László Góth
Department of Clinical Biochemistry and Molecular Pathology
University of Debrecen Medical School
PO Box 40
Debrecen
Hungary
Name/email consistency: high
- Detection of a novel familial catalase mutation (Hungarian type D) and the possible risk of inherited catalase deficiency for diabetes mellitus. Góth, L., Vitai, M., Rass, P., Sükei, E., Páy, A. Electrophoresis (2005)
- Blood catalase activity in gestational diabetes is decreased but not associated with pregnancy complications. Góth, L., Tóth, Z., Tarnai, I., Bérces, M., Török, P., Bigler, W.N. Clin. Chem. (2005)
- The effects of hydrogen peroxide promoted by homocysteine and inherited catalase deficiency on human hypocatalasemic patients. Góth, L., Vitai, M. Free Radic. Biol. Med. (2003)
- 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. Góth, L., Rass, P., Madarasi, I. Electrophoresis (2001)
- A new type of inherited catalase deficiencies: its characterization and comparison to the Japanese and Swiss type of acatalasemia. Góth, L. Blood Cells Mol. Dis. (2001)
- Lipid and carbohydrate metabolism in acatalasemia. Góth, L. Clin. Chem. (2000)
- A simple PCR-heteroduplex screening method for detection of a common mutation of the catalase gene in Hungary. Góth, L., Gorzsás, A., Kalmár, T. Clin. Chem. (2000)
