These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

128 related articles for article (PubMed ID: 35843247)

  • 61. 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]  

  • 62. Breaking the spatial constraint between neighboring zinc fingers: a new germline mutation in GATA2 deficiency syndrome.
    Cavalcante de Andrade Silva M; Katsumura KR; Mehta C; Velloso EDRP; Bresnick EH; Godley LA
    Leukemia; 2021 Jan; 35(1):264-268. PubMed ID: 32286542
    [No Abstract]   [Full Text] [Related]  

  • 63. CENTRAL RETINAL VEIN OCCLUSION IN GATA2 DEFICIENCY.
    Berry D; Fekrat S
    Retin Cases Brief Rep; 2019 Spring; 13(2):181-184. PubMed ID: 28248742
    [TBL] [Abstract][Full Text] [Related]  

  • 64. Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome).
    Ostergaard P; Simpson MA; Connell FC; Steward CG; Brice G; Woollard WJ; Dafou D; Kilo T; Smithson S; Lunt P; Murday VA; Hodgson S; Keenan R; Pilz DT; Martinez-Corral I; Makinen T; Mortimer PS; Jeffery S; Trembath RC; Mansour S
    Nat Genet; 2011 Sep; 43(10):929-31. PubMed ID: 21892158
    [TBL] [Abstract][Full Text] [Related]  

  • 65. GATA2 deficiency in a patient with a somatic mutation of GATA2.
    Liu Q; Ju X; Peng H
    QJM; 2024 Feb; 117(1):66-68. PubMed ID: 37802913
    [No Abstract]   [Full Text] [Related]  

  • 66. Hematopoietic stem cell transplantation in children and adolescents with GATA2-related myelodysplastic syndrome.
    Bortnick R; Wlodarski M; de Haas V; De Moerloose B; Dworzak M; Hasle H; Masetti R; Starý J; Turkiewicz D; Ussowicz M; Kozyra E; Albert M; Bader P; Bordon V; Cario G; Beier R; Schulte J; Bresters D; Müller I; Pichler H; Sedlacek P; Sauer MG; Zecca M; Göhring G; Yoshimi A; Noellke P; Erlacher M; Locatelli F; Niemeyer CM; Strahm B;
    Bone Marrow Transplant; 2021 Nov; 56(11):2732-2741. PubMed ID: 34244664
    [TBL] [Abstract][Full Text] [Related]  

  • 67. MonoMAC Syndrome Caused by a Novel GATA2 Mutation Successfully Treated by Allogeneic Hematopoietic Stem Cell Transplantation.
    Moraes-Fontes MF; Caramalho Í; Hsu AP; Holland SM; Abecasis M
    J Clin Immunol; 2019 Jan; 39(1):4-6. PubMed ID: 30478525
    [No Abstract]   [Full Text] [Related]  

  • 68. Clinical and biological characteristics and prognostic impact of somatic GATA2 mutations in myeloid malignancies: a single institution experience.
    Nanaa A; Viswanatha D; Xie Z; Jevremovic D; Nguyen P; Salama ME; Greipp P; Bessonen K; Gangat N; Patnaik M; Pardanani A; Alkhateeb HB; Shah M; Hogan W; Tefferi A; Litzow M; He R; Al-Kali A
    Blood Cancer J; 2021 Jun; 11(6):122. PubMed ID: 34193836
    [No Abstract]   [Full Text] [Related]  

  • 69. GATA2 deficiency associated with copy number variation: A reference for considering inborn errors of immunity.
    Freeman CM; Barry TD; Bauer CS; Miller HK; Rukasin CR; Wright BL
    J Allergy Clin Immunol Pract; 2022 Sep; 10(9):2476-2478.e9. PubMed ID: 35654370
    [No Abstract]   [Full Text] [Related]  

  • 70. Heritable GATA2 mutations associated with familial myelodysplastic syndrome and acute myeloid leukemia.
    Hahn CN; Chong CE; Carmichael CL; Wilkins EJ; Brautigan PJ; Li XC; Babic M; Lin M; Carmagnac A; Lee YK; Kok CH; Gagliardi L; Friend KL; Ekert PG; Butcher CM; Brown AL; Lewis ID; To LB; Timms AE; Storek J; Moore S; Altree M; Escher R; Bardy PG; Suthers GK; D'Andrea RJ; Horwitz MS; Scott HS
    Nat Genet; 2011 Sep; 43(10):1012-7. PubMed ID: 21892162
    [TBL] [Abstract][Full Text] [Related]  

