Observation of c.260A > G mutation in superoxide dismutase 1 that causes p.Asn86Ser in Iranian amyotrophic lateral sclerosis patient and absence of genotype/phenotype correlation

por Khani, Marzieh, Alavi, Afagh, Nafissi, Shahriar, Elahi, Elahe
Publicado 2015

Challenge accepted: uncovering the role of rare genetic variants in Alzheimer’s disease

por Khani, Marzieh, Gibbons, Elizabeth, Bras, Jose, Guerreiro, Rita
Publicado 2022

Correction: Challenge accepted: Uncovering the role of rare genetic variants in Alzheimer’s disease

por Khani, Marzieh, Gibbons, Elizabeth, Bras, Jose, Guerreiro, Rita
Publicado 2022

An Iranian familial amyotrophic lateral sclerosis pedigree with p.Val48Phe causing mutation in SOD1: a genetic and clinical report

por Alavi, Afagh, Khani, Marzieh, Nafissi, Shahriar, Shamshiri, Hosein, Elahi, Elahe
Publicado 2014

Water uptake by gecko β-keratin and the influence of relative humidity on its mechanical and volumetric properties

por Khani, Marzieh, Materzok, Tobias, Eslami, Hossein, Gorb, Stanislav, Müller-Plathe, Florian
Publicado 2022

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

por Khani, Marzieh, Shamshiri, Hosein, Fatehi, Farzad, Rohani, Mohammad, Haghi Ashtiani, Bahram, Akhoundi, Fahimeh Haji, Alavi, Afagh, Moazzeni, Hamidreza, Taheri, Hanieh, Ghani, Mina Tolou, Javanparast, Leila, Hashemi, Seyyed Saleh, Haji‐Seyed‐Javadi, Ramona, Heidari, Matineh, Nafissi, Shahriar, Elahi, Elahe
Publicado 2020