Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Anthonie P. C. van der Maas"'
Autor:
Ralph Tiedt, Patricia Frank, Kun Liu, Anthonie P. C. van der Maas, Robert Kralovics, Andreas Buser, Krzysztof Okoń, Heinz Gisslinger, Barbara Grabowska, Damla Olcaydu, Radek C. Skoda, Zbigniew Rudzki
Publikováno v:
Haematologica. 93:706-714
Background Hereditary thrombocythemia is an autosomal dominant disorder with clinical features resembling sporadic essential thrombocythemia. Germline mutations in families with hereditary thrombocythemia have been identified in the gene for thrombop
Autor:
Soon-Siong Teo, Anthonie P. C. van der Maas, André Tichelli, Andreas Buser, Robert Kralovics, Joern Coers, Radek C. Skoda
Publikováno v:
Blood. 102:1869-1871
Decreased expression of c-MPL protein in platelets, increased expression of polycythemia rubra vera 1 (PRV-1) and nuclear factor I-B (NFIB) mRNA in granulocytes, and loss of heterozygosity on chromosome 9p (9pLOH) were described as molecular markers
Autor:
Eduardus F. M. Posthuma, Anthonie P. C. van der Maas, Peter J. M. Valk, Frank A. Jacob, Hidde L. A. Posthuma, Radek C. Skoda
Publikováno v:
Blood, 116(17), 3375-3376. American Society of Hematology
To the editor: Essential thrombocythemia (ET) is frequently characterized by clonal hematopoiesis and an acquired JAK2-V617F mutation. Mutations in the thrombopoietin gene ( THPO ) and in the thrombopoietin receptor gene ( MPL ) can cause hereditary