Novel mutation of the notch3 gene in arabic family with CADASIL

par Bohlega, Saeed
Publié 2011

The Burden of Musculoskeletal Conditions at the Start of the New Millennium

par Bohlega, Saeed
Publié dans Ann Saudi Med (2004)

Ataxia and Hypogonadotropic Hypogonadism with Intrafamilial Variability Caused by RNF216 Mutation

par Alqwaifly, Mohammed, Bohlega, Saeed
Publié dans Neurol Int (2016)

Riboflavin Has Neuroprotective Potential: Focus on Parkinson’s Disease and Migraine

par Marashly, Eyad T., Bohlega, Saeed A.
Publié dans Front Neurol (2017)

Absence of mtDNA mutations in leukocytes of CADASIL patients

par Abu-Amero, Khaled K, Hellani, Ali, Bohlega, Saeed
Publié 2008

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

par Bohlega, Saeed, Al-Ajlan, Huda, Al-Saif, Amr
Publié 2014

Oromandibular Dystonia in Yemeni Patients with Khat Chewing: A Response to Botulinum Toxin Treatment

par Shehata, Hatem S., El-Tamawy, Mohamed S., Mohieldin, Nevin, Edrees, Mohammed, Bohlega, Saeed
Publié 2014

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

par Alshubaili, Asmahan, Abou-Al-Shaar, Hussam, Santhamoorthy, Ponnusamy, Attia, Hosam, Bohlega, Saeed
Publié dans BMC Neurol (2016)

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

par Abu-Amero, Khaled K, Al-Dhalaan, Hesham, Bohlega, Saeed, Hellani, Ali, Taylor, Robert W
Publié 2009

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

par Hdiji, Olfa, Turki, Emna, Bouzidi, Nouha, Bouchhima, Imen, Damak, Mariem, Bohlega, Saeed, Mhiri, Chokri
Publié dans J Mov Disord (2016)

Multiple sclerosis in the Arabian Gulf countries: a consensus statement

par Bohlega, Saeed, Inshasi, Jihad, Al Tahan, Abdel Rahman, Madani, Abu Bakr, Qahtani, Hussien, Rieckmann, Peter
Publié 2013

Neurobrucellosis: Clinical and Neuroimaging Correlation

par Al-Sous, M. Walid, Bohlega, Saeed, Al-Kawi, M. Zuheir, Alwatban, Jehad, McLean, Donald R.
Publié dans AJNR Am J Neuroradiol (2004)

Clinical and genetic features of anoctaminopathy in Saudi Arabia

par Bohlega, Saeed, Monies, Dorothy M., Abulaban, Ahmad A., Murad, Hatem N., Alhindi, Hindi N., Meyer, Brian F.
Publié dans Neurosciences (Riyadh) (2015)

Clinical and Molecular Characterization of Ataxia with Oculomotor Apraxia Patients In Saudi Arabia

par Bohlega, Saeed A, Shinwari, Jameela M, Al Sharif, Latifa J, Khalil, Dania S, Alkhairallah, Thamer S, Al Tassan, Nada A
Publié 2011

CADASIL in Arabs: clinical and genetic findings

par Bohlega, Saeed, Al Shubili, Asmahan, Edris, Abdulrahman, Alreshaid, Abdulrahman, AlKhairallah, Thamer, AlSous, M Walid, Farah, Samir, Abu-Amero, Khaled K
Publié 2007

LGMD1D myopathy with cytoplasmic and nuclear inclusions in a Saudi family due to DNAJB6 mutation

par BOHLEGA, SAEED A., ALFAWAZ, SARAH, ABOU-AL-SHAAR, HUSSAM, AL-HINDI, HINDI N., MURAD, HATEM N., BOHLEGA, MOHAMED S., MEYER, BRIAN F., MONIES, DOROTA
Publié dans Acta Myol (2018)

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

par 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.
Publié dans BMC Med Genet (2019)

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

par 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
Publié 2013

Exome Sequencing: Mutilating Sensory Neuropathy with Spastic Paraplegia due to a Mutation in FAM134B Gene

par Wakil, Salma M., Monies, Dorota, Hagos, Samya, Al-Ajlan, Fahad, Finsterer, Josef, Al Qahtani, Aisha, Ramzan, Khushnooda, Al Humaidy, Rawan, Al-Muhaizea, Mohamed A., Meyer, Brian, Bohlega, Saeed A.
Publié dans Case Rep Genet (2018)

Future of Management of Multiple Sclerosis in the Middle East: A Consensus View from Specialists in Ten Countries

par 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
Publié 2013