BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

197 related articles for article (PubMed ID: 14074060)

  • 1. [HEMOGLOBINOSES IN THE CONGO (L'EOPOLDVILLE) AND IN RUANDA-URUNDI].
    VANDEPITTE J; STIJNS J
    Ann Soc Belg Med Trop (1920); 1963 Jun; 43():271-81. PubMed ID: 14074060
    [No Abstract]   [Full Text] [Related]  

  • 2. [IMPORTED BLOOD DYSCRASIAS].
    BRUMPT LC
    Bull Soc Pathol Exot Filiales; 1964 Jun; 57():841-8. PubMed ID: 14279607
    [No Abstract]   [Full Text] [Related]  

  • 3. HEREDITARY RED CELL TRAITS AND MALARIA.
    MOTULSKY AG
    Am J Trop Med Hyg; 1964 Jan; 13():SUPPL147-58. PubMed ID: 14106725
    [No Abstract]   [Full Text] [Related]  

  • 4. STUDIES IN ISOLATES.
    FRASER GR
    J Genet Hum; 1964; 13():32-46. PubMed ID: 14192062
    [No Abstract]   [Full Text] [Related]  

  • 5. CORRELATION OF S HEMOGLOBIN WITH GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY AND ITS SIGNIFICANCE.
    LEWIS RA; HATHORN M
    Blood; 1965 Aug; 26():176-80. PubMed ID: 14332479
    [No Abstract]   [Full Text] [Related]  

  • 6. 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]  

  • 7. GLUCOSE-6-PHOSPHATE DEHYDROGENASE (G6PD) DEFICIENCY, THALASSAEMIA, AND ABNORMAL HAEMOGLOBINS IN TAIWAN.
    MOTULSKY AG; LEE TC; FRASER GR
    J Med Genet; 1965 Mar; 2(1):18-20. PubMed ID: 14296917
    [No Abstract]   [Full Text] [Related]  

  • 8. HEREDITARY AND ACQUIRED BLOOD FACTORS IN THE NEGROID POPULATION OF SURINAM. II. THE INCIDENCE OF HAEMOGLOBIN ANOMALIES AND THE DEFICIENCY OF GLUCOSE-6-PHOSPHATE DEHYDROGENASE.
    PIK C; LOOS JA; JONXIS JH; PRINS HK
    Trop Geogr Med; 1965 Mar; 17():61-8. PubMed ID: 14317229
    [No Abstract]   [Full Text] [Related]  

  • 9. THALASSEMIAS, ABNORMAL HEMOGLOBINS AND GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY IN THE ARTA AREA OF GREECE: DIAGNOSTIC AND GENETIC ASPECTS OF COMPLETE VILLAGE STUDIES.
    FRASER GR; STAMATOYANNOPOULOS G; KATTAMIS C; LOUKOPOULOS D; DEFARANAS B; KITSOS C; ZANNOS-MARIOLEA L; CHOREMIS C; FESSAS P; MOTULSKY AG
    Ann N Y Acad Sci; 1964 Oct; 119():415-35. PubMed ID: 14219423
    [No Abstract]   [Full Text] [Related]  

  • 10. OBSERVATIONS ON THE RESISTANCE IN HB E THALASSAEMIA DISEASE TO INDUCED INFECTION WITH PLASMODIUM VIVAX.
    RAY RN; CHATTERJEA JB; CHAUDHURI RN
    Bull World Health Organ; 1964; 30(1):51-5. PubMed ID: 14122440
    [TBL] [Abstract][Full Text] [Related]  

  • 11. CLINICAL MANIFESTATIONS OF PRIMAQUINE-SENSITIVE ANEMIA.
    BERRY DH; VIETTI TJ
    Am J Dis Child; 1965 Aug; 110():166-71. PubMed ID: 14320767
    [No Abstract]   [Full Text] [Related]  

  • 12. MALARIA AND HAEMOGLOBIN E IN THAILAND.
    FLATZ G; PIK C; SUNDHARAGIATI B
    Lancet; 1964 Aug; 2(7356):385-7. PubMed ID: 14173627
    [No Abstract]   [Full Text] [Related]  

  • 13. STUDIES ON THE DISTRIBUTION OF GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY, THALASSEMIA, AND OTHER GENETIC TRAITS IN THE COASTAL AND MOUNTAIN VILLAGES OF CYPRUS.
    PLATO CC; RUCKNAGEL DL; GERSHOWITZ H
    Am J Hum Genet; 1964 Sep; 16(3):267-83. PubMed ID: 14204777
    [No Abstract]   [Full Text] [Related]  

  • 14. GLUCOSE-6-PHOSPHATE DEHYDROGENASE (G6PD) DEFICIENCY, THALASSAEMIA, AND ABNORMAL HAEMOGLOBINS IN THE PHILIPPINES.
    MOTULSKY AG; STRANSKY E; FRASER GR
    J Med Genet; 1964 Dec; 1(2):102-6. PubMed ID: 14234103
    [No Abstract]   [Full Text] [Related]  

  • 15. THALASSAEMIA, GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY, SICKLING, AND MALARIAL ENDEMICITY IN GREECE: A STUDY OF FIVE AREAS.
    STAMATOYANNOPOULOS G; FESSAS P
    Br Med J; 1964 Apr; 1(5387):875-9. PubMed ID: 14102772
    [No Abstract]   [Full Text] [Related]  

  • 16. FREQUENCY OF HAEMOGLOBIN S AND GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY IN SOUTHERN TANZANIA.
    MARTI HR; SCHOEPF K; GSELL OR
    Br Med J; 1965 Jun; 1(5448):1475-6. PubMed ID: 14288087
    [No Abstract]   [Full Text] [Related]  

  • 17. TRIPLE ERYTHROPOIETIC ANOMALY: PORPHYRIA, GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY AND HETEROZYGOUS STATE OF HAEMOGLOBIN E.
    CHATTERJI AK
    Bull Calcutta Sch Trop Med; 1963 Apr; 11():75-6. PubMed ID: 14301738
    [No Abstract]   [Full Text] [Related]  

  • 18. CONGENITAL HEINZ-BODY ANAEMIA. FURTHER EVIDENCE ON THE CAUSE OF HEINZ-BODY PRODUCTION IN RED CELLS.
    GRIMES AJ; MEISLER A; DACIE JV
    Br J Haematol; 1964 Jul; 10():281-90. PubMed ID: 14179483
    [No Abstract]   [Full Text] [Related]  

  • 19. STUDIES ON SEVERAL GENETIC HEMATOLOGICAL TRAITS OF THE MEXICAN POPULATION. 8. HEMOGLOBIN S, GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY, AND OTHER CHARACTERISTICS IN A MALARIAL REGION.
    LISKER R; LORIA A; CORDOVA MS
    Am J Hum Genet; 1965 Mar; 17(2):179-87. PubMed ID: 14262135
    [No Abstract]   [Full Text] [Related]  

  • 20. GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY IN RED CELLS. INCIDENCE IN THE CURA CAO POPULATION, ITS CLINICAL AND GENETIC ASPECTS.
    VAN DER SAR A; SCHOUTEN H; BOUDIER AM
    Enzymologia; 1964 Oct; 27():289-310. PubMed ID: 14228390
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 10.