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Morteza Heidari

Showing results (61-70 of 121) with videos related to

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European Journal of Pediatrics|August 29, 2025
Combination therapies in spinal muscular atrophy: a systematic reviewMaryam Bemanalizadeh, Leida Heidary, Mohammad Sedigh Dakkali, et al.
Iranian Journal of Child Neurology|November 10, 2025
Learning Outcomes of Virtual Journal Clubs in Comparison to Real Ones in Pediatric Neurology FellowsMahmoud Mohammadi, Mitra Zolfaghari, Reza Shervin Badv, et al.
International Journal for Quality in Health Care : Journal of the International Society for Quality in Health Care|December 28, 2020
Developing a charter of spiritual care for patientsAkram Heidari, Abdolhasan Kazemi, Mohammad Abbasi, et al.
Pediatric Neurology|July 16, 2014
Efficacy and safety of cinnarizine in the prophylaxis of migraine in children: a double-blind placebo-controlled randomized trialMahmoud Reza Ashrafi, Soodeh Salehi, Reza Azizi Malamiri, et al.
European Journal of Medical Genetics|March 13, 2026
Genetic and Clinical Insights into Pontocerebellar Hypoplasia: Identification of Novel Variants in an Iranian CohortZahra Rezaei, Farnoosh Emami, Morteza Heidari, et al.
Clinical Case Reports|January 28, 2025
Primary Diffuse Leptomeningeal Melanomatosis Leading to Raised Intracranial Pressure in a Pediatric PatientShiva Sareh, Zohreh Habibi, Mohammad Vasei, et al.
Molecular Biology Reports|June 1, 2024
Distinct neurological phenotypes associated with biallelic loss of NOTCH3 function: evidence for recessive inheritanceBehnoosh Tasharrofi, Ali Najafi, Elham Pourbakhtyaran, et al.
Journal of Child Neurology|November 19, 2024
Death Causes Among Iranian Children With LeukodystrophiesMahsa Shiva, Sareh Hosseinpour, Mahmoud Reza Ashrafi, et al.
Journal of Molecular Neuroscience : MN|April 30, 2026
Expanding the Clinical Spectrum of LYRM7-Associated Mitochondrial Complex III Deficiency: Insights from New Cases and Literature ReviewGolazin Shahbodagh Khan, Shiva Bayat, Reza Azizimalamiri, et al.
Clinical Case Reports|December 10, 2025
A Novel Mutation of CADHERIN (<i>CDH15</i>) in an Iranian Boy With Borderline Intelligence Without Dysmorphism-A Case ReportMahmoud Reza Ashrafi, Ali Nikkhah, Morteza Heidari, et al.
Pageof 13

Showing results (61-70 of 121) with videos related to

Sort By:
Pageof 13
European Journal of Pediatrics|August 29, 2025
Combination therapies in spinal muscular atrophy: a systematic reviewMaryam Bemanalizadeh, Leida Heidary, Mohammad Sedigh Dakkali, et al.
Iranian Journal of Child Neurology|November 10, 2025
Learning Outcomes of Virtual Journal Clubs in Comparison to Real Ones in Pediatric Neurology FellowsMahmoud Mohammadi, Mitra Zolfaghari, Reza Shervin Badv, et al.
International Journal for Quality in Health Care : Journal of the International Society for Quality in Health Care|December 28, 2020
Developing a charter of spiritual care for patientsAkram Heidari, Abdolhasan Kazemi, Mohammad Abbasi, et al.
Pediatric Neurology|July 16, 2014
Efficacy and safety of cinnarizine in the prophylaxis of migraine in children: a double-blind placebo-controlled randomized trialMahmoud Reza Ashrafi, Soodeh Salehi, Reza Azizi Malamiri, et al.
European Journal of Medical Genetics|March 13, 2026
Genetic and Clinical Insights into Pontocerebellar Hypoplasia: Identification of Novel Variants in an Iranian CohortZahra Rezaei, Farnoosh Emami, Morteza Heidari, et al.
Clinical Case Reports|January 28, 2025
Primary Diffuse Leptomeningeal Melanomatosis Leading to Raised Intracranial Pressure in a Pediatric PatientShiva Sareh, Zohreh Habibi, Mohammad Vasei, et al.
Molecular Biology Reports|June 1, 2024
Distinct neurological phenotypes associated with biallelic loss of NOTCH3 function: evidence for recessive inheritanceBehnoosh Tasharrofi, Ali Najafi, Elham Pourbakhtyaran, et al.
Journal of Child Neurology|November 19, 2024
Death Causes Among Iranian Children With LeukodystrophiesMahsa Shiva, Sareh Hosseinpour, Mahmoud Reza Ashrafi, et al.
Journal of Molecular Neuroscience : MN|April 30, 2026
Expanding the Clinical Spectrum of LYRM7-Associated Mitochondrial Complex III Deficiency: Insights from New Cases and Literature ReviewGolazin Shahbodagh Khan, Shiva Bayat, Reza Azizimalamiri, et al.
Clinical Case Reports|December 10, 2025
A Novel Mutation of CADHERIN (<i>CDH15</i>) in an Iranian Boy With Borderline Intelligence Without Dysmorphism-A Case ReportMahmoud Reza Ashrafi, Ali Nikkhah, Morteza Heidari, et al.
Pageof 13