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Aida Ghasemi

Showing results (11-20 of 23) with videos related to

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Neurogenetics|November 26, 2024
Clinical and genetic diversity in Iranian individuals with RAPSN-related congenital myasthenic syndromeAida Ghasemi, Seyed Jalaleddin Hadei, Sara KamaliZonouzi, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|July 6, 2023
The first reports of FA2H-associated neurodegeneration from two unrelated Iranian familiesNarges Hashemi, Reza Nejad Shahrokh Abadi, Afagh Alavi, et al.
Neuromuscular Disorders : NMD|January 15, 2026
Clinical and molecular spectrum of an Iranian Charcot-Marie-Tooth 2T cohort, and the diagnostic importance of whole exome sequencing in identifying co-occurrence inherited disordersZahra Salami, Mahsa Mohammadi, Aida Ghasemi, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|June 26, 2024
Phenotypic and genotyping spectrum of two Iranian cases with RBCK1-associated polyglucosan body myopathyMarzieh Babaee, Yalda Nilipour, Sahar Alijanpour, et al.
Orphanet Journal of Rare Diseases|March 13, 2024
COLQ-Congenital myasthenic syndrome in an Iranian cohort: the clinical and genetics spectrumOmid Hesami, Mahtab Ramezani, Aida Ghasemi, et al.
Molecular Genetics and Genomics : MGG|December 5, 2024
Beginning at the ends: telomere and telomere-based cancer therapeuticsZahra Sadr, Masoumeh Ghasemi, Soheyla Jafarpour, et al.
Neurogenetics|November 28, 2024
Three Iranian patients with rare subtypes of hereditary spastic paraplegia (HSP): SPG76, SPG56, and SPG69Zahra Sadr, Aida Ghasemi, Mohammad Rohani, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|March 27, 2024
A Novel Homozygous Variant in the <i>MCOLN1</i> Gene Associated With Severe Oromandibular Dystonia and ParkinsonismAida Ghasemi, Mahdieh Eslami Ardakani, Mansoureh Togha, et al.
Muscle & Nerve|November 28, 2025
A Cohort of Iranian Patients With Congenital Myasthenic Syndrome due to Glycosylation DefectsMahtab Ramezani, Ali Asghar Okhovat, Yalda Nilipour, 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.
Pageof 3

Showing results (11-20 of 23) with videos related to

Sort By:
Pageof 3
Neurogenetics|November 26, 2024
Clinical and genetic diversity in Iranian individuals with RAPSN-related congenital myasthenic syndromeAida Ghasemi, Seyed Jalaleddin Hadei, Sara KamaliZonouzi, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|July 6, 2023
The first reports of FA2H-associated neurodegeneration from two unrelated Iranian familiesNarges Hashemi, Reza Nejad Shahrokh Abadi, Afagh Alavi, et al.
Neuromuscular Disorders : NMD|January 15, 2026
Clinical and molecular spectrum of an Iranian Charcot-Marie-Tooth 2T cohort, and the diagnostic importance of whole exome sequencing in identifying co-occurrence inherited disordersZahra Salami, Mahsa Mohammadi, Aida Ghasemi, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|June 26, 2024
Phenotypic and genotyping spectrum of two Iranian cases with RBCK1-associated polyglucosan body myopathyMarzieh Babaee, Yalda Nilipour, Sahar Alijanpour, et al.
Orphanet Journal of Rare Diseases|March 13, 2024
COLQ-Congenital myasthenic syndrome in an Iranian cohort: the clinical and genetics spectrumOmid Hesami, Mahtab Ramezani, Aida Ghasemi, et al.
Molecular Genetics and Genomics : MGG|December 5, 2024
Beginning at the ends: telomere and telomere-based cancer therapeuticsZahra Sadr, Masoumeh Ghasemi, Soheyla Jafarpour, et al.
Neurogenetics|November 28, 2024
Three Iranian patients with rare subtypes of hereditary spastic paraplegia (HSP): SPG76, SPG56, and SPG69Zahra Sadr, Aida Ghasemi, Mohammad Rohani, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|March 27, 2024
A Novel Homozygous Variant in the <i>MCOLN1</i> Gene Associated With Severe Oromandibular Dystonia and ParkinsonismAida Ghasemi, Mahdieh Eslami Ardakani, Mansoureh Togha, et al.
Muscle & Nerve|November 28, 2025
A Cohort of Iranian Patients With Congenital Myasthenic Syndrome due to Glycosylation DefectsMahtab Ramezani, Ali Asghar Okhovat, Yalda Nilipour, 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.
Pageof 3