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A patient with typical clinical features of mitochondrial encephalopathy, lactic acidosis and stroke-like episodes (MELAS) but without an obvious genetic cause: a case report
A patient with typical clinical features of mitochondrial encephalopathy, lactic acidosis and stroke-like episodes (MELAS) but without an obvious genetic cause: a case report
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A patient with typical clinical features of mitochondrial encephalopathy, lactic acidosis and stroke-like episodes (MELAS) but without an obvious genetic cause: a case report

Abu-Amero, Khaled K ; Al-Dhalaan, Hesham ; Bohlega, Saeed ; Hellani, Ali ; Taylor, Robert W

Journal of medical case reports, 2009-10, Vol.3 (1), p.77-77, Article 77 [Periódico revisado por pares]

England: BioMed Central Ltd

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2
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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3
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, 2011-04, Vol.3 (1) [Periódico revisado por pares]

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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
In silico analysis of influence of the missense mutation P629S on the molecular interaction and 3D properties of PIK3R5
In silico analysis of influence of the missense mutation P629S on the molecular interaction and 3D properties of PIK3R5
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In silico analysis of influence of the missense mutation P629S on the molecular interaction and 3D properties of PIK3R5

Shinwari, Jameela ; Tahir, Asma I. ; Bohlega, Saeed ; AlTassan, Nada

Advances in biological chemistry, 2013, Vol.3 (4), p.408-417

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6
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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7
Natalizumab treatment for multiple sclerosis: Middle East and North Africa regional recommendations for patient selection and monitoring
Natalizumab treatment for multiple sclerosis: Middle East and North Africa regional recommendations for patient selection and monitoring
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Natalizumab treatment for multiple sclerosis: Middle East and North Africa regional recommendations for patient selection and monitoring

Alroughani, Raed A ; Aref, Hany M ; Bohlega, Saeed A ; Dahdaleh, Maurice P ; Feki, Imed ; Al Jumah, Mohammed A ; Al-Kawi, Muhammad Z ; Koussa, Salam F ; Sahraian, Mohamad A ; Alsharoqi, Isa A ; Yamout, Bassem I

BMC neurology, 2014-02, Vol.14 (1), p.27-27, Article 27 [Periódico revisado por pares]

England: BioMed Central

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8
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, 2014-05, Vol.22 (5), p.640-643 [Periódico revisado por pares]

England: Nature Publishing Group

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9
Oromandibular dystonia in yemeni patients with khat chewing: a response to botulinum toxin treatment
Oromandibular dystonia in yemeni patients with khat chewing: a response to botulinum toxin treatment
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Oromandibular dystonia in yemeni patients with khat chewing: a response to botulinum toxin treatment

Shehata, Hatem S ; El-Tamawy, Mohamed S ; Mohieldin, Nevin ; Edrees, Mohammed ; Bohlega, Saeed

Neurology international, 2014-06, Vol.6 (2), p.5385-5385 [Periódico revisado por pares]

Italy: MDPI AG

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10
INTERNATIONAL CONSENSUS PROJECT: NEURO-BEHCET DISEASE
INTERNATIONAL CONSENSUS PROJECT: NEURO-BEHCET DISEASE
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INTERNATIONAL CONSENSUS PROJECT: NEURO-BEHCET DISEASE

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

Journal of neurology, neurosurgery and psychiatry, 2014-10, Vol.85 (10), p.e4.69-e4 [Periódico revisado por pares]

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