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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
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 [Periódico revisado por pares]

Italy: MDPI AG

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

Cheshire: Springer Healthcare

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4
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 [Periódico revisado por pares]

Italy: MDPI AG

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5
Integrated Analysis of Whole Exome Sequencing and Copy Number Evaluation in Parkinson's Disease
Integrated Analysis of Whole Exome Sequencing and Copy Number Evaluation in Parkinson's Disease
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Integrated Analysis of Whole Exome Sequencing and Copy Number Evaluation in Parkinson's Disease

Yemni, Eman Al ; Monies, Dorota ; Alkhairallah, Thamer ; Bohlega, Saeed ; Abouelhoda, Mohamed ; Magrashi, Amna ; Mustafa, Abeer ; AlAbdulaziz, Basma ; Alhamed, Mohamed ; Baz, Batoul ; Goljan, Ewa ; Albar, Renad ; Jabaan, Amjad ; Faquih, Tariq ; Subhani, Shazia ; Ali, Wafa ; Shinwari, Jameela ; Al-Mubarak, Bashayer ; Al-Tassan, Nada

Scientific reports, 2019-03, Vol.9 (1), p.3344-3344, Article 3344 [Periódico revisado por pares]

England: Nature Publishing Group

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6
Methanol-induced parkinsonism and cerebral vasculopathy due to perfume inhalation
Methanol-induced parkinsonism and cerebral vasculopathy due to perfume inhalation
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Methanol-induced parkinsonism and cerebral vasculopathy due to perfume inhalation

B Mohammed, Walaa ; Tarabzouni, Salma ; Bohlega, Saeed

BMJ neurology open, 2022-05, Vol.4 (1), p.e000221-e000221 [Periódico revisado por pares]

England: BMJ Publishing Group Ltd

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7
Clinical, Neurophysiological, Radiological, Pathological, and Genetic Features of Dysferlinopathy in Saudi Arabia
Clinical, Neurophysiological, Radiological, Pathological, and Genetic Features of Dysferlinopathy in Saudi Arabia
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Clinical, Neurophysiological, Radiological, Pathological, and Genetic Features of Dysferlinopathy in Saudi Arabia

Alharbi, Norah ; Matar, Rawan ; Cupler, Edward ; Al-Hindi, Hindi ; Murad, Hatem ; Alhomud, Iftteah ; Monies, Dorota ; Alshehri, Ali ; Alyahya, Mossaed ; Meyer, Brian ; Bohlega, Saeed

Frontiers in neuroscience, 2022-02, Vol.16, p.815556-815556 [Periódico revisado por pares]

Switzerland: Frontiers Research Foundation

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8
Truncating ARL6IP1 variant as the genetic cause of fatal complicated hereditary spastic paraplegia
Truncating ARL6IP1 variant as the genetic cause of fatal complicated hereditary spastic paraplegia
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Truncating ARL6IP1 variant as the genetic cause of fatal complicated hereditary spastic paraplegia

Wakil, Salma M ; Alhissi, Safa ; Al Dossari, Haya ; Alqahtani, Ayesha ; Shibin, Sherin ; Melaiki, Brahim T ; Finsterer, Josef ; Al-Hashem, Amal ; Bohlega, Saeed ; Alazami, Anas M

BMC medical genetics, 2019-07, Vol.20 (1), p.119-119, Article 119 [Periódico revisado por pares]

England: BioMed Central Ltd

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9
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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10
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 Ltd

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