Gergics P - 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. 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

MEN1 gene mutations in Hungarian patients with multiple endocrine neoplasia type 1.

Balogh K, Hunyady L, Patocs A, Gergics P, Valkusz Z, Toth M, Racz K. Balogh K, et al. Among authors: gergics p. Clin Endocrinol (Oxf). 2007 Nov;67(5):727-34. doi: 10.1111/j.1365-2265.2007.02953.x. Clin Endocrinol (Oxf). 2007. PMID: 17953629

3

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: gergics p. BMC Med Genet. 2008 Apr 16;9:29. doi: 10.1186/1471-2350-9-29. BMC Med Genet. 2008. PMID: 18416845 Free PMC article.

4

[Methods for the analysis of large gene deletions and their application in some hereditary diseases].

Gergics P, Toke J, Szilágyi A, Szappanos A, Kender Z, Barta G, Tóth M, Igaz P, Rácz K, Patócs A. Gergics P, et al. Orv Hetil. 2009 Dec 13;150(50):2258-64. doi: 10.1556/OH.2009.28755. Orv Hetil. 2009. PMID: 19951857 Review. Hungarian.

5

Novel mutation of the CYP17 gene in two unrelated patients with combined 17alpha-hydroxylase/17,20-lyase deficiency: demonstration of absent enzyme activity by expressing the mutant CYP17 gene and by three-dimensional modeling.

Patocs A, Liko I, Varga I, Gergics P, Boros A, Futo L, Kun I, Bertalan R, Toth S, Pazmany T, Toth M, Szücs N, Horanyi J, Glaz E, Racz K. Patocs A, et al. Among authors: gergics p. J Steroid Biochem Mol Biol. 2005 Nov;97(3):257-65. doi: 10.1016/j.jsbmb.2005.06.035. Epub 2005 Sep 19. J Steroid Biochem Mol Biol. 2005. PMID: 16176874

6

[Clinical symptoms, diagnosis and treatment of multiple endocrine neoplasia type 1. Results of genetic screening in Hungarian patients].

Balogh K, Hunyady L, Patócs A, Valkusz Z, Bertalan R, Gergics P, Majnik J, Toke J, Tóth M, Szucs N, Gláz E, Futo L, Horányi J, Rácz K, Tulassay Z. Balogh K, et al. Among authors: gergics p. Orv Hetil. 2005 Oct 23;146(43):2191-7. Orv Hetil. 2005. PMID: 16323565 Review. Hungarian.

7

Overrepresentation of the N363S variant of the glucocorticoid receptor gene in patients with bilateral adrenal incidentalomas.

Majnik J, Patocs A, Balogh K, Toth M, Gergics P, Szappanos A, Mondok A, Borgulya G, Panczel P, Prohaszka Z, Racz K. Majnik J, et al. Among authors: gergics p. J Clin Endocrinol Metab. 2006 Jul;91(7):2796-9. doi: 10.1210/jc.2006-0066. Epub 2006 Apr 24. J Clin Endocrinol Metab. 2006. PMID: 16636127

8

Genotype-phenotype correlations in Hungarian patients with hereditary medullary thyroid cancer.

Patocs A, Klein I, Szilvasi A, Gergics P, Toth M, Valkusz Z, Forizs E, Igaz P, Al-Farhat Y, Tordai A, Varadi A, Racz K, Esik O. Patocs A, et al. Among authors: gergics p. Wien Klin Wochenschr. 2006 Jul;118(13-14):417-21. doi: 10.1007/s00508-006-0635-9. Wien Klin Wochenschr. 2006. PMID: 16865647

9

Neonatal severe hyperparathyroidism associated with a novel de novo heterozygous R551K inactivating mutation and a heterozygous A986S polymorphism of the calcium-sensing receptor gene.

Tõke J, Czirják G, Patócs A, Enyedi B, Gergics P, Csákváry V, Enyedi P, Tóth M. Tõke J, et al. Among authors: gergics p. Clin Endocrinol (Oxf). 2007 Sep;67(3):385-92. doi: 10.1111/j.1365-2265.2007.02896.x. Epub 2007 Jun 7. Clin Endocrinol (Oxf). 2007. PMID: 17555508

10

Parathyroid hormone-dependent hypercalcemia.

Toke J, Patócs A, Balogh K, Gergics P, Stenczer B, Rácz K, Tóth M. Toke J, et al. Among authors: gergics p. Wien Klin Wochenschr. 2009;121(7-8):236-45. doi: 10.1007/s00508-009-1149-z. Wien Klin Wochenschr. 2009. PMID: 19562279 Review.

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