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568 related items for PubMed ID: 10772881

  • 1. Molecular characterization of a German variant of glucose-6-phosphate dehydrogenase deficiency (G6PD Aachen).
    Efferth T, Osieka R, Beutler E.
    Blood Cells Mol Dis; 2000 Feb; 26(1):101-4. PubMed ID: 10772881
    [Abstract] [Full Text] [Related]

  • 2. Genotype and phenotype correlation in glucose-6-phosphate dehydrogenase deficiency.
    Pietrapertosa A, Palma A, Campanale D, Delios G, Vitucci A, Tannoia N.
    Haematologica; 2001 Jan; 86(1):30-5. PubMed ID: 11146567
    [Abstract] [Full Text] [Related]

  • 3. DNA damage and apoptosis in mononuclear cells from glucose-6-phosphate dehydrogenase-deficient patients (G6PD Aachen variant) after UV irradiation.
    Efferth T, Fabry U, Osieka R.
    J Leukoc Biol; 2001 Mar; 69(3):340-2. PubMed ID: 11261779
    [Abstract] [Full Text] [Related]

  • 4. [Identification of molecular variants of the enzyme glucose-6-phosphate dehydrogenase by the polymerase chain reaction technique].
    Rovira A, Vives Corrons JL, Estrada M, Gutiérrez A, Pujades MA, Colomer D, Corbella M, Aymerich M.
    Med Clin (Barc); 1994 Mar 05; 102(8):281-4. PubMed ID: 8170224
    [Abstract] [Full Text] [Related]

  • 5. Molecular heterogeneity of glucose-6-phosphate dehydrogenase (G6PD) variants in the south of Thailand and identification of a novel variant (G6PD Songklanagarind).
    Laosombat V, Sattayasevana B, Janejindamai W, Viprakasit V, Shirakawa T, Nishiyama K, Matsuo M.
    Blood Cells Mol Dis; 2005 Mar 05; 34(2):191-6. PubMed ID: 15727905
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  • 6. Two distinct Indian G6PD variants G6PD Jamnagar and G6PD Rohini caused by the same 949 G-->A mutation.
    Sukumar S, Mukherjee MB, Colah RB, Mohanty D.
    Blood Cells Mol Dis; 2005 Mar 05; 35(2):193-5. PubMed ID: 15996881
    [Abstract] [Full Text] [Related]

  • 7. Neonatal jaundice and molecular mutations in glucose-6-phosphate dehydrogenase deficient newborn infants.
    Huang CS, Hung KL, Huang MJ, Li YC, Liu TH, Tang TK.
    Am J Hematol; 1996 Jan 05; 51(1):19-25. PubMed ID: 8571933
    [Abstract] [Full Text] [Related]

  • 8. [Molecular analysis of glucose-6-dehydrogenase deficiency in Spain].
    Vives Corrons JL, Zarza R, Aymerich JM, Boixadera J, Carrera A, Colomer D, Corbella M, Castro M, Crespo JM, Del Arco A, Erkiaga S, Font L, González I, Juncá J, Lausin A, Manrubia E, Martín Núñez G, Murga MJ, Oliva E, Pérez de Mendiguren B, Pujades MA, Remacha A, Rovira A, Villegas A.
    Sangre (Barc); 1997 Oct 05; 42(5):391-8. PubMed ID: 9424740
    [Abstract] [Full Text] [Related]

  • 9. Molecular characterization of glucose-6-phosphate dehydrogenase deficiency in Pakistani population.
    Moiz B, Nasir A, Moatter T, Naqvi ZA, Khurshid M.
    Int J Lab Hematol; 2011 Dec 05; 33(6):570-8. PubMed ID: 21507207
    [Abstract] [Full Text] [Related]

  • 10. Several mutations including two novel mutations of the glucose-6-phosphate dehydrogenase gene in Polish G6PD deficient subjects with chronic nonspherocytic hemolytic anemia, acute hemolytic anemia, and favism.
    Jablonska-Skwiecinska E, Lewandowska I, Plochocka D, Topczewski J, Zimowski JG, Klopocka J, Burzynska B.
    Hum Mutat; 1999 Dec 05; 14(6):477-84. PubMed ID: 10571945
    [Abstract] [Full Text] [Related]

  • 11. Molecular characterization of glucose-6-phosphate dehydrogenase deficiency in the Kurdish population of Western Iran.
    Rahimi Z, Vaisi-Raygani A, Nagel RL, Muniz A.
    Blood Cells Mol Dis; 2006 Dec 05; 37(2):91-4. PubMed ID: 16938474
    [Abstract] [Full Text] [Related]

  • 12. Chronic nonspherocytic hemolytic anemia due to glucose-6-phosphate dehydrogenase deficiency: report of two families with novel mutations causing G6PD Bangkok and G6PD Bangkok Noi.
    Tanphaichitr VS, Hirono A, Pung-amritt P, Treesucon A, Wanachiwanawin W.
    Ann Hematol; 2011 Jul 05; 90(7):769-75. PubMed ID: 21302115
    [Abstract] [Full Text] [Related]

  • 13. Incidence and complete molecular characterization of glucose-6-phosphate dehydrogenase deficiency in the Guangxi Zhuang autonomous region of southern China: description of four novel mutations.
    Yan T, Cai R, Mo O, Zhu D, Ouyang H, Huang L, Zhao M, Huang F, Li L, Liang X, Xu X.
    Haematologica; 2006 Oct 05; 91(10):1321-8. PubMed ID: 17018380
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  • 16. Molecular and biochemical data on some glucose-6-phosphate dehydrogenase variants from southern Sardinia.
    Frigerio R, Sole G, Lovicu M, Passiu G.
    Haematologica; 1994 Oct 05; 79(4):319-21. PubMed ID: 7806085
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  • 17. Molecular characterization of erythrocyte glucose-6-phosphate dehydrogenase deficiency in Tunisia.
    Daoud BB, Mosbehi I, Préhu C, Chaouachi D, Hafsia R, Abbes S.
    Pathol Biol (Paris); 2008 Jul 05; 56(5):260-7. PubMed ID: 18226470
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  • 19. Association of glucose-6-phosphate dehydrogenase deficiency and X-linked chronic granulomatous disease in a child with anemia and recurrent infections.
    Agudelo-Flórez P, Costa-Carvalho BT, López JA, Redher J, Newburger PE, Olalla-Saad ST, Condino-Neto A.
    Am J Hematol; 2004 Mar 05; 75(3):151-6. PubMed ID: 14978696
    [Abstract] [Full Text] [Related]

  • 20. Description of a novel missense mutation of glucose-6-phosphate dehydrogenase gene associated with asymptomatic high enzyme deficiency.
    Minucci A, Concolino P, Antenucci M, Santonocito C, Ameglio F, Zuppi C, Giardina B, Capoluongo E.
    Clin Biochem; 2007 Aug 05; 40(12):856-8. PubMed ID: 17524386
    [Abstract] [Full Text] [Related]

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