Prchal JT - Search Results

1

Endemic polycythemia in Russia: mutation in the VHL gene.

Ang SO, Chen H, Gordeuk VR, Sergueeva AI, Polyakova LA, Miasnikova GY, Kralovics R, Stockton DW, Prchal JT. Ang SO, et al. Among authors: prchal jt. Blood Cells Mol Dis. 2002 Jan-Feb;28(1):57-62. doi: 10.1006/bcmd.2002.0488. Blood Cells Mol Dis. 2002. PMID: 11987242

2

Congenital polycythemia in Chuvashia.

Sergeyeva A, Gordeuk VR, Tokarev YN, Sokol L, Prchal JF, Prchal JT. Sergeyeva A, et al. Among authors: prchal jf, prchal jt. Blood. 1997 Mar 15;89(6):2148-54. Blood. 1997. PMID: 9058738 Free article.

3

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. Among authors: prchal jf, prchal jt. Blood. 1997 Sep 1;90(5):2057-61. Blood. 1997. PMID: 9292543 Free article.

4

The erythropoietin receptor gene is not linked with the polycythemia phenotype in a family with autosomal dominant primary polycythemia.

Kralovics R, Sokol L, Broxson EH Jr, Prchal JT. Kralovics R, et al. Among authors: prchal jt. Proc Assoc Am Physicians. 1997 Nov;109(6):580-5. Proc Assoc Am Physicians. 1997. PMID: 9394420

5

Absence of polycythemia in a child with a unique erythropoietin receptor mutation in a family with autosomal dominant primary polycythemia.

Kralovics R, Sokol L, Prchal JT. Kralovics R, et al. Among authors: prchal jt. J Clin Invest. 1998 Jul 1;102(1):124-9. doi: 10.1172/JCI2886. J Clin Invest. 1998. PMID: 9649565 Free PMC article.

6

Haematopoietic progenitors and signal transduction in polycythaemia vera and primary thrombocythaemia.

Kralovics R, Prchal JT. Kralovics R, et al. Among authors: prchal jt. Baillieres Clin Haematol. 1998 Dec;11(4):803-18. doi: 10.1016/s0950-3536(98)80040-1. Baillieres Clin Haematol. 1998. PMID: 10640218 Review.

7

Congenital and inherited polycythemia.

Kralovics R, Prchal JT. Kralovics R, et al. Among authors: prchal jt. Curr Opin Pediatr. 2000 Feb;12(1):29-34. doi: 10.1097/00008480-200002000-00006. Curr Opin Pediatr. 2000. PMID: 10676771 Review.

8

A polymorphism of the X-linked gene IDS increases the number of females informative for transcriptional clonality assays.

Gregg XT, Kralovics R, Prchal JT. Gregg XT, et al. Among authors: prchal jt. Am J Hematol. 2000 Apr;63(4):184-91. doi: 10.1002/(sici)1096-8652(200004)63:4<184::aid-ajh4>3.0.co;2-i. Am J Hematol. 2000. PMID: 10706761 Free article.

9

Genetic heterogeneity of primary familial and congenital polycythemia.

Kralovics R, Prchal JT. Kralovics R, et al. Among authors: prchal jt. Am J Hematol. 2001 Oct;68(2):115-21. doi: 10.1002/ajh.1162. Am J Hematol. 2001. PMID: 11559951 Free article.

10

Acquired uniparental disomy of chromosome 9p is a frequent stem cell defect in polycythemia vera.

Kralovics R, Guan Y, Prchal JT. Kralovics R, et al. Among authors: prchal jt. Exp Hematol. 2002 Mar;30(3):229-36. doi: 10.1016/s0301-472x(01)00789-5. Exp Hematol. 2002. PMID: 11882360 Free article.

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