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11
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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12
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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13
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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14
Nine Hereditary Movement Disorders First Described in Asia: Their History and Evolution
Nine Hereditary Movement Disorders First Described in Asia: Their History and Evolution
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Nine Hereditary Movement Disorders First Described in Asia: Their History and Evolution

Jagota, Priya ; Ugawa, Yoshikazu ; Aldaajani, Zakiyah ; Ibrahim, Norlinah Mohamed ; Ishiura, Hiroyuki ; Nomura, Yoshiko ; Tsuji, Shoji ; Diesta, Cid ; Hattori, Nobutaka ; Onodera, Osamu ; Bohlega, Saeed ; AlDin, Amir S N ; Lim, Shen-Yang ; Lee, Jee-Young ; Jeon, Beomseok ; Pal, Pramod Kumar ; Shang, Huifang ; Fujioka, Shinsuke ; Kukkle, Prashanth Lingappa ; Phokaewvarangkul, Onanong ; Lin, Chin-Hsien ; Shambetova, Cholpon ; Bhidayasiri, Roongroj

Journal Of Movement Disorders, 2023, 16(3), , pp.231-247 [Periódico revisado por pares]

Korea (South): The Korean Movement Disorder Society

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15
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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16
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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17
Absence of mtDNA mutations in leukocytes of CADASIL patients
Absence of mtDNA mutations in leukocytes of CADASIL patients
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Absence of mtDNA mutations in leukocytes of CADASIL patients

Abu-Amero, Khaled K ; Hellani, Ali ; Bohlega, Saeed

BMC research notes, 2008-05, Vol.1 (1), p.16-16 [Periódico revisado por pares]

England: BioMed Central Ltd

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18
A Prospective Multicenter Study for Assessing MusiQoL Validity among Arabic-Speaking MS Patients Treated with Subcutaneous Interferon β-1a
A Prospective Multicenter Study for Assessing MusiQoL Validity among Arabic-Speaking MS Patients Treated with Subcutaneous Interferon β-1a
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A Prospective Multicenter Study for Assessing MusiQoL Validity among Arabic-Speaking MS Patients Treated with Subcutaneous Interferon β-1a

Al Jumah, Mohammed ; Kojan, Suleiman ; Alroughani, Raed ; Cupler, Edward ; Bohlega, Saeed ; Daif, Abdulkader ; Al Mujalli, Mousa ; Al Harbi, Talal ; El Tamawy, Mohamed ; Ashour, Samia ; Mhiri, Chokri ; Gouider, Riadh ; Jawhary, Ayah ; El Boghdady, Ahmed ; Hussein, Mohamed Ghezzi, Angelo ; Angelo Ghezzi

Multiple sclerosis international, 2021-03, Vol.2021, p.6681431-7 [Periódico revisado por pares]

Egypt: Hindawi

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19
Tremor in Parkinson’s Disease: From Pathophysiology to Advanced Therapies
Tremor in Parkinson’s Disease: From Pathophysiology to Advanced Therapies
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Tremor in Parkinson’s Disease: From Pathophysiology to Advanced Therapies

Abusrair, Ali H. ; Elsekaily, Walaa ; Bohlega, Saeed

Tremor and other hyperkinetic movements (New York, N.Y.), 2022-09, Vol.12 (1) [Periódico revisado por pares]

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20
Woodhouse-Sakati Syndrome: Report of the First Tunisian Family with the C2orf37 Gene Mutation
Woodhouse-Sakati Syndrome: Report of the First Tunisian Family with the C2orf37 Gene Mutation
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Woodhouse-Sakati Syndrome: Report of the First Tunisian Family with the C2orf37 Gene Mutation

Hdiji, Olfa ; Turki, Emna ; Bouzidi, Nouha ; Bouchhima, Imen ; Damak, Mariem ; Bohlega, Saeed ; Mhiri, Chokri

Journal Of Movement Disorders, 2016, 9(2), , pp.120-123 [Periódico revisado por pares]

Korea (South): The Korean Movement Disorders Society

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