Works by Rohani, Mohammad


Results: 116
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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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    Correction: Phenotype and genotype heterogeneity of PLA2G6-associated neurodegeneration in a cohort of pediatric and adult patients.

    Published in:
    Orphanet Journal of Rare Diseases, 2023, v. 18, n. 1, p. 1, doi. 10.1186/s13023-023-02794-3
    By:
    • Dehnavi, Ali Zare;
    • Bemanalizadeh, Maryam;
    • Kahani, Seyyed Mohammad;
    • Ashrafi, Mahmoud Reza;
    • Rohani, Mohammad;
    • Toosi, Mehran Beiraghi;
    • Heidari, Morteza;
    • Hosseinpour, Sareh;
    • Amini, Behnam;
    • Zokaei, Shaghayegh;
    • Rezaei, Zahra;
    • Aryan, Hajar;
    • Amanat, Man;
    • Vahidnezhad, Hassan;
    • Mohammadi, Pouria;
    • Garshasbi, Masoud;
    • Tavasoli, Ali Reza
    Publication type:
    Article
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    Phenotype and genotype heterogeneity of PLA2G6-associated neurodegeneration in a cohort of pediatric and adult patients.

    Published in:
    Orphanet Journal of Rare Diseases, 2023, v. 18, n. 1, p. 1, doi. 10.1186/s13023-023-02780-9
    By:
    • Dehnavi, Ali Zare;
    • Bemanalizadeh, Maryam;
    • Kahani, Seyyed Mohammad;
    • Ashrafi, Mahmoud Reza;
    • Rohani, Mohammad;
    • Toosi, Mehran Beiraghi;
    • Heidari, Morteza;
    • Hosseinpour, Sareh;
    • Amini, Behnam;
    • Zokaei, Shaghayegh;
    • Rezaei, Zahra;
    • Aryan, Hajar;
    • Amanat, Man;
    • Vahidnezhad, Hassan;
    • Mohammadi, Pouria;
    • Garshasbi, Masoud;
    • Tavasoli, Ali Reza
    Publication type:
    Article
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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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    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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    Familial Hypermanganesemia in Iran.

    Published in:
    Movement Disorders Clinical Practice, 2023, v. 10, n. 5, p. 850, doi. 10.1002/mdc3.13723
    By:
    • Tabatabaee, Seyedeh Narges;
    • Effat Nejad, Sajjad;
    • Nikkhah, Ali;
    • Hashemi, Narges;
    • Alavi, Afagh;
    • Lang, Anthony E.;
    • Rohani, Mohammad;
    • Emamikhah, Maziar
    Publication type:
    Article
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    Diplopia in Progressive Supranuclear Palsy.

    Published in:
    Movement Disorders Clinical Practice, 2020, v. 7, n. 2, p. 232, doi. 10.1002/mdc3.12890
    By:
    • Yazdi, Narges;
    • Ghamsari, Mona Ramezani;
    • Shoeibi, Ali;
    • Rohani, Mohammad
    Publication type:
    Article
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    Gelastic Cataplexy in Niemann Pick Type C.

    Published in:
    Movement Disorders Clinical Practice, 2019, v. 6, n. 6, p. 498, doi. 10.1002/mdc3.12786
    By:
    • Yazdi, Narges;
    • Fasano, Alfonso;
    • Lang, Anthony E.;
    • Rohani, Mohammad
    Publication type:
    Article
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    Action Myoclonus and Seizure in Kufor‐Rakeb Syndrome.

    Published in:
    Movement Disorders Clinical Practice, 2018, v. 5, n. 2, p. 195, doi. 10.1002/mdc3.12570
    By:
    • Sina, Farzad;
    • Rohani, Mohammad;
    • Lang, Anthony E.;
    • Fasano, Alfonso;
    • Elahi, Elahe;
    • Hardy, John;
    • Bras, Jose;
    • Alavi, Afagh
    Publication type:
    Article
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