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Journal Abstract Search

88 related items for PubMed ID: 101006

  • 1. beta-Thalassemia in Sicily: hematological and biosynthetic studies.
    Schilirò G, Musumeci S, Pizzarelli G, Di Gregorio L, Fischer A, Russo G.
    Acta Haematol; 1978; 60(4):193-200. PubMed ID: 101006
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  • 2. Hemoglobin G San José [beta 2 7 (A4) Glu to Gly alpha 2], beta thalassemia, and alpha thalassemia in a Sicilian family.
    Musumeci S, Schilirò G, Pizzarelli G, Tentori L, Marinucci M, Fontanarosa PP, Russo G.
    Hum Genet; 1979 Nov; 52(2):239-47. PubMed ID: 511180
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  • 3. Alpha thalassaemia in Sicily: haematological and biosynthetic studies.
    Musumeci S, Schiliro G, Pizzarelli G, D'Agata A, Fischer A, Russo G.
    Br J Haematol; 1979 Nov; 43(3):413-22. PubMed ID: 497118
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  • 4. C3 polymorphism in beta-thalassemia.
    Germenis A, Kalantzi M, Karamerou A, Politi C, Fertakis A.
    Acta Haematol; 1984 Nov; 71(1):45-8. PubMed ID: 6419525
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  • 7. Unusual combination of genetic defects in a Sicilian boy: G gamma delta beta thalassemia, G gamma A gamma heterocellular HPFH, beta (0) thalassemia, and albinism.
    Schilirò G, Pavone L, Romeo MA, Russo A, Musumeci S, Russo G.
    Am J Med Genet; 1983 Jun; 15(2):225-31. PubMed ID: 6192718
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  • 8. Heterogeneity of haplotypes among patients with severe Cooley disease in Eastern Sicily.
    Lombardo M, Ragusa A, Sortino G, Cacciola E, Lombardo T, Labie D.
    Hum Genet; 1986 Feb; 72(2):145-7. PubMed ID: 3002959
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  • 9. Hemoglobin D Ibadan trait in combination with sigma beta thalassemia.
    Castro O, Winter WP, Bullock WH, Jilly PN, Gvozden AB, Rucknagel DL.
    Hemoglobin; 1979 Feb; 3(1):77-82. PubMed ID: 457424
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  • 10. Molecular basis of alpha-thalassemia in Sicily.
    Fichera M, Spalletta A, Fiorenza F, Lombardo T, Schilirò G, Tamouza R, Lapouméroulie C, Labie D, Ragusa A.
    Hum Genet; 1997 Mar; 99(3):381-6. PubMed ID: 9050927
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  • 11. Beta-thalassemia in Brazil.
    Zago MA, Costa F, Bottura C.
    Braz J Med Biol Res; 1981 Dec; 14(6):383-8. PubMed ID: 6086110
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  • 12. [Heterogeneity of globin protein synthesis in bone marrow cells of patients with homozygous beta-thalassemia from Tadzhikistan].
    Nasyrova FIu, Mirakilova AM, Ryzhova IB, Sabzanova RB, Limborskaia SA.
    Mol Gen Mikrobiol Virusol; 1988 Oct; (10):34-40. PubMed ID: 2976480
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  • 14. Molecular mechanisms underlying thalassemia intermedia in Iran.
    Neishabury M, Azarkeivan A, Oberkanins C, Esteghamat F, Amirizadeh N, Najmabadi H.
    Genet Test; 2008 Dec; 12(4):549-56. PubMed ID: 18939939
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  • 16. Types of thalassemia in Sicily.
    Russo G.
    Birth Defects Orig Artic Ser; 1982 Dec; 18(7):185-8. PubMed ID: 7159728
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  • 17. Biosynthetic studies and gamma-chain composition in the Greek type of hereditary persistence of fetal hemoglobin and in its association with beta-thalassemia.
    Camaschella C, Ciocca-Vasino MA, Guerrasio A, Balegno G, Barberis E, Delponte D, Saglio G.
    Acta Haematol; 1979 Dec; 61(5):272-7. PubMed ID: 111454
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  • 19. Silent thalassemias: genotypes and phenotypes.
    Bianco I, Cappabianca MP, Foglietta E, Lerone M, Deidda G, Morlupi L, Grisanti P, Ponzini D, Rinaldi S, Graziani B.
    Haematologica; 1997 Dec; 82(3):269-80. PubMed ID: 9234571
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  • 20. Genotype-phenotype correlation and report of novel mutations in β-globin gene in thalassemia patients.
    Nagar R, Sinha S, Raman R.
    Blood Cells Mol Dis; 2015 Jun; 55(1):10-4. PubMed ID: 25976460
    [Abstract] [Full Text] [Related]

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