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Genetic identification of members of the prominent Báthory aristocratic family.
Gînguță A, Kovács B, Schütz O, Tihanyi B, Nyerki E, Maár K, Maróti Z, Varga GIB, Băcueț-Crișan D, Keresztes T, Török T, Neparáczki E. Gînguță A, et al. Among authors: maroti z. iScience. 2023 Sep 14;26(10):107911. doi: 10.1016/j.isci.2023.107911. eCollection 2023 Oct 20. iScience. 2023. PMID: 37810237 Free PMC article.
Novel heterozygous STUB1 gene mutation causes SCA48 in a Hungarian patient.
Klivényi P, Szpisjak L, Salamon A, Németh VL, Szépfalusi N, Maróti Z, Kalmár T, Zimmermann A, Zádori D. Klivényi P, et al. Among authors: maroti z. Ideggyogy Sz. 2023 Jan 30;76(1-2):63-72. doi: 10.18071/isz.76.0063. Ideggyogy Sz. 2023. PMID: 36892293 Free article. English.
Partial RAG deficiency in a patient with varicella infection, autoimmune cytopenia, and anticytokine antibodies.
Goda V, Malik A, Kalmar T, Maroti Z, Patel B, Ujhazi B, Csomos K, Hale JE, Chen K, Bleesing J, Palma P, Cancrini C, Comeau AM, Krivan G, Walter JE. Goda V, et al. Among authors: maroti z. J Allergy Clin Immunol Pract. 2018 Sep-Oct;6(5):1769-1771.e2. doi: 10.1016/j.jaip.2018.01.015. Epub 2018 Feb 2. J Allergy Clin Immunol Pract. 2018. PMID: 29410113 Free PMC article. No abstract available.
Comprehensive genetic testing in children with a clinical diagnosis of ARPKD identifies phenocopies.
Szabó T, Orosz P, Balogh E, Jávorszky E, Máttyus I, Bereczki C, Maróti Z, Kalmár T, Szabó AJ, Reusz G, Várkonyi I, Marián E, Gombos É, Orosz O, Madar L, Balla G, Kappelmayer J, Tory K, Balogh I. Szabó T, et al. Among authors: maroti z. Pediatr Nephrol. 2018 Oct;33(10):1713-1721. doi: 10.1007/s00467-018-3992-5. Epub 2018 Jun 28. Pediatr Nephrol. 2018. PMID: 29956005
64 results