Kralovics R - Search Results

1

Germline genetic factors influence the outcome of interferon-α therapy in polycythemia vera.

Jäger R, Gisslinger H, Fuchs E, Bogner E, Milosevic Feenstra JD, Weinzierl J, Schischlik F, Gisslinger B, Schalling M, Zörer M, Krejcy K, Klade C, Kralovics R. Jäger R, et al. Among authors: kralovics r. Blood. 2021 Jan 21;137(3):387-391. doi: 10.1182/blood.2020005792. Blood. 2021. PMID: 32814349 Free PMC article. Clinical Trial.

2

Two new EPO receptor mutations: truncated EPO receptors are most frequently associated with primary familial and congenital polycythemias.

Kralovics R, Indrak K, Stopka T, Berman BW, Prchal JF, Prchal JT. Kralovics R, et al. Blood. 1997 Sep 1;90(5):2057-61. Blood. 1997. PMID: 9292543 Free article.

3

Clonal hematopoiesis in familial polycythemia vera suggests the involvement of multiple mutational events in the early pathogenesis of the disease.

Kralovics R, Stockton DW, Prchal JT. Kralovics R, et al. Blood. 2003 Nov 15;102(10):3793-6. doi: 10.1182/blood-2003-03-0885. Epub 2003 Jun 26. Blood. 2003. PMID: 12829587 Free article.

4

Somatic mutations of JAK2 exon 12 in patients with JAK2 (V617F)-negative myeloproliferative disorders.

Pietra D, Li S, Brisci A, Passamonti F, Rumi E, Theocharides A, Ferrari M, Gisslinger H, Kralovics R, Cremonesi L, Skoda R, Cazzola M. Pietra D, et al. Among authors: kralovics r. Blood. 2008 Feb 1;111(3):1686-9. doi: 10.1182/blood-2007-07-101576. Epub 2007 Nov 5. Blood. 2008. PMID: 17984312 Free article.

5

Clonal heterogeneity in polycythemia vera patients with JAK2 exon12 and JAK2-V617F mutations.

Li S, Kralovics R, De Libero G, Theocharides A, Gisslinger H, Skoda RC. Li S, et al. Among authors: kralovics r. Blood. 2008 Apr 1;111(7):3863-6. doi: 10.1182/blood-2007-09-111971. Epub 2008 Jan 14. Blood. 2008. PMID: 18195094 Free article.

6

A de novo splice donor mutation in the thrombopoietin gene causes hereditary thrombocythemia in a Polish family.

Liu K, Kralovics R, Rudzki Z, Grabowska B, Buser AS, Olcaydu D, Gisslinger H, Tiedt R, Frank P, Okoñ K, van der Maas AP, Skoda RC. Liu K, et al. Among authors: kralovics r. Haematologica. 2008 May;93(5):706-14. doi: 10.3324/haematol.11801. Epub 2008 Mar 26. Haematologica. 2008. PMID: 18367486 Free article.

7

Acquired resistance to interferon alpha therapy associated with homozygous MPL-W515L mutation and chromosome 20q deletion in primary myelofibrosis.

Buxhofer-Ausch V, Gisslinger H, Berg T, Gisslinger B, Kralovics R. Buxhofer-Ausch V, et al. Among authors: kralovics r. Eur J Haematol. 2009 Feb;82(2):161-3. doi: 10.1111/j.1600-0609.2008.01183.x. Epub 2008 Nov 10. Eur J Haematol. 2009. PMID: 19018861 No abstract available.

8

Clonal analysis of deletions on chromosome 20q and JAK2-V617F in MPD suggests that del20q acts independently and is not one of the predisposing mutations for JAK2-V617F.

Schaub FX, Jäger R, Looser R, Hao-Shen H, Hermouet S, Girodon F, Tichelli A, Gisslinger H, Kralovics R, Skoda RC. Schaub FX, et al. Among authors: kralovics r. Blood. 2009 Feb 26;113(9):2022-7. doi: 10.1182/blood-2008-07-167056. Epub 2008 Dec 1. Blood. 2009. PMID: 19047681 Free article.

9

A common JAK2 haplotype confers susceptibility to myeloproliferative neoplasms.

Olcaydu D, Harutyunyan A, Jäger R, Berg T, Gisslinger B, Pabinger I, Gisslinger H, Kralovics R. Olcaydu D, et al. Among authors: kralovics r. Nat Genet. 2009 Apr;41(4):450-4. doi: 10.1038/ng.341. Epub 2009 Mar 15. Nat Genet. 2009. PMID: 19287385

10

Molecular basis and clonal evolution of myeloproliferative neoplasms.

Jäger R, Kralovics R. Jäger R, et al. Among authors: kralovics r. Haematologica. 2010 Apr;95(4):526-9. doi: 10.3324/haematol.2009.019570. Haematologica. 2010. PMID: 20378573 Free PMC article. No abstract available.

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