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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, Vol.8 (2), p.6444-6444 [Periódico revisado por pares]

Italy: MDPI AG

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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, Vol.64, p.145-149 [Periódico revisado por pares]

England: Elsevier Ltd

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3
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, Vol.9 (1), p.11-23 [Periódico revisado por pares]

Cheshire: Springer Healthcare

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4
Ultrasound-guided botulinum toxin A injection in the treatment of belly dancer's dyskinesia
Ultrasound-guided botulinum toxin A injection in the treatment of belly dancer's dyskinesia
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Ultrasound-guided botulinum toxin A injection in the treatment of belly dancer's dyskinesia

Alshubaili, Asmahan ; Abou-Al-Shaar, Hussam ; Santhamoorthy, Ponnusamy ; Attia, Hosam ; Bohlega, Saeed

BMC neurology, 2016, Vol.16 (1), p.226-226 [Periódico revisado por pares]

England: BioMed Central Ltd

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5
SET binding factor 1 (SBF1) mutation causes Charcot-Marie-Tooth disease type 4B3
SET binding factor 1 (SBF1) mutation causes Charcot-Marie-Tooth disease type 4B3
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SET binding factor 1 (SBF1) mutation causes Charcot-Marie-Tooth disease type 4B3

Alazami, Anas M ; Alzahrani, Fatema ; Bohlega, Saeed ; Alkuraya, Fowzan S

Neurology, 2014, Vol.82 (18), p.1665-1666 [Periódico revisado por pares]

United States: American Academy of Neurology

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6
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, Vol.8, p.333-333 [Periódico revisado por pares]

Switzerland: Frontiers Media S.A

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7
Mutation of fibulin-1 causes a novel syndrome involving the central nervous system and connective tissues
Mutation of fibulin-1 causes a novel syndrome involving the central nervous system and connective tissues
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Mutation of fibulin-1 causes a novel syndrome involving the central nervous system and connective tissues

Bohlega, Saeed ; Al-Ajlan, Huda ; Al-Saif, Amr

European journal of human genetics : EJHG, 2014, Vol.22 (5), p.640-643 [Periódico revisado por pares]

England: Nature Publishing Group

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8
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, Vol.16 (6), p.773-778 [Periódico revisado por pares]

Başkent Üniversitesi

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9
Diagnosis and management of Neuro-Behçet’s disease: international consensus recommendations
Diagnosis and management of Neuro-Behçet’s disease: international consensus recommendations
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Diagnosis and management of Neuro-Behçet’s disease: international consensus recommendations

Kalra, Seema ; Silman, Alan ; Akman-Demir, Gulsen ; Bohlega, Saeed ; Borhani-Haghighi, Afshin ; Constantinescu, Cris S. ; Houman, Habib ; Mahr, Alfred ; Salvarani, Carlos ; Sfikakis, Petros P. ; Siva, Aksel ; Al-Araji, Adnan

Journal of neurology, 2014, Vol.261 (9), p.1662-1676 [Periódico revisado por pares]

Berlin/Heidelberg: Springer Berlin Heidelberg

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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, Vol.3 (2), p.e6-e6 [Periódico revisado por pares]

Italy: MDPI AG

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