Works by Badv, Reza Shervin

Results: 61
    1
    2
    3

    Correction to: High genetic heterogeneity of leukodystrophies in Iranian children: the first report of Iranian Leukodystrophy Registry.

    Published in:
    2023
    By:
    • Ashrafi, Mahmoudreza;
    • Kameli, Reyhaneh;
    • Hosseinpour, Sareh;
    • Razmara, Ehsan;
    • Zamani, Zahra;
    • Rezaei, Zahra;
    • Mashayekhi, Raziyeh;
    • Pak, Neda;
    • Barzegar, Mohammad;
    • Azizimalamiri, Reza;
    • Kashani, Morteza Rezvani;
    • Khosroshahi, Nahideh;
    • Rasulinezhad, Maryam;
    • Heidari, Morteza;
    • Amanat, Man;
    • Abdi, Alireza;
    • Mohammadi, Bahram;
    • Mohammadi, Mahmoud;
    • Zamani, Gholam Reza;
    • Badv, Reza Shervin
    Publication type:
    Correction Notice
    4

    High genetic heterogeneity of leukodystrophies in Iranian children: the first report of Iranian Leukodystrophy Registry.

    Published in:
    Neurogenetics, 2023, v. 24, n. 4, p. 279, doi. 10.1007/s10048-023-00730-y
    By:
    • Ashrafi, Mahmoudreza;
    • Kameli, Reyhaneh;
    • Hosseinpour, Sareh;
    • Razmara, Ehsan;
    • Zamani, Zahra;
    • Rezaei, Zahra;
    • Mashayekhi, Raziyeh;
    • Pak, Neda;
    • Barzegar, Mohammad;
    • Azizimalamiri, Reza;
    • Kashani, Morteza Rezvani;
    • Khosroshahi, Nahideh;
    • Rasulinezhad, Maryam;
    • Heidari, Morteza;
    • Amanat, Man;
    • Abdi, Alireza;
    • Mohammadi, Bahram;
    • Mohammadi, Mahmoud;
    • Zamani, Gholam Reza;
    • Badv, Reza Shervin
    Publication type:
    Article
    5
    6

    Molecular characterization of a large cohort of mucopolysaccharidosis patients: Iran Mucopolysaccharidosis RE‐diagnosis study (IMPRESsion).

    Published in:
    Human Mutation, 2022, v. 43, n. 4, p. e1, doi. 10.1002/humu.24328
    By:
    • Ghaffari, Saeed R.;
    • Rafati, Maryam;
    • Shadnoush, Mahdi;
    • Pourbabaee, Shokooh;
    • Aghighi, Mohammad;
    • Mirab Samiee, Siamak;
    • Kermanchi, Jamshid;
    • Alaei, Mohammad R.;
    • Salehpour, Shadab;
    • Amirkashani, Davoud;
    • Setoodeh, Aria;
    • Sarkhail, Peymaneh;
    • Badv, Reza Shervin;
    • Aminzadeh, Majid;
    • Shiva, Siamak;
    • Eshraghi, Peyman;
    • Moravej, Hossein;
    • Hashemipour, Mahin;
    • Rostampour, Noushin;
    • Hamidieh, َAmir Ali
    Publication type:
    Article
    7
    8
    9

    The First Comprehensive Cohort of the Duchenne Muscular Dystrophy in Iranian Population: Mutation Spectrum of 314 Patients and Identifying Two Novel Nonsense Mutations.

    Published in:
    Journal of Molecular Neuroscience, 2020, v. 70, n. 10, p. 1565, doi. 10.1007/s12031-020-01594-9
    By:
    • Zamani, Gholamreza;
    • Hosseini Bereshneh, Ali;
    • Azizi Malamiri, Reza;
    • Bagheri, Sayna;
    • Moradi, Kamyar;
    • Ashrafi, Mahmoud Reza;
    • Tavasoli, Ali Reza;
    • Mohammadi, Mahmoud;
    • Badv, Reza Shervin;
    • Ghahvechi Akbari, Masood;
    • Heidari, Morteza
    Publication type:
    Article
    10
    11
    12
    13
    14
    15
    16
    17
    18

    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
    19

    Clinical and imaging outcomes after intrathecal injection of umbilical cord tissue mesenchymal stem cells in cerebral palsy: a randomized double-blind sham-controlled clinical trial.

    Published in:
    Stem Cell Research & Therapy, 2021, v. 12, n. 1, p. 1, doi. 10.1186/s13287-021-02513-4
    By:
    • Amanat, Man;
    • Majmaa, Anahita;
    • Zarrabi, Morteza;
    • Nouri, Masoumeh;
    • Akbari, Masood Ghahvechi;
    • Moaiedi, Ali Reza;
    • Ghaemi, Omid;
    • Zamani, Fatemeh;
    • Najafi, Sharif;
    • Badv, Reza Shervin;
    • Vosough, Massoud;
    • Hamidieh, Amir Ali;
    • Salehi, Mona;
    • Montazerlotfelahi, Hadi;
    • Tavasoli, Ali Reza;
    • Heidari, Morteza;
    • Mohebi, Hossein;
    • Fatemi, Ali;
    • Garakani, Amir;
    • Ashrafi, Mahmoud Reza
    Publication type:
    Article
    20
    21
    22
    23
    24
    25

    Patterns of Antiepileptic Drug Reactions in Children: A Multicenter Study.

