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Moez Ravanbod

Showing results (1-10 of 6) with videos related to

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Pediatric Neurology|January 23, 2025
Genetic Homogeneity of a TDP1 Variant, c.1478A>G, as the Main Disease-Causing Variant of Spinocerebellar Ataxia With Axonal Neuropathy 1 (SCAN1) in the Middle East: A Systematic ReviewMahsa Mohammadi, Moez Ravanbod, Aida Ghasemi, et al.
Gene|April 2, 2025
Clinical and molecular assessment of a spastic ataxia 4 (SPAX4) patient with a novel variant in the MTPAP gene, and a systematic reviewMoez Ravanbod, Mahsa Mohammadi, Parsa Soleimani, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|June 10, 2026
A novel homozygous variant in the POLR1A gene: a complicated hereditary spastic paraplegia (c-HSP) or a hypomyelinating leukodystrophy type-27 (HLD27) phenotype?Masoud Tajamolian, Moez Ravanbod, Shahryar Alavi, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|June 22, 2026
Introducing a novel variant in the FTH1 gene; A closer look at FTH1-related neuroferritinopathy as a neurodegeneration with brain iron accumulation (NBIA) disorderMohammad Rohani, Moez Ravanbod, Davood Zare-Abdollahi, et al.
Journal of the Peripheral Nervous System : JPNS|July 25, 2025
GDAP1-Related Charcot-Marie-Tooth Disease: Axonal or Demyelinating Subtype? Autosomal Recessive or Autosomal Dominant Inheritance?Moez Ravanbod, Mahsa Mohammadi, Aida Ghasemi, et al.
Orphanet Journal of Rare Diseases|May 12, 2026
Expanding the genetic and clinical landscapes of hereditary spastic paraplegia (HSP): a cohort study of 103 familiesAtefeh Davarzani, Moez Ravanbod, Aida Ghasemi, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Pediatric Neurology|January 23, 2025
Genetic Homogeneity of a TDP1 Variant, c.1478A>G, as the Main Disease-Causing Variant of Spinocerebellar Ataxia With Axonal Neuropathy 1 (SCAN1) in the Middle East: A Systematic ReviewMahsa Mohammadi, Moez Ravanbod, Aida Ghasemi, et al.
Gene|April 2, 2025
Clinical and molecular assessment of a spastic ataxia 4 (SPAX4) patient with a novel variant in the MTPAP gene, and a systematic reviewMoez Ravanbod, Mahsa Mohammadi, Parsa Soleimani, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|June 10, 2026
A novel homozygous variant in the POLR1A gene: a complicated hereditary spastic paraplegia (c-HSP) or a hypomyelinating leukodystrophy type-27 (HLD27) phenotype?Masoud Tajamolian, Moez Ravanbod, Shahryar Alavi, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|June 22, 2026
Introducing a novel variant in the FTH1 gene; A closer look at FTH1-related neuroferritinopathy as a neurodegeneration with brain iron accumulation (NBIA) disorderMohammad Rohani, Moez Ravanbod, Davood Zare-Abdollahi, et al.
Journal of the Peripheral Nervous System : JPNS|July 25, 2025
GDAP1-Related Charcot-Marie-Tooth Disease: Axonal or Demyelinating Subtype? Autosomal Recessive or Autosomal Dominant Inheritance?Moez Ravanbod, Mahsa Mohammadi, Aida Ghasemi, et al.
Orphanet Journal of Rare Diseases|May 12, 2026
Expanding the genetic and clinical landscapes of hereditary spastic paraplegia (HSP): a cohort study of 103 familiesAtefeh Davarzani, Moez Ravanbod, Aida Ghasemi, et al.
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