Fazakas F - Search Results

1

Germline VHL gene mutations in Hungarian families with von Hippel-Lindau disease and patients with apparently sporadic unilateral pheochromocytomas.

Gergics P, Patocs A, Toth M, Igaz P, Szucs N, Liko I, Fazakas F, Szabo I, Kovacs B, Glaz E, Racz K. Gergics P, et al. Among authors: fazakas f. Eur J Endocrinol. 2009 Sep;161(3):495-502. doi: 10.1530/EJE-09-0399. Epub 2009 Jul 2. Eur J Endocrinol. 2009. PMID: 19574279

2

Ser80Ile mutation and a concurrent Pro25Leu variant of the VHL gene in an extended Hungarian von Hippel-Lindau family.

Patocs A, Gergics P, Balogh K, Toth M, Fazakas F, Liko I, Racz K. Patocs A, et al. Among authors: fazakas f. BMC Med Genet. 2008 Apr 16;9:29. doi: 10.1186/1471-2350-9-29. BMC Med Genet. 2008. PMID: 18416845 Free PMC article.

3

Three novel germ-line VHL mutations in Hungarian von Hippel-Lindau patients, including a nonsense mutation in a fifteen-year-old boy with renal cell carcinoma.

Losonczy G, Fazakas F, Pfliegler G, Komáromi I, Balázs E, Pénzes K, Berta A. Losonczy G, et al. Among authors: fazakas f. BMC Med Genet. 2013 Jan 8;14:3. doi: 10.1186/1471-2350-14-3. BMC Med Genet. 2013. PMID: 23298237 Free PMC article.

4

GJB2 mutations in patients with non-syndromic hearing loss from Northeastern Hungary.

Tóth T, Kupka S, Haack B, Riemann K, Braun S, Fazakas F, Zenner HP, Muszbek L, Blin N, Pfister M, Sziklai I. Tóth T, et al. Among authors: fazakas f. Hum Mutat. 2004 Jun;23(6):631-2. doi: 10.1002/humu.9250. Hum Mutat. 2004. PMID: 15146474

5

Coincidence of mutations in different connexin genes in Hungarian patients.

Tóth T, Kupka S, Haack B, Fazakas F, Muszbek L, Blin N, Pfister M, Sziklai I. Tóth T, et al. Among authors: fazakas f. Int J Mol Med. 2007 Sep;20(3):315-21. Int J Mol Med. 2007. PMID: 17671735

6

Decreased blood catalase activity is not related to specific beta-thalassemia mutations in Hungary.

Kósa Z, Nagy T, Nagy E, Fazakas F, Góth L. Kósa Z, et al. Among authors: fazakas f. Int J Lab Hematol. 2012 Apr;34(2):172-8. doi: 10.1111/j.1751-553X.2011.01377.x. Epub 2011 Oct 10. Int J Lab Hematol. 2012. PMID: 21985133

7

TGFBI (BIGH3) gene mutations in Hungary--report of the novel F547S mutation associated with polymorphic corneal amyloidosis.

Takács L, Losonczy G, Matesz K, Balogh I, Sohajda Z, Tóth K, Fazakas F, Vereb G, Berta A. Takács L, et al. Among authors: fazakas f. Mol Vis. 2007 Oct 18;13:1976-83. Mol Vis. 2007. PMID: 17982422

8

Changes of KRAS Exon 2 Codon 12/13 Mutation Status in Recurrent Colorectal Cancer.

Dócs O, Fazakas F, Horváth NL, Tóth L, András C, Horváth Z, Méhes G. Dócs O, et al. Among authors: fazakas f. Pathol Oncol Res. 2015 Apr;21(2):399-404. doi: 10.1007/s12253-014-9834-2. Epub 2014 Sep 24. Pathol Oncol Res. 2015. PMID: 25248721 Free article.

9

A new mutation in the human pres gene and its effect on prestin function.

Toth T, Deak L, Fazakas F, Zheng J, Muszbek L, Sziklai I. Toth T, et al. Among authors: fazakas f. Int J Mol Med. 2007 Oct;20(4):545-50. Int J Mol Med. 2007. PMID: 17786286

10

Variant type Glanzmann thrombasthenia caused by homozygous p.724R>X mutation in beta3 integrin.

Bagoly Z, Fazakas F, Marosi A, Török O, Bereczky Z, Haramura G, Tóth J, Kappelmayer J, Muszbek L. Bagoly Z, et al. Among authors: fazakas f. Thromb Res. 2010 May;125(5):427-31. doi: 10.1016/j.thromres.2010.01.002. Epub 2010 Jan 27. Thromb Res. 2010. PMID: 20106508 No abstract available.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

19 results

Search Page

Filters