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Reza Ashrafi

Showing results (141-150 of 222) with videos related to

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Journal of Molecular Neuroscience : MN|April 30, 2026
Expanding the Clinical Spectrum of LYRM7-Associated Mitochondrial Complex III Deficiency: Insights from New Cases and Literature ReviewGolazin Shahbodagh Khan, Shiva Bayat, Reza Azizimalamiri, et al.
Irish Journal of Medical Science|January 15, 2022
Novel phenotype and genotype spectrum of WDR62 in two patients with associated primary autosomal recessive microcephalyHajar Aryan, Shaghayegh Zokaei, Dariush Farhud, et al.
Acta Medica Iranica|August 28, 2017
Association of the Single Nucleotide Polymorphisms of the Genes Encoding IL-2 and IFN-γ With Febrile SeizureAmin Shahrokhi, Ameneh Zare-Shahabadi, Mohammad Naeimi Poor, et al.
International Journal of Biological Macromolecules|December 18, 2017
Can any "non-specific charge modification within microtubule binding domains of Tau" be a prerequisite of the protein amyloid aggregation? An in vitro study on the 1N4R isoformAbolfazl Jangholi, Mohammad Reza Ashrafi-Kooshk, Seyed Shahriar Arab, et al.
Molecular Syndromology|August 7, 2025
A Report of Dual Presentations of Pseudo-TORCH Syndrome 1 and MCC2 Deficiency and Review of the LiteratureAli Talea, Shiva Bayat, Golazin Shahbodagh Khan, et al.
Molecular Genetics & Genomic Medicine|February 20, 2025
Trichothiodystrophy due to ERCC2 Variants: Uncommon Contributor to Progressive Hypomyelinating LeukodystrophyAli Reza Tavasoli, Arastoo Kaki, Maedeh Ganji, et al.
Pediatric Neurology|December 13, 2006
Selenium and intractable epilepsy: is there any correlation?Mahmood Reza Ashrafi, Reza Shabanian, Ali Abbaskhanian, et al.
BMC Neurology|August 5, 2020
Novel imaging and clinical phenotypes of CONDSIAS disorder caused by a homozygous frameshift variant of ADPRHL2: a case reportHajar Aryan, Ehsan Razmara, Dariush Farhud, et al.
American Journal of Medical Genetics. Part A|October 22, 2014
First description of a patient with Vici syndrome due to a mutation affecting the penultimate exon of EPG5 and review of the literatureNadja Ehmke, Nima Parvaneh, Peter Krawitz, et al.
Journal of Neurogenetics|July 9, 2017
LGMD2E is the most common type of sarcoglycanopathies in the Iranian populationAfagh Alavi, Sara Esmaeili, Yalda Nilipour, et al.
Pageof 23

Showing results (141-150 of 222) with videos related to

Sort By:
Pageof 23
Journal of Molecular Neuroscience : MN|April 30, 2026
Expanding the Clinical Spectrum of LYRM7-Associated Mitochondrial Complex III Deficiency: Insights from New Cases and Literature ReviewGolazin Shahbodagh Khan, Shiva Bayat, Reza Azizimalamiri, et al.
Irish Journal of Medical Science|January 15, 2022
Novel phenotype and genotype spectrum of WDR62 in two patients with associated primary autosomal recessive microcephalyHajar Aryan, Shaghayegh Zokaei, Dariush Farhud, et al.
Acta Medica Iranica|August 28, 2017
Association of the Single Nucleotide Polymorphisms of the Genes Encoding IL-2 and IFN-γ With Febrile SeizureAmin Shahrokhi, Ameneh Zare-Shahabadi, Mohammad Naeimi Poor, et al.
International Journal of Biological Macromolecules|December 18, 2017
Can any "non-specific charge modification within microtubule binding domains of Tau" be a prerequisite of the protein amyloid aggregation? An in vitro study on the 1N4R isoformAbolfazl Jangholi, Mohammad Reza Ashrafi-Kooshk, Seyed Shahriar Arab, et al.
Molecular Syndromology|August 7, 2025
A Report of Dual Presentations of Pseudo-TORCH Syndrome 1 and MCC2 Deficiency and Review of the LiteratureAli Talea, Shiva Bayat, Golazin Shahbodagh Khan, et al.
Molecular Genetics & Genomic Medicine|February 20, 2025
Trichothiodystrophy due to ERCC2 Variants: Uncommon Contributor to Progressive Hypomyelinating LeukodystrophyAli Reza Tavasoli, Arastoo Kaki, Maedeh Ganji, et al.
Pediatric Neurology|December 13, 2006
Selenium and intractable epilepsy: is there any correlation?Mahmood Reza Ashrafi, Reza Shabanian, Ali Abbaskhanian, et al.
BMC Neurology|August 5, 2020
Novel imaging and clinical phenotypes of CONDSIAS disorder caused by a homozygous frameshift variant of ADPRHL2: a case reportHajar Aryan, Ehsan Razmara, Dariush Farhud, et al.
American Journal of Medical Genetics. Part A|October 22, 2014
First description of a patient with Vici syndrome due to a mutation affecting the penultimate exon of EPG5 and review of the literatureNadja Ehmke, Nima Parvaneh, Peter Krawitz, et al.
Journal of Neurogenetics|July 9, 2017
LGMD2E is the most common type of sarcoglycanopathies in the Iranian populationAfagh Alavi, Sara Esmaeili, Yalda Nilipour, et al.
Pageof 23