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Bader Shirah

Showing results (91-100 of 111) with videos related to

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Intractable & Rare Diseases Research|August 27, 2020
A novel variant c.3706C>T p.(Avg 1236Cys) in the <i>ABCA7</i> gene in a Saudi patient with susceptibility to Alzheimer's disease 9Hussein Algahtani, Bader Shirah, Alhusain Alshareef, et al.
Genes & Diseases|February 11, 2021
Autosomal recessive cerebellar ataxia with spasticity due to a rare mutation in <i>GBA2</i> gene in a large consanguineous Saudi familyHussein Algahtani, Bader Shirah, Ikram Ullah, et al.
Maedica|December 21, 2022
Adult-Onset Hereditary Spastic Paraplegia 15 in a Saudi Patient with A Compound Heterozygous Variant in the <i>ZFYVE26</i>GeneHussein Algahtani, Bader Shirah, Rahaf Aljohani, et al.
The International Journal of Neuroscience|March 17, 2020
A novel mutation in <i>ATM</i> gene in a Saudi female with ataxia telangiectasiaHussein Algahtani, Bader Shirah, Raghad Algahtani, et al.
Aging Cell|January 12, 2026
Astronauts as a Human Aging Model: Epigenetic Age Responses to Space ExposureMatías Fuentealba, JangKeun Kim, Jeremy Wain Hirschberg, et al.
Journal of Stroke and Cerebrovascular Diseases : the Official Journal of National Stroke Association|May 17, 2020
A Novel Heterozygous Variant in Exon 19 of NOTCH3 in a Saudi Family with Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and LeukoencephalopathyHussein Algahtani, Bader Shirah, Suzan Y Alharbi, et al.
Cureus|June 13, 2022
Migraine Prevalence and Analysis of Dietary Habits in Relation to Headache in the Female Population: A Single-Center Study From Jeddah, Saudi ArabiaYasser S Aladdin, Rawaf Alsharif, Weaam Mattar, et al.
International Journal of Health Sciences|January 18, 2021
Congenital hypothyroidism in Saudi population in two major cities: A retrospective study on prevalence and therapeutic outcomesAdnan Al Shaikh, Areej Alsofyani, Bader Shirah, et al.
Saudi Journal of Biological Sciences|June 6, 2022
Clinical whole exome sequencing revealed <i>de novo</i> heterozygous stop-gain and missense variants in the <i>STXBP1</i> gene associated with epilepsy in Saudi familiesMuhammad Imran Naseer, Angham Abdulrhman Abdulkareem, Mahmood Rasool, et al.
Seizure|April 30, 2019
A very rare form of autosomal dominant progressive myoclonus epilepsy caused by a novel variant in the PRICKLE1 geneHussein Algahtani, Fahad Al-Hakami, Mohammed Al-Shehri, et al.
Pageof 12

Showing results (91-100 of 111) with videos related to

Sort By:
Pageof 12
Intractable & Rare Diseases Research|August 27, 2020
A novel variant c.3706C>T p.(Avg 1236Cys) in the <i>ABCA7</i> gene in a Saudi patient with susceptibility to Alzheimer's disease 9Hussein Algahtani, Bader Shirah, Alhusain Alshareef, et al.
Genes & Diseases|February 11, 2021
Autosomal recessive cerebellar ataxia with spasticity due to a rare mutation in <i>GBA2</i> gene in a large consanguineous Saudi familyHussein Algahtani, Bader Shirah, Ikram Ullah, et al.
Maedica|December 21, 2022
Adult-Onset Hereditary Spastic Paraplegia 15 in a Saudi Patient with A Compound Heterozygous Variant in the <i>ZFYVE26</i>GeneHussein Algahtani, Bader Shirah, Rahaf Aljohani, et al.
The International Journal of Neuroscience|March 17, 2020
A novel mutation in <i>ATM</i> gene in a Saudi female with ataxia telangiectasiaHussein Algahtani, Bader Shirah, Raghad Algahtani, et al.
Aging Cell|January 12, 2026
Astronauts as a Human Aging Model: Epigenetic Age Responses to Space ExposureMatías Fuentealba, JangKeun Kim, Jeremy Wain Hirschberg, et al.
Journal of Stroke and Cerebrovascular Diseases : the Official Journal of National Stroke Association|May 17, 2020
A Novel Heterozygous Variant in Exon 19 of NOTCH3 in a Saudi Family with Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and LeukoencephalopathyHussein Algahtani, Bader Shirah, Suzan Y Alharbi, et al.
Cureus|June 13, 2022
Migraine Prevalence and Analysis of Dietary Habits in Relation to Headache in the Female Population: A Single-Center Study From Jeddah, Saudi ArabiaYasser S Aladdin, Rawaf Alsharif, Weaam Mattar, et al.
International Journal of Health Sciences|January 18, 2021
Congenital hypothyroidism in Saudi population in two major cities: A retrospective study on prevalence and therapeutic outcomesAdnan Al Shaikh, Areej Alsofyani, Bader Shirah, et al.
Saudi Journal of Biological Sciences|June 6, 2022
Clinical whole exome sequencing revealed <i>de novo</i> heterozygous stop-gain and missense variants in the <i>STXBP1</i> gene associated with epilepsy in Saudi familiesMuhammad Imran Naseer, Angham Abdulrhman Abdulkareem, Mahmood Rasool, et al.
Seizure|April 30, 2019
A very rare form of autosomal dominant progressive myoclonus epilepsy caused by a novel variant in the PRICKLE1 geneHussein Algahtani, Fahad Al-Hakami, Mohammed Al-Shehri, et al.
Pageof 12