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22. Prevalence, clinical characteristics, and prognosis of GATA2-related myelodysplastic syndromes in children and adolescents. Wlodarski MW; Hirabayashi S; Pastor V; Starý J; Hasle H; Masetti R; Dworzak M; Schmugge M; van den Heuvel-Eibrink M; Ussowicz M; De Moerloose B; Catala A; Smith OP; Sedlacek P; Lankester AC; Zecca M; Bordon V; Matthes-Martin S; Abrahamsson J; Kühl JS; Sykora KW; Albert MH; Przychodzien B; Maciejewski JP; Schwarz S; Göhring G; Schlegelberger B; Cseh A; Noellke P; Yoshimi A; Locatelli F; Baumann I; Strahm B; Niemeyer CM; Blood; 2016 Mar; 127(11):1387-97; quiz 1518. PubMed ID: 26702063 [TBL] [Abstract][Full Text] [Related]
23. Loss of B cells and their precursors is the most constant feature of GATA-2 deficiency in childhood myelodysplastic syndrome. Nováková M; Žaliová M; Suková M; Wlodarski M; Janda A; Froňková E; Campr V; Lejhancová K; Zapletal O; Pospíšilová D; Černá Z; Kuhn T; Švec P; Pelková V; Zemanová Z; Kerndrup G; van den Heuvel-Eibrink M; van der Velden V; Niemeyer C; Kalina T; Trka J; Starý J; Hrušák O; Mejstříková E Haematologica; 2016 Jun; 101(6):707-16. PubMed ID: 27013649 [TBL] [Abstract][Full Text] [Related]
24. MDS-associated mutations in germline GATA2 mutated patients with hematologic manifestations. McReynolds LJ; Yang Y; Yuen Wong H; Tang J; Zhang Y; Mulé MP; Daub J; Palmer C; Foruraghi L; Liu Q; Zhu J; Wang W; West RR; Yohe ME; Hsu AP; Hickstein DD; Townsley DM; Holland SM; Calvo KR; Hourigan CS Leuk Res; 2019 Jan; 76():70-75. PubMed ID: 30578959 [TBL] [Abstract][Full Text] [Related]
25. GATA2 mutation in long stand Mycobacterium kansasii infection, myelodysplasia and MonoMAC syndrome: a case-report. Mendes-de-Almeida DP; Andrade FG; Borges G; Dos Santos-Bueno FV; Vieira IF; da Rocha LKMDS; Mendes-da-Cruz DA; Zancopé-Oliveira RM; Calado RT; Pombo-de-Oliveira MS BMC Med Genet; 2019 Apr; 20(1):64. PubMed ID: 31035956 [TBL] [Abstract][Full Text] [Related]
26. Connecting the Dots From Fever of Unknown Origin to Myelodysplastic Syndrome: GATA2 Haploinsufficiency. Montiel-Esparza R; Reys B; Rogers ZR; Evans AS; Wysocki CA; Timmons C; Dickerson KE J Pediatr Hematol Oncol; 2020 Jul; 42(5):e365-e368. PubMed ID: 31033783 [TBL] [Abstract][Full Text] [Related]
27. Mutational profiling of a MonoMAC syndrome family with GATA2 deficiency. Ding LW; Ikezoe T; Tan KT; Mori M; Mayakonda A; Chien W; Lin DC; Jiang YY; Lill M; Yang H; Sun QY; Koeffler HP Leukemia; 2017 Jan; 31(1):244-245. PubMed ID: 27680514 [No Abstract] [Full Text] [Related]
28. Fifty Shades of GATA2 Mutation: A Case of Plasmablastic Lymphoma, Nontuberculous Mycobacterial Infection, and Myelodysplastic Syndrome. Fakhri B; Cashen AF; Duncavage EJ; Watkins MP; Wartman LD; Bartlett NL Clin Lymphoma Myeloma Leuk; 2019 Sep; 19(9):e532-e535. PubMed ID: 31279773 [No Abstract] [Full Text] [Related]
29. A case of GATA2-related myelodysplastic syndrome with unbalanced translocation der(1;7)(q10;p10). Kurata T; Shigemura T; Muramatsu H; Okuno Y; Nakazawa Y Pediatr Blood Cancer; 2017 Aug; 64(8):. PubMed ID: 28066994 [No Abstract] [Full Text] [Related]
30. [Clinical and genetic background of familial myelodysplasia and acute myeloid leukemia]. Király PA; Kállay K; Marosvári D; Benyó G; Szőke A; Csomor J; Bödör C Orv Hetil; 2016 Feb; 157(8):283-9. PubMed ID: 26876264 [TBL] [Abstract][Full Text] [Related]
31. Monozygotic twins with shared de novo GATA2 mutation but dissimilar phenotypes due to differential promoter methylation. Kim N; Choi S; Kim SM; Lee AC; Im K; Park HS; Kim JA; Kim K; Kim I; Chang YH; Lee DS Leuk Lymphoma; 2019 Apr; 60(4):1053-1061. PubMed ID: 30714451 [TBL] [Abstract][Full Text] [Related]