Szalay F - Search Results

1

[ATP7B gene mutations in Hungarian patients with Wilson disease--case reports to illustrate the diverse clinical presentations].

Folhoffer A, Horváth A, Hegedüs D, Firneisz G, Dunkel K, Willheim C, Ferenci P, Szönyi L, Abonyi M, Lakatos PL, Szalay F. Folhoffer A, et al. Among authors: szalay f. Orv Hetil. 2003 Dec 21;144(51):2509-15. Orv Hetil. 2003. PMID: 14974157 Hungarian.

2

[Genetic aspects of liver diseases].

Pár A, Szalay F, Lakatos PL, Nagy Z, Mózsik G. Pár A, et al. Among authors: szalay f. Orv Hetil. 2002 Jan 6;143(1):3-12. Orv Hetil. 2002. PMID: 11816376 Review. Hungarian.

3

[Gene therapy in liver diseases].

Pár A, Lakatos PL, Abonyi M, Szalay F, Nagy Z, Mózsik G. Pár A, et al. Among authors: szalay f. Orv Hetil. 2002 Jan 20;143(3):125-9. Orv Hetil. 2002. PMID: 11883109 Review. Hungarian.

4

[Decreased bone mineral density and gene polymorphism in primary biliary cirrhosis].

Lakatos PL, Bajnok E, Tornai I, Folhoffer A, Horváth A, Lakatos P, Szalay F. Lakatos PL, et al. Among authors: szalay f. Orv Hetil. 2004 Feb 15;145(7):331-6. Orv Hetil. 2004. PMID: 15049048 Hungarian.

5

Novel mutations of the ATP7B gene among 109 Hungarian patients with Wilson's disease.

Folhoffer A, Ferenci P, Csak T, Horvath A, Hegedus D, Firneisz G, Osztovits J, Kosa JP, Willheim-Polli C, Szonyi L, Abonyi M, Lakatos PL, Szalay F. Folhoffer A, et al. Among authors: szalay f. Eur J Gastroenterol Hepatol. 2007 Feb;19(2):105-11. doi: 10.1097/01.meg.0000223904.70492.0b. Eur J Gastroenterol Hepatol. 2007. PMID: 17272994

6

[Liver transplantation in Wilson's disease patients, 1996-2017].

Németh D, Folhoffer A, László SB, Kóbori L, Görög D, Fehérvári I, Fazakas J, Gerlei Z, Máthé Z, Szalay F. Németh D, et al. Among authors: szalay f. Orv Hetil. 2019 Dec;160(51):2021-2025. doi: 10.1556/650.2019.31582. Orv Hetil. 2019. PMID: 31838861 Hungarian.

7

Common mutations of ATP7B in Wilson disease patients from Hungary.

Firneisz G, Lakatos PL, Szalay F, Polli C, Glant TT, Ferenci P. Firneisz G, et al. Among authors: szalay f. Am J Med Genet. 2002 Feb 15;108(1):23-8. doi: 10.1002/ajmg.10220. Am J Med Genet. 2002. PMID: 11857545

8

[Wilson disease in 2003].

Szalay F. Szalay F. Orv Hetil. 2003 Dec 14;144(50):2451-8. Orv Hetil. 2003. PMID: 15067983 Review. Hungarian.

9

Insulin-like growth factor I gene microsatellite repeat, collagen type Ialpha1 gene Sp1 polymorphism, and bone disease in primary biliary cirrhosis.

Lakatos PL, Bajnok E, Tornai I, Folhoffer A, Horvath A, Lakatos P, Habior A, Szalay F. Lakatos PL, et al. Among authors: szalay f. Eur J Gastroenterol Hepatol. 2004 Aug;16(8):753-9. doi: 10.1097/01.meg.0000108364.41221.d0. Eur J Gastroenterol Hepatol. 2004. PMID: 15256976

10

[NOD2/CARD15 mutations and genotype-phenotype correlations in patients with Crohn's disease. Hungarian multicenter study].

Lakatos L, Lakatos PL, Willheim-Polli C, Reinisch W, Ferenci P, Tulassay Z, Molnár T, Kovács A, Papp J, Szalay F; Hungarian IBD Study Group. Lakatos L, et al. Among authors: szalay f. Orv Hetil. 2004 Jul 4;145(27):1403-11. Orv Hetil. 2004. PMID: 15320482 Hungarian.

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