BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

823 related articles for article (PubMed ID: 14084634)

  • 1. THE FIRST OBSERVATION OF HOMOZYGOUS HEMOGLOBIN S-ALPHA THALASSEMIA DISEASE AND TWO TYPES OF SICKLE CELL THALASSEMIA DISEASE: (A) SICKLE CELL-ALPHA THALASSEMIA DISEASE, (B) SICKLE CELL-BETA THALASSEMIA DISEASE.
    AKSOY M
    Blood; 1963 Dec; 22():757-69. PubMed ID: 14084634
    [No Abstract]   [Full Text] [Related]  

  • 2. Clinical manifestations of inherited abnormal hemoglobins. I. The interaction of hemoglobin-S with hemoglobin-D.
    STURGEON P; ITANO HA; BERGREN WR
    Blood; 1955 May; 10(5):389-404. PubMed ID: 14363320
    [No Abstract]   [Full Text] [Related]  

  • 3. [TYPES OF SICKLE CELL- THALASSEMIC DISEASES. A. SICKLE CELL-BETA THALASSEMIA. B. SICKLE CELL-ALPHA THALASSEMIA. STUDY OF 6 CASES IN 5 FAMILIES].
    AKSOY M
    Turk Tip Cemiy Mecm; 1963 Jun; 29():313-20. PubMed ID: 14047038
    [No Abstract]   [Full Text] [Related]  

  • 4. Studies on abnormal hemoglobins. XI. Sickle cell-thalassemia disease in the Negro; the significance of the S+A+F and S+A patterns obtained by hemoglobin analysis.
    SINGER K; SINGER L; GOLDBERG SR
    Blood; 1955 May; 10(5):405-15. PubMed ID: 14363321
    [No Abstract]   [Full Text] [Related]  

  • 5. Sickle cell haemoglobin and two types of thalassaemia in the same family.
    RUSSO G; MOLLICA F
    Acta Haematol; 1962; 28():329-40. PubMed ID: 13975667
    [No Abstract]   [Full Text] [Related]  

  • 6. Studies on abnormal hemoglobins. XIII. Hemoglobin S-thalassemia disease and hemoglobin C-thalassemia disease in siblings.
    SINGER K; JOSEPHSON AM; SINGER L; HELLER P; ZIMMERMAN HJ
    Blood; 1957 Jul; 12(7):593-602. PubMed ID: 13436515
    [No Abstract]   [Full Text] [Related]  

  • 7. [HOMOZYGOUS HEMOGLOBIN S AND ALPHA THALASSEMIC DISEASE].
    AKSOY M
    Turk Tip Cemiy Mecm; 1963 Jun; 29():299-305. PubMed ID: 14047036
    [No Abstract]   [Full Text] [Related]  

  • 8. [On the behavior of different types of hemoglobin (Hb A, A2, F, S and "Bart's") in thalassemia, drepanocytosis and microdrepanocythemia].
    VENTRUTO V; DE ROSA L; CIMINO R; QUATTRIN N
    Schweiz Med Wochenschr; 1962 Oct; 92():1322-4. PubMed ID: 13996677
    [No Abstract]   [Full Text] [Related]  

  • 9. Abnormal hemoglobins; clinical disorders resulting from various combinations.
    LAWRENCE JS; VALENTINE WN
    Calif Med; 1955 Jan; 82(1):1-5. PubMed ID: 13230906
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Studies on abnormal hemoglobins. VI. Electrophoretic demonstration of type S (sickle cell) hemoglobin in erythrocytes incapable of showing the sickle cell phenomenon.
    SINGER K; FISHER B
    Blood; 1953 Mar; 8(3):270-5. PubMed ID: 13032196
    [No Abstract]   [Full Text] [Related]  

  • 11. OCCURRENCE OF HAEMOGLOBIN H AND HAEMOGLOBIN BART'S IN ALPHA-THALASSEMIA: A FAMILY WITH 2 POSSIBLE HOMOZYGOUS CASES WITH G-6-PD-DEFICIENCY.
    HELLEMAN PW; PUNT K; VERLOOP MC
    Nature; 1964 Mar; 201():1039-40. PubMed ID: 14191584
    [No Abstract]   [Full Text] [Related]  

  • 12. Sickle cell syndromes. II. The sickle cell anemia-alpha-thalassemia syndrome.
    Honig GR; Koshy M; Mason RG; Vida LN
    J Pediatr; 1978 Apr; 92(4):556-61. PubMed ID: 633012
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genetic Background of the Sickle Cell Disease Pediatric Population of Dakar, Senegal, and Characterization of a Novel Frameshift β-Thalassemia Mutation [HBB: c.265_266del; p.Leu89Glufs*2].
    Gueye Tall F; Martin C; Malick Ndour EH; Déme Ly I; Renoux C; Chillotti L; Veyrenche N; Connes P; Madieye Gueye P; Ndiaye Diallo R; Lacan P; Diagne I; Amadou Diop P; Cissé A; Lopez Sall P; Joly P
    Hemoglobin; 2017 Mar; 41(2):89-95. PubMed ID: 28670947
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Sickle cell anemia and α-thalassemia: a modulating factor in homozygous HbS/S patients in Oman.
    Hassan SM; Al Muslahi M; Al Riyami M; Bakker E; Harteveld CL; Giordano PC
    Eur J Med Genet; 2014; 57(11-12):603-6. PubMed ID: 25266642
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Studies on abnormal hemoglobins. III. The interrelationship of type S (sickle cell) hemoglobin and type F (alkali resistant) hemoglobin in sickle cell anemia.
    SINGER K; CHERNOFF AI
    Blood; 1952 Jan; 7(1):47-52. PubMed ID: 14886409
    [No Abstract]   [Full Text] [Related]  

  • 16. Analysis of mRNA from red cells of patients with thalassemia and hemoglobin variants.
    Smetanina NS; Molchanova TP; Huisman TH
    Hemoglobin; 1997 Sep; 21(5):437-67. PubMed ID: 9322078
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [A CASE OF MICRODREPANOCYTIC DISEASE DUE TO S HEMOGLOBIN AND A VARIETY OF MICROCYTHEMIA WITH NORMAL QUOTA OF A2 HEMOGLOBIN AND ELEVATED QUOTA OF F HEMOGLOBIN (THIRD VARIETY OF MICRODREPANOCYTIC DISEASE)].
    SILVESTRONI E; BIANCO I
    Prog Med (Napoli); 1964 Aug; 20():509-13. PubMed ID: 14235120
    [No Abstract]   [Full Text] [Related]  

  • 18. [Serological research on the antigen power of some types of normal and pathological human hemoglobin. I. Hemoglobin of Cooley's anemia and of sickle cell anemia].
    VECCHIO F; BARBAGALLO E
    Pediatria (Napoli); 1950; 58(7-8):481-97. PubMed ID: 14797314
    [No Abstract]   [Full Text] [Related]  

  • 19. [THALASSEMIA MINOR HB-S. BASED ON CASES IN ONE FAMILY].
    OBRADOV S; MUSAFIJA A; DUGUMOVIC Z
    Med Arh; 1964; 18():47-56. PubMed ID: 14311906
    [No Abstract]   [Full Text] [Related]  

  • 20. Modification of hemoglobin H disease by sickle trait.
    Matthay KK; Mentzer WC; Dozy AM; Kan YW; Bainton DF
    J Clin Invest; 1979 Oct; 64(4):1024-32. PubMed ID: 479366
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 42.