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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

270 related items for PubMed ID: 5046623

  • 1. Serum iron and unsaturated iron-binding capacity in the -thalassaemia trait: their relation to the levels of haemoglobins A, A 2 , and F.
    Kattamis C, Lagos P, Metaxotou-Mavromati A, Matsaniotis N.
    J Med Genet; 1972 Jun; 9(2):154-9. PubMed ID: 5046623
    [No Abstract] [Full Text] [Related]

  • 2. Haematological data in 312 cases of -thalassaemia trait in Thailand.
    Pootrakul P, Wasi P, Na-Nakorn S.
    Br J Haematol; 1973 Jun; 24(6):703-12. PubMed ID: 4716054
    [No Abstract] [Full Text] [Related]

  • 3. Comparison of Price-Jones curves obtained with an electronic corpuscle counter in normal subjects and in patients with thalassaemia and iron deficiency.
    Cazzavillan M, Barbui T, Franchi F, Chisesi T, Dini E.
    Haematologia (Budap); 1973 Jun; 7(3):333-7. PubMed ID: 4790072
    [No Abstract] [Full Text] [Related]

  • 4. Beta-thalassaemia in Cuba.
    de la Torre E, Hernandez P, Martinez G, Srarch E, Colombo B.
    Haematologia (Budap); 1974 Jun; 8(1-4):71-9. PubMed ID: 4461439
    [No Abstract] [Full Text] [Related]

  • 5. New mutation leading to -thalassaemia minor.
    Tönz O, Winterhalter KH, Glatthaar BE.
    Nat New Biol; 1973 Jan 24; 241(108):127-8. PubMed ID: 4512457
    [No Abstract] [Full Text] [Related]

  • 6. [Thalassemia trait in the pediatric age and body iron status].
    Abreu de Miani MS, Calvo EB, Sanchís ME, Peñalver JA.
    Sangre (Barc); 1986 Jan 24; 31(1):1-6. PubMed ID: 3704880
    [No Abstract] [Full Text] [Related]

  • 7. Homozygous delta-thalassemia first discovered in Japanese family with hereditary persistence of fetal hemoglobin.
    Ota Y, Yamaoka K, Sumida I, Fujita S, Fujimura T.
    Blood; 1971 Jun 24; 37(6):706-15. PubMed ID: 5162313
    [No Abstract] [Full Text] [Related]

  • 8. Hereditary persistence of fetal hemoglobin and beta-thalassemia in a Turkish child.
    Yamak B, Ozsoylu S, Altay C, Hiçsönmez G, Say B.
    Acta Haematol; 1973 Jun 24; 50(2):124-8. PubMed ID: 4200806
    [No Abstract] [Full Text] [Related]

  • 9. Comprehensive testing for thalassemia trait.
    Pearson HA, McPhedran P, O'Brien RT, Aspnes GT, McIntosh S, Guiliotis DK.
    Ann N Y Acad Sci; 1974 Jun 24; 232(0):135-44. PubMed ID: 4528485
    [No Abstract] [Full Text] [Related]

  • 10. Discrimination between iron deficiency and heterozygous thalassaemia.
    Walford DM, McPherson K, Deacon R.
    Lancet; 1979 Feb 10; 1(8111):323. PubMed ID: 84973
    [No Abstract] [Full Text] [Related]

  • 11. Various aspects of alpha-thalassemia.
    Lehmann H, Lang A.
    Ann N Y Acad Sci; 1974 Feb 10; 232(0):152-8. PubMed ID: 4370548
    [No Abstract] [Full Text] [Related]

  • 12. Hb D punjab--alpha thalassaemia combination in a Turkish family.
    Cavdar AO, Arcasoy A.
    Scand J Haematol; 1974 Feb 10; 13(4):313-9. PubMed ID: 4445829
    [No Abstract] [Full Text] [Related]

  • 13. Serum ferritin in beta-thalassemia trait.
    Loria A, Konijn AM, Hershko C.
    Isr J Med Sci; 1978 Nov 10; 14(11):1127-31. PubMed ID: 750537
    [Abstract] [Full Text] [Related]

  • 14. Some problems of hemoglobin patterns in different thalassemic syndromes showing the heterogeneity of beta-thalassemia genes.
    Aksoy M, Erdem S.
    Ann N Y Acad Sci; 1969 Nov 20; 165(1):13-24. PubMed ID: 5260139
    [No Abstract] [Full Text] [Related]

  • 15. Heterozygous beta-thalassaemia in pregnancy.
    Whiteside MG, Smith MB.
    Med J Aust; 1973 Sep 08; 2(10):487-90. PubMed ID: 4750543
    [No Abstract] [Full Text] [Related]

  • 16. Automated measurement of red blood cell microcytosis and hypochromia in iron deficiency and beta-thalassemia trait.
    d'Onofrio G, Zini G, Ricerca BM, Mancini S, Mango G.
    Arch Pathol Lab Med; 1992 Jan 08; 116(1):84-9. PubMed ID: 1734838
    [Abstract] [Full Text] [Related]

  • 17. A further observation on the possible association between haemoglobin G alpha-Philadelphia and alpha-thalassaemia.
    Martinez G, Vidal H, Colombo B.
    Hum Hered; 1973 Jan 08; 23(2):157-63. PubMed ID: 4756854
    [No Abstract] [Full Text] [Related]

  • 18. The silent carrier of beta thalassemia.
    Schwartz E.
    N Engl J Med; 1969 Dec 11; 281(24):1327-33. PubMed ID: 5355437
    [No Abstract] [Full Text] [Related]

  • 19. The micromeasurement of free erythrocyte protoporphyrin as a means of differentiating alpha thalassemia trait from iron deficiency anemia.
    Koenig HM, Lightsey AL, Schanberger JE.
    J Pediatr; 1975 Apr 11; 86(4):539-41. PubMed ID: 1127499
    [Abstract] [Full Text] [Related]

  • 20. The starch gel quantitative electrophoresis of haemoglobin as screening in the thalassaemia syndromes.
    Ricco G, Gallo E, Mazza U, Bianco G, Prato V.
    Acta Haematol; 1969 Apr 11; 42(2):99-105. PubMed ID: 4982583
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 14.