Catalase deficiency and type 2 diabetes von Góth, László

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Inherited catalase deficiency: Is it benign or a factor in various age related disorders? von Góth, László, Nagy, Teréz

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Acatalasemia and diabetes mellitus von Góth, László, Nagy, Teréz

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A simple method for examination of polymorphisms of catalase exon 9: rs769217 in Hungarian microcytic anemia and beta-thalassemia patients von Nagy, Teréz, Csordás, Melinda, Kósa, Zsuzsanna, Góth, László

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Reactive oxygen species, hydrogen peroxide, catalase and diabetes mellitus von Góth, László

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The effects of hydrogen peroxide promoted by homocysteine and inherited catalase deficiency on human hypocatalasemic patients von Góth, László, Vitai, Márta

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Catalase deficiency may complicate urate oxidase (rasburicase) therapy von Góth, László, Bigler, N. William

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Catalase −262C>T polymorphisms in Hungarian vitiligo patients and in controls: further acatalasemia mutations in Hungary von Kósa, Zsuzsanna, Fejes, Zsolt, Nagy, Teréz, Csordás, Melinda, Simics, Enikő, Remenyik, Éva, Góth, László

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Rare isoform of alkaline phosphatase in necrotic granulomatous inflammation of liver von Góth, László, Asztalos, László, Dezső, Balázs

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Genetic heterogeneity of the 5′ uncoding region of the catalase gene in Hungarian acatalasemic and hypocatalasemic subjects von GOTH, L

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A Novel Catalase Mutation (a GA Insertion) Causes the Hungarian Type of Acatalasemia von Góth, László, Shemirani, Amir, Kalmár, Tibor

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Polymorphism of 5′ of the catalase gene in Hungarian acatalasemia and hypocatalasemia von Góth, László, Vitai, Márta

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Hereditary catalase deficiencies and increased risk of diabetes von Goth, Laszlo, Eaton, John W

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Lipid and Carbohydrate Metabolism in Acatalasemia von Góth, László

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Lipid and carbohydrate metabolism in acatalasemia von GOTH, L

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A novel catalase mutation (a G insertion in exon 2) causes the type B of the Hungarian acatalasemia von GOTH, Laszlo

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A New Type of Inherited Catalase Deficiencies: Its Characterization and Comparison to the Japanese and Swiss Type of Acatalasemia von Góth, László

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Detection of a novel familial catalase mutation (Hungarian type D) and the possible risk of inherited catalase deficiency for diabetes mellitus von Góth, László, Vitai, Márta, Rass, Péter, Sükei, Eszter, Páy, Anikó

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A novel catalase mutation detected by polymerase chain reaction-single strand conformation polymorphism, nucleotide sequencing, and Western blot analyses is responsible for the typ... von Góth, László, Rass, Péter, Madarasi, Irén

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Blood catalase deficiency and diabetes in Hungary von Góth, L, Lenkey A, Bigler, W N

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