Shahriar Nafissi

Publication Activity (10 Years)

Years Active: 2021-2024
Publications (10 Years): 23

Top Topics

Myasthenia Gravis

Top Venues

Clinical case reports

Basic and clinical neuroscience

Orphanet journal of rare diseases

NPJ genomic medicine

This page only lists publications with an associated author ORCID identifier.

Publications

Omid Hesami, Mahtab Ramezani, Aida Ghasemi, Farzad Fatehi, Ali Asghar Okhovat, Bentolhoda Ziaadini, Ariana Kariminejad, Shahriar Nafissi
COLQ-Congenital myasthenic syndrome in an Iranian cohort: the clinical and genetics spectrum. Orphanet journal of rare diseases 19 (1) (2024)
Marzieh Khani, Hosein Shamshiri, Shahriar Nafissi, Najmeh Salehi, Hamidreza Moazzeni, Hanieh Taheri, Elahe Elahi
Identification of a mutation in TNRC18 in a patient with clinical features of Fazio-Londe disease. Clinical case reports 12 (1) (2024)
Marzieh Khani, Hosein Shamshiri, Shahriar Nafissi, Najmeh Salehi, Hamidreza Moazzeni, Hanieh Taheri, Elahe Elahi
Identification of a mutation in TNRC18 in a patient with clinical features of Fazio-Londe disease. Clinical case reports 12 (1) (2024)
Omid Hesami, Mahtab Ramezani, Aida Ghasemi, Farzad Fatehi, Ali Asghar Okhovat, Bentolhoda Ziaadini, Ariana Kariminejad, Shahriar Nafissi
COLQ-Congenital myasthenic syndrome in an Iranian cohort: the clinical and genetics spectrum. Orphanet journal of rare diseases 19 (1) (2024)
Ayda Abolhassani, Zohreh Fattahi, Maryam Beheshtian, Mahsa Fadaee, Raheleh Vazehan, Fatemeh Ahangari, Shima Dehdahsi, Mehrshid Faraji Zonooz, Elham Parsimehr, Zahra Kalhor, Fatemeh Peymani, Maryam Mozaffarpour Nouri, Mojgan Babanejad, Khadijeh Noudehi, Fatemeh Fatehi, Shima Zamanian Najafabadi, Fariba Afroozan, Hilda Yazdan, Bita Bozorgmehr, Azita Azarkeivan, Shokouh Sadat Mahdavi, Pooneh Nikuei, Farzad Fatehi, Payman Jamali, Mahmoud Reza Ashrafi, Parvaneh Karimzadeh, Haleh Habibi, Kimia Kahrizi, Shahriar Nafissi, Ariana Kariminejad, Hossein Najmabadi
Clinical application of next generation sequencing for Mendelian disease diagnosis in the Iranian population. NPJ genomic medicine 9 (1) (2024)
Omid Hesami, Mahtab Ramezani, Aida Ghasemi, Farzad Fatehi, Ali Asghar Okhovat, Bentolhoda Ziaadini, Ariana Kariminejad, Shahriar Nafissi
COLQ-Congenital myasthenic syndrome in an Iranian cohort: the clinical and genetics spectrum. Orphanet journal of rare diseases 19 (1) (2024)
Ayda Abolhassani, Zohreh Fattahi, Maryam Beheshtian, Mahsa Fadaee, Raheleh Vazehan, Fatemeh Ahangari, Shima Dehdahsi, Mehrshid Faraji Zonooz, Elham Parsimehr, Zahra Kalhor, Fatemeh Peymani, Maryam Mozaffarpour Nouri, Mojgan Babanejad, Khadijeh Noudehi, Fatemeh Fatehi, Shima Zamanian Najafabadi, Fariba Afroozan, Hilda Yazdan, Bita Bozorgmehr, Azita Azarkeivan, Shokouh Sadat Mahdavi, Pooneh Nikuei, Farzad Fatehi, Payman Jamali, Mahmoud Reza Ashrafi, Parvaneh Karimzadeh, Haleh Habibi, Kimia Kahrizi, Shahriar Nafissi, Ariana Kariminejad, Hossein Najmabadi
Clinical application of next generation sequencing for Mendelian disease diagnosis in the Iranian population. NPJ genomic medicine 9 (1) (2024)
Marzieh Khani, Hosein Shamshiri, Shahriar Nafissi, Najmeh Salehi, Hamidreza Moazzeni, Hanieh Taheri, Elahe Elahi
Identification of a mutation in TNRC18 in a patient with clinical features of Fazio-Londe disease. Clinical case reports 12 (1) (2024)
Farzad Fatehi, Parisa Khaghani, Ali Asghar Okhovat, Kamyar Moradi, Farzad Teimouri, Mahsa Mortaja, Mahsa Layegh, Akram Panahi, Shahriar Nafissi
Investigating the Association Between Muscular Ultrasonographic Alterations and Clinical Symptoms in Patients With Inflammatory Myopathy. Basic and clinical neuroscience 14 (5) (2023)
Farzad Fatehi, Parisa Khaghani, Ali Asghar Okhovat, Kamyar Moradi, Farzad Teimouri, Mahsa Mortaja, Mahsa Layegh, Akram Panahi, Shahriar Nafissi
Investigating the Association Between Muscular Ultrasonographic Alterations and Clinical Symptoms in Patients With Inflammatory Myopathy. Basic and clinical neuroscience 14 (5) (2023)
Alireza Haghighi, Zahra Alvandi, Yalda Nilipour, Amirreza Haghighi, Ruth Kornreich, Shahriar Nafissi, Robert J Desnick
