Search Results - Fatemeh Vand Rajabpour

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    Lipoid Proteinosis Due to Homozygous Deletion Mutation (c.735delTG) in the ECM1 Gene Presents with Seizures and Hoarseness but No Skin Involvement by Hassan Vahidnezhad, Leila Youssefian, Abbas Tafakhori, Qiaoli Li, Jouni Uitto, Fatemeh Vand Rajabpour, Morteza Pishnamazi, Amirhossein Modabbernia, Mina Tabrizi

    Published 2020
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    Decreased Sox2 messenger RNA expression in basal cell carcinoma by Reza Ahmadi-Beni, Fatemeh Vand-Rajabpour, Mohamadreza Ahmadifard, Maryam Daneshpazhooh, Pedram Noormohammadpour, Javad Rahmati, Kambiz Kamyab Hesari, Mehdi Yaseri, Mina Tabrizi

    Published 2020
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