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Journal Abstract Search

67 related items for PubMed ID: 1243190

  • 1. Hemoglobin O Arabia. Considerations on the first nine cases discovered in Romania.
    Bratu V, Predescu C, Pâtea N, Apăteanu V, Lehmann H.
    Med Interne; 1975; 13(2):141-5. PubMed ID: 1243190
    [Abstract] [Full Text] [Related]

  • 2. Spectrum of hemoglobinopathies in the state of Orissa, India: a ten years cohort study.
    Balgir RS.
    J Assoc Physicians India; 2005 Dec; 53():1021-6. PubMed ID: 16572956
    [Abstract] [Full Text] [Related]

  • 3. HbS in nine Romanian families.
    Predescu C, Bratu V, Popa V, Chicioreanu-Orza G, Tudosie H.
    Med Interne; 1975 Dec; 13(2):135-40. PubMed ID: 1243189
    [Abstract] [Full Text] [Related]

  • 4. [Familial case of Genova 28 (B10) Leu-Pro hemoglobin. Clinical, hematological, genetic and biochemical study of a French family].
    Labie D, Bernadou A, Wajcman H, Bilsqui-Pasquier G.
    Nouv Rev Fr Hematol; 1972 Dec; 12(4):502-6. PubMed ID: 4264206
    [No Abstract] [Full Text] [Related]

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  • 7. Clinical phenotypes and genotypes diagnosis of thalassemia in children.
    Torcharus K, Sriphaisal T, Krutvecho T, Suwanasophon C, Intarapakawong J.
    Southeast Asian J Trop Med Public Health; 1995 Dec; 26 Suppl 1():275-7. PubMed ID: 8629123
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  • 8. [Association of Hbo Arab/beta-thalassemia discovered fortuitously in 2 brothers].
    Mongalgi MA, Debbabi A, Guemira F, Fattoum S.
    Ann Pediatr (Paris); 1992 Apr; 39(4):268-70. PubMed ID: 1616242
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  • 9. "Minor" hemoglobinopathies: a risk factor for asthma.
    Palma-Carlos AG, Palma-Carlos ML, Costa AC.
    Eur Ann Allergy Clin Immunol; 2005 May; 37(5):177-82. PubMed ID: 15984316
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  • 10. [First cases of hemoglobin C diseases in Rumania].
    Bratu V, Predescu C, Roizman N.
    Stud Cercet Med Interna; 1968 May; 9(1):55-9. PubMed ID: 5665105
    [No Abstract] [Full Text] [Related]

  • 11. Family studies of alpha-thalassemia and hemoglobin H disease in Eastern Saudi Arabia.
    Mcniel JR.
    J Med Assoc Thai; 1971 Mar; 54(3):153-66. PubMed ID: 4101839
    [No Abstract] [Full Text] [Related]

  • 12. [Study of hemoglobinopathy in Kashi district of Xinjiang].
    Yu W, Zhang Z, Li H.
    Zhonghua Xue Ye Xue Za Zhi; 1998 Apr; 19(4):198-200. PubMed ID: 11243136
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  • 15. Survey of thalassemias and hemoglobinopathies in the Dai nationality of southern China.
    Zhao SC, Lu DP, Shi HL.
    Chin Med J (Engl); 1988 Apr; 101(4):237-40. PubMed ID: 3138080
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  • 16. [Heterozygous beta thalassemia with increased HbF: independent segregation of beta thalassemia and hereditary persistent fetal hemoglobin (Swiss type) in a Spanish family].
    De Blas JM, Martín E, Martínez ML, Caso F.
    Sangre (Barc); 1985 Apr; 30(1):28-36. PubMed ID: 2408346
    [No Abstract] [Full Text] [Related]

  • 17. A non-deletion hereditary persistence of fetal hemoglobin (HPFH) determinant not linked to the beta-globin gene complex.
    Thein SL, Weatherall DJ.
    Prog Clin Biol Res; 1989 Apr; 316B():97-111. PubMed ID: 2482508
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  • 18. [Hemoglobinopathies in Tunisia. An updated review of the epidemiologic and molecular data].
    Fattoum S.
    Tunis Med; 2006 Nov; 84(11):687-96. PubMed ID: 17294892
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  • 19. [New cases of O-Arabia hemoglobinopathy in the Burgas district].
    Cholakov B, Kunchev KN.
    Vutr Boles; 1974 Nov; 13(3):51-4. PubMed ID: 4446583
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