Search Results - Mirna Lechpammer

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    A rare case of centronuclear myopathy with DNM2 mutation: genotype-phenotype correlation by Amir Ghorbani Aghbolaghi, Mirna Lechpammer

    Published 2017
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    An extremely rare case of concurrent BRAF V600E mutation driven hairy cell leukemia and melanoma: case report and review of literature by Amir Ghorbani-Aghbolaghia, Mirna Lechpammer, Saba F. Ali, Nam K. Ku, Denis M. Dwyre, Hooman H. Rashidi

    Published 2017
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