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Journal Abstract Search

236 related items for 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 15; 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 15; 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 15; 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 20; 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 Oct 20; 56():485-506. PubMed ID: 14081707
    [No Abstract] [Full Text] [Related]

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  • 8. THREE INHERITED INTRA-ERYTHROCYTIC DEFECTS: HEREDITARY SPHEROCYTOSIS, HB S AND HB C.
    THOMPSON RB, ROBERTSON MG.
    Acta Haematol; 1964 Oct 20; 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 Oct 20; 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 20; 8(3):270-5. PubMed ID: 13032196
    [No Abstract] [Full Text] [Related]

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  • 12. [ANEMIAS CAUSED BY ABNORMAL HEMOGLOBINS].
    DREYFUS JC.
    Sem Hop; 1964 Apr 20; 40():1161-9. PubMed ID: 14146499
    [No Abstract] [Full Text] [Related]

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  • 15. Abnormal hemoglobins; clinical disorders resulting from various combinations.
    LAWRENCE JS, VALENTINE WN.
    Calif Med; 1955 Jan 20; 82(1):1-5. PubMed ID: 13230906
    [Abstract] [Full Text] [Related]

  • 16. [RELATIONS BETWEEN ANOMALIES OF HEMOGLOBIN SYNTHESIS AND HUMAN DISEASE].
    PAULUZZI S.
    Recenti Prog Med; 1964 Dec 20; 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 20; 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 17; 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 17; 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 23; 186():745-8. PubMed ID: 14078086
    [No Abstract] [Full Text] [Related]

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