100 related articles for article (PubMed ID: 8790601)
1. Clonal hematopoiesis and acquired thalassemia in common variable immunodeficiency.
Belickova M; Schroeder HW; Guan YL; Brierre J; Berney S; Cooper MD; Prchal JT
Mol Med; 1994 Nov; 1(1):56-61. PubMed ID: 8790601
[TBL] [Abstract][Full Text] [Related]
2. High prevalence of hemoglobin disorders and glucose-6-phosphate dehydrogenase (G6PD) deficiency in the Republic of Guinea (West Africa).
Millimono TS; Loua KM; Rath SL; Relvas L; Bento C; Diakite M; Jarvis M; Daries N; Ribeiro LM; Manco L; Kaeda JS
Hemoglobin; 2012; 36(1):25-37. PubMed ID: 21929367
[TBL] [Abstract][Full Text] [Related]
3. Aberrant X chromosome skewing and acquired clonal hematopoiesis in adult-onset common variable immunodeficiency.
Wong GK; Barmettler S; Heather JM; Millar D; Penny SA; Huissoon A; Richter A; Cobbold M
JCI Insight; 2019 Jul; 4(14):. PubMed ID: 31341110
[TBL] [Abstract][Full Text] [Related]
4. Hemoglobin messenger RNA from human bone marrow. Isolation and translation in homozygous and heterozygous beta-thalassemia.
Nienhuis AW; Canfield PH; Anderson WF
J Clin Invest; 1973 Jul; 52(7):1735-45. PubMed ID: 4718962
[TBL] [Abstract][Full Text] [Related]
5. Defective IL-4 signaling in T cells defines severe common variable immunodeficiency.
Taraldsrud E; Fevang B; Jørgensen SF; Moltu K; Hilden V; Taskén K; Aukrust P; Myklebust JH; Olweus J
J Autoimmun; 2017 Jul; 81():110-119. PubMed ID: 28476239
[TBL] [Abstract][Full Text] [Related]
6. Late-onset combined immune deficiency: a subset of common variable immunodeficiency with severe T cell defect.
Malphettes M; Gérard L; Carmagnat M; Mouillot G; Vince N; Boutboul D; Bérezné A; Nove-Josserand R; Lemoing V; Tetu L; Viallard JF; Bonnotte B; Pavic M; Haroche J; Larroche C; Brouet JC; Fermand JP; Rabian C; Fieschi C; Oksenhendler E;
Clin Infect Dis; 2009 Nov; 49(9):1329-38. PubMed ID: 19807277
[TBL] [Abstract][Full Text] [Related]
7. Translation of -globin m-RNA in -thalassemia and the S and C hemoglobinopathies.
Rieder RF
J Clin Invest; 1972 Feb; 51(2):364-72. PubMed ID: 5009120
[TBL] [Abstract][Full Text] [Related]
8. Further evidence of a quantitative deficiency of chain-specific globin mRNA in the thalassemia syndromes.
Kazazian HH; Ginder GD; Snyder PG; Van Beneden RJ; Woodhead AP
Proc Natl Acad Sci U S A; 1975 Feb; 72(2):567-71. PubMed ID: 1054838
[TBL] [Abstract][Full Text] [Related]
9. Gene regulation in hematopoiesis: new lessons from thalassemia.
Higgs DR
Hematology Am Soc Hematol Educ Program; 2004; ():1-13. PubMed ID: 15561673
[TBL] [Abstract][Full Text] [Related]
10. Common variable immunodeficiency: the immune system in chaos.
Bayry J; Hermine O; Webster DA; Lévy Y; Kaveri SV
Trends Mol Med; 2005 Aug; 11(8):370-6. PubMed ID: 15996517
[TBL] [Abstract][Full Text] [Related]
11. Autoimmunity and infection in common variable immunodeficiency (CVID).
Patuzzo G; Barbieri A; Tinazzi E; Veneri D; Argentino G; Moretta F; Puccetti A; Lunardi C
Autoimmun Rev; 2016 Sep; 15(9):877-82. PubMed ID: 27392505
[TBL] [Abstract][Full Text] [Related]
12. Erythroid marrow activity and functional anemia in patients with the rare interaction of a single functional a-globin and beta-globin gene.
Traeger-Synodinos J; Papassotiriou I; Vrettou C; Skarmoutsou C; Stamoulakatou A; Kanavakis E
Haematologica; 2001 Apr; 86(4):363-7. PubMed ID: 11325640
[TBL] [Abstract][Full Text] [Related]
13. Genetic patterns in thalassemia intermedia (constitutional microcytic anemia). Familial, hematologic and biosynthetic studies.
Bianco I; Graziani B; Carboni C
Hum Hered; 1977; 27(4):257-72. PubMed ID: 892805
[TBL] [Abstract][Full Text] [Related]
14. Concurrent sickle-cell anemia and alpha-thalassemia: effect on severity of anemia.
Embury SH; Dozy AM; Miller J; Davis JR; Kleman KM; Preisler H; Vichinsky E; Lande WN; Lubin BH; Kan YW; Mentzer WC
N Engl J Med; 1982 Feb; 306(5):270-4. PubMed ID: 6172710
[TBL] [Abstract][Full Text] [Related]
15. Clonal and constricted T cell repertoire in Common Variable Immune Deficiency.
Ramesh M; Hamm D; Simchoni N; Cunningham-Rundles C
Clin Immunol; 2017 May; 178():1-9. PubMed ID: 25596453
[TBL] [Abstract][Full Text] [Related]
16. Genetic modifiers of sickle cell anemia in the BABY HUG cohort: influence on laboratory and clinical phenotypes.
Sheehan VA; Luo Z; Flanagan JM; Howard TA; Thompson BW; Wang WC; Kutlar A; Ware RE;
Am J Hematol; 2013 Jul; 88(7):571-6. PubMed ID: 23606168
[TBL] [Abstract][Full Text] [Related]
17. [Successful cord blood transplantation in a patient with adult-onset common variable immunodeficiency].
Harutani Y; Tamura S; Kobata H; Oiwa T; Yamashita Y; Mushino T; Hosoi H; Murata S; Nishikawa A; Imai K; Morio T; Sonoki T
Rinsho Ketsueki; 2018; 59(3):293-299. PubMed ID: 29618687
[TBL] [Abstract][Full Text] [Related]
18. Common variable immunodeficiency: test indications and interpretations.
Weiler CR; Bankers-Fulbright JL
Mayo Clin Proc; 2005 Sep; 80(9):1187-200. PubMed ID: 16178499
[TBL] [Abstract][Full Text] [Related]
19. Chromosomal radiosensitivity in patients with common variable immunodeficiency.
Aghamohammadi A; Moin M; Kouhi A; Mohagheghi MA; Shirazi A; Rezaei N; Tavassoli S; Esfahani M; Cheraghi T; Dastan J; Nersesian J; Ghaffari SR
Immunobiology; 2008; 213(5):447-54. PubMed ID: 18472053
[TBL] [Abstract][Full Text] [Related]
20. A short-term trial of butyrate to stimulate fetal-globin-gene expression in the beta-globin disorders.
Perrine SP; Ginder GD; Faller DV; Dover GH; Ikuta T; Witkowska HE; Cai SP; Vichinsky EP; Olivieri NF
N Engl J Med; 1993 Jan; 328(2):81-6. PubMed ID: 7677966
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]