Bertalan R - Search Results

1

[The prevalence of SHOX gene deletion in children with idiopathic short stature. A multicentric study].

Dávid A, Butz H, Halász Z, Török D, Nyirő G, Muzsnai Á, Csákváry V, Luczay A, Sallai Á, Hosszú É, Felszeghy E, Tar A, Szántó Z, Fekete GL, Kun I, Patócs A, Bertalan R. Dávid A, et al. Among authors: bertalan r. Orv Hetil. 2017 Aug;158(34):1351-1356. doi: 10.1556/650.2017.30829. Orv Hetil. 2017. PMID: 28823207 Hungarian.

2

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: bertalan r. 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

3

[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: bertalan r. Orv Hetil. 2005 Oct 23;146(43):2191-7. Orv Hetil. 2005. PMID: 16323565 Review. Hungarian.

4

[Nucleotide sequence variants of the glucocorticoid receptor gene and their significance in determining glucocorticoid sensitivity].

Majnik J, Patócs A, Balogh K, Luczay A, Török D, Szabó V, Borgulya G, Gergics P, Szappanos A, Bertalan R, Belema B, Toke J, Sereg M, Nagy ZZ, Sólyom J, Tóth M, Gláz E, Rácz K, Németh J, Fekete G, Tulassay Z. Majnik J, et al. Among authors: bertalan r. Orv Hetil. 2006 Nov 5;147(44):2107-15. Orv Hetil. 2006. PMID: 17209299 Review. Hungarian.

5

High prevalence of PROP1 gene mutations in Hungarian patients with childhood-onset combined anterior pituitary hormone deficiency.

Halász Z, Toke J, Patócs A, Bertalan R, Tömböl Z, Sallai A, Hosszú E, Muzsnai A, Kovács L, Sólyom J, Fekete G, Rácz K. Halász Z, et al. Among authors: bertalan r. Endocrine. 2006 Dec;30(3):255-60. doi: 10.1007/s12020-006-0002-7. Endocrine. 2006. PMID: 17526936

6

Maternal hyperandrogenism beginning from early pregnancy and progressing until delivery does not produce virilization of a female newborn.

Bertalan R, Csabay L, Blazovics A, Rigo J Jr, Varga I, Halasz Z, Toldy E, Boyle B, Racz K. Bertalan R, et al. Gynecol Endocrinol. 2007 Oct;23(10):581-3. doi: 10.1080/09513590701553571. Gynecol Endocrinol. 2007. PMID: 17852424

7

The 9th European congress of endocrinology.

Luczay A, Bertalan R, Racz K. Luczay A, et al. Among authors: bertalan r. Pediatr Endocrinol Rev. 2007 Dec;5(2):686-7. Pediatr Endocrinol Rev. 2007. PMID: 18084164 No abstract available.

8

Laterality disturbance and hypopituitarism. A case report of co-existing situs inversus totalis and combined pituitary hormone deficiency.

Halász Z, Bertalan R, Toke J, Patócs A, Tóth M, Fekete G, Gláz E, Rácz K. Halász Z, et al. Among authors: bertalan r. J Endocrinol Invest. 2008 Jan;31(1):74-8. doi: 10.1007/BF03345570. J Endocrinol Invest. 2008. PMID: 18296909

9

The protective effect of the ER22/23EK polymorphism against an excessive weight gain during pregnancy.

Bertalan R, Patócs A, Boyle B, Rigó J, Rácz K. Bertalan R, et al. Gynecol Endocrinol. 2009 Jun;25(6):379-82. doi: 10.1080/09513590902730762. Gynecol Endocrinol. 2009. PMID: 19241242

10

Overrepresentation of BclI polymorphism of the glucocorticoid receptor gene in pregnant women with HELLP syndrome.

Bertalan R, Patocs A, Nagy B, Derzsy Z, Gullai N, Szappanos A, Rigo J Jr, Racz K. Bertalan R, et al. Clin Chim Acta. 2009 Jul;405(1-2):148-52. doi: 10.1016/j.cca.2009.03.046. Epub 2009 Mar 29. Clin Chim Acta. 2009. PMID: 19336230

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