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

Morteza Heidari

Showing results (81-90 of 121) with videos related to

Pageof 13
Sort By:
BMC Pediatrics|December 12, 2022
The quality of life in children with spinal muscular atrophy: a case-control studyGholamreza Zamani, Mahmoud Reza Ashrafi, Homa Ghabeli, et al.
Molecular Genetics & Genomic Medicine|March 3, 2023
Expanding the genetic spectrum of giant axonal neuropathy: Two novel variants in Iranian familiesMahmoud Reza Ashrafi, Ali Zare Dehnavi, Ali Reza Tavasoli, et al.
Cephalalgia : an International Journal of Headache|November 12, 2019
Cinnarizine and sodium valproate as the preventive agents of pediatric migraine: A randomized double-blind placebo-controlled trialMan Amanat, Mansoureh Togha, Elmira Agah, et al.
Journal of Molecular Neuroscience : MN|January 4, 2022
Primary and Secondary Microcephaly, Global Developmental Delay, and Seizure in Two Siblings Caused by a Novel Missense Variant in the ZNF335 GeneAli Reza Tavasoli, Elmira Haji Esmaeil Memar, Mahmoud Reza Ashrafi, et al.
BMC Neurology|May 3, 2022
Characteristics of disease progression and genetic correlation in ambulatory Iranian boys with Duchenne muscular dystrophyGholamreza Zamani, Sareh Hosseinpour, Mahmoud Reza Ashrafi, et al.
Pediatric Rheumatology Online Journal|June 13, 2023
A case series of ten plus one deficiency of adenosine deaminase 2 (DADA2) patients in IranKosar Asna Ashari, Nahid Aslani, Nima Parvaneh, et al.
Neuromuscular Disorders : NMD|May 29, 2016
The quality of life in boys with Duchenne muscular dystrophyGholamreza Zamani, Morteza Heidari, Reza Azizi Malamiri, et al.
Iranian Journal of Child Neurology|May 8, 2026
Hyperventilation-Induced High-Amplitude Rhythmic Slowing and Its Impact on Migraine Frequency in Children: A Retrospective Observational Cohort StudyMahmoud Mohammadi, Reza Shervin Badv, Zahra Rezaei, et al.
Journal of Molecular Neuroscience : MN|February 26, 2022
Genetic Analysis of Forty MLPA-Negative Duchenne Muscular Dystrophy Patients by Whole-Exome SequencingGholam Reza Zamani, Mohammad Farid Mohammadi, Ali Reza Tavasoli, et al.
Iranian Journal of Child Neurology|October 31, 2024
Exploring the Phenotypic Profile of Acute Flaccid Paralysis: Insights from a Third-Level Pediatric Emergency RoomSareh Hosseinpour, Roxana Pazouki, Mahmoud Reza Ashrafi, et al.
Pageof 13

Showing results (81-90 of 121) with videos related to

Sort By:
Pageof 13
BMC Pediatrics|December 12, 2022
The quality of life in children with spinal muscular atrophy: a case-control studyGholamreza Zamani, Mahmoud Reza Ashrafi, Homa Ghabeli, et al.
Molecular Genetics & Genomic Medicine|March 3, 2023
Expanding the genetic spectrum of giant axonal neuropathy: Two novel variants in Iranian familiesMahmoud Reza Ashrafi, Ali Zare Dehnavi, Ali Reza Tavasoli, et al.
Cephalalgia : an International Journal of Headache|November 12, 2019
Cinnarizine and sodium valproate as the preventive agents of pediatric migraine: A randomized double-blind placebo-controlled trialMan Amanat, Mansoureh Togha, Elmira Agah, et al.
Journal of Molecular Neuroscience : MN|January 4, 2022
Primary and Secondary Microcephaly, Global Developmental Delay, and Seizure in Two Siblings Caused by a Novel Missense Variant in the ZNF335 GeneAli Reza Tavasoli, Elmira Haji Esmaeil Memar, Mahmoud Reza Ashrafi, et al.
BMC Neurology|May 3, 2022
Characteristics of disease progression and genetic correlation in ambulatory Iranian boys with Duchenne muscular dystrophyGholamreza Zamani, Sareh Hosseinpour, Mahmoud Reza Ashrafi, et al.
Pediatric Rheumatology Online Journal|June 13, 2023
A case series of ten plus one deficiency of adenosine deaminase 2 (DADA2) patients in IranKosar Asna Ashari, Nahid Aslani, Nima Parvaneh, et al.
Neuromuscular Disorders : NMD|May 29, 2016
The quality of life in boys with Duchenne muscular dystrophyGholamreza Zamani, Morteza Heidari, Reza Azizi Malamiri, et al.
Iranian Journal of Child Neurology|May 8, 2026
Hyperventilation-Induced High-Amplitude Rhythmic Slowing and Its Impact on Migraine Frequency in Children: A Retrospective Observational Cohort StudyMahmoud Mohammadi, Reza Shervin Badv, Zahra Rezaei, et al.
Journal of Molecular Neuroscience : MN|February 26, 2022
Genetic Analysis of Forty MLPA-Negative Duchenne Muscular Dystrophy Patients by Whole-Exome SequencingGholam Reza Zamani, Mohammad Farid Mohammadi, Ali Reza Tavasoli, et al.
Iranian Journal of Child Neurology|October 31, 2024
Exploring the Phenotypic Profile of Acute Flaccid Paralysis: Insights from a Third-Level Pediatric Emergency RoomSareh Hosseinpour, Roxana Pazouki, Mahmoud Reza Ashrafi, et al.
Pageof 13