370 related articles for article (PubMed ID: 15217714)
1. Polycythemia and oxygen sensing.
Maran J; Prchal J
Pathol Biol (Paris); 2004 Jun; 52(5):280-4. PubMed ID: 15217714
[TBL] [Abstract][Full Text] [Related]
2. "Benign erythrocytosis" and other familial and congenital polycythemias.
Prchal JT; Sokol L
Eur J Haematol; 1996 Oct; 57(4):263-8. PubMed ID: 8982288
[TBL] [Abstract][Full Text] [Related]
3. Mutation in the negative regulatory element of the erythropoietin receptor gene in a case of sporadic primary polycythemia.
Sokol L; Prchal JF; D'Andrea A; Rado TA; Prchal JT
Exp Hematol; 1994 May; 22(5):447-53. PubMed ID: 8174675
[TBL] [Abstract][Full Text] [Related]
4. 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
Blood; 1997 Sep; 90(5):2057-61. PubMed ID: 9292543
[TBL] [Abstract][Full Text] [Related]
5. Erythropoietin-independent erythroid colony formation by bone marrow progenitors exposed to interleukin-11 and interleukin-8.
Corre-Buscail I; Pineau D; Boissinot M; Hermouet S
Exp Hematol; 2005 Nov; 33(11):1299-308. PubMed ID: 16263414
[TBL] [Abstract][Full Text] [Related]
6. 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; Prchal JT
Proc Assoc Am Physicians; 1997 Nov; 109(6):580-5. PubMed ID: 9394420
[TBL] [Abstract][Full Text] [Related]
7. Childhood polycythemias/erythrocytoses: classification, diagnosis, clinical presentation, and treatment.
Cario H
Ann Hematol; 2005 Mar; 84(3):137-45. PubMed ID: 15599750
[TBL] [Abstract][Full Text] [Related]
8. Lessons from familial myeloproliferative disorders.
Skoda R; Prchal JT
Semin Hematol; 2005 Oct; 42(4):266-73. PubMed ID: 16210040
[TBL] [Abstract][Full Text] [Related]
9. Prediction of clinical course in patients with idiopathic erythrocytosis by endogenous erythroid colony assay but not by serum erythropoietin levels.
Shih LY; Lee CT; Ou YC
Exp Hematol; 1997 Apr; 25(4):288-92. PubMed ID: 9131002
[TBL] [Abstract][Full Text] [Related]
10. Endogenous erythroid colony assay in patients with polycythemia vera and its clinical significance.
Bai J; Shao ZH; Liu H; Shi J; He GS; Cao YR; Cui ZZ; Wu YH; Sun J; Tian Z; Jia HR; Qian LS; Yang TY; Yang CL
Chin Med J (Engl); 2004 May; 117(5):668-72. PubMed ID: 15161531
[TBL] [Abstract][Full Text] [Related]
11. [Polycythemia: primary or secondary? The differential diagnostic value of stem cell cultures].
Küng C; Huxol H; Müller R; Speck B; Nissen C
Schweiz Med Wochenschr; 1993 Jan; 123(3):53-6. PubMed ID: 8426948
[TBL] [Abstract][Full Text] [Related]
12. Multiple signaling pathways are involved in erythropoietin-independent differentiation of erythroid progenitors in polycythemia vera.
Ugo V; Marzac C; Teyssandier I; Larbret F; Lécluse Y; Debili N; Vainchenker W; Casadevall N
Exp Hematol; 2004 Feb; 32(2):179-87. PubMed ID: 15102479
[TBL] [Abstract][Full Text] [Related]
13. Congenital polycythemias/erythrocytoses.
Gordeuk VR; Stockton DW; Prchal JT
Haematologica; 2005 Jan; 90(1):109-16. PubMed ID: 15642677
[TBL] [Abstract][Full Text] [Related]
14. Erythropoietin hypersensitivity in primary familial and congenital polycythemia: role of tyrosines Y285 and Y344 in erythropoietin receptor cytoplasmic domain.
Arcasoy MO; Karayal AF
Biochim Biophys Acta; 2005 Apr; 1740(1):17-28. PubMed ID: 15878737
[TBL] [Abstract][Full Text] [Related]
15. In vitro erythropoiesis in polycythemia vera and other myeloproliferative disorders.
Weinberg RS
Semin Hematol; 1997 Jan; 34(1):64-9. PubMed ID: 9025164
[TBL] [Abstract][Full Text] [Related]
16. The gene encoding hematopoietic cell phosphatase (SHP-1) is structurally and transcriptionally intact in polycythemia vera.
Asimakopoulos FA; Hinshelwood S; Gilbert JG; Delibrias CC; Göttgens B; Fearon DT; Green AR
Oncogene; 1997 Mar; 14(10):1215-22. PubMed ID: 9121771
[TBL] [Abstract][Full Text] [Related]
17. 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
J Clin Invest; 1998 Jul; 102(1):124-9. PubMed ID: 9649565
[TBL] [Abstract][Full Text] [Related]
18. The complete evaluation of erythrocytosis: congenital and acquired.
Patnaik MM; Tefferi A
Leukemia; 2009 May; 23(5):834-44. PubMed ID: 19295544
[TBL] [Abstract][Full Text] [Related]
19. Erythroid cultures and erythropoietin assay. Clinical and diagnostic value.
Casadevall N; Lacombe C; Varet B
Nouv Rev Fr Hematol (1978); 1990; 32(1):77-81. PubMed ID: 2112239
[TBL] [Abstract][Full Text] [Related]
20. Molecular study of congenital erythrocytosis in 70 unrelated patients revealed a potential causal mutation in less than half of the cases (Where is/are the missing gene(s)?).
Bento C; Almeida H; Maia TM; Relvas L; Oliveira AC; Rossi C; Girodon F; Fernandez-Lago C; Aguado-Diaz A; Fraga C; Costa RM; Araújo AL; Silva J; Vitória H; Miguel N; Silveira MP; Martin-Nuñez G; Ribeiro ML
Eur J Haematol; 2013 Oct; 91(4):361-8. PubMed ID: 23859443
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]