Nemaline myopathy: reclassification of previously reported variants according to ACMG guidelines, and report of novel genetic variants. European journal of human genetics : EJHG (2023)
Franziska Paul, Calista Ng, Umar Bin Mohamad Sahari, Shahriar Nafissi, Yalda Nilipoor, Ali Reza Tavasoli, Carine Bonnard, Pui-Mun Wong, Nasrinsadat Nabavizadeh, Umut Altunoğlu, Mehrdad A Estiar, Charles B L M Majoie, Hane Lee, Stanley F Nelson, Ziv Gan Or, Guy A Rouleau, Paul P Van Veldhoven, Rami Massie, Raoul C Hennekam, Ariana Kariminejad, Bruno Reversade
RABENOSYN separation-of-function mutations uncouple endosomal recycling from lysosomal degradation, causing a distinct Mendelian disorder. Human molecular genetics 31 (21) (2022)
Niayesh Mohebbi, Maryam Taghizadeh-Ghehi, Seyed Mehrdad Savar, Siamak Abdi, Romina Kouhsari, Kheirollah Gholami, Shahriar Nafissi
Adverse drug reactions of Rituximab in patients suffering from autoimmune neurological diseases. Daru : journal of Faculty of Pharmacy, Tehran University of Medical Sciences 30 (2) (2022)
Marzieh Khani, Shahriar Nafissi, Hosein Shamshiri, Hamidreza Moazzeni, Hanieh Taheri, Mehdi Sadeghi, Najmeh Salehi, Fereshteh Chitsazian, Elahe Elahi
Identification of UBA1 as the causative gene of an X-linked non-Kennedy spinal-bulbar muscular atrophy. European journal of neurology 29 (12) (2022)
Shahriar Nafissi, Ali Asghar Okhovat, Farnaz Sinaei, Behnaz Ansari, Hormoz Ayramloo, Keyvan Basiri, Reza Boostani, Bahram Haghi Ashtiani, Payam Sarraf, Farzad Fatehi
Iranian Consensus Recommendations for Treatment of Myasthenia Gravis. Archives of Iranian medicine 25 (1) (2022)
Ali Asghar Okhovat, Soroor Advani, Bentolhoda Ziaadini, Akram Panahi, Saeideh Salehizadeh, Shahriar Nafissi, Bahram Haghi Ashtiani, Yusuf A Rajabally, Farzad Fatehi
The value of MUNIX as an objective electrophysiological biomarker of disease progression in chronic inflammatory demyelinating polyneuropathy. Muscle & nerve 65 (4) (2022)
Farnaz Sinaei, Farzad Fatehi, Shahram Oveis Gharan, Soroush Ehsan, Koorosh Kamali, Shahriar Nafissi
Disease severity and response to treatment in Iranian patients with myasthenia gravis. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology (2021)
Farzad Fatehi, Ali Asghar Okhovat, Akram Panahi, Bentolhoda Ziaaddini, Yusuf A Rajabally, Shahriar Nafissi
Retrospective analysis of response to rituximab in chronic inflammatory demyelinating polyneuropathy refractory to first-line therapy. Journal of the peripheral nervous system : JPNS 26 (4) (2021)
Narges Karimi, Reza Boostani, Farzad Fatehi, Akram Panahi, Ali Asghar Okhovat, Bentolhoda Ziaadini, Keivan Basiri, Siamak Abdi, Farnaz Sinaei, Mojtaba Rezaei, Gholamreza Shamsaei, Behnaz Ansari, Shahriar Nafissi
Guillain-Barre Syndrome and COVID-19 Vaccine: A Report of Nine Patients. Basic and clinical neuroscience 12 (5) (2021)
Mahdieh Pashaei, Atefeh Davarzani, Reza Hajati, Babak Zamani, Shahriar Nafissi, Farzaneh Larti, Yalda Nilipour, Mohammad Rohani, Afagh Alavi
Description of clinical features and genetic analysis of one ultra-rare (SPG64) and two common forms (SPG5A and SPG15) of hereditary spastic paraplegia families. Journal of neurogenetics 35 (2) (2021)
Elmira Agah, Shahriar Nafissi, Fatemeh Saleh, Payam Sarraf, Abbas Tafakhori, Seyed Vahid Mousavi, Amene Saghazadeh, Maryam Sadr, Farnaz Sinaei, Bahareh Mohebbi, Mahdi Mahmoudi, Hamideh Shadi, Nima Rezaei
Investigating the possible association between NLRP3 gene polymorphisms and myasthenia gravis. Muscle & nerve 63 (5) (2021)
Helia Mojtabavi, Farzad Fatehi, Sepideh Shahkarami, Nima Rezaei, Shahriar Nafissi
Novel Mutations of the TYMP Gene in Mitochondrial Neurogastrointestinal Encephalomyopathy: Case Series and Literature Review. Journal of molecular neuroscience : MN 71 (12) (2021)
Helia Mojtabavi, Shahriar Nafissi, Behrooz Mahmoodi-Bakhtiari, Davood Fathi, Farzad Fatehi
Persian adaptation of Edinburgh Cognitive and Behavioural Screen (ECAS). Amyotrophic lateral sclerosis & frontotemporal degeneration 22 (5-6) (2021)