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Page 1
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: kalmar t. Ideggyogy Sz. 2023 Jan 30;76(1-2):63-72. doi: 10.18071/isz.76.0063. Ideggyogy Sz. 2023. PMID: 36892293 Free article. English.
Hemizygous nonsense variant in the moesin gene (MSN) leads to a new autoimmune phenotype of Immunodeficiency 50.
Kovács AL, Kárteszi J, Prohászka Z, Kalmár T, Késmárky G, Koltai K, Nagy Z, Sebők J, Vas T, Molnár K, Berki T, Böröcz K, Gyömörei C, Szalma J, Egyed M, Horváth S, Oláh P, Csuka D, Németh V, Gyulai R. Kovács AL, et al. Among authors: kalmar t. Front Immunol. 2022 Sep 1;13:919411. doi: 10.3389/fimmu.2022.919411. eCollection 2022. Front Immunol. 2022. PMID: 36119109 Free PMC article.
[CYP24A1 gene defect manifesting with gestational hypercalcemia].
Györkös A, Tőke J, Sohár G, Kovács M, Goldfinger J, Vajda G, Kalmár T, Tóth M. Györkös A, et al. Among authors: kalmar t. Orv Hetil. 2022 Jul 31;163(31):1237-1242. doi: 10.1556/650.2022.32520. Print 2022 Jul 31. Orv Hetil. 2022. PMID: 35908214 Hungarian.
The genetic origin of Huns, Avars, and conquering Hungarians.
Maróti Z, Neparáczki E, Schütz O, Maár K, Varga GIB, Kovács B, Kalmár T, Nyerki E, Nagy I, Latinovics D, Tihanyi B, Marcsik A, Pálfi G, Bernert Z, Gallina Z, Horváth C, Varga S, Költő L, Raskó I, Nagy PL, Balogh C, Zink A, Maixner F, Götherström A, George R, Szalontai C, Szenthe G, Gáll E, Kiss AP, Gulyás B, Kovacsóczy BN, Gál SS, Tomka P, Török T. Maróti Z, et al. Among authors: kalmar t. Curr Biol. 2022 Jul 11;32(13):2858-2870.e7. doi: 10.1016/j.cub.2022.04.093. Epub 2022 May 25. Curr Biol. 2022. PMID: 35617951 Free article.
49 results