Torthaí cuardaigh - Nahid Aslani

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  1. 1
    Íomhá chlúdaigh

    TNFAIP3 mutation causing haploinsufficiency of A20 with a hemophagocytic lymphohistiocytosis phenotype: a report of two cases de réir Nahid Aslani, Kosar Asnaashari, Nima Parvaneh, Mohammad Shahrooei, Maryam Sotoudeh-Anvari, Farhad Shahram, Vahid Ziaee

    Foilsithe / Cruthaithe 2022
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  2. 2
    Íomhá chlúdaigh

    A case series of ten plus one deficiency of adenosine deaminase 2 (DADA2) patients in Iran de réir Kosar Asna Ashari, Nahid Aslani, Nima Parvaneh, Raheleh Assari, Morteza Heidari, Mohammadreza Fathi, Fatemeh Tahghighi Sharabian, Alireza Ronagh, Mohammad Shahrooei, Alireza Moafi, Nima Rezaei, Vahid Ziaee

    Foilsithe / Cruthaithe 2023
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