205 related articles for article (PubMed ID: 31132167)
21. Congenital polycythemia with homozygous and heterozygous mutations of von Hippel-Lindau gene: five new Caucasian patients.
Bento MC; Chang KT; Guan Y; Liu E; Caldas G; Gatti RA; Prchal JT
Haematologica; 2005 Jan; 90(1):128-9. PubMed ID: 15642680
[TBL] [Abstract][Full Text] [Related]
22. Chuvash-type congenital polycythemia in 4 families of Asian and Western European ancestry.
Percy MJ; McMullin MF; Jowitt SN; Potter M; Treacy M; Watson WH; Lappin TR
Blood; 2003 Aug; 102(3):1097-9. PubMed ID: 12702509
[TBL] [Abstract][Full Text] [Related]
23. The worldwide distribution of the VHL 598C>T mutation indicates a single founding event.
Liu E; Percy MJ; Amos CI; Guan Y; Shete S; Stockton DW; McMullin MF; Polyakova LA; Ang SO; Pastore YD; Jedlickova K; Lappin TR; Gordeuk V; Prchal JT
Blood; 2004 Mar; 103(5):1937-40. PubMed ID: 14604959
[TBL] [Abstract][Full Text] [Related]
24. 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]
25. Disruption of oxygen homeostasis underlies congenital Chuvash polycythemia.
Ang SO; Chen H; Hirota K; Gordeuk VR; Jelinek J; Guan Y; Liu E; Sergueeva AI; Miasnikova GY; Mole D; Maxwell PH; Stockton DW; Semenza GL; Prchal JT
Nat Genet; 2002 Dec; 32(4):614-21. PubMed ID: 12415268
[TBL] [Abstract][Full Text] [Related]
26. Erythrocytosis associated with
Gangat N; Oliveira JL; Porter TR; Hoyer JD; Al-Kali A; Patnaik MM; Pardanani A; Tefferi A
Haematologica; 2022 May; 107(5):1201-1204. PubMed ID: 35142155
[No Abstract] [Full Text] [Related]
27. 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]
28. Novel High Oxygen Affinity Hemoglobin Variant in a Patient with Polycythemia: Hb Kennisis [β85(F1)Phe→Leu (TT
Nabhani IA; Aneke JC; Verhovsek M; Eng B; Kuo KHM; Rudinskas LC; Waye JS
Hemoglobin; 2020 Jan; 44(1):10-12. PubMed ID: 32151172
[TBL] [Abstract][Full Text] [Related]
29. 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]
30. An Additional Case of Hb Saint Nazaire [β103(G5)Phe→Ile;
Bobée V; Feugray G; Brunel V; Joly P; Lahary A
Hemoglobin; 2019 Jan; 43(1):50-51. PubMed ID: 30700173
[TBL] [Abstract][Full Text] [Related]
31. The phenotype of polycythemia due to Croatian homozygous VHL (571C>G:H191D) mutation is different from that of Chuvash polycythemia (VHL 598C>T:R200W).
Tomasic NL; Piterkova L; Huff C; Bilic E; Yoon D; Miasnikova GY; Sergueeva AI; Niu X; Nekhai S; Gordeuk V; Prchal JT
Haematologica; 2013 Apr; 98(4):560-7. PubMed ID: 23403324
[TBL] [Abstract][Full Text] [Related]
32. 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]
33. Decreased serum glucose and glycosylated hemoglobin levels in patients with Chuvash polycythemia: a role for HIF in glucose metabolism.
McClain DA; Abuelgasim KA; Nouraie M; Salomon-Andonie J; Niu X; Miasnikova G; Polyakova LA; Sergueeva A; Okhotin DJ; Cherqaoui R; Okhotin D; Cox JE; Swierczek S; Song J; Simon MC; Huang J; Simcox JA; Yoon D; Prchal JT; Gordeuk VR
J Mol Med (Berl); 2013 Jan; 91(1):59-67. PubMed ID: 23015148
[TBL] [Abstract][Full Text] [Related]
34. Ten Years of Routine α- and β-Globin Gene Sequencing in UK Hemoglobinopathy Referrals Reveals 60 Novel Mutations.
Henderson SJ; Timbs AT; McCarthy J; Gallienne AE; Proven M; Rugless MJ; Lopez H; Eglinton J; Dziedzic D; Beardsall M; Khalil MS; Old JM
Hemoglobin; 2016; 40(2):75-84. PubMed ID: 26635043
[TBL] [Abstract][Full Text] [Related]
35. Altered cytokine profiles in patients with Chuvash polycythemia.
Niu X; Miasnikova GY; Sergueeva AI; Polyakova LA; Okhotin DJ; Tuktanov NV; Nouraie M; Ammosova T; Nekhai S; Gordeuk VR
Am J Hematol; 2009 Feb; 84(2):74-8. PubMed ID: 19062180
[TBL] [Abstract][Full Text] [Related]
36. 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]
37. Genetic analysis of erythrocytosis reveals possible causative and modifier gene mutations.
Gurnari C; Lombardi AM; Cosi E; Biagetti G; Buccisano F; Franceschini L; Di Veroli A; Falconi G; Fabiani E; Cantonetti M; Nasso D; Lo-Coco F; Randi ML; Voso MT
Br J Haematol; 2019 Aug; 186(4):e100-e103. PubMed ID: 31016714
[No Abstract] [Full Text] [Related]
38. Hb Tarrant [α126(H9)Asp→Asn; HBA2: c.379G > A (or HBA1)] in a Chinese Family as a Cause of Familial Erythrocytosis.
Ip KL; So JC; Law MF; Wong RS; Tam HC; Ng MH
Hemoglobin; 2016 Aug; 40(4):260-3. PubMed ID: 27240426
[TBL] [Abstract][Full Text] [Related]
39. EPAS1 p.M535T mutation in a Bulgarian family with congenital erythrocytosis.
Alaikov T; Ivanova M; Shivarov V
Hematology; 2016 Dec; 21(10):619-622. PubMed ID: 27292716
[TBL] [Abstract][Full Text] [Related]
40. Congenital polycythemias/erythrocytoses.
Gordeuk VR; Stockton DW; Prchal JT
Haematologica; 2005 Jan; 90(1):109-16. PubMed ID: 15642677
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
