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Reza Ashrafi

Showing results (211-220 of 222) with videos related to

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Iranian Journal of Allergy, Asthma, and Immunology|May 11, 2026
The Value of Anti-Drug Antibody Detection in Discriminating Patients from Healthy Controls and Predicting the Gross Motor Functional State in Patients with Pompe DiseaseSolmaz Aziz-Ahari, Mahdi Aminian, Aliasghar Rahimian, et al.
Archives of Iranian Medicine|August 6, 2023
Neurologic Manifestations of Coronavirus Disease 2019 in Children: An Iranian Hospital-Based StudyElmira Haji Esmaeil Memar, Morteza Heidari, Homa Ghabeli, et al.
Genome Medicine|December 24, 2017
B3GALNT2 mutations associated with non-syndromic autosomal recessive intellectual disability reveal a lack of genotype-phenotype associations in the muscular dystrophy-dystroglycanopathiesReza Maroofian, Moniek Riemersma, Lucas T Jae, et al.
Epilepsy Research|July 6, 2026
Genetic heterogeneity, movement disorders, and white matter abnormalities in pediatric developmental and epileptic encephalopathies: A retrospective cohort study from a National Neurodegenerative and Leukodystrophy RegistryPouria Mohammadi, Sahand Fateh Tehrani, Reza Shervin Badv, et al.
Neuromolecular Medicine|July 2, 2024
A Comprehensive Overview of NF1 Mutations in Iranian PatientsShahram Savad, Mohammad-Hossein Modarressi, Sarang Younesi, et al.
Brain & Development|December 21, 2023
A comprehensive study of mutation and phenotypic heterogeneity of childhood mitochondrial leukodystrophiesSareh Hosseinpour, Ehsan Razmara, Morteza Heidari, et al.
NPJ Genomic Medicine|February 19, 2024
Clinical application of next generation sequencing for Mendelian disease diagnosis in the Iranian populationAyda Abolhassani, Zohreh Fattahi, Maryam Beheshtian, et al.
Human Genomics|April 3, 2024
The genetic basis of early-onset hereditary ataxia in Iran: results of a national registry of a heterogeneous populationNejat Mahdieh, Morteza Heidari, Zahra Rezaei, et al.
Frontiers in Neurology|July 12, 2021
The ARCA Registry: A Collaborative Global Platform for Advancing Trial Readiness in Autosomal Recessive Cerebellar AtaxiasAndreas Traschütz, Selina Reich, Astrid D Adarmes, et al.
Journal of Neuromuscular Diseases|February 19, 2025
Comparative efficacy of risdiplam and nusinersen in Type 2 and 3 spinal muscular atrophy patients: A cohort study using real-world dataMahmoud Reza Ashrafi, Marzieh Babaee, Seyed Saeed Hashemi Nazari, et al.
Pageof 23

Showing results (211-220 of 222) with videos related to

Sort By:
Pageof 23
Iranian Journal of Allergy, Asthma, and Immunology|May 11, 2026
The Value of Anti-Drug Antibody Detection in Discriminating Patients from Healthy Controls and Predicting the Gross Motor Functional State in Patients with Pompe DiseaseSolmaz Aziz-Ahari, Mahdi Aminian, Aliasghar Rahimian, et al.
Archives of Iranian Medicine|August 6, 2023
Neurologic Manifestations of Coronavirus Disease 2019 in Children: An Iranian Hospital-Based StudyElmira Haji Esmaeil Memar, Morteza Heidari, Homa Ghabeli, et al.
Genome Medicine|December 24, 2017
B3GALNT2 mutations associated with non-syndromic autosomal recessive intellectual disability reveal a lack of genotype-phenotype associations in the muscular dystrophy-dystroglycanopathiesReza Maroofian, Moniek Riemersma, Lucas T Jae, et al.
Epilepsy Research|July 6, 2026
Genetic heterogeneity, movement disorders, and white matter abnormalities in pediatric developmental and epileptic encephalopathies: A retrospective cohort study from a National Neurodegenerative and Leukodystrophy RegistryPouria Mohammadi, Sahand Fateh Tehrani, Reza Shervin Badv, et al.
Neuromolecular Medicine|July 2, 2024
A Comprehensive Overview of NF1 Mutations in Iranian PatientsShahram Savad, Mohammad-Hossein Modarressi, Sarang Younesi, et al.
Brain & Development|December 21, 2023
A comprehensive study of mutation and phenotypic heterogeneity of childhood mitochondrial leukodystrophiesSareh Hosseinpour, Ehsan Razmara, Morteza Heidari, et al.
NPJ Genomic Medicine|February 19, 2024
Clinical application of next generation sequencing for Mendelian disease diagnosis in the Iranian populationAyda Abolhassani, Zohreh Fattahi, Maryam Beheshtian, et al.
Human Genomics|April 3, 2024
The genetic basis of early-onset hereditary ataxia in Iran: results of a national registry of a heterogeneous populationNejat Mahdieh, Morteza Heidari, Zahra Rezaei, et al.
Frontiers in Neurology|July 12, 2021
The ARCA Registry: A Collaborative Global Platform for Advancing Trial Readiness in Autosomal Recessive Cerebellar AtaxiasAndreas Traschütz, Selina Reich, Astrid D Adarmes, et al.
Journal of Neuromuscular Diseases|February 19, 2025
Comparative efficacy of risdiplam and nusinersen in Type 2 and 3 spinal muscular atrophy patients: A cohort study using real-world dataMahmoud Reza Ashrafi, Marzieh Babaee, Seyed Saeed Hashemi Nazari, et al.
Pageof 23