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Results: 1-8 |
Results: 8

Authors: Goth, L
Citation: L. Goth, A new type of inherited catalase deficiencies: Its characterization and comparison to the Japanese and Swiss type of acatalasemia, BL CELL M D, 27(2), 2001, pp. 512-517

Authors: Goth, L Rass, P Madarasi, I
Citation: L. Goth et al., A novel catalase mutation detected by polymerase chain reaction-single strand conformation polymorphism, nucleotide sequencing, and Western blot analyses is responsible for the type C of Hungarian acatalasemia, ELECTROPHOR, 22(1), 2001, pp. 49-51

Authors: Goth, L Lenkey, A Bigler, WN
Citation: L. Goth et al., Blood catalase deficiency and diabetes in Hungary, DIABET CARE, 24(10), 2001, pp. 1839-1840

Authors: Goth, L
Citation: L. Goth, A novel catalase mutation (a G insertion in exon 2) causes the type B of the Hungarian acatalasemia, CLIN CHIM A, 311(2), 2001, pp. 161

Authors: Goth, L Shemirani, A Kalmar, T
Citation: L. Goth et al., A novel catalase mutation (a GA insertion) causes the Hungarian type of acatalasemia, BL CELL M D, 26(2), 2000, pp. 151-154

Authors: Goth, L Eaton, JW
Citation: L. Goth et Jw. Eaton, Hereditary catalase deficiencies and increased risk of diabetes, LANCET, 356(9244), 2000, pp. 1820-1821

Authors: Goth, L Gorzsas, A Kalmar, T
Citation: L. Goth et al., A simple PCR-heteroduplex screening method for detection of a common mutation of the catalase gene in Hungary, CLIN CHEM, 46(8), 2000, pp. 1199-1200

Authors: Goth, L
Citation: L. Goth, Lipid and carbohydrate metabolism in acatalasemia, CLIN CHEM, 46(4), 2000, pp. 564-566
Risultati: 1-8 |