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Amir Bahreini

Showing results (1-10 of 29) with videos related to

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Annals of Neurology|March 19, 2011
Interferon-beta and toll-like receptor-9 processingHamid Zahednasab, Seyed Amir Bahreini
Journal of the Neurological Sciences|March 16, 2010
DNA hypomethylation in multiple sclerosis diseaseHamid Zahednasab, Seyed Amir Bahreini
Advanced Biomedical Research|November 27, 2025
Novel SQSTM1 (c.838G>T) Mutation Identified in Two Unrelated Cases of Cerebellar Ataxia and Gaze PalsyNeda Hosseini Moshkenani, Azin Momeni, Amir Bahreini
Functional Neurology|March 13, 2015
Co-occurrence of multiple sclerosis and Thomsen's myotonia: a report of two casesFereshteh Ashtari, Seyed Amir Bahreini, Hamid Zahednasab
Epilepsy Research|October 25, 2021
Clinical and genetic profile of children with unexplained intellectual disability/developmental delay and epilepsyNayereh Nouri, Amir Bahreini, Jafar Nasiri, et al.
Journal of the Neurological Sciences|September 11, 2010
The role of MEFV gene mutations in Multiple Sclerosis susceptibilityHamid Zahednasab, Mohammad Saadatnia, M Reza Jabalameli, et al.
Journal of Neuroimmunology|September 14, 2010
The role of non-HLA single nucleotide polymorphisms in multiple sclerosis susceptibilitySeyed Amir Bahreini, M Reza Jabalameli, Mohammad Saadatnia, et al.
Life Sciences|November 15, 2020
A novel carcinogenic PI3Kα mutation suggesting the role of helical domain in transmitting nSH2 regulatory signals to kinase domainSafoura Ghalamkari, Shahryar Alavi, Hamidreza Mianesaz, et al.
Immunogenetics|July 18, 2024
The sufficiency of genetic diagnosis in managing patients with inborn errors of immunity during prenatal care and childbearingNegin Salemi, Shima Bakhshesh, Amir Bahreini, et al.
Journal of Neuroimmunology|October 22, 2010
Controversial role of MMP-9 gene in MS diseaseHamid Zahednasab, Mohammad Saadatnia, M Reza Jabalameli, et al.
Pageof 3

Showing results (1-10 of 29) with videos related to

Sort By:
Pageof 3
Annals of Neurology|March 19, 2011
Interferon-beta and toll-like receptor-9 processingHamid Zahednasab, Seyed Amir Bahreini
Journal of the Neurological Sciences|March 16, 2010
DNA hypomethylation in multiple sclerosis diseaseHamid Zahednasab, Seyed Amir Bahreini
Advanced Biomedical Research|November 27, 2025
Novel SQSTM1 (c.838G>T) Mutation Identified in Two Unrelated Cases of Cerebellar Ataxia and Gaze PalsyNeda Hosseini Moshkenani, Azin Momeni, Amir Bahreini
Functional Neurology|March 13, 2015
Co-occurrence of multiple sclerosis and Thomsen's myotonia: a report of two casesFereshteh Ashtari, Seyed Amir Bahreini, Hamid Zahednasab
Epilepsy Research|October 25, 2021
Clinical and genetic profile of children with unexplained intellectual disability/developmental delay and epilepsyNayereh Nouri, Amir Bahreini, Jafar Nasiri, et al.
Journal of the Neurological Sciences|September 11, 2010
The role of MEFV gene mutations in Multiple Sclerosis susceptibilityHamid Zahednasab, Mohammad Saadatnia, M Reza Jabalameli, et al.
Journal of Neuroimmunology|September 14, 2010
The role of non-HLA single nucleotide polymorphisms in multiple sclerosis susceptibilitySeyed Amir Bahreini, M Reza Jabalameli, Mohammad Saadatnia, et al.
Life Sciences|November 15, 2020
A novel carcinogenic PI3Kα mutation suggesting the role of helical domain in transmitting nSH2 regulatory signals to kinase domainSafoura Ghalamkari, Shahryar Alavi, Hamidreza Mianesaz, et al.
Immunogenetics|July 18, 2024
The sufficiency of genetic diagnosis in managing patients with inborn errors of immunity during prenatal care and childbearingNegin Salemi, Shima Bakhshesh, Amir Bahreini, et al.
Journal of Neuroimmunology|October 22, 2010
Controversial role of MMP-9 gene in MS diseaseHamid Zahednasab, Mohammad Saadatnia, M Reza Jabalameli, et al.
Pageof 3