  • 71. A Nationwide Study of GATA2 Deficiency in Norway-the Majority of Patients Have Undergone Allo-HSCT.
    Jørgensen SF; Buechner J; Myhre AE; Galteland E; Spetalen S; Kulseth MA; Sorte HS; Holla ØL; Lundman E; Alme C; Heier I; Flægstad T; Fløisand Y; Benneche A; Fevang B; Aukrust P; Stray-Pedersen A; Gedde-Dahl T; Nordøy I
    J Clin Immunol; 2022 Feb; 42(2):404-420. PubMed ID: 34893945
    [TBL] [Abstract][Full Text] [Related]  

  • 72. Transcription factors implicated in late megakaryopoiesis as markers of outcome after azacitidine and allogeneic stem cell transplantation in myelodysplastic syndrome.
    Falconi G; Fabiani E; Criscuolo M; Fianchi L; Finelli C; Cerqui E; Pelosi E; Screnci M; Gurnari C; Zangrilli I; Postorino M; Laurenti L; Piciocchi A; Testa U; Lo-Coco F; Voso MT
    Leuk Res; 2019 Sep; 84():106191. PubMed ID: 31386932
    [TBL] [Abstract][Full Text] [Related]  

  • 73. Comparison of Outcomes of Myeloablative Allogeneic Stem Cell Transplantation for Pediatric Patients with Bone Marrow Failure, Myelodysplastic Syndrome and Acute Myeloid Leukemia with and without Germline GATA2 Mutations.
    Hofmann I; Avagyan S; Stetson A; Guo D; Al-Sayegh H; London WB; Lehmann L
    Biol Blood Marrow Transplant; 2020 Jun; 26(6):1124-1130. PubMed ID: 32088370
    [TBL] [Abstract][Full Text] [Related]  

  • 74. [MonoMAC syndrome patient developing myelodysplastic syndrome following persistent EBV infection].
    Yamamoto H; Hattori H; Takagi E; Morishita T; Ishikawa Y; Terakura S; Nishida T; Ito Y; Murata M; Kiyoi H
    Rinsho Ketsueki; 2018; 59(3):315-322. PubMed ID: 29618691
    [TBL] [Abstract][Full Text] [Related]  

  • 75. Folliculotropic mycosis fungoides associated with GATA2 deficiency: a new skin manifestation.
    Fertitta L; Fontbrune FS; Battistella M; De Masson A; Bergeron A; Ranta D; Vignon-Pennamen MD; Bagot M; Bouaziz JD
    Br J Dermatol; 2018 Dec; 179(6):1420-1421. PubMed ID: 30101490
    [No Abstract]   [Full Text] [Related]  

  • 76. Primary Lymphedema and Viral Warts in GATA2 Haploinsufficiency.
    Perez Botero J; Rodriguez V
    Mayo Clin Proc; 2017 Mar; 92(3):482. PubMed ID: 28259234
    [No Abstract]   [Full Text] [Related]  

  • 77. Prevalence of germline GATA2 and SAMD9/9L variants in paediatric haematological disorders with monosomy 7.
    Yoshida M; Tanase-Nakao K; Shima H; Shirai R; Yoshida K; Osumi T; Deguchi T; Mori M; Arakawa Y; Takagi M; Miyamura T; Sakaguchi K; Toyoda H; Ishida H; Sakata N; Imamura T; Kawahara Y; Morimoto A; Koike T; Yagasaki H; Ito S; Tomizawa D; Kiyokawa N; Narumi S; Kato M
    Br J Haematol; 2020 Dec; 191(5):835-843. PubMed ID: 32770553
    [TBL] [Abstract][Full Text] [Related]  

  • 78. Marked genetic heterogeneity in familial myelodysplasia/acute myeloid leukaemia.
    Holme H; Hossain U; Kirwan M; Walne A; Vulliamy T; Dokal I
    Br J Haematol; 2012 Jul; 158(2):242-248. PubMed ID: 22533337
    [TBL] [Abstract][Full Text] [Related]  

  • 79. Successful umbilical cord blood hematopoietic stem cell transplantation in pediatric patients with MDS/AML associated with underlying GATA2 mutations: two case reports and review of literature.
    Mallhi K; Dix DB; Niederhoffer KY; Armstrong L; Rozmus J
    Pediatr Transplant; 2016 Nov; 20(7):1004-1007. PubMed ID: 27416790
    [TBL] [Abstract][Full Text] [Related]  

  • 80. Disseminated Mycosis by Arthrocladium fulminans Jeopardizing a Patient with GATA2 Deficiency.
    Egenlauf B; Schuhmann M; Giese T; Junghanss T; Stojkovic M; Tintelnot K; de Hoog S; Greil J; Richter E; Vehresschild M; Heussel CP; Herth FJF; Kreuter M
    Respiration; 2019; 97(5):472-475. PubMed ID: 30928982
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.