BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

112 related articles for article (PubMed ID: 10465943)

  • 1. [Diagnosis and therapy of hemoglobinopathies].
    Hattori Y
    Nihon Naika Gakkai Zasshi; 1999 Jun; 88(6):1010-5. PubMed ID: 10465943
    [No Abstract]   [Full Text] [Related]  

  • 2. [Study of hemoglobinopathies found in Belgium].
    Fondu P
    Bull Mem Acad R Med Belg; 1995; 150(10-11):367-75; discussion 376-8. PubMed ID: 8845787
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The impact of molecular biology on the diagnosis and treatment of hemoglobin disorders.
    Berg PE; Schechter AN
    Mol Genet Med; 1992; 2():1-38. PubMed ID: 1458221
    [No Abstract]   [Full Text] [Related]  

  • 4. Molecular biologic diagnosis of the hemoglobinopathies.
    Schwartz E; Surrey S
    Hosp Pract (Off Ed); 1986 Sep; 21(9):163-78. PubMed ID: 3091617
    [No Abstract]   [Full Text] [Related]  

  • 5. [Abnormal hemoglobin and thalassemia].
    Hattori Y; Harano T
    Nihon Rinsho; 2001 Nov; 59 Suppl 7():437-51. PubMed ID: 11808151
    [No Abstract]   [Full Text] [Related]  

  • 6. [Prenatal diagnosis of hereditary hemoglobinopathies].
    Cao A; Pirastu M; Rosatelli C
    Haematologica; 1989 Oct; 74(5 Suppl):213-22. PubMed ID: 2574134
    [No Abstract]   [Full Text] [Related]  

  • 7. Treatment of thalassemia with hydroxyurea: an indispensable alternative therapy.
    Kattamis A
    J Pediatr Hematol Oncol; 2007 Nov; 29(11):729-30. PubMed ID: 17984687
    [No Abstract]   [Full Text] [Related]  

  • 8. Beta-globin gene disorders in Italy and the Mediterranean area.
    Ottolenghi S; Carestia C
    Horiz Biochem Biophys; 1986; 8():257-98. PubMed ID: 2875932
    [No Abstract]   [Full Text] [Related]  

  • 9. The interactions of alpha-thalassemia with hemoglobinopathies.
    Steinberg MH
    Hematol Oncol Clin North Am; 1991 Jun; 5(3):453-73. PubMed ID: 1864819
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Haemoglobinopathies.
    Old J
    Prenat Diagn; 1996 Dec; 16(13):1181-6. PubMed ID: 9061749
    [TBL] [Abstract][Full Text] [Related]  

  • 11. New treatments of sickle cell disease.
    Embury SH
    West J Med; 1996 May; 164(5):444. PubMed ID: 8686307
    [No Abstract]   [Full Text] [Related]  

  • 12. Mutations in the A gamma-globin promoter in hereditary persistence of fetal hemoglobin and delta beta zero-thalassemia.
    Ottolenghi S; Giglioni B; Comi P; Mantovani R; Malgaretti N; Nicolis S; Longinotti M; Sciarratta GV; Pirastu M; Camaschella C
    Prog Clin Biol Res; 1987; 251():373-82. PubMed ID: 2448807
    [No Abstract]   [Full Text] [Related]  

  • 13. delta beta-Thalassemia and HPFH.
    Ottolenghi S; Giglioni B; Taramelli R; Comi P; Gianni AM
    Birth Defects Orig Artic Ser; 1982; 18(7):65-7. PubMed ID: 6186314
    [No Abstract]   [Full Text] [Related]  

  • 14. [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]  

  • 15. Prenatal diagnosis of hemoglobin disorders.
    Kan YW
    Prog Hematol; 1977; 10():91-104. PubMed ID: 337367
    [No Abstract]   [Full Text] [Related]  

  • 16. Management of sickle cell disease.
    Steinberg MH
    N Engl J Med; 1999 Apr; 340(13):1021-30. PubMed ID: 10099145
    [No Abstract]   [Full Text] [Related]  

  • 17. Beta-globin-like gene cluster haplotypes in hemoglobinopathies.
    Muralitharan S; Krishnamoorthy R; Nagel RL
    Methods Mol Med; 2003; 82():195-211. PubMed ID: 12669645
    [No Abstract]   [Full Text] [Related]  

  • 18. [Population genetics study of hemoglobinopathies in Uzbekistan. II. Population dynamics of hemoglobinopathies].
    Asanov AIu; Ginter EK; Bakhramov SM; Gar'kavtseva RF; Revazov AA
    Genetika; 1987 Jul; 23(7):1328-33. PubMed ID: 2958388
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Molecular diagnosis of hemoglobinopathies and thalassemia.
    Kan YW; Chang JC
    Prenat Diagn; 2010 Jul; 30(7):608-10. PubMed ID: 20572100
    [No Abstract]   [Full Text] [Related]  

  • 20. [Heterozygous beta thalassemia with increased HbF: independent segregation of beta thalassemia and hereditary persistent fetal hemoglobin (Swiss type) in a Spanish family].
    De Blas JM; Martín E; Martínez ML; Caso F
    Sangre (Barc); 1985; 30(1):28-36. PubMed ID: 2408346
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.