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Aida Ghasemi

Showing results (1-10 of 23) with videos related to

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Neuromuscular Disorders : NMD|March 5, 2023
NMNAT1 and hereditary spastic paraplegia (HSP): expanding the phenotypic spectrum of NMNAT1 variantsZahra Sadr, Aida Ghasemi, Mohammad Rohani, et al.
Neuromuscular Disorders : NMD|December 3, 2023
Corrigendum to "NMNAT1 and hereditary spastic paraplegia (HSP): Expanding the phenotypic spectrum of NMNAT1 variants" [Neuromuscular Disorders, 33(2023) 295-301]Zahra Sadr, Aida Ghasemi, Mohammad Rohani, et al.
Neuromuscular Disorders : NMD|March 29, 2025
Identifying novel AGRN variants in congenital myasthenic syndrome: insights from three Iranian familiesHadi Gharebaghian, Aida Ghasemi, Omid Hesami, et al.
Molecular Syndromology|December 7, 2023
Copy Number Variations in Hereditary Spastic Paraplegia-Related Genes: Evaluation of an Iranian Hereditary Spastic Paraplegia Cohort and Literature ReviewAida Ghasemi, Zahra Sadr, Mojgan Babanejad, et al.
Neuromuscular Disorders : NMD|November 17, 2024
CHRNE-related congenital myasthenic syndrome in Iran: Clinical and molecular insightsNarges Karimi, Aida Ghasemi, Akram Panahi, et al.
Molecular Syndromology|November 2, 2023
Description of Phenotypic Heterogeneity in a <i>GJC2</i>-Related Family and Literature ReviewAida Ghasemi, Ali Reza Tavasoli, Mana Khojasteh, et al.
Journal of Human Genetics|March 1, 2026
Expanding the phenotypic spectrum of LAMA2-related disorders: Axonal neuropathy in the absence of muscular dystrophyMahsa Mohammadi, Mahdieh Rahimoghli, Aida Ghasemi, et al.
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.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|March 22, 2025
Mutation spectrum and clinical features of MYORG in Iranian patients with Primary Familial Brain Calcification (PFBC)Parsa Soleimani, Mana Khojasteh, Aida Ghasemi, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|March 5, 2024
JAM2 variants can be more common in primary familial brain calcification (PFBC) cases than those appear; may be due to a founder mutationMana Khojasteh, Parsa Soleimani, Aida Ghasemi, et al.
Pageof 3

Showing results (1-10 of 23) with videos related to

Sort By:
Pageof 3
Neuromuscular Disorders : NMD|March 5, 2023
NMNAT1 and hereditary spastic paraplegia (HSP): expanding the phenotypic spectrum of NMNAT1 variantsZahra Sadr, Aida Ghasemi, Mohammad Rohani, et al.
Neuromuscular Disorders : NMD|December 3, 2023
Corrigendum to "NMNAT1 and hereditary spastic paraplegia (HSP): Expanding the phenotypic spectrum of NMNAT1 variants" [Neuromuscular Disorders, 33(2023) 295-301]Zahra Sadr, Aida Ghasemi, Mohammad Rohani, et al.
Neuromuscular Disorders : NMD|March 29, 2025
Identifying novel AGRN variants in congenital myasthenic syndrome: insights from three Iranian familiesHadi Gharebaghian, Aida Ghasemi, Omid Hesami, et al.
Molecular Syndromology|December 7, 2023
Copy Number Variations in Hereditary Spastic Paraplegia-Related Genes: Evaluation of an Iranian Hereditary Spastic Paraplegia Cohort and Literature ReviewAida Ghasemi, Zahra Sadr, Mojgan Babanejad, et al.
Neuromuscular Disorders : NMD|November 17, 2024
CHRNE-related congenital myasthenic syndrome in Iran: Clinical and molecular insightsNarges Karimi, Aida Ghasemi, Akram Panahi, et al.
Molecular Syndromology|November 2, 2023
Description of Phenotypic Heterogeneity in a <i>GJC2</i>-Related Family and Literature ReviewAida Ghasemi, Ali Reza Tavasoli, Mana Khojasteh, et al.
Journal of Human Genetics|March 1, 2026
Expanding the phenotypic spectrum of LAMA2-related disorders: Axonal neuropathy in the absence of muscular dystrophyMahsa Mohammadi, Mahdieh Rahimoghli, Aida Ghasemi, et al.
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.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|March 22, 2025
Mutation spectrum and clinical features of MYORG in Iranian patients with Primary Familial Brain Calcification (PFBC)Parsa Soleimani, Mana Khojasteh, Aida Ghasemi, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|March 5, 2024
JAM2 variants can be more common in primary familial brain calcification (PFBC) cases than those appear; may be due to a founder mutationMana Khojasteh, Parsa Soleimani, Aida Ghasemi, et al.
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