    Published in:
    Iranian Journal of Child Neurology, 2022, v. 16, n. 3, p. 133, doi. 10.22037/ijcn.v16i3.32872
    By:
    • Sedighi, Parinaz;
    • Khalili, Neda;
    • Khalili, Nastaran;
    • Doosti-Irani, Amin;
    • Moradi, Atefeh;
    • Moghadam, Samira;
    • Nemati, Meshkat;
    • Jorjafki, Sobhan Mohammadi;
    • Badv, Reza Shervin;
    • Sedighi, Iraj
    Publication type:
    Article
    26
    27
    28
    29
    30
    31
    32

    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
    33
    34
    35
    36
    37

    Reevaluation of the Impact of the Novel Likely Pathogenic Variant c.1286_1288delAGA in the ATP8A2 Gene: A 7‐Year Follow‐Up With Clinical, Genetic, and ACMG Insights in an Iranian Family.

    Published in:
    Molecular Genetics & Genomic Medicine, 2025, v. 13, n. 2, p. 1, doi. 10.1002/mgg3.70081
    By:
    • Kalayinia, Samira;
    • Hesami, Hamed;
    • Badv, Reza Shervin;
    • Rabbani, Maryam;
    • Rezaei, Zahra;
    • Hosseinkhani, Zohreh;
    • Nikbakht, Sedighe;
    • Sharifi, Ameneh;
    • Akbari, Bahman;
    • Mirab Samiee, Siamak;
    • Mahdieh, Nejat
    Publication type:
    Article
    38
    39

    Neurologic Manifestations of Coronavirus Disease 2019 in Children: An Iranian Hospital-Based Study.

    Published in:
    Archives of Iranian Medicine (AIM), 2023, v. 26, n. 3, p. 166, doi. 10.34172/aim.2023.25
    By:
    • Esmaeil Memar, Elmira Haji;
    • Heidari, Morteza;
    • Ghabeli, Homa;
    • Pourbakhtyaran, Elham;
    • Haghighi, Roya;
    • Mahdi Hosseiny, Seyyed Mohammad;
    • Mamishi, Setareh;
    • Mahmoudi, Shima;
    • Eshaghi, Hamid;
    • Tavasoli, Ali Reza;
    • Mohammadi, Mahmoud;
    • Badv, Reza Shervin;
    • Zamani, Gholamreza;
    • Akbari, Masood Ghahvehchi;
    • Yarali, Bahram;
    • Shirzadi, Rohola;
    • Mohammadpour, Masoud;
    • Yaghmaei, Bahareh;
    • Ekbatani, Meisam Sharifzadeh;
    • Najafi, Zeynab
    Publication type:
    Article
    40

    Photoclinic.

    Published in:
    2022
    By:
    • Badv, Reza Shervin;
    • Akbari, Masood Ghahvechi;
    • Heidari, Morteza;
    • Safavi, Moeinadin
    Publication type:
    Test/Instrument
    41
    42
    43
    44
    45
    46

    Investigation of Chromosomal Abnormalities and Microdeletion/ Microduplication(s) in Fifty Iranian Patients with Multiple Congenital Anomalies.

    Published in:
    Cell Journal (Yakhteh), 2019, v. 21, n. 3, p. 337, doi. 10.22074/cellj.2019.6053
    By:
    • Mohammadzadeh, Akbar;
    • Akbaroghli, Susan;
    • Aghaei-Moghadam, Ehsan;
    • Mahdieh, Nejat;
    • Badv, Reza Shervin;
    • Jamali, Payman;
    • Kariminejad, Roxana;
    • Chavoshzadeh, Zahra;
    • Firouzabadi, Saghar Ghasemi;
    • Ghanaie, Roxana Mansour;
    • Nozari, Ahoura;
    • Banihashemi, Sussan;
    • Hadipour, Fatemeh;
    • Hadipour, Zahra;
    • Kariminejad, Ariana;
    • Najmabadi, Hossein;
    • Shafeghati, Yousef;
    • Behjati, Farkhondeh
    Publication type:
    Article
    47

    Sexual Dimorphism in Telomere Length in Childhood Autism.

    Published in:
    Journal of Autism & Developmental Disorders, 2023, v. 53, n. 5, p. 2050, doi. 10.1007/s10803-022-05486-2
    By:
    • Panahi, Yasin;
    • Salasar Moghaddam, Fahimeh;
    • Babaei, Khadijeh;
    • Eftekhar, Mohammad;
    • Shervin Badv, Reza;
    • Eskandari, Mohammad Reza;
    • Vafaee-Shahi, Mohammad;
    • Pezeshk, Hamid;
    • Pedram, Mehrdad
    Publication type:
    Article
    48
    49
    50

    The First Report of Iranian Registry of Patients with Spinal Muscular Atrophy.

    Published in:
    Journal of Neuromuscular Diseases, 2023, v. 10, n. 2, p. 211, doi. 10.3233/JND-221614
    By:
    • Mansouri, Vahid;
    • Heidari, Morteza;
    • Bemanalizadeh, Maryam;
    • Azizimalamiri, Reza;
    • Nafissi, Shahriar;
    • Akbari, Masood Ghahvechi;
    • Barzegar, Mohammad;
    • Moayedi, Ali Reza;
    • Badv, Reza Shervin;
    • Mohamadi, Mahmood;
    • Tavasoli, Ali Reza;
    • Amirsalari, Susan;
    • Khajeh, Ali;
    • Inaloo, Soroor;
    • Fatehi, Farzad;
    • Hosseinpour, Sareh;
    • Babaei, Meisam;
    • Hosseini, Seyed Ahmad;
    • Mahdi Hosseiny, Seyyed Mohammad;
    • Fayyazi, Afshin
    Publication type:
    Article