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 *

148 related articles for article (PubMed ID: 6083725)

  • 21. The importance of the genetic picture and globin synthesis in determining the clinical and haematological features of thalassaemia intermedia.
    Gallo E; Massaro P; Miniero R; David D; Tarella C
    Br J Haematol; 1979 Feb; 41(2):211-21. PubMed ID: 427031
    [TBL] [Abstract][Full Text] [Related]  

  • 22. The German sickle cell disease registry reveals a surprising risk of acute splenic sequestration and an increased transfusion requirement in patients with compound heterozygous sickle cell disease HbS/β-thalassaemia and no or low HbA expression.
    Allard P; Tagliaferri L; Weru V; Cario H; Lobitz S; Grosse R; Bleeke M; Oevermann L; Hakimeh D; Jarisch A; Kopp-Schneider A; Kulozik AE; Kunz JB; ; Lassay L
    Eur J Haematol; 2024 Oct; 113(4):501-509. PubMed ID: 38946051
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Sickle Cell Disease in Jordan: The Experience of a Major Referral Center.
    Oudat RI; Abualruz HS; Al-Shiek NKA; Al-Mashaqba EA; Al-Hiari RA; Alsoukhni HA; Hammad MAA
    Med Arch; 2021 Feb; 75(1):27-30. PubMed ID: 34012195
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Sickle cell disease in Sudan.
    Bayoumi RA; Abu Zeid YA; Abdul Sadig A; Awad Elkarim O
    Trans R Soc Trop Med Hyg; 1988; 82(1):164-8. PubMed ID: 2459819
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Sickle cell-hereditary persistence of fetal haemoglobin and its differentiation from other sickle cell syndromes.
    Murray N; Serjeant BE; Serjeant GR
    Br J Haematol; 1988 May; 69(1):89-92. PubMed ID: 2454649
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Globin synthetic ratios in homozygous beta-thalassemia patients from Lebanon.
    Chehab FF; Khouri FP; Deeb SS
    Hemoglobin; 1984; 8(2):151-62. PubMed ID: 6206028
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Beta-thalassemia in Brazil.
    Zago MA; Costa F; Bottura C
    Braz J Med Biol Res; 1981 Dec; 14(6):383-8. PubMed ID: 6086110
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Application of cellulose acetate electrophoresis to globin chain separation for antenatal diagnosis of beta thalassemia.
    Boccacci M; Massa A; Tentori L
    Clin Chim Acta; 1981 Oct; 116(2):137-42. PubMed ID: 7296882
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Beta-thalassemia intermedia with exceptionally high hemoglobin A2: relationship to mutations in the beta-gene promoter.
    Coleman MB; Adams JG; Plonczynski MW; Harrell AH; Walker AM; Fairbanks V; Steinberg MH
    Am J Med Sci; 1992 Aug; 304(2):73-8. PubMed ID: 1380206
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Heterogeneity of beta/alpha ratio in Italian beta-thalassaemia heterozygotes.
    Sampietro M; Cappellini MD; Taddei MT; Fiorelli G
    Haematologica; 1983; 68(6):703-11. PubMed ID: 6199264
    [No Abstract]   [Full Text] [Related]  

  • 31. Hemoglobin A2 levels in healthy persons, sickle cell disease, sickle cell trait, and beta-thalassemia by capillary isoelectric focusing.
    Craver RD; Abermanis JG; Warrier RP; Ode DL; Hempe JM
    Am J Clin Pathol; 1997 Jan; 107(1):88-91. PubMed ID: 8980373
    [TBL] [Abstract][Full Text] [Related]  

  • 32. The cellular basis for different fetal hemoglobin levels among sickle cell individuals with two, three, and four alpha-globin genes.
    Dover GJ; Chang VT; Boyer SH; Serjeant GR; Antonarakis S; Higgs DR
    Blood; 1987 Jan; 69(1):341-4. PubMed ID: 2431731
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Amelioration of clinical severity through raised fetal hemoglobin in sickle cell anaemia.
    Ponnazhagan S; Sarkar R
    Indian J Pediatr; 1992; 59(1):85-90. PubMed ID: 1377179
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Fetal hemoglobin and alpha thalassemia modulate the phenotypic expression of HbSD-Punjab.
    Patel DK; Purohit P; Dehury S; Das P; Dutta A; Meher S; Patel S; Bag S; Mashon RS; Das K
    Int J Lab Hematol; 2014 Aug; 36(4):444-50. PubMed ID: 24245819
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Effects of alpha-thalassemia and sickle polymerization tendency on the urine-concentrating defect of individuals with sickle cell trait.
    Gupta AK; Kirchner KA; Nicholson R; Adams JG; Schechter AN; Noguchi CT; Steinberg MH
    J Clin Invest; 1991 Dec; 88(6):1963-8. PubMed ID: 1752955
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Sickle cell traits in Canada. Trimodal distribution of Hb S as a result of interaction with alpha-thalassaemia gene.
    Wong SC; Ali MA; Boyadjian SE
    Acta Haematol; 1981; 65(3):157-63. PubMed ID: 6165216
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Hemoglobin S-O Arab-alpha-thalassemia: globin biosynthesis and clinical picture.
    Ballas SK; Atwater J; Burka ER
    Hemoglobin; 1977; 1(7):651-62. PubMed ID: 914640
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Association of fetal hemoglobin level with frequency of acute pain episodes in sickle cell disease (HbS-only phenotype) patients.
    Jit BP; Mohanty PK; Purohit P; Das K; Patel S; Meher S; Mohanty JR; Sinha S; Behera RK; Das P
    Blood Cells Mol Dis; 2019 Mar; 75():30-34. PubMed ID: 30597429
    [TBL] [Abstract][Full Text] [Related]  

  • 39. High Hb A2 beta-thalassemia due to a 468 bp deletion in a patient with Hb S/beta-thalassemia.
    Patterson M; Walker L; Eng B; Waye JS
    Hemoglobin; 2005; 29(4):293-5. PubMed ID: 16370492
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Beta + thalassemia--Portuguese type: clinical, haematological and molecular studies of a newly defined form of beta thalassaemia.
    Tamagnini GP; Lopes MC; Castanheira ME; Wainscoat JS; Wood WG
    Br J Haematol; 1983 Jun; 54(2):189-200. PubMed ID: 6189507
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.