Works matching AU Rohani, Mohammad

Results: 117
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    Amyotrophic lateral sclerosis progression: Iran-ALS clinical registry, a multicentre study.

    Published in:
    Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration, 2015, v. 16, n. 7/8, p. 506, doi. 10.3109/21678421.2015.1074698
    By:
    • Shamshiri, Hosein;
    • Fatehi, Farzad;
    • Davoudi, Farnoush;
    • Mir, Elham;
    • Pourmirza, Behin;
    • Abolfazli, Roya;
    • Etemadifar, Masoud;
    • Harirchian, Mohammad Hossein;
    • Gharagozli, Koroush;
    • Ayromlou, Hormoz;
    • Basiri, Keivan;
    • Zamani, Babak;
    • Rohani, Mohammad;
    • Sedighi, Behnaz;
    • Roudbari, Ali;
    • Delavar Kasmaei, Hossein;
    • Nikkhah, Karim;
    • Ranjbar Naeini, Alireza;
    • Nafissi, Shahriar
    Publication type:
    Article
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    Follow‐up of 25 patients with treatable ataxia: A comprehensive case series study.

    Published in:
    Clinical Case Reports, 2022, v. 10, n. 4, p. 1, doi. 10.1002/ccr3.5777
    By:
    • Ashrafi, Mahmoud Reza;
    • Pourbakhtyaran, Elham;
    • Rohani, Mohammad;
    • Shalbafan, Bita;
    • Tavasoli, Ali Reza;
    • Hosseinpour, Sareh;
    • Rasulinezhad, Maryam;
    • Rezaei, Zahra;
    • Zare Dehnavi, Ali;
    • Hosseiny, Seyyed Mohammad Mahdi;
    • Haghighi, Roya;
    • Ghabeli, Homa;
    • Heidari, Morteza
    Publication type:
    Article
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    Clinical and Molecular Findings of Autosomal Recessive Spastic Ataxia of Charlevoix Saguenay: an Iranian Case Series Expanding the Genetic and Neuroimaging Spectra.

    Published in:
    Cerebellum, 2023, v. 22, n. 4, p. 640, doi. 10.1007/s12311-022-01430-3
    By:
    • Ashrafi, Mahmoud Reza;
    • Mohammadi, Pouria;
    • Tavasoli, Ali Reza;
    • Heidari, Morteza;
    • Hosseinpour, Sareh;
    • Rasulinejad, Maryam;
    • Rohani, Mohammad;
    • Akbari, Masoud Ghahvechi;
    • Malamiri, Reza Azizi;
    • Badv, Reza Shervin;
    • Fathi, Davood;
    • Dehnavi, Ali Zare;
    • Savad, Shahram;
    • Rabbani, Ali;
    • Synofzik, Matthis;
    • Mahdieh, Nejat;
    • Rezaei, Zahra
    Publication type:
    Article
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    Clinical spectrum in multiple families with primary COQ<sub>10</sub> deficiency.

    Published in:
    American Journal of Medical Genetics. Part A, 2021, v. 185, n. 2, p. 440, doi. 10.1002/ajmg.a.61983
    By:
    • Hashemi, Seyyed S.;
    • Zare‐Abdollahi, Davood;
    • Bakhshandeh, Mohammad K.;
    • Vafaee, Amirreza;
    • Abolhasani, Sona;
    • Inanloo Rahatloo, Kolsoum;
    • DanaeeFard, Fardad;
    • Farboodi, Niloofar;
    • Rohani, Mohammad;
    • Alavi, Afagh
    Publication type:
    Article
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    The genetic basis of early-onset hereditary ataxia in Iran: results of a national registry of a heterogeneous population.

    Published in:
    Human Genomics, 2024, v. 18, n. 1, p. 1, doi. 10.1186/s40246-024-00598-5
    By:
    • Mahdieh, Nejat;
    • Heidari, Morteza;
    • Rezaei, Zahra;
    • Tavasoli, Ali Reza;
    • Hosseinpour, Sareh;
    • Rasulinejad, Maryam;
    • Dehnavi, Ali Zare;
    • Ghahvechi Akbari, Masoud;
    • Badv, Reza Shervin;
    • Vafaei, Elahe;
    • Mohebbi, Ali;
    • Mohammadi, Pouria;
    • Hosseiny, Seyyed Mohammad Mahdi;
    • Azizimalamiri, Reza;
    • Nikkhah, Ali;
    • Pourbakhtyaran, Elham;
    • Rohani, Mohammad;
    • Khanbanha, Narges;
    • Nikbakht, Sedigheh;
    • Movahedinia, Mojtaba
    Publication type:
    Article
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    Description of combined ARHSP/JALS phenotype in some patients with SPG11 mutations.

    Published in:
    Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 7, p. 1, doi. 10.1002/mgg3.1240
    By:
    • 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
    Publication type:
    Article
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    Cost‐utility analysis of a coadjutant telemedicine intervention for fall prevention in Parkinson's disease.

    Published in:
    European Journal of Neurology, 2025, v. 32, n. 1, p. 1, doi. 10.1111/ene.16561
    By:
    • Cubo, Esther;
    • Rohani, Mohammad;
    • Eissazade, Negin;
    • Garcia‐Bustillo, Álvaro;
    • Ramírez‐Sanz, José Miguel;
    • Garrido‐Labrador, José Luis;
    • Olivares‐Gil, Alicia;
    • Valiñas‐Sieiro Rn, Florita;
    • Allende‐Río Rn, Marta;
    • Gonzalez‐Santos, Josefa;
    • Gonzalez‐Bernal, Jerónimo Javier;
    • Trejo, José;
    • Calvo‐Simal, Sara;
    • Diez‐Pastor, José Francisco;
    • García‐García, David;
    • Arnaiz‐González, Álvar
    Publication type:
    Article
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    Fulminant multiple sclerosis (MS).

    Published in:
    Neurological Sciences, 2011, v. 32, n. 5, p. 953, doi. 10.1007/s10072-011-0723-0
    By:
    • Rohani, Mohammad;
    • Ghourchian, Shadi
    Publication type:
    Article
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