BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

187 related articles for article (PubMed ID: 12111766)

  • 1. Outcome in hemoglobin SC disease: a four-decade observational study of clinical, hematologic, and genetic factors.
    Powars DR; Hiti A; Ramicone E; Johnson C; Chan L
    Am J Hematol; 2002 Jul; 70(3):206-15. PubMed ID: 12111766
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Sickle cell disease as a cause of osteonecrosis of the femoral head.
    Milner PF; Kraus AP; Sebes JI; Sleeper LA; Dukes KA; Embury SH; Bellevue R; Koshy M; Moohr JW; Smith J
    N Engl J Med; 1991 Nov; 325(21):1476-81. PubMed ID: 1944426
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Beta-globin gene haplotype in Hb SC disease.
    Steinberg MH; Nagel RL; Lawrence C; Swaminathan V; Lu ZH; Plonczynski M; Harrell A
    Am J Hematol; 1996 Jul; 52(3):189-91. PubMed ID: 8756085
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Beta-cluster haplotypes, alpha-gene status, and hematological data from SS, SC, and S-beta-thalassemia patients in southern California.
    Schroeder WA; Powars DR; Kay LM; Chan LS; Huynh V; Shelton JB; Shelton JR
    Hemoglobin; 1989; 13(4):325-53. PubMed ID: 2473969
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Pain in sickle cell disease. Rates and risk factors.
    Platt OS; Thorington BD; Brambilla DJ; Milner PF; Rosse WF; Vichinsky E; Kinney TR
    N Engl J Med; 1991 Jul; 325(1):11-6. PubMed ID: 1710777
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The influence of uridine diphosphate glucuronosyl transferase 1A promoter polymorphisms, beta-globin gene haplotype, co-inherited alpha-thalassemia trait and Hb F on steady-state serum bilirubin levels in sickle cell anemia.
    Adekile A; Kutlar F; McKie K; Addington A; Elam D; Holley L; Clair B; Kutlar A
    Eur J Haematol; 2005 Aug; 75(2):150-5. PubMed ID: 16004608
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Hemoglobin H disease in the eastern region of Saudi Arabia.
    Qadri MI; Islam SA
    Saudi Med J; 2000 Jul; 21(7):666-71. PubMed ID: 11500731
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Effect of alpha-thalassemia and beta-globin gene cluster haplotypes on the hematological and clinical features of sickle-cell anemia in Brazil.
    Figueiredo MS; Kerbauy J; Gonçalves MS; Arruda VR; Saad ST; Sonati MF; Stoming T; Costa FF
    Am J Hematol; 1996 Oct; 53(2):72-6. PubMed ID: 8892730
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Hemoglobin F concentration as a function of age in Kuwaiti sickle cell disease patients.
    Adekile A; Al-Kandari M; Haider M; Rajaa M; D'Souza M; Sukumaran J
    Med Princ Pract; 2007; 16(4):286-90. PubMed ID: 17541294
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Molecular characteristics of pediatric patients with sickle cell anemia and stroke.
    Sarnaik SA; Ballas SK
    Am J Hematol; 2001 Jul; 67(3):179-82. PubMed ID: 11391715
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Hearing impairment in persons with the hemoglobin SC genotype.
    Onakoya PA; Nwaorgu OG; Shokunbi WA
    Ear Nose Throat J; 2010 Jul; 89(7):306-10. PubMed ID: 20628988
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Interaction of the alpha alpha alpha globin gene haplotype and sickle haemoglobin.
    Higgs DR; Clegg JB; Weatherall DJ; Serjeant BE; Serjeant GR
    Br J Haematol; 1984 Aug; 57(4):671-8. PubMed ID: 6331494
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Beta-S gene cluster haplotypes modulate hematologic and hemorheologic expression in sickle cell anemia. Use in predicting clinical severity.
    Powars DR; Meiselman HJ; Fisher TC; Hiti A; Johnson C
    Am J Pediatr Hematol Oncol; 1994 Feb; 16(1):55-61. PubMed ID: 7508688
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Diagnostic complication and molecular characteristics of Hb SC-Chicago disease with alpha-thal-2 (-alpha3.7 deletion): effects of multiple variant on patient's phenotype.
    Hughes HY; McKie K; Carmichael H; Bora K; Kutlar A; Kutlar F
    Ann Hematol; 2009 Nov; 88(11):1151-3. PubMed ID: 19373463
    [No Abstract]   [Full Text] [Related]  

  • 15. Genetic Blood Disorders Survey in the Sultanate of Oman.
    Al-Riyami A; Ebrahim GJ
    J Trop Pediatr; 2003 Jul; 49 Suppl 1():i1-20. PubMed ID: 12934793
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mortality in sickle cell disease. Life expectancy and risk factors for early death.
    Platt OS; Brambilla DJ; Rosse WF; Milner PF; Castro O; Steinberg MH; Klug PP
    N Engl J Med; 1994 Jun; 330(23):1639-44. PubMed ID: 7993409
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Effect of alpha-globin genotype on the pathophysiology of sickle cell disease.
    Ballas SK
    Pediatr Pathol Mol Med; 2001; 20(2):107-21. PubMed ID: 12673836
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Incidence and natural history of proliferative sickle cell retinopathy: observations from a cohort study.
    Downes SM; Hambleton IR; Chuang EL; Lois N; Serjeant GR; Bird AC
    Ophthalmology; 2005 Nov; 112(11):1869-75. PubMed ID: 16171867
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Coinheritance of the different copy numbers of alpha-globin gene modifies severity of beta-thalassemia/Hb E disease.
    Sripichai O; Munkongdee T; Kumkhaek C; Svasti S; Winichagoon P; Fucharoen S
    Ann Hematol; 2008 May; 87(5):375-9. PubMed ID: 18026953
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Comparison of red blood cell hematology among normal, alpha-thalassemia-1 trait, and hemoglobin Bart's fetuses at mid-pregnancy.
    Srisupundit K; Piyamongkol W; Tongsong T
    Am J Hematol; 2008 Dec; 83(12):908-10. PubMed ID: 18932192
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.