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 *

114 related articles for article (PubMed ID: 23128329)

  • 41. Pregnancy in patients with beta-thalassemia intermedia: outcome of mothers and newborns.
    Nassar AH; Usta IM; Rechdan JB; Koussa S; Inati A; Taher AT
    Am J Hematol; 2006 Jul; 81(7):499-502. PubMed ID: 16755576
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Dominantly Inherited beta-Thalassemia.
    Efremov GD
    Hemoglobin; 2007; 31(2):193-207. PubMed ID: 17486503
    [TBL] [Abstract][Full Text] [Related]  

  • 43. [Molecular aspects of alpha dn beta thalassemias].
    Ibarra B; Perea FJ; Hernández-Córdova A
    Arch Invest Med (Mex); 1990; 21(4):357-62. PubMed ID: 1669226
    [TBL] [Abstract][Full Text] [Related]  

  • 44. [Changes in hemoglobin in patients with hemolytic anemia].
    Pérez G; de la Peña ME; Esparza A; Mejía A; Vázquez V; Aguilar Luna JC; González J; López-Guido B; Ornelas ML; Ibarra B
    Arch Invest Med (Mex); 1990; 21(4):385-8. PubMed ID: 1669229
    [TBL] [Abstract][Full Text] [Related]  

  • 45. [Neonatal hemolytic anemias: genetic aspects and prevention].
    Pace DP
    G Clin Med; 1974 Jun; 55(6):417-29. PubMed ID: 4478154
    [No Abstract]   [Full Text] [Related]  

  • 46. Genetic modifiers of beta-thalassemia.
    Thein SL
    Haematologica; 2005 May; 90(5):649-60. PubMed ID: 15921380
    [TBL] [Abstract][Full Text] [Related]  

  • 47. [Splenectomy in a patient with beta thalassemia intermedia and severe hemolytic anemia].
    Pérez JA; Padilla J; Rodríguez MA; Cura S; Sánchez S; Cutillas MJ; Sanz J
    Rev Esp Anestesiol Reanim; 2001; 48(6):288-91. PubMed ID: 11446945
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Distinct phenotypic expression associated with a new hyperunstable alpha globin variant (Hb heraklion, alpha1cd37(C2)Pro>0): comparison to other alpha-thalassemic hemoglobinopathies.
    Traeger-Synodinos J; Papassotiriou I; Metaxotou-Mavrommati A; Vrettou C; Stamoulakatou A; Kanavakis E
    Blood Cells Mol Dis; 2000 Aug; 26(4):276-84. PubMed ID: 11042028
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Development of severe anemia during fever episodes in patients with hemoglobin E trait and hemoglobin H disease combinations.
    Jetsrisuparb A; Sanchaisuriya K; Fucharoen G; Fucharoen S; Wiangnon S; Jetsrisuparb C; Sirijirachai J; Chansoong K
    J Pediatr Hematol Oncol; 2006 Apr; 28(4):249-53. PubMed ID: 16679924
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Homozygous hereditary elliptocytosis as the cause of haemolytic anemia in infancy.
    Nielsen JA; Praktitioner S
    Scand J Haematol; 1968; 5(6):486-96. PubMed ID: 5731934
    [No Abstract]   [Full Text] [Related]  

  • 51. Moyamoya disease associated with hemoglobin Fairfax and beta-thalassemia.
    Marden FA; Putman CM; Grant JM; Greenberg J
    Pediatr Neurol; 2008 Feb; 38(2):130-2. PubMed ID: 18206795
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Globin chain synthesis in hemolytic anemia reticulocytes. A case of hemoglobin Burke.
    Suzuki H; Wada C; Kamata K; Takahashi E; Sato N; Kunitomo T
    Biochem Mol Biol Int; 1993 Jul; 30(3):425-31. PubMed ID: 8401300
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Neonatal malaria--a clinico-hematological profile.
    Patwari A; Aneja S; Berry AM; Ghosh S
    Indian Pediatr; 1978 Oct; 15(10):847-9. PubMed ID: 730310
    [No Abstract]   [Full Text] [Related]  

  • 54. Diagnosis of concurrent hemoglobin H disease and heterozygous beta-thalassemia.
    Ma ES; Chan AY; Au WY; Yeung YM; Chan LC
    Haematologica; 2001 Apr; 86(4):432-3. PubMed ID: 11325652
    [TBL] [Abstract][Full Text] [Related]  

  • 55. [Detection of beta thalassemia by the technique of refractory amplification of mutation systems (ARMS-PCR)].
    Bravo M; Salazar R; Arends A; Alvarez M; Velázquez D; Guevara JM; Castillo O
    Invest Clin; 1999 Sep; 40(3):203-13. PubMed ID: 10531753
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Fatal hemolytic anemia presumably due to the combination of sickle cell and thalassemia gene; case report.
    NAIL SK; KOTHARI BV; JHAVERI CL; SUKUMARAN PK; SANGHVI LD
    Indian J Med Sci; 1957 Apr; 11(4):244-9. PubMed ID: 13428325
    [No Abstract]   [Full Text] [Related]  

  • 57. Oral phosphodiesterase type 5 inhibitors alleviate recurrent priapism complicating thalassemia intermedia: a case report.
    Tzortzis V; Mitrakas L; Gravas S; Mamoulakis C; Meissner A; Kyriakou D; Melekos MD
    J Sex Med; 2009 Jul; 6(7):2068-71. PubMed ID: 19453903
    [TBL] [Abstract][Full Text] [Related]  

  • 58. [The congenital anomalies of the erythrocytes and blood pigments].
    BETKE K
    Monatsschr Kinderheilkd (1902); 1962 Mar; 110():159-63. PubMed ID: 13868623
    [No Abstract]   [Full Text] [Related]  

  • 59. Neonatal hemolytic anemia due to pyknocytosis.
    Vos MJ; Martens D; van de Leur SJ; van Wijk R
    Eur J Pediatr; 2014 Dec; 173(12):1711-4. PubMed ID: 25001230
    [TBL] [Abstract][Full Text] [Related]  

  • 60. A Rare Cause of Neonatal Hemolytic Anemia: Glutathione Synthetase Deficiency.
    Soylu Ustkoyuncu P; Mutlu FT; Kiraz A; Tag Balkis Z; Yel S
    J Pediatr Hematol Oncol; 2018 Jan; 40(1):e45-e49. PubMed ID: 28267090
    [TBL] [Abstract][Full Text] [Related]  

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