Shahriar Nafissi
19PUBLICATIONS
49CO-AUTHORS
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Publications (19)
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|Nov 28, 2025
A Cohort of Iranian Patients With Congenital Myasthenic Syndrome due to Glycosylation Defects.Mahtab Ramezani, Ali Asghar Okhovat, Yalda Nilipour
|May 18, 2025
First Iranian Family with a Novel Missense Variant in MYO9B Gene Causing Charcot-Marie-Tooth Disease.Maryam Beheshtian, Maryam Mozaffarpour Nouri, Fatemeh Ahangari
|Apr 17, 2024
Investigating the Association Between Muscular Ultrasonographic Alterations and Clinical Symptoms in Patients With Inflammatory Myopathy.Farzad Fatehi, Parisa Khaghani, Ali Asghar Okhovat
|Mar 13, 2024
COLQ-Congenital myasthenic syndrome in an Iranian cohort: the clinical and genetics spectrum.Omid Hesami, Mahtab Ramezani, Aida Ghasemi
|Feb 19, 2024
Clinical application of next generation sequencing for Mendelian disease diagnosis in the Iranian population.Ayda Abolhassani, Zohreh Fattahi, Maryam Beheshtian
|Jan 08, 2024
Identification of a mutation in TNRC18 in a patient with clinical features of Fazio-Londe disease.Marzieh Khani, Hosein Shamshiri, Shahriar Nafissi
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Frequent Collaborators
6 joint publications
Farzad Fatehi
6 joint publications
Ali Asghar Okhovat
2 joint publications
Hossein Najmabadi
2 joint publications
Yusuf A Rajabally
2 joint publications
Elahe Elahi
2 joint publications
Akram Panahi
2 joint publications
Ariana Kariminejad
1 joint publications
Bahareh Mohebbi
1 joint publications
Helia Mojtabavi
1 joint publications
Bahram Haghi Ashtiani
