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BMC Pediatrics
|
December 12, 2022
The quality of life in children with spinal muscular atrophy: a case-control study
Gholamreza 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 families
Mahmoud 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 trial
Man 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 Gene
Ali 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 dystrophy
Gholamreza 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 Iran
Kosar Asna Ashari, Nahid Aslani, Nima Parvaneh, et al.
Neuromuscular Disorders : NMD
|
May 29, 2016
The quality of life in boys with Duchenne muscular dystrophy
Gholamreza 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 Study
Mahmoud 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 Sequencing
Gholam 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 Room
Sareh Hosseinpour, Roxana Pazouki, Mahmoud Reza Ashrafi, et al.
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of 13
Search research articles
Search
Showing results (81-90 of 121) with videos related to
Sort By:
Page
of 13
BMC Pediatrics
|
December 12, 2022
The quality of life in children with spinal muscular atrophy: a case-control study
Gholamreza 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 families
Mahmoud 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 trial
Man 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 Gene
Ali 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 dystrophy
Gholamreza 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 Iran
Kosar Asna Ashari, Nahid Aslani, Nima Parvaneh, et al.
Neuromuscular Disorders : NMD
|
May 29, 2016
The quality of life in boys with Duchenne muscular dystrophy
Gholamreza 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 Study
Mahmoud 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 Sequencing
Gholam 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 Room
Sareh Hosseinpour, Roxana Pazouki, Mahmoud Reza Ashrafi, et al.
Page
of 13