169 related articles for article (PubMed ID: 37428608)
1. Whole Exome Sequencing Reveals Novel Variants in Unexplained Erythrocytosis.
Khurana H; Muthusamy B; Yanamandra U; Garapati K; Premdeep H; Subramanian S; Pandey A
OMICS; 2023 Jul; 27(7):299-304. PubMed ID: 37428608
[TBL] [Abstract][Full Text] [Related]
2. Mutational Landscape of Patients Referred for Elevated Hemoglobin Level.
Bhai P; Chin-Yee B; Pope V; Cheong I; Matyashin M; Levy MA; Foroutan A; Stuart A; Hsia CC; Lin H; Sadikovic B; Chin-Yee I
Curr Oncol; 2022 Sep; 29(10):7209-7217. PubMed ID: 36290845
[No Abstract] [Full Text] [Related]
3. Phenotypic variations and new mutations in JAK2 V617F-negative polycythemia vera, erythrocytosis, and idiopathic myelofibrosis.
Williams DM; Kim AH; Rogers O; Spivak JL; Moliterno AR
Exp Hematol; 2007 Nov; 35(11):1641-6. PubMed ID: 17920755
[TBL] [Abstract][Full Text] [Related]
4. Genetic basis of unexplained erythrocytosis in Indian patients.
Mallik N; Sharma P; Kaur Hira J; Chhabra S; Sreedharanunni S; Kumar N; Naseem S; Sachdeva MUS; Ahluwalia J; Malhotra P; Varma N; Varma S; Das R
Eur J Haematol; 2019 Aug; 103(2):124-130. PubMed ID: 31132167
[TBL] [Abstract][Full Text] [Related]
5. Erythrocytosis: genes and pathways involved in disease development.
Gašperšič J; Kristan A; Kunej T; Zupan IP; Debeljak N
Blood Transfus; 2021 Nov; 19(6):518-532. PubMed ID: 33370224
[TBL] [Abstract][Full Text] [Related]
6. Diagnostic Approaches to Investigate JAK2-Unmutated Erythrocytosis Based on a Single Tertiary Center Experience.
Lee Y; Seo SH; Kim J; Kim SA; Lee JY; Lee JO; Bang SM; Park KU; Hwang SM
Mol Diagn Ther; 2024 May; 28(3):311-318. PubMed ID: 38568469
[TBL] [Abstract][Full Text] [Related]
7. The frequency of JAK2 exon 12 mutations in idiopathic erythrocytosis patients with low serum erythropoietin levels.
Percy MJ; Scott LM; Erber WN; Harrison CN; Reilly JT; Jones FG; Green AR; McMullin MF
Haematologica; 2007 Dec; 92(12):1607-14. PubMed ID: 18055983
[TBL] [Abstract][Full Text] [Related]
8. Germline JAK2 E846D Substitution as the Cause of Erythrocytosis?
Maaziz N; Garrec C; Airaud F; Bobée V; Contentin N; Cayssials E; Rimbert A; Aral B; Bézieau S; Gardie B; Girodon F
Genes (Basel); 2023 May; 14(5):. PubMed ID: 37239426
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. Detection of JAK2 exon 12 mutations in 15 patients with JAK2V617F negative polycythemia vera.
Schnittger S; Bacher U; Haferlach C; Geer T; Müller P; Mittermüller J; Petrides P; Schlag R; Sandner R; Selbach J; Slawik HR; Tessen HW; Wehmeyer J; Kern W; Haferlach T
Haematologica; 2009 Mar; 94(3):414-8. PubMed ID: 19252176
[TBL] [Abstract][Full Text] [Related]
12. Idiopathic erythrocytosis: a germline disease?
Elli EM; Mauri M; D'Aliberti D; Crespiatico I; Fontana D; Redaelli S; Pelucchi S; Spinelli S; Manghisi B; Cavalca F; Aroldi A; Ripamonti A; Ferrari S; Palamini S; Mottadelli F; Massimino L; Ramazzotti D; Cazzaniga G; Piperno A; Gambacorti-Passerini C; Piazza R
Clin Exp Med; 2024 Jan; 24(1):11. PubMed ID: 38244120
[TBL] [Abstract][Full Text] [Related]
13. JAK2 exon 12 mutations in polycythemia vera or idiopathic erythrocytosis.
Martínez-Avilés L; Besses C; Alvarez-Larrán A; Cervantes F; Hernández-Boluda JC; Bellosillo B
Haematologica; 2007 Dec; 92(12):1717-8. PubMed ID: 18056003
[TBL] [Abstract][Full Text] [Related]
14. Detection of low allele burden of JAK2 exon 12 mutations using TA-cloning in patients with erythrocytosis.
Ohyashiki JH; Hisatomi H; Shimizu S; Sugaya M; Ohyashiki K
Jpn J Clin Oncol; 2009 Aug; 39(8):509-13. PubMed ID: 19491085
[TBL] [Abstract][Full Text] [Related]
15. Characteristics of JAK2 unmutated erythrocytosis: Distinctive traits between polycythemia vera and non-polycythemia vera patients.
Ernest V; Abbou N; Tichadou A; Arcani R; Venton G
Eur J Intern Med; 2023 Jan; 107():113-115. PubMed ID: 36096924
[No Abstract] [Full Text] [Related]
16. Diagnostic Performance of Erythropoietin Levels in Polycythemia Vera: Experience at a Comprehensive Cancer Center.
Davila-Gonzalez D; Barrios-Ruiz A; Fountain E; Cheng L; Masarova L; Verstovsek S; Rojas-Hernandez CM
Clin Lymphoma Myeloma Leuk; 2021 Apr; 21(4):224-229. PubMed ID: 33349602
[TBL] [Abstract][Full Text] [Related]
17. JAK2 unmutated erythrocytosis: 2023 Update on diagnosis and management.
Gangat N; Szuber N; Tefferi A
Am J Hematol; 2023 Jun; 98(6):965-981. PubMed ID: 36966432
[TBL] [Abstract][Full Text] [Related]
18. Whole-exome sequencing identifies novel candidate predisposition genes for familial polycythemia vera.
Hirvonen EAM; Pitkänen E; Hemminki K; Aaltonen LA; Kilpivaara O
Hum Genomics; 2017 Apr; 11(1):6. PubMed ID: 28427458
[TBL] [Abstract][Full Text] [Related]
19. Identification of Variants Associated With Rare Hematological Disorder Erythrocytosis Using Targeted Next-Generation Sequencing Analysis.
Kristan A; Pajič T; Maver A; Režen T; Kunej T; Količ R; Vuga A; Fink M; Žula Š; Podgornik H; Anžej Doma S; Preložnik Zupan I; Rozman D; Debeljak N
Front Genet; 2021; 12():689868. PubMed ID: 34349782
[TBL] [Abstract][Full Text] [Related]
20. Identification of Two Novel
Lo Riso L; Vargas-Parra G; Navarro G; Arenillas L; Fernández-Ibarrondo L; Robredo B; Ballester C; López B; Perez-Montaña A; Sampol A; Florensa L; Besses C; Duran MA; Bellosillo B
Genes (Basel); 2022 Sep; 13(10):. PubMed ID: 36292571
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
