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Saeed Bohlega

Showing results (11-20 of 64) with videos related to

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BMC Research Notes|August 20, 2008
Absence of mtDNA mutations in leukocytes of CADASIL patientsKhaled K Abu-Amero, Ali Hellani, Saeed Bohlega
Ophthalmic Genetics|April 13, 2005
Mitochondrial T9957C mutation in association with NAION and seizures but not MELASKhaled K Abu-Amero, Thomas M Bosley, Saeed Bohlega, et al.
BMC Neurology|November 19, 2016
Ultrasound-guided botulinum toxin A injection in the treatment of belly dancer's dyskinesiaAsmahan Alshubaili, Hussam Abou-Al-Shaar, Ponnusamy Santhamoorthy, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 28, 2026
Long-Term Outcomes of Deep Brain Stimulation in Woodhouse-Sakati SyndromeHend Alhodaif, Yara Alkhodair, Faisal Alotaibi, et al.
Neurology International|July 3, 2014
Oromandibular dystonia in yemeni patients with khat chewing: a response to botulinum toxin treatmentHatem S Shehata, Mohamed S El-Tamawy, Nevin Mohieldin, et al.
Journal of Movement Disorders|June 1, 2016
Woodhouse-Sakati Syndrome: Report of the First Tunisian Family with the C2orf37 Gene MutationOlfa Hdiji, Emna Turki, Nouha Bouzidi, et al.
European Neurology|December 1, 2015
Levodopa-Carbidopa Intestinal Gel Infusion Therapy in Advanced Parkinson's Disease: Single Middle Eastern Center ExperienceSaeed Bohlega, Hussam Abou Al-Shaar, Thamer Alkhairallah, et al.
AJNR. American Journal of Neuroradiology|March 24, 2004
Neurobrucellosis: clinical and neuroimaging correlationM Walid Al-Sous, Saeed Bohlega, M Zuheir Al-Kawi, et al.
Journal of Medical Case Reports|December 1, 2009
A patient with typical clinical features of mitochondrial encephalopathy, lactic acidosis and stroke-like episodes (MELAS) but without an obvious genetic cause: a case reportKhaled K Abu-Amero, Hesham Al-Dhalaan, Saeed Bohlega, et al.
Journal of the Neurological Sciences|July 18, 2016
Phenotypic comparison of individuals with homozygous or heterozygous mutation of NOTCH3 in a large CADASIL familyHussam Abou Al-Shaar, Najeeb Qadi, Mohamed H Al-Hamed, et al.
Pageof 7

Showing results (11-20 of 64) with videos related to

Sort By:
Pageof 7
BMC Research Notes|August 20, 2008
Absence of mtDNA mutations in leukocytes of CADASIL patientsKhaled K Abu-Amero, Ali Hellani, Saeed Bohlega
Ophthalmic Genetics|April 13, 2005
Mitochondrial T9957C mutation in association with NAION and seizures but not MELASKhaled K Abu-Amero, Thomas M Bosley, Saeed Bohlega, et al.
BMC Neurology|November 19, 2016
Ultrasound-guided botulinum toxin A injection in the treatment of belly dancer's dyskinesiaAsmahan Alshubaili, Hussam Abou-Al-Shaar, Ponnusamy Santhamoorthy, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 28, 2026
Long-Term Outcomes of Deep Brain Stimulation in Woodhouse-Sakati SyndromeHend Alhodaif, Yara Alkhodair, Faisal Alotaibi, et al.
Neurology International|July 3, 2014
Oromandibular dystonia in yemeni patients with khat chewing: a response to botulinum toxin treatmentHatem S Shehata, Mohamed S El-Tamawy, Nevin Mohieldin, et al.
Journal of Movement Disorders|June 1, 2016
Woodhouse-Sakati Syndrome: Report of the First Tunisian Family with the C2orf37 Gene MutationOlfa Hdiji, Emna Turki, Nouha Bouzidi, et al.
European Neurology|December 1, 2015
Levodopa-Carbidopa Intestinal Gel Infusion Therapy in Advanced Parkinson's Disease: Single Middle Eastern Center ExperienceSaeed Bohlega, Hussam Abou Al-Shaar, Thamer Alkhairallah, et al.
AJNR. American Journal of Neuroradiology|March 24, 2004
Neurobrucellosis: clinical and neuroimaging correlationM Walid Al-Sous, Saeed Bohlega, M Zuheir Al-Kawi, et al.
Journal of Medical Case Reports|December 1, 2009
A patient with typical clinical features of mitochondrial encephalopathy, lactic acidosis and stroke-like episodes (MELAS) but without an obvious genetic cause: a case reportKhaled K Abu-Amero, Hesham Al-Dhalaan, Saeed Bohlega, et al.
Journal of the Neurological Sciences|July 18, 2016
Phenotypic comparison of individuals with homozygous or heterozygous mutation of NOTCH3 in a large CADASIL familyHussam Abou Al-Shaar, Najeeb Qadi, Mohamed H Al-Hamed, et al.
Pageof 7