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Morteza Heidari

Showing results (71-80 of 121) with videos related to

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Molecular Genetics & Genomic Medicine|February 20, 2025
Trichothiodystrophy due to ERCC2 Variants: Uncommon Contributor to Progressive Hypomyelinating LeukodystrophyAli Reza Tavasoli, Arastoo Kaki, Maedeh Ganji, et al.
Molecular Syndromology|August 7, 2025
A Report of Dual Presentations of Pseudo-TORCH Syndrome 1 and MCC2 Deficiency and Review of the LiteratureAli Talea, Shiva Bayat, Golazin Shahbodagh Khan, et al.
Acta Neurologica Belgica|December 9, 2016
The efficacy of the ketogenic diet in infants and young children with refractory epilepsies using a formula-based powderMahmoud Reza Ashrafi, Seyed Ahmad Hosseini, Gholam Reza Zamani, et al.
European Journal of Neurology|May 20, 2023
Efficacy and safety of miglustat in the treatment of GM2 gangliosidosis: A systematic reviewVahid Mansouri, Ali Reza Tavasoli, Masoud Khodarahmi, et al.
Physics in Medicine and Biology|July 17, 2018
Prediction of chemotherapy response in ovarian cancer patients using a new clustered quantitative image markerAbolfazl Zargari, Yue Du, Morteza Heidari, et al.
Journal of Molecular Neuroscience : MN|March 11, 2022
Epilepsia Partialis Continua a Clinical Feature of a Missense Variant in the ADCK3 Gene and Poor Response to TherapyMahmoud Reza Ashrafi, Roya Haghighi, Reza Shervin Badv, et al.
Neurogenetics|January 12, 2023
Expanding the neuroimaging findings of guanidinoacetate methyltransferase deficiency in an Iranian girl with a homozygous frameshift variant in the GAMTSeyedeh Atiyeh Afjei, Mohammad Farid Mohammadi, Elham Pourbakhtyaran, et al.
Acta Neurologica Belgica|August 15, 2024
Unraveling neuroimaging insights in developmental epileptic encephalopathy type 25: a comprehensive review of reported cases and a novel SLC13A5 variantMohammad Farid Mohammadi, Sahand Tehrani Fateh, Maedeh Ganji, et al.
Molecular Syndromology|February 15, 2024
<i>TPP1</i> Variants in Iranian patients: A Novel Pathogenic Homozygous Variant Causing Neuronal Ceroid Lipofuscinosis 2Nahid Vafaei, Ali Mohebbi, Zahra Rezaei, et al.
Irish Journal of Medical Science|July 31, 2023
Persistent basal ganglia involvement in aminoacylase-1 deficiency: expanding imaging findings and review of literatureMohammad Farid Mohammadi, Ali Dehghani, Kiana Zarabadi, et al.
Pageof 13

Showing results (71-80 of 121) with videos related to

Sort By:
Pageof 13
Molecular Genetics & Genomic Medicine|February 20, 2025
Trichothiodystrophy due to ERCC2 Variants: Uncommon Contributor to Progressive Hypomyelinating LeukodystrophyAli Reza Tavasoli, Arastoo Kaki, Maedeh Ganji, et al.
Molecular Syndromology|August 7, 2025
A Report of Dual Presentations of Pseudo-TORCH Syndrome 1 and MCC2 Deficiency and Review of the LiteratureAli Talea, Shiva Bayat, Golazin Shahbodagh Khan, et al.
Acta Neurologica Belgica|December 9, 2016
The efficacy of the ketogenic diet in infants and young children with refractory epilepsies using a formula-based powderMahmoud Reza Ashrafi, Seyed Ahmad Hosseini, Gholam Reza Zamani, et al.
European Journal of Neurology|May 20, 2023
Efficacy and safety of miglustat in the treatment of GM2 gangliosidosis: A systematic reviewVahid Mansouri, Ali Reza Tavasoli, Masoud Khodarahmi, et al.
Physics in Medicine and Biology|July 17, 2018
Prediction of chemotherapy response in ovarian cancer patients using a new clustered quantitative image markerAbolfazl Zargari, Yue Du, Morteza Heidari, et al.
Journal of Molecular Neuroscience : MN|March 11, 2022
Epilepsia Partialis Continua a Clinical Feature of a Missense Variant in the ADCK3 Gene and Poor Response to TherapyMahmoud Reza Ashrafi, Roya Haghighi, Reza Shervin Badv, et al.
Neurogenetics|January 12, 2023
Expanding the neuroimaging findings of guanidinoacetate methyltransferase deficiency in an Iranian girl with a homozygous frameshift variant in the GAMTSeyedeh Atiyeh Afjei, Mohammad Farid Mohammadi, Elham Pourbakhtyaran, et al.
Acta Neurologica Belgica|August 15, 2024
Unraveling neuroimaging insights in developmental epileptic encephalopathy type 25: a comprehensive review of reported cases and a novel SLC13A5 variantMohammad Farid Mohammadi, Sahand Tehrani Fateh, Maedeh Ganji, et al.
Molecular Syndromology|February 15, 2024
<i>TPP1</i> Variants in Iranian patients: A Novel Pathogenic Homozygous Variant Causing Neuronal Ceroid Lipofuscinosis 2Nahid Vafaei, Ali Mohebbi, Zahra Rezaei, et al.
Irish Journal of Medical Science|July 31, 2023
Persistent basal ganglia involvement in aminoacylase-1 deficiency: expanding imaging findings and review of literatureMohammad Farid Mohammadi, Ali Dehghani, Kiana Zarabadi, et al.
Pageof 13