408 related articles for article (PubMed ID: 19295544)
21. Algorithmic evaluation of hereditary erythrocytosis: Pathways and caveats.
Oliveira JL
Int J Lab Hematol; 2019 May; 41 Suppl 1():89-94. PubMed ID: 31069987
[TBL] [Abstract][Full Text] [Related]
22. Congenital erythrocytosis with elevated erythropoietin level: an incorrectly set "erythrostat"?
Manglani MV; DeGroff CG; Dukes PP; Ettinger LJ
J Pediatr Hematol Oncol; 1998; 20(6):560-2. PubMed ID: 9856679
[TBL] [Abstract][Full Text] [Related]
23. Mutations in the von Hippel-Lindau (VHL) tumor suppressor gene and VHL-haplotype analysis in patients with presumable congenital erythrocytosis.
Cario H; Schwarz K; Jorch N; Kyank U; Petrides PE; Schneider DT; Uhle R; Debatin KM; Kohne E
Haematologica; 2005 Jan; 90(1):19-24. PubMed ID: 15642664
[TBL] [Abstract][Full Text] [Related]
24. Determination of serum immunoreactive erythropoietin in the investigation of erythrocytosis.
Cotes PM; Doré CJ; Yin JA; Lewis SM; Messinezy M; Pearson TC; Reid C
N Engl J Med; 1986 Jul; 315(5):283-7. PubMed ID: 3724821
[TBL] [Abstract][Full Text] [Related]
25. Congenital polycythemias/erythrocytoses.
Gordeuk VR; Stockton DW; Prchal JT
Haematologica; 2005 Jan; 90(1):109-16. PubMed ID: 15642677
[TBL] [Abstract][Full Text] [Related]
26. 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]
27. [Systematic diagnosis of erythrocytosis].
de Heer K; Silbermann MH; Koene HR; Biemond BJ; Muller HP; van Oers MH
Ned Tijdschr Geneeskd; 2007 Aug; 151(32):1770-6. PubMed ID: 17822247
[TBL] [Abstract][Full Text] [Related]
28. Congenital erythrocytosis and polycythemia vera in childhood and adolescence.
Cario H; Schwarz K; Debatin KM; Kohne E
Klin Padiatr; 2004; 216(3):157-62. PubMed ID: 15175960
[TBL] [Abstract][Full Text] [Related]
29. The role of a low erythropoietin level for the polycythemia vera diagnosis.
Lupak O; Han X; Xie P; Mahmood S; Mohammed H; Donthireddy V
Blood Cells Mol Dis; 2020 Feb; 80():102355. PubMed ID: 31525610
[TBL] [Abstract][Full Text] [Related]
30. rs779805 Von Hippel-Lindau Gene Polymorphism Induced/Related Polycythemia Entity, Clinical Features, Cancer Association, and Familiar Characteristics.
Remenyi G; Bereczky Z; Gindele R; Ujfalusi A; Illes A; Udvardy M
Pathol Oncol Res; 2021; 27():1609987. PubMed ID: 34899081
[TBL] [Abstract][Full Text] [Related]
31. Genetic basis of congenital erythrocytosis: mutation update and online databases.
Bento C; Percy MJ; Gardie B; Maia TM; van Wijk R; Perrotta S; Della Ragione F; Almeida H; Rossi C; Girodon F; Aström M; Neumann D; Schnittger S; Landin B; Minkov M; Randi ML; Richard S; Casadevall N; Vainchenker W; Rives S; Hermouet S; Ribeiro ML; McMullin MF; Cario H; ; Chauveau A; Gimenez-Roqueplo AP; Bressac-de-Paillerets B; Altindirek D; Lorenzo F; Lambert F; Dan H; Gad-Lapiteau S; Catarina Oliveira A; Rossi C; Fraga C; Taradin G; Martin-Nuñez G; Vitória H; Diaz Aguado H; Palmblad J; Vidán J; Relvas L; Ribeiro ML; Luigi Larocca M; Luigia Randi M; Pedro Silveira M; Percy M; Gross M; Marques da Costa R; Beshara S; Ben-Ami T; Ugo V;
Hum Mutat; 2014 Jan; 35(1):15-26. PubMed ID: 24115288
[TBL] [Abstract][Full Text] [Related]
32. The JAK2 V617F mutation is absent in patients with erythrocytosis due to high oxygen affinity hemoglobin variants.
McClure RF; Hoyer JD; Mai M
Hemoglobin; 2006; 30(4):487-9. PubMed ID: 16987804
[TBL] [Abstract][Full Text] [Related]
33. The clinical and laboratory evaluation of the patient with erythrocytosis.
Lee G; Arcasoy MO
Eur J Intern Med; 2015 Jun; 26(5):297-302. PubMed ID: 25837692
[TBL] [Abstract][Full Text] [Related]
34. Loss of the JAK2 intramolecular auto-inhibition mechanism is predicted by structural modelling of a novel exon 12 insertion mutation in a case of idiopathic erythrocytosis.
Albiero E; Madeo D; Ruggeri M; Bernardi M; Giorgetti A; Rodeghiero F
Br J Haematol; 2008 Sep; 142(6):986-90. PubMed ID: 18671703
[TBL] [Abstract][Full Text] [Related]
35. Secondary Hypertension, Erythrocytosis, and Unilateral Renal Cystic Disease in a Submariner: A Case Report.
Forbes AS; Yeo FE
J Spec Oper Med; 2016; 16(4):1-5. PubMed ID: 28088811
[TBL] [Abstract][Full Text] [Related]
36. Erythrocytosis: Diagnosis and investigation.
Noumani I; Harrison CN; McMullin MF
Int J Lab Hematol; 2024 May; 46 Suppl 1():55-62. PubMed ID: 38695361
[TBL] [Abstract][Full Text] [Related]
37. Genetic basis of congenital erythrocytosis.
Bento C
Int J Lab Hematol; 2018 May; 40 Suppl 1():62-67. PubMed ID: 29741264
[TBL] [Abstract][Full Text] [Related]
38. 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]
39. Hereditary gene mutations in Korean patients with isolated erythrocytosis.
Jang JH; Seo JY; Jang J; Jung CW; Lee KO; Kim SH; Kim HJ
Ann Hematol; 2014 Jun; 93(6):931-5. PubMed ID: 24482100
[TBL] [Abstract][Full Text] [Related]
40. Prevalence and clinicopathologic correlates of JAK2 exon 12 mutations in JAK2V617F-negative polycythemia vera.
Pardanani A; Lasho TL; Finke C; Hanson CA; Tefferi A
Leukemia; 2007 Sep; 21(9):1960-3. PubMed ID: 17597810
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]