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Journal Abstract Search

104 related items for PubMed ID: 1701619

  • 1. [Thalassemia intermedia. Report of two cases].
    Khaldi F, Hassine F, Guemira F, Bennaceur B, Fattoum S.
    Ann Pediatr (Paris); 1990 Sep; 37(7):455-7. PubMed ID: 1701619
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  • 3. Heterogeneity of beta/alpha ratio in Italian beta-thalassaemia heterozygotes.
    Sampietro M, Cappellini MD, Taddei MT, Fiorelli G.
    Haematologica; 1983 Sep; 68(6):703-11. PubMed ID: 6199264
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  • 4. beta-Thalassemia intermedia homozygous for normal hemoglobin A2 beta-thalassemia. Study in four families.
    Aksoy M, Bermek E, Almiş G, Kutlar A.
    Acta Haematol; 1982 Sep; 67(1):57-61. PubMed ID: 6174012
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  • 5. [Intermediate thalassemia. Study of 5 cases in their clinical, ferrokinetic and erythrokinetic aspects].
    Muñoz JA, Martín MV, Risueño CE, Freire J, Pajares M, Campos J.
    Sangre (Barc); 1989 Oct; 34(5):346-9. PubMed ID: 2482545
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  • 6. Diagnostic efficacy of haemoglobin A2 in heterozygous beta thalassaemia.
    Saraya AK, Kumar R, Choudhry VP, Tyagi RS, Sehgal AK.
    Indian J Med Res; 1984 Aug; 80():203-8. PubMed ID: 6210250
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  • 7. Thalassemia types in Calabria (Southern Italy).
    Brancati C, Tagarelli A.
    Birth Defects Orig Artic Ser; 1982 Aug; 18(7):147-55. PubMed ID: 6186309
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  • 8. [Changes in hemoglobin fractions of pregnant women with heterozygous beta-thalassemia and iron deficiency anemia].
    Tikhonova LV.
    Akush Ginekol (Mosk); 1983 Dec; (12):41-3. PubMed ID: 6198936
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  • 9. Haemoglobin A2 is elevated in hyperthyroid patients.
    Krishnamoorthy R, Elion J, Kuhn JM, Lagrange JL, Rochette J, Luton JP, Bricaire H, Labie D.
    Nouv Rev Fr Hematol (1978); 1982 Dec; 24(1):39-40. PubMed ID: 6175951
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  • 10. Globin chain synthesis analysis in obligate beta 0-thalassemia heterozygotes with isolated increase of hemoglobin A2 levels.
    Galanello R, Melis MA, Furbetta M, Angius A, Scalas MT, Paglietti E, Cao A.
    Nouv Rev Fr Hematol (1978); 1981 Dec; 23(4):193-5. PubMed ID: 7312613
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  • 18. Erythroleukemia manifesting delta beta-thalassemia.
    Markham RE, Butler F, Goh K, Rowley PT.
    Hemoglobin; 1983 Dec; 7(1):71-8. PubMed ID: 6188718
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  • 19. [Double heterozygous Hb O ARAB/beta+ thalassemia (in a Tunisian family)].
    Ben Abdeladhim A, Ben Othman T, Grira F, Ayssaoui B, Fattoum S, Boussen M.
    Tunis Med; 1988 Dec; 66(8-9):631-5. PubMed ID: 2462760
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  • 20. Partial mispairing and crossing-over between beta 0 and delta genes as the origin of the delta beta 0 thalassemia gene. A single mutational event hypothesis.
    Cantú JM, Ibarra B, Vaca G, Ramirez ML, Sánchez-Corona J.
    Hum Genet; 1979 Jun 19; 49(2):191-8. PubMed ID: 468250
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