Nagy, T., Góth, L.: Catalase and Its Applications.
In: The Blood Catalase in the Human Body. Ed.: Mariana R. Lauar, Débora S. A. Colombari, Eduardo Colombari, Patrícia M. De Paula, Laurival A. De Luca Jr., Carina A. F. Andrade, José V. Menani, I. Ryzhik, M. Makarov, Mouna Ghorbel, Faical Brini, Teréz Nagy, László Góth, Safija Herenda, Edhem Haskovic, Nova Science Publishers, New York, 77-92, 2022. ISBN: 9798886974218

Káplár, M., Nagy, T., Góth, L.: Association of Catalase Gene rs769217 Polymorphism with Carotid Intima-media Thickness in Diabetic Patients.
Int. J. Diabetes Metab. Disord. 3 (1), 1-5, 2018.

Nagy, T., Góth, L.: Decreased blood catalase activity in diabetes.
J. Diabetes Care Endocrin. 1 e001, 2017.

Góth, L., Zabolai, E., Nagy, T.: Fast screening method for polymorphisms in exon 9 of the catalase gene.
JDRR. 1 (1), 50-59, 2017.

Góth, L., Nagy, T., Paragh, G., Káplár, M.: Blood Catalase Activities, Catalase Gene Polymorphisms and Acatalasemia Mutations in Hungarian Patients with Diabetes Mellitus.
Glob. J. Obes. Diabetes. Metab. Syndr. 3 (1), 001-005, 2016.

Góth, L., Nagy, T.: Are the catalase Gene mutations Responsible for the Decreased Blood catalase Activity?.
Int. J. Clin. Chem. Labor. Med. 1 (1), 15-17, 2015.

Góth, L., Nagy, T., Káplár, M.: A veleszületett katalázhiány (acatalasaemia) és a 2-es típusú diabetes mellitus.
Orvosi Hetilap. 156 (10), 393-398, 2015.

Nagy, T., Pászti, E., Káplár, M., Bhattoa, H., Góth, L.: Further acatalasemia mutations in human patients from Hungary with diabetes and microcytic anemia.
Mutat. Res. Fundam. Mol. Mech. Mutagen. 772 10-14, 2015.

Góth, L., Nagy, T.: Inherited catalase deficiency: is it benign or a factor in various age related disorders?.
Mutat. Res.-Rev. Mutat. Res. 753 (2), 147-154, 2013.

Góth, L., Nagy, T.: Acatalasemia and diabetes mellitus.
Arch. Biochem. Biophys. 525 (2), 195-200, 2012.

Nagy, T., Csordás, M., Kósa, Z., Góth, L.: A simple method for examination of polymorphisms of catalase exon 9: rs769217 in Hungarian microcytic anemia and beta-thalassemia patients.
Arch. Biochem. Biophys. 525 (2), 201-206, 2012.

Kósa, Z., Fejes, Z., Nagy, T., Csordás, M., Simics, E., Remenyik, É., Góth, L.: Catalase - 262C>T polymorphisms in Hungarian vitiligo patients and in controls: further acatalasemia mutations in Hungary.
Mol. Biol. Rep. 39 (4), 4787-4795, 2012.

Kósa, Z., Nagy, T., Nagy, E., Fazakas, F., Góth, L.: Decreased blood catalase activity is not related to specific beta-thalassemia mutations in Hungary.
Int. J. Lab. Hematol. 34 (2), 172-178, 2012.

Góth, L., Nagy, T., Kósa, Z., Fejes, Z., Bhattoa, H., Paragh, G., Káplár, M.: Effects of rs769217 and rs1001179 polymorphisms of catalase gene on blood catalase, carbohydrate and lipid biomarkers in diabetes mellitus.
Free Radic. Res. 46 (10), 1249-1257, 2012.