Afagh Alavi

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 17

Top Venues

Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology

The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques

Movement disorders clinical practice

Molecular genetics & genomic medicine

University of Social Welfare and Rehabilitation Science

University of Tehran (PHD)

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

Affiliation History

University of Social Welfare and Rehabilitation Science

Iran

Assistant Prof. :: Genetics Research Center

Education History

University of Tehran

Iran

PHD :: Cellular and Molecular Biology

Publications

Aida Ghasemi, Mahdieh Eslami Ardakani, Mansoureh Togha, Narges Yazdi, Anthony E Lang, Elahe Amini, Mohammad Rohani, Afagh Alavi
A novel homozygous variant in the MCOLN1 gene associated with severe oromandibular dystonia and Parkinsonism. The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques (2024)
Aida Ghasemi, Mahdieh Eslami Ardakani, Mansoureh Togha, Narges Yazdi, Anthony E Lang, Elahe Amini, Mohammad Rohani, Afagh Alavi
A Novel Homozygous Variant in the MCOLN1 Gene Associated With Severe Oromandibular Dystonia and Parkinsonism. The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques (2024)
Mana Khojasteh, Parsa Soleimani, Aida Ghasemi, Peyman Taghizadeh, Mohammad Rohani, Afagh Alavi
JAM2 variants can be more common in primary familial brain calcification (PFBC) cases than those appear; may be due to a founder mutation. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 45 (8) (2024)
Mana Khojasteh, Parsa Soleimani, Aida Ghasemi, Peyman Taghizadeh, Mohammad Rohani, Afagh Alavi
JAM2 variants can be more common in primary familial brain calcification (PFBC) cases than those appear; may be due to a founder mutation. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology (2024)
Mana Khojasteh, Parsa Soleimani, Aida Ghasemi, Peyman Taghizadeh, Mohammad Rohani, Afagh Alavi
JAM2 variants can be more common in primary familial brain calcification (PFBC) cases than those appear; may be due to a founder mutation. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 45 (8) (2024)
Elahe Amini, Mohammad Rohani, Anthony E Lang, Zahra Azad, Seyed Amir Hassan Habibi, Afagh Alavi, Gholam Ali Shahidi, Maziar Emamikhah, Ahmad Chitsaz
Estimation of Ambulation and Survival in Neurodegeneration with Brain Iron Accumulation Disorders. Movement disorders clinical practice 11 (1) (2023)
Ali Akbar Asadi-Pooya, Leila Simani, Marjan Asadollahi, Fatemeh Sadat Rashidi, Ehsan Ahmadipour, Afagh Alavi, Mehrdad Roozbeh, Nayyereh Akbari, Negar Firouzabadi
Potential role of FKBP5 single-nucleotide polymorphisms in functional seizures. Epilepsia open (2023)
Elahe Amini, Mohammad Rohani, Anthony E Lang, Zahra Azad, Seyed Amir Hassan Habibi, Afagh Alavi, Gholam Ali Shahidi, Maziar Emamikhah, Ahmad Chitsaz
Estimation of Ambulation and Survival in Neurodegeneration with Brain Iron Accumulation Disorders. Movement disorders clinical practice 11 (1) (2023)
Zahra Sadr, Davood Zare-Abdollahi, Mohammad Rohani, Afagh Alavi
A founder mutation in COQ7, p.(Leu111Pro), causes pure hereditary spastic paraplegia (HSP) in the Iranian population. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology (2023)
Elahe Amini, Mohammad Rohani, Anthony E Lang, Zahra Azad, Seyed Amir Hassan Habibi, Afagh Alavi, Gholam Ali Shahidi, Maziar Emamikhah, Ahmad Chitsaz
Estimation of Ambulation and Survival in Neurodegeneration with Brain Iron Accumulation Disorders. Movement disorders clinical practice 11 (1) (2023)
Atefeh Davarzani, Amin Shahrokhi, Seyyed Saleh Hashemi, Aida Ghasemi, Mohammad Reza Habibi Kavashkohei, Niloofar Farboodi, Anthony E Lang, Maryam Ghiasi, Mohammad Rohani, Afagh Alavi
The second family affected with a PRDM8-related disease. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 43 (6) (2022)
Seyyed-Saleh Hashemi, Reza Hajati, Atefeh Davarzani, Mohammad Rohani, Fardad DanaeeFard, Mohammad Masoud Rahimi Bidgoli, Farzad Fatehi, Ariana Kariminejad, Hossein Najmabadi, Shahriar Nafissi, Afagh Alavi
Anticipation Can Be More Common in Hereditary Spastic Paraplegia with SPAST Mutations Than It Appears. The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques (2021)
Reza Hajati, Maziar Emamikhah, Fardad Danaee Fard, Mohammad Rohani, Afagh Alavi
Neurodegeneration with Brain Iron Accumulation and a Brief Report of the Disease in Iran. The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques (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)
Marzieh Khani, Hosein Shamshiri, Farzad Fatehi, Mohammad Rohani, Bahram Haghi Ashtiani, Fahimeh Haji Akhoundi, Afagh Alavi, Hamidreza Moazzeni, Hanieh Taheri, Mina Tolou Ghani, Leila Javanparast, Seyyed Saleh Hashemi, Ramona Haji-Seyed-Javadi, Matineh Heidari, Shahriar Nafissi, Elahe Elahi
Description of combined ARHSP/JALS phenotype in some patients with SPG11 mutations. Molecular genetics & genomic medicine 8 (7) (2020)
Seyyed S Hashemi, Davood Zare-Abdollahi, Mohammad K Bakhshandeh, Amirreza Vafaee, Sona Abolhasani, Kolsoum Inanloo Rahatloo, Fardad DanaeeFard, Niloofar Farboodi, Mohammad Rohani, Afagh Alavi
Clinical spectrum in multiple families with primary COQ10 deficiency. American journal of medical genetics. Part A 185 (2) (2020)
Mohammad Rohani, Alfonso Fasano, Anthony E Lang, Babak Zamani, Leila Javanparast, Mohammad-Masoud Rahimi Bidgoli, Afagh Alavi
Pantothenate kinase-associated neurodegeneration mimicking Tourette syndrome: a case report and review of the literature. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 39 (10) (2018)

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Publication Activity (10 Years)

Top Topics

Top Venues

Afagh Alavi