notch3 gene in arabic family with CADASIL

Bohlega, Saeed

Neurology international, 2011-07, Vol.3 (2), p.e6-e6 [Peer Reviewed Journal]

Italy: MDPI AG

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