Bilaketaren emaitzak - Afagh Alavi

An Iranian familial amyotrophic lateral sclerosis pedigree with p.Val48Phe causing mutation in SOD1: a genetic and clinical report nork Afagh Alavi, Marzieh Khani, Shahriar Nafissi, Hosein Shamshiri, Elahe Elahi

Testu osoa

Intellectual disability associated with craniofacial dysmorphism due to POLR3B mutation and defect in spliceosomal machinery nork Mostafa Saghi, Kolsoum InanlooRahatloo, Afagh Alavi, Kimia Kahrizi, Hossein Najmabadi

Testu osoa

A novel nonsense mutation in WNK1/HSN2 associated with sensory neuropathy and limb destruction in four siblings of a large Iranian pedigree nork Behrouz Rahmani, Fatemeh Fekrmandi, Keivan Ahadi, Tannaz Ahadi, Afagh Alavi, Abolhassan Ahmadiani, Sareh Asadi

Testu osoa

Identification of let-7f and miR-338 as plasma-based biomarkers for sporadic amyotrophic lateral sclerosis using meta-analysis and empirical validation nork Narges Daneshafrooz, Mohammad Taghi Joghataei, Mehdi Mehdizadeh, Afagh Alavi, Mahmood Barati, Bahman Panahi, Shahram Teimourian, Babak Zamani

Testu osoa

A Pathogenic Homozygous Mutation In The Pleckstrin Homology Domain Of RASA1 Is Responsible For Familial Tricuspid Atresia In An Iranian Consanguineous Family nork Ahoura Nozari, Ehsan Aghaei-Moghadam, Aliakbar Zeinaloo, Afagh Alavi, Saghar Ghasemi Firouzabad, Shohre Minaee, Marzeieh Eskandari Hesari, Farkhondeh Behjati

Testu osoa

Potential role of FKBP5 single‐nucleotide polymorphisms in functional seizures nork Ali A. Asadi‐Pooya, Leila Simani, Marjan Asadollahi, Fatemeh Sadat Rashidi, Ehsan Ahmadipour, Afagh Alavi, Mehrdad Roozbeh, Nayyereh Akbari, Negar Firouzabadi

Testu osoa

Expanding the genetic and clinical landscapes of hereditary spastic paraplegia (HSP): a cohort study of 103 families nork Atefeh Davarzani, Moez Ravanbod, Aida Ghasemi, Mahsa Mohammadi, Mohammad Rohani, Shahriar Nafissi, Payman Jamali, Hossein Najmabadi, Farzad Fatehi, Shahryar Alavi, Zahra Firoozfar, Fariba Zemorshidi, Mohammad Reza Habibi-Kavashkohie, Afagh Alavi

Testu osoa

Description of combined ARHSP/JALS phenotype in some patients with SPG11 mutations nork 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

Testu osoa