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PUBMED FOR HANDHELDS

Journal Abstract Search


229 related items for PubMed ID: 7349757

  • 1. [Alpha thalassemia in Macedonia].
    Efremov G, Stojanovski N, Nastev B, Zisovska C.
    Bilt Hematol Transfuz; 1981; 9(1-3):3-15. PubMed ID: 7349757
    [Abstract] [Full Text] [Related]

  • 2. Comparison of red blood cell hematology among normal, alpha-thalassemia-1 trait, and hemoglobin Bart's fetuses at mid-pregnancy.
    Srisupundit K, Piyamongkol W, Tongsong T.
    Am J Hematol; 2008 Dec; 83(12):908-10. PubMed ID: 18932192
    [Abstract] [Full Text] [Related]

  • 3. Modification of hemoglobin H disease by sickle trait.
    Matthay KK, Mentzer WC, Dozy AM, Kan YW, Bainton DF.
    J Clin Invest; 1979 Oct; 64(4):1024-32. PubMed ID: 479366
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  • 4. Prevalence of hemoglobin E, alpha-thalassemia and glucose-6-phosphate dehydrogenase deficiency in 1,000 cord bloods studied in Bangkok.
    Tanphaichitr VS, Mahasandana C, Suvatte V, Yodthong S, Pung-amritt P, Seeloem J.
    Southeast Asian J Trop Med Public Health; 1995 Oct; 26 Suppl 1():271-4. PubMed ID: 8629122
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  • 5. Determination of hemoglobin Bart's in alpha thalassemia traits by two-site immunoradiometric assay. II. Detection of hemoglobin Bart's in alpha thalassemia traits.
    Makonkawkeyoon L, Ongchai S, Sanguansermsri T.
    J Med Assoc Thai; 1992 Oct; 75(10):565-9. PubMed ID: 1306192
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  • 6. Hb Bart's level in cord blood and deletions of alpha-globin genes.
    Lie-Injo LE, Solai A, Herrera AR, Nicolaisen L, Kan YW, Wan WP, Hasan K.
    Blood; 1982 Feb; 59(2):370-6. PubMed ID: 6895707
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  • 7. Alpha-thalassemia in premature newborns.
    Maccioni L, Galanello R, Ruggeri R, Puddu R, Rosatelli D, Marras A, Chiappe S, Macciotta A, Cao A.
    Pediatr Res; 1986 Nov; 20(11):1077-81. PubMed ID: 3797101
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  • 8. Haemoglobin synthesis in 28 obligatory cases for alpha-thalassemia traits.
    Pootrakul S, Sapprapa S, Wasi P, Na-Nakorn S, Suwanik R.
    Humangenetik; 1975 Sep 10; 29(2):121-6. PubMed ID: 1176133
    [Abstract] [Full Text] [Related]

  • 9. Hb Bart's in cord blood: an accurate indicator of alpha-thalassemia.
    Rugless MJ, Fisher CA, Stephens AD, Amos RJ, Mohammed T, Old JM.
    Hemoglobin; 2006 Sep 10; 30(1):57-62. PubMed ID: 16540417
    [Abstract] [Full Text] [Related]

  • 10. Haemolytic disease of the newborn and chronic anaemia induced by gamma beta thalassaemia in a Dutch family.
    Oort M, Heerspink W, Roos D, Flavell RA, Bernini LF.
    Br J Haematol; 1981 Jun 10; 48(2):251-62. PubMed ID: 7195273
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  • 11. Gene mapping of Malaysian alpha thalassemias with alpha and zeta globin gene probes.
    Lie-Injo LE, Herrera AR, Lebo RV, Hassan K, Lopez CG.
    Am J Hematol; 1985 Mar 10; 18(3):289-96. PubMed ID: 2983536
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  • 12. Quantitative analysis of Hb Bart's in cord blood by capillary electrophoresis system.
    Munkongdee T, Pichanun D, Butthep P, Klamchuen S, Chalermpolprapa V, Winichagoon P, Svasti S, Fucharoen S.
    Ann Hematol; 2011 Jul 10; 90(7):741-6. PubMed ID: 21188378
    [Abstract] [Full Text] [Related]

  • 13. [Alpha-thalassemia in Puglia. II. Neonatal screening for Bart's hemoglobin].
    Izzo P, Pasculli D, Schonauer S, Mudoni A, De Mattia D, Constantino R, Melpignano A, Saccia M.
    Boll Soc Ital Biol Sper; 1979 Apr 15; 55(7):703-8. PubMed ID: 550897
    [Abstract] [Full Text] [Related]

  • 14. Sickle cell anemia associated with alpha-thalassemia in Malaysian Indians.
    Lie-Injo LE, Hassan K, Joishy SK, Lim ML.
    Am J Hematol; 1986 Jul 15; 22(3):265-74. PubMed ID: 2424302
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  • 16. Thalassemia intermedia associated with the Hb Constant Spring EE Bart's disease in pregnancy: a molecular and hematological analysis.
    Fucharoen S, Fucharoen G, Sae-ung N, Sanchaisuriya K.
    Blood Cells Mol Dis; 2007 Jul 15; 39(2):195-8. PubMed ID: 17587614
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  • 20. Variability in the interaction of beta-thalassemia with the alpha-chain variants Hb G-Philadelphia and Hb Rampa.
    Huisman TH, Gravely ME, Henson J, Felice A, Wilson JB, Abraham EC, Vella F, Little MW.
    J Lab Clin Med; 1978 Aug 15; 92(2):311-20. PubMed ID: 681817
    [Abstract] [Full Text] [Related]


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