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Bader Shirah

Showing results (81-90 of 111) with videos related to

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Encephalitis (Seoul, Korea)|October 31, 2024
Multifocal disseminated necrotizing leukoencephalopathy as severe central nervous system toxicity from nivolumab therapy for Hodgkin lymphoma: a case reportHussein Algahtani, Bader Shirah, Mohamed Najm Aldeen Alameen, et al.
Cureus|January 23, 2020
Assessment of the Burden of Multiple Sclerosis Patients' Caregivers in Saudi ArabiaHussein Algahtani, Bader Shirah, Abdulrahman Bayazeed, et al.
Journal of Back and Musculoskeletal Rehabilitation|July 4, 2018
Limb-girdle muscular dystrophy type 2B: An unusual cause of proximal muscular weakness in Saudi ArabiaHussein Algahtani, Bader Shirah, Ali H Alassiri, et al.
Bioinformation|October 9, 2023
Leber hereditary optic neuropathy presenting as bilateral visual loss and white matter diseaseHussein Algahtani, Bader Shirah, Angham Abdulrhman Abdulkareem, et al.
Journal of the Neurological Sciences|October 25, 2016
Congenital insensitivity to pain with anhidrosis: A report of two siblings with a novel mutation in (TrkA) NTRK1 gene in a Saudi familyHussein Algahtani, Muhammad Imran Naseer, Mohammad Al-Qahtani, et al.
Intractable & Rare Diseases Research|June 21, 2019
A novel mutation in <i>TTN</i> gene in a Saudi patient with bilateral facial weakness and scapular wingingHussein Algahtani, Bader Shirah, Raghad Algahtani, et al.
Journal of Epilepsy Research|September 28, 2020
A Novel Intronic Variant in <i>SLC2A1</i> Gene in a Saudi Patient with Myoclonic EpilepsyHussein Algahtani, Bader Shirah, Ahmad Albarakaty, et al.
Neurological Research|October 5, 2020
A Novel Variant in CWF19L1 Gene in a Family with Late-Onset Autosomal Recessive Cerebellar Ataxia 17Hussein Algahtani, Bader Shirah, Samah Almatrafi, et al.
Intractable & Rare Diseases Research|December 19, 2018
Ataxia with ocular apraxia type 2 not responding to 4-aminopyridine: A rare mutation in the <i>SETX</i> gene in a Saudi patientHussein Algahtani, Bader Shirah, Raghad Algahtani, et al.
Intractable & Rare Diseases Research|March 19, 2019
A novel mutation in <i>CACNA1A</i> gene in a Saudi female with episodic ataxia type 2 with no response to acetazolamide or 4-aminopyridineHussein Algahtani, Bader Shirah, Raghad Algahtani, et al.
Pageof 12

Showing results (81-90 of 111) with videos related to

Sort By:
Pageof 12
Encephalitis (Seoul, Korea)|October 31, 2024
Multifocal disseminated necrotizing leukoencephalopathy as severe central nervous system toxicity from nivolumab therapy for Hodgkin lymphoma: a case reportHussein Algahtani, Bader Shirah, Mohamed Najm Aldeen Alameen, et al.
Cureus|January 23, 2020
Assessment of the Burden of Multiple Sclerosis Patients' Caregivers in Saudi ArabiaHussein Algahtani, Bader Shirah, Abdulrahman Bayazeed, et al.
Journal of Back and Musculoskeletal Rehabilitation|July 4, 2018
Limb-girdle muscular dystrophy type 2B: An unusual cause of proximal muscular weakness in Saudi ArabiaHussein Algahtani, Bader Shirah, Ali H Alassiri, et al.
Bioinformation|October 9, 2023
Leber hereditary optic neuropathy presenting as bilateral visual loss and white matter diseaseHussein Algahtani, Bader Shirah, Angham Abdulrhman Abdulkareem, et al.
Journal of the Neurological Sciences|October 25, 2016
Congenital insensitivity to pain with anhidrosis: A report of two siblings with a novel mutation in (TrkA) NTRK1 gene in a Saudi familyHussein Algahtani, Muhammad Imran Naseer, Mohammad Al-Qahtani, et al.
Intractable & Rare Diseases Research|June 21, 2019
A novel mutation in <i>TTN</i> gene in a Saudi patient with bilateral facial weakness and scapular wingingHussein Algahtani, Bader Shirah, Raghad Algahtani, et al.
Journal of Epilepsy Research|September 28, 2020
A Novel Intronic Variant in <i>SLC2A1</i> Gene in a Saudi Patient with Myoclonic EpilepsyHussein Algahtani, Bader Shirah, Ahmad Albarakaty, et al.
Neurological Research|October 5, 2020
A Novel Variant in CWF19L1 Gene in a Family with Late-Onset Autosomal Recessive Cerebellar Ataxia 17Hussein Algahtani, Bader Shirah, Samah Almatrafi, et al.
Intractable & Rare Diseases Research|December 19, 2018
Ataxia with ocular apraxia type 2 not responding to 4-aminopyridine: A rare mutation in the <i>SETX</i> gene in a Saudi patientHussein Algahtani, Bader Shirah, Raghad Algahtani, et al.
Intractable & Rare Diseases Research|March 19, 2019
A novel mutation in <i>CACNA1A</i> gene in a Saudi female with episodic ataxia type 2 with no response to acetazolamide or 4-aminopyridineHussein Algahtani, Bader Shirah, Raghad Algahtani, et al.
Pageof 12