Search Results - Alyasin, Soheila Sadat

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  1. 1
    A rare case of SRD5A3‐CDG in a patient with ataxia and telangiectasia: A case report

    A rare case of SRD5A3‐CDG in a patient with ataxia and telangiectasia: A case report by Nabavizadeh, Sayyed Hesamedin, Noeiaghdam, Rafat, Johari, Leila, Hosseini, Seyed Ali, Esmaeilzadeh, Hossein, Alyasin, Soheila Sadat

    Published in Clinical case reports
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  2. 2
    Homozygous Autosomal Recessive DIAPH1 Mutation Associated with Central Nervous System Involvement and Aspergillosis: A Rare Case

    Homozygous Autosomal Recessive DIAPH1 Mutation Associated with Central Nervous System Involvement and Aspergillosis: A Rare Case by Esmaeilzadeh, Hossein, Noeiaghdam, Rafat, Johari, Leila, Hosseini, Seyed Ali, Nabavizadeh, Sayyed Hesamedin, Alyasin, Soheila Sadat

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    Homozygous Autosomal Recessive DIAPH1 Mutation Associated with Central Nervous System Involvement and Aspergillosis: A Rare Case

    Homozygous Autosomal Recessive DIAPH1 Mutation Associated with Central Nervous System Involvement and Aspergillosis: A Rare Case by Esmaeilzadeh, Hossein, Noeiaghdam, Rafat, Johari, Leila, Hosseini, Seyed Ali, Nabavizadeh, Sayyed Hesamedin, Alyasin, Soheila Sadat

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    Exome-first Approach Identified Novel Homozygous Dedicator of Cytokinesis 8 (DOCK8) Mutations in Three Unrelated Iranian Pedigrees Suspected with Hyper-IgE Syndrome

    Exome-first Approach Identified Novel Homozygous Dedicator of Cytokinesis 8 (DOCK8) Mutations in Three Unrelated Iranian Pedigrees Suspected with Hyper-IgE Syndrome by Aghebati-Maleki, Ali, Shahani, Tina, Momen, Tooba, Alyasin, Soheila, Changi-Ashtiani, Majid, Biglari, Alireza, Shahrooei, Mohammad, Javanian, Asiyeh Sadat, Amini, Suzan, Bossuyt, Xavier, Rokni-Zadeh, Hassan

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