Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Reza Ghasemi

Showing results (121-130 of 139) with videos related to

Pageof 14
Sort By:
Molecular Genetics & Genomic Medicine|January 21, 2025
Clinical Features and Genetic Characteristics of XLID Patients With KDM5C Gene Mutations: Insights on Phenotype-Genotype Correlations From 175 Previous Cases and Identification of a Novel VariantMohammad-Reza Ghasemi, Zahra Esmaeilizadeh, Sahand Tehrani Fateh, et al.
Neurosurgical Review|March 17, 2025
Customized 3D-printed Poly ether ether ketone cranial implant for cranioplasty of skull defectsFarid Qoorchi Moheb Seraj, Daniel Kheradmand, Sajjad Najafi, et al.
Biochemical Genetics|April 19, 2025
Exome Sequencing in 9 Iranian Patients Expands the Mutational and Clinical Spectrum of Bardet-Biedl SyndromeMohammad Reza Seyedtaghia, Mohsen Habibi, Farzad Hashemi-Gorji, et al.
Journal of Education and Health Promotion|October 16, 2025
Association of backpacks carriage manner (BCM) and musculoskeletal symptoms among students facilitating health promotion: Ergonomics design-based qualitative content analysis studyAli Askari, Malih Babahaji, Hesamedin Askari Majdabadi, et al.
Clinical Genetics|December 4, 2024
Comprehensive Analysis of TEK Variants in Patients With Vascular MalformationsReza Ghasemi, Meagan M Corliss, Kevin M Bowling, et al.
BMC Medical Genomics|January 12, 2024
Comprehensive review and expanding the genetic landscape of Cornelia-de-Lange spectrum: insights from novel mutations and skin biopsy in exome-negative casesSahand Tehrani Fateh, Nadia Mohammad Zadeh, Shadab Salehpour, et al.
Heliyon|March 19, 2024
Identification of novel mutations in <i>TPK1</i> and <i>SLC19A3</i> genes in families exhibiting thiamine metabolism dysfunction syndromeFatemeh Norouzi Rostami, Hossein Sadeghi, Farzad Hashemi-Gorji, et al.
Iranian Journal of Child Neurology|May 2, 2022
Analysis of Cytogenetic Abnormalities in Iranian Patients with Syndromic Autism Spectrum Disorder: A Case SeriesMohammad Reza Ghasemi, Peyman Zargari, Hossein Sadeghi, et al.
Experimental Physiology|April 18, 2018
Eccentric exercise increases circulating fibroblast activation protein α but not bioactive fibroblast growth factor 21 in healthy humansBiraj Parmar, Jo E Lewis, Ricardo J Samms, et al.
JIMD Reports|August 1, 2025
Glycine <i>N</i>-Acyltransferase Deficiency due to a Homozygous Nonsense Variant in the <i>GLYAT</i>: A Novel Inborn Error of MetabolismMona Nourbakhsh, Mohammad Miryounesi, Ali Tale, et al.
Pageof 14

Showing results (121-130 of 139) with videos related to

Sort By:
Pageof 14
Molecular Genetics & Genomic Medicine|January 21, 2025
Clinical Features and Genetic Characteristics of XLID Patients With KDM5C Gene Mutations: Insights on Phenotype-Genotype Correlations From 175 Previous Cases and Identification of a Novel VariantMohammad-Reza Ghasemi, Zahra Esmaeilizadeh, Sahand Tehrani Fateh, et al.
Neurosurgical Review|March 17, 2025
Customized 3D-printed Poly ether ether ketone cranial implant for cranioplasty of skull defectsFarid Qoorchi Moheb Seraj, Daniel Kheradmand, Sajjad Najafi, et al.
Biochemical Genetics|April 19, 2025
Exome Sequencing in 9 Iranian Patients Expands the Mutational and Clinical Spectrum of Bardet-Biedl SyndromeMohammad Reza Seyedtaghia, Mohsen Habibi, Farzad Hashemi-Gorji, et al.
Journal of Education and Health Promotion|October 16, 2025
Association of backpacks carriage manner (BCM) and musculoskeletal symptoms among students facilitating health promotion: Ergonomics design-based qualitative content analysis studyAli Askari, Malih Babahaji, Hesamedin Askari Majdabadi, et al.
Clinical Genetics|December 4, 2024
Comprehensive Analysis of TEK Variants in Patients With Vascular MalformationsReza Ghasemi, Meagan M Corliss, Kevin M Bowling, et al.
BMC Medical Genomics|January 12, 2024
Comprehensive review and expanding the genetic landscape of Cornelia-de-Lange spectrum: insights from novel mutations and skin biopsy in exome-negative casesSahand Tehrani Fateh, Nadia Mohammad Zadeh, Shadab Salehpour, et al.
Heliyon|March 19, 2024
Identification of novel mutations in <i>TPK1</i> and <i>SLC19A3</i> genes in families exhibiting thiamine metabolism dysfunction syndromeFatemeh Norouzi Rostami, Hossein Sadeghi, Farzad Hashemi-Gorji, et al.
Iranian Journal of Child Neurology|May 2, 2022
Analysis of Cytogenetic Abnormalities in Iranian Patients with Syndromic Autism Spectrum Disorder: A Case SeriesMohammad Reza Ghasemi, Peyman Zargari, Hossein Sadeghi, et al.
Experimental Physiology|April 18, 2018
Eccentric exercise increases circulating fibroblast activation protein α but not bioactive fibroblast growth factor 21 in healthy humansBiraj Parmar, Jo E Lewis, Ricardo J Samms, et al.
JIMD Reports|August 1, 2025
Glycine <i>N</i>-Acyltransferase Deficiency due to a Homozygous Nonsense Variant in the <i>GLYAT</i>: A Novel Inborn Error of MetabolismMona Nourbakhsh, Mohammad Miryounesi, Ali Tale, et al.
Pageof 14