Kralovics R - Search Results

1

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.

2

Comparison of molecular markers in a cohort of patients with chronic myeloproliferative disorders.

Kralovics R, Buser AS, Teo SS, Coers J, Tichelli A, van der Maas AP, Skoda RC. Kralovics R, et al. Blood. 2003 Sep 1;102(5):1869-71. doi: 10.1182/blood-2003-03-0744. Epub 2003 May 1. Blood. 2003. PMID: 12730106 Free article.

3

Molecular pathogenesis of Philadelphia chromosome negative myeloproliferative disorders.

Kralovics R, Skoda RC. Kralovics R, et al. Blood Rev. 2005 Jan;19(1):1-13. doi: 10.1016/j.blre.2004.02.002. Blood Rev. 2005. PMID: 15572213 Review.

4

A gain-of-function mutation of JAK2 in myeloproliferative disorders.

Kralovics R, Passamonti F, Buser AS, Teo SS, Tiedt R, Passweg JR, Tichelli A, Cazzola M, Skoda RC. Kralovics R, et al. N Engl J Med. 2005 Apr 28;352(17):1779-90. doi: 10.1056/NEJMoa051113. N Engl J Med. 2005. PMID: 15858187 Free article.

5

Altered gene expression in myeloproliferative disorders correlates with activation of signaling by the V617F mutation of Jak2.

Kralovics R, Teo SS, Buser AS, Brutsche M, Tiedt R, Tichelli A, Passamonti F, Pietra D, Cazzola M, Skoda RC. Kralovics R, et al. Blood. 2005 Nov 15;106(10):3374-6. doi: 10.1182/blood-2005-05-1889. Epub 2005 Aug 4. Blood. 2005. PMID: 16081684 Free article.

6

Acquisition of the V617F mutation of JAK2 is a late genetic event in a subset of patients with myeloproliferative disorders.

Kralovics R, Teo SS, Li S, Theocharides A, Buser AS, Tichelli A, Skoda RC. Kralovics R, et al. Blood. 2006 Aug 15;108(4):1377-80. doi: 10.1182/blood-2005-11-009605. Epub 2006 May 4. Blood. 2006. PMID: 16675710 Free article. Clinical Trial.

7

The JAK2-V617F mutation is frequently present at diagnosis in patients with essential thrombocythemia and polycythemia vera.

Lippert E, Boissinot M, Kralovics R, Girodon F, Dobo I, Praloran V, Boiret-Dupré N, Skoda RC, Hermouet S. Lippert E, et al. Among authors: kralovics r. Blood. 2006 Sep 15;108(6):1865-7. doi: 10.1182/blood-2006-01-013540. Epub 2006 May 25. Blood. 2006. PMID: 16728702 Free article.

8

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.

9

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.

10

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.

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