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Journal of Genetics
|
September 21, 2023
A novel <i>METTL5</i> variant disrupting a donor splice site leads to primary microcephaly-related intellectual disability in an Iranian family: clinical features and literature review
Fatemeh Shakarami, Zahra Nouri, Hossein Khanahmad, et al.
Neuromuscular Disorders : NMD
|
August 21, 2022
Whole exome sequencing identified a novel LAMA2 frameshift variant causing merosin-deficient congenital muscular dystrophy in a patient with cardiomyopathy, and autism-like behavior
Zahra Nouri, Akram Sarmadi, Sina Narrei, et al.
Clinical Neurology and Neurosurgery
|
January 3, 2025
Coagulopathy at admission in traumatic brain injury and its association with hematoma progression: A systematic review and meta-analysis of 2411 patients
Ibrahim Mohammadzadeh, Behnaz Niroomand, Amin Tajerian, et al.
Journal of Education and Health Promotion
|
March 2, 2022
Comparison of the effect of two teaching methods on surgical technologist students' learning and satisfaction (flashcards vs. mobile-based learning)
Leila Sadati, Mehran Nafar, Sahar Karami, et al.
BMC Medical Genomics
|
July 3, 2024
Clinical characterizations and molecular genetic study of two co-segregating variants in PDZD7 and PDE6C genes leading simultaneously to non-syndromic hearing loss and achromatopsia
Zahra Nouri, Akram Sarmadi, Sina Narrei, et al.
NPJ Biofilms and Microbiomes
|
April 5, 2022
The microbiota-gut-kidney axis mediates host osmoregulation in a small desert mammal
Zahra Nouri, Xue-Ying Zhang, Saeid Khakisahneh, et al.
Medical Journal of the Islamic Republic of Iran
|
August 21, 2023
A Comparative Study of the Effect of Two Methods of Online Education Based on Sweller'S Cognitive Load Theory and Online Education in A Common Way on the Academic Engagement of Medical Students in Anatomy
Zohreh Sohrabi, Sohrab Nosrati, Zahra Nouri Khaneghah, et al.
Molecular Biology Reports
|
July 6, 2020
Whole exome sequencing identifies novel compound heterozygous pathogenic variants in the MYO15A gene leading to autosomal recessive non-syndromic hearing loss
Akram Sarmadi, Samane Nasrniya, Sina Narrei, et al.
Medical Journal of the Islamic Republic of Iran
|
July 31, 2025
A Scoping Review of Quasi-experimental Studies on Simulation-Based Learning in Medical Education: Trends and Insights from the Last Decade
Zohreh Sohrabi, Samane Ghasemi, Zahra Nouri Khaneghah, et al.
Advanced Biomedical Research
|
October 19, 2020
Molecular Genetic Study in a Cohort of Iranian Families Suspected to Maturity-Onset Diabetes of the Young, Reveals a Recurrent Mutation and a High-Risk Variant in the <i>CEL</i> Gene
Akram Sarmadi, Aliasgar Mohammadi, Fatemeh Tabatabaei, et al.
Page
of 5
Search research articles
Search
Showing results (11-20 of 45) with videos related to
Sort By:
Page
of 5
Journal of Genetics
|
September 21, 2023
A novel <i>METTL5</i> variant disrupting a donor splice site leads to primary microcephaly-related intellectual disability in an Iranian family: clinical features and literature review
Fatemeh Shakarami, Zahra Nouri, Hossein Khanahmad, et al.
Neuromuscular Disorders : NMD
|
August 21, 2022
Whole exome sequencing identified a novel LAMA2 frameshift variant causing merosin-deficient congenital muscular dystrophy in a patient with cardiomyopathy, and autism-like behavior
Zahra Nouri, Akram Sarmadi, Sina Narrei, et al.
Clinical Neurology and Neurosurgery
|
January 3, 2025
Coagulopathy at admission in traumatic brain injury and its association with hematoma progression: A systematic review and meta-analysis of 2411 patients
Ibrahim Mohammadzadeh, Behnaz Niroomand, Amin Tajerian, et al.
Journal of Education and Health Promotion
|
March 2, 2022
Comparison of the effect of two teaching methods on surgical technologist students' learning and satisfaction (flashcards vs. mobile-based learning)
Leila Sadati, Mehran Nafar, Sahar Karami, et al.
BMC Medical Genomics
|
July 3, 2024
Clinical characterizations and molecular genetic study of two co-segregating variants in PDZD7 and PDE6C genes leading simultaneously to non-syndromic hearing loss and achromatopsia
Zahra Nouri, Akram Sarmadi, Sina Narrei, et al.
NPJ Biofilms and Microbiomes
|
April 5, 2022
The microbiota-gut-kidney axis mediates host osmoregulation in a small desert mammal
Zahra Nouri, Xue-Ying Zhang, Saeid Khakisahneh, et al.
Medical Journal of the Islamic Republic of Iran
|
August 21, 2023
A Comparative Study of the Effect of Two Methods of Online Education Based on Sweller'S Cognitive Load Theory and Online Education in A Common Way on the Academic Engagement of Medical Students in Anatomy
Zohreh Sohrabi, Sohrab Nosrati, Zahra Nouri Khaneghah, et al.
Molecular Biology Reports
|
July 6, 2020
Whole exome sequencing identifies novel compound heterozygous pathogenic variants in the MYO15A gene leading to autosomal recessive non-syndromic hearing loss
Akram Sarmadi, Samane Nasrniya, Sina Narrei, et al.
Medical Journal of the Islamic Republic of Iran
|
July 31, 2025
A Scoping Review of Quasi-experimental Studies on Simulation-Based Learning in Medical Education: Trends and Insights from the Last Decade
Zohreh Sohrabi, Samane Ghasemi, Zahra Nouri Khaneghah, et al.
Advanced Biomedical Research
|
October 19, 2020
Molecular Genetic Study in a Cohort of Iranian Families Suspected to Maturity-Onset Diabetes of the Young, Reveals a Recurrent Mutation and a High-Risk Variant in the <i>CEL</i> Gene
Akram Sarmadi, Aliasgar Mohammadi, Fatemeh Tabatabaei, et al.
Page
of 5