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 *

235 related articles for article (PubMed ID: 14129142)

  • 1. [ON A CASE OF DOUBLE DREPANOCYTOSIS-MICROCYTHEMIA HETEROZYGOSITY WITH DIMINUTION OF FRACTION A2].
    CUTILLO S; MIRAGLIADELGIUDICE M; DEBELLIS U
    Rass Int Clin Ter; 1963 Dec; 43():1251-64. PubMed ID: 14129142
    [No Abstract]   [Full Text] [Related]  

  • 2. INTERACTION OF HEMOGLOBIN LEPORE WITH SICKLE CELL TRAIT AND MICROCYTHEMIA (THALASSEMIA) IN A SOUTHERN ITALIAN FAMILY.
    SILVESTRONI E; BIANCO I; BAGLIONI C
    Blood; 1965 Apr; 25():457-69. PubMed ID: 14284335
    [No Abstract]   [Full Text] [Related]  

  • 3. [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]  

  • 4. [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]  

  • 5. [1ST CASE IN GUADELOUPE OF GENOTYPIC HEMOLYTIC ANEMIA WITH DREPANOCYTOSIS AND HEMOGLOBINOSIS D. HISTORY OF A DIAGNOSIS].
    PINEAU A
    Bull Soc Pathol Exot Filiales; 1963; 56():485-506. PubMed ID: 14081707
    [No Abstract]   [Full Text] [Related]  

  • 6. Familial differences in the proportion of abnormal hemoglobin present in the sickle cell trait.
    NEEL JV; WELLS IC; ITANO HA
    J Clin Invest; 1951 Oct; 30(10):1120-4. PubMed ID: 14888690
    [No Abstract]   [Full Text] [Related]  

  • 7. Variation in the amount of hemoglobin S in a patient with sickle cell trait and megaloblastic anemia.
    HELLER P; YAKULIS VJ; EPSTEIN RB; FRIEDLAND S
    Blood; 1963 Apr; 21():479-83. PubMed ID: 13953594
    [No Abstract]   [Full Text] [Related]  

  • 8. THREE INHERITED INTRA-ERYTHROCYTIC DEFECTS: HEREDITARY SPHEROCYTOSIS, HB S AND HB C.
    THOMPSON RB; ROBERTSON MG
    Acta Haematol; 1964 Oct; 32():233-8. PubMed ID: 14252557
    [No Abstract]   [Full Text] [Related]  

  • 9. [On a case of thalasso-drepanocytosis (Silvestroni-Bianco disease). Study of the hemoglobins and of the genetics. Splenectomy].
    MARCHAL G; BILSKI-PASQUIER G; de GROUCHY ; COMBRISSON A; DEPLANTE R
    Rev Hematol; 1960; 15():291-306. PubMed ID: 13766452
    [No 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. SIMULTANEOUS RADIOACTIVE TRACER STUDIES OF ERYTHROPOIESIS AND RED-CELL DESTRUCTION IN SICKLE-CELL DISEASE AND SICKLE-CELL HAEMOGLOBIN/THALASSAEMIA.
    MALAMOS B; BELCHER EH; GYFTAKI E; BINOPOULOS D
    Br J Haematol; 1963 Oct; 9():487-98. PubMed ID: 14076131
    [No Abstract]   [Full Text] [Related]  

  • 12. [ANEMIAS CAUSED BY ABNORMAL HEMOGLOBINS].
    DREYFUS JC
    Sem Hop; 1964 Apr; 40():1161-9. PubMed ID: 14146499
    [No Abstract]   [Full Text] [Related]  

  • 13. EFFECT OF IRON-DEFICIENCY ANAEMIA ON THE METABOLISM OF THE HETEROGENIC HAEMOGLOBINS IN SICKLE CELL TRAIT.
    LEVERE RD; LICHTMAN HC; LEVINE J
    Nature; 1964 May; 202():499-501. PubMed ID: 14167840
    [No Abstract]   [Full Text] [Related]  

  • 14. [A NEW KIND OF DREPANOCYTIC ANEMIA: HEMOGLOBIN A-HEMOGLOBIN LEPORE DISEASE].
    SILVESTRONI E; BIANCO I
    Prog Med (Napoli); 1963 Sep; 19():545-8. PubMed ID: 14122941
    [No Abstract]   [Full Text] [Related]  

  • 15. 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]  

  • 16. [RELATIONS BETWEEN ANOMALIES OF HEMOGLOBIN SYNTHESIS AND HUMAN DISEASE].
    PAULUZZI S
    Recenti Prog Med; 1964 Dec; 37():533-76. PubMed ID: 14262942
    [No Abstract]   [Full Text] [Related]  

  • 17. QUANTITATIVE STUDIES ON A2, SICKLE CELL, AND FETAL HEMOGLOBINS IN NEGROES WITH MONGOLISM, WITH OBSERVATIONS ON TRANSLOCATION MONGOLISM IN NEGROES.
    WEINSTEIN ED; RUCKNAGEL DL; SHAW MW
    Am J Hum Genet; 1965 Sep; 17(5):443-56. PubMed ID: 14334744
    [No Abstract]   [Full Text] [Related]  

  • 18. Sickle cell disease in a patient with sickle cell trait and compound heterozygosity for hemoglobin S and hemoglobin Quebec-Chori.
    Witkowska HE; Lubin BH; Beuzard Y; Baruchel S; Esseltine DW; Vichinsky EP; Kleman KM; Bardakdjian-Michau J; Pinkoski L; Cahn S
    N Engl J Med; 1991 Oct; 325(16):1150-4. PubMed ID: 1891024
    [No Abstract]   [Full Text] [Related]  

  • 19. Mutation rates of the abnormal hemoglobin genes.
    FROTA-PESSOA O; WAJNTAL A
    Am J Hum Genet; 1963 Jun; 15(2):123-5. PubMed ID: 13945846
    [No Abstract]   [Full Text] [Related]  

  • 20. SPLENECTOMY FOR HYPERSPLENISM IN SICKLE CELL ANEMIA.
    EGDAHL RH; MARTIN WW; HILKOVITZ G
    JAMA; 1963 Nov; 186():745-8. PubMed ID: 14078086
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 12.