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 *

119 related articles for article (PubMed ID: 23128329)

  • 21. Co-inheritance of compound heterozygous Hb Constant Spring and a single -alpha(3.7) gene deletion with heterozygous deltabeta thalassaemia: a diagnostic challenge.
    Azma RZ; Othman A; Azman N; Alauddin H; Ithnin A; Yusof N; Razak NF; Sardi NH; Hussin NH
    Malays J Pathol; 2012 Jun; 34(1):57-62. PubMed ID: 22870600
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Characterization of a novel β-globin gene cluster deletion causing (
    Wu MY; Li J; Yan JM; Zhang Y; Li DZ
    Int J Lab Hematol; 2017 Feb; 39(1):e19-e22. PubMed ID: 27997753
    [No Abstract]   [Full Text] [Related]  

  • 23. 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]  

  • 24. Severe fetal and neonatal hemolytic anemia due to a 198 kb deletion removing the complete β-globin gene cluster.
    Verhovsek M; Shah NR; Wilcox I; Koenig SC; Barros T; Thornburg CD; Steinberg MH; Luo HY; Chui DH
    Pediatr Blood Cancer; 2012 Nov; 59(5):941-4. PubMed ID: 22294483
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Infantile pyknocytosis: an under-recognized form of neonatal hemolytic anemia?
    Coutinho M; Costa E; Monteiro T; Silva G; Costa H; Guedes A; Freitas I; Barbot J
    Lab Hematol; 2012 Dec; 18(4):27-9. PubMed ID: 23253864
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Infantile Pyknocytosis: An Uncommon Cause of Newborn Hemolytic Anemia.
    Castillo J; Ness TE; Mehta PS
    J Pediatr Hematol Oncol; 2020 May; 42(4):e251-e253. PubMed ID: 30933020
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Clinical and molecular characterization of novel deletions causing epsilon gamma delta beta thalassemia: Report of two cases.
    Repnikova E; Roberts J; Mc Dermott S; Farooqi MS; Iqbal NT; Silvey M; Nolen J; Taboada E; Li W
    Pathol Res Pract; 2019 Oct; 215(10):152578. PubMed ID: 31451289
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Genotype-phenotype relationship of the δ-thalassemia and Hb A(2) variants: observation of 52 genotypes.
    Lacerra G; Scarano C; Lagona LF; Testa R; Caruso DG; Medulla E; Friscia MG; Mastrullo L; Caldora M; Prezioso R; Gaudiano C; Magnano C; Romeo MA; Musollino G; Di Noce F; Carestia C
    Hemoglobin; 2010; 34(5):407-23. PubMed ID: 20854114
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [A cause of post-natal anemia, urinary infection].
    Etienne M; Debauchez C; Caillet R
    Ann Pediatr (Paris); 1977; 24(6-7):503-10. PubMed ID: 16211932
    [No Abstract]   [Full Text] [Related]  

  • 30. Autoimmune hemolytic anemia in patients with β-thalassemia major.
    Xu LH; Fang JP; Weng WJ; Huang K; Zhang YT
    Pediatr Hematol Oncol; 2012 Apr; 29(3):235-40. PubMed ID: 22475299
    [TBL] [Abstract][Full Text] [Related]  

  • 31. A rare example that coinheritance of a severe form of beta-thalassemia and alpha-thalassemia interact in a "synergistic" manner to balance the phenotype of classic thalassemic syndromes.
    Kanavakis E; Traeger-Synodinos J; Lafioniatis S; Lazaropoulou C; Liakopoulou T; Paleologos G; Metaxotou-Mavrommati A; Stamoulakatou A; Papassotiriou I
    Blood Cells Mol Dis; 2004; 32(2):319-24. PubMed ID: 15003825
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Infantile pyknocytosis: a rare form of neonatal anemia.
    Kraus D; Yacobovich J; Hoffer V; Scheuerman O; Tamary H; Garty BZ
    Isr Med Assoc J; 2010 Mar; 12(3):188-9. PubMed ID: 20684190
    [No Abstract]   [Full Text] [Related]  

  • 33. [Hemolytic disease of the newborn and chronic hypochromic microcytic anemia in one family: gamma-delta-beta thalassemia].
    Oort M; Heerspink W; Roos D; Bernini LF
    Tijdschr Kindergeneeskd; 1981 Dec; 49(6):199-207. PubMed ID: 7330840
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Detection of unknown deletions in beta-globin gene cluster using relative quantitative PCR methods.
    Babashah S; Jamali S; Mahdian R; Nosaeid MH; Karimipoor M; Alimohammadi R; Raeisi M; Maryami F; Masoudifar M; Zeinali S
    Eur J Haematol; 2009 Sep; 83(3):261-9. PubMed ID: 19341428
    [TBL] [Abstract][Full Text] [Related]  

  • 35. High frequency of deletional alpha-thalassemia in beta-thalassemia trait: implications for genetic counseling.
    Panigrahi I; Rafeeq PH; Choudhry VP; Saxena R
    Am J Hematol; 2004 Jul; 76(3):297-9. PubMed ID: 15224373
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Use of capillary electrophoresis to determine hemoglobin A2 in healthy adults and alpha- and beta-thalassemia carriers].
    Hua L; Li J; Liu ZY; Zhong HZ; Liao C; Xu XM
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Oct; 20(5):421-4. PubMed ID: 14556197
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Hemolytic anemia in the newborn.
    Matsunaga AT; Lubin BH
    Clin Perinatol; 1995 Sep; 22(3):803-28. PubMed ID: 8521694
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Infantile pyknocytosis: a rare form of neonatal hemolytic anemia. 5 case-studies].
    Limme B; Dresse MF; Ketelslegers O; Rigo V; Hoyoux C
    Arch Pediatr; 2008 Dec; 15(12):1765-8. PubMed ID: 18995999
    [TBL] [Abstract][Full Text] [Related]  

  • 39. β-globin gene cluster haplotypes in a cohort of 221 children with sickle cell anemia or Sβ⁰-thalassemia and their association with clinical and hematological features.
    Belisário AR; Martins ML; Brito AM; Rodrigues CV; Silva CM; Viana MB
    Acta Haematol; 2010; 124(3):162-70. PubMed ID: 20938172
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Blueberry muffin rash, hyperbilirubinemia, and hypoglycemia: a case of hemolytic disease of the fetus and newborn due to anti-Kp(a).
    Brumbaugh JE; Morgan S; Beck JC; Zantek N; Kearney S; Bendel CM; Roberts KD
    J Perinatol; 2011 May; 31(5):373-6. PubMed ID: 21525882
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.