Hasil Pencarian - Mohammad Vafaee‐Shahi

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  1. 1
    A fulminant presentation of post‐COVID‐19 necrotizing pneumonia and ischemic stroke in an 8‐year‐old girl: A case report and literature review

    A fulminant presentation of post‐COVID‐19 necrotizing pneumonia and ischemic stroke in an 8‐year‐old girl: A case report and literature review oleh Fahimeh Ehsanipur, Pouya Ebrahimi, Leila Tahernia, Mohammad Vafaee‐Shahi

    Diterbitkan 2024-08-01
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  2. 2
    A boy with blistering of sun-exposed skin and finger shortening: the first case of Variegate Porphyria with a novel mutation in protoporphyrinogen oxidase (PPOX) gene in Iran: a case report and literature review

    A boy with blistering of sun-exposed skin and finger shortening: the first case of Variegate Porphyria with a novel mutation in protoporphyrinogen oxidase (PPOX) gene in Iran: a ca... oleh Mohammad Vafaee-Shahi, Saeide Ghasemi, Aina Riahi, Zahra Sadr

    Diterbitkan 2022-02-01
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  3. 3
    Is a Brain Stroke Caused by COVID-19 Seen Under Two Years of Age? A Case Report

    Is a Brain Stroke Caused by COVID-19 Seen Under Two Years of Age? A Case Report oleh Mohammad Vafaee Shahi, Sedigheh Yousefzadegan, Ramin Zare Mahmoudabadi, Fatemeh Ahmadi, Aina Riahi

    Diterbitkan 2021-12-01
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  4. 4
    The effect of Rosa canina L. and a polyherbal formulation syrup in patients with attention-deficit/hyperactivity disorder: a study protocol for a multicenter randomized controlled trial

    The effect of Rosa canina L. and a polyherbal formulation syrup in patients with attention-deficit/hyperactivity disorder: a study protocol for a multicenter randomized controlled... oleh Haide Golsorkhi, Mostafa Qorbani, Mohammad Kamalinejad, Saeideh Sabbaghzadegan, Mohsen Bahrami, Mohammad Vafaee-Shahi, Hadi Montazerlotfelahi, Elham Abniki, Majid Dadmehr

    Diterbitkan 2022-05-01
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  5. 5
    Bilateral horizontal gaze palsy in an 8‐year‐old girl: A rare case with NDUFS4 gene mutation

    Bilateral horizontal gaze palsy in an 8‐year‐old girl: A rare case with NDUFS4 gene mutation oleh Mohammad Vafaee‐Shahi, Saeide Ghasemi, Mehran Beiraghi Toosi, Mahmoud Reza Ashrafi, Reza Shervin Badv, Ali Reza Tavasoli, Leila Tahernia

    Diterbitkan 2021-09-01
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  6. 6
    Immunodeficiency, Centromeric Region Instability, and Facial Anomalies Syndrome (ICF) in a Boy with Variable Clinical and Immunological Presentations

    Immunodeficiency, Centromeric Region Instability, and Facial Anomalies Syndrome (ICF) in a Boy with Variable Clinical and Immunological Presentations oleh Mohammad Hassan Bemanian, Saba Arshi, Mohammad Nabavi, Mohammad Vafaee-Shahi, Morteza Fallahpour, Sima Shokri, Afshin Rezaeifar, Hossein Shahzadi, Fatemeh Atashrazm

    Diterbitkan 2021-04-01
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  7. 7
    Genetic insights into PHARC syndrome: identification of a novel frameshift mutation in ABHD12

    Genetic insights into PHARC syndrome: identification of a novel frameshift mutation in ABHD12 oleh Ahmad Daneshi, Masoud Garshasbi, Mohammad Farhadi, Khalil Ghasemi Falavarjani, Mohammad Vafaee-Shahi, Navid Almadani, MohammadSina Zabihi, Mohammad Amin Ghalavand, Masoumeh Falah

    Diterbitkan 2023-10-01
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