Fekete G - Search Results

1

Y-chromosome markers in Turner syndrome: Screening of 130 patients.

Sallai A, Sólyom J, Dobos M, Szabó J, Halász Z, Ságodi L, Niederland T, Kozári A, Bertalan R, Ugocsai P, Fekete G. Sallai A, et al. Among authors: fekete g. J Endocrinol Invest. 2010 Apr;33(4):222-7. doi: 10.1007/BF03345783. Epub 2009 Jul 21. J Endocrinol Invest. 2010. PMID: 19625757

2

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: fekete g. J Endocrinol Invest. 2008 Jan;31(1):74-8. doi: 10.1007/BF03345570. J Endocrinol Invest. 2008. PMID: 18296909

3

Limited value of serum steroid measurements in identification of mild form of 21-hydroxylase deficiency.

Török D, Halász Z, Garami M, Homoki J, Fekete G, Sólyom J. Török D, et al. Among authors: fekete g. Exp Clin Endocrinol Diabetes. 2003 Feb;111(1):27-32. doi: 10.1055/s-2003-37497. Exp Clin Endocrinol Diabetes. 2003. PMID: 12605347

4

Screening for mutations of 21-hydroxylase gene in Hungarian patients with congenital adrenal hyperplasia.

Ferenczi A, Garami M, Kiss E, Pék M, Sasvári-Székely M, Barta C, Staub M, Sólyom J, Fekete G. Ferenczi A, et al. Among authors: fekete g. J Clin Endocrinol Metab. 1999 Jul;84(7):2369-72. doi: 10.1210/jcem.84.7.5835. J Clin Endocrinol Metab. 1999. PMID: 10404805 Free article.

5

[Androgen insensitivity syndrome. Clinical features and molecular genetics].

Sólyom J, Scheiber D, Fekete G. Sólyom J, et al. Among authors: fekete g. Orv Hetil. 2001 Aug 5;142(31):1659-65. Orv Hetil. 2001. PMID: 11556259 Review. Hungarian.

6

Potential advantage of N363S glucocorticoid receptor polymorphism in 21-hydroxylase deficiency.

Luczay A, Török D, Ferenczi A, Majnik J, Sólyom J, Fekete G. Luczay A, et al. Among authors: fekete g. Eur J Endocrinol. 2006 Jun;154(6):859-64. doi: 10.1530/eje.1.02162. Eur J Endocrinol. 2006. PMID: 16728546

7

Prenatal diagnosis of steroid 21-hydroxylase deficiency by allele-specific amplification.

Theodoropoulou M, Barta C, Szoke M, Guttman A, Staub M, Niederland T, Sólyom J, Fekete G, Sasvari-Szekely M. Theodoropoulou M, et al. Among authors: fekete g. Fetal Diagn Ther. 2001 Jul-Aug;16(4):237-40. doi: 10.1159/000053918. Fetal Diagn Ther. 2001. PMID: 11399887

8

[Aberrations of chromosome 18 and their significance in genetic counseling].

Eggermann T, Bujdosó G, Haug T, Heidrich-Kaul C, Hofmann D, Fekete G, Dobos M, Schwanitz G. Eggermann T, et al. Among authors: fekete g. Orv Hetil. 2000 Jul 23;141(30):1667-71. Orv Hetil. 2000. PMID: 10962904 Hungarian.

9

[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: fekete gl. Orv Hetil. 2017 Aug;158(34):1351-1356. doi: 10.1556/650.2017.30829. Orv Hetil. 2017. PMID: 28823207 Hungarian.

10

National registry of patients with juvenile idiopathic inflammatory myopathies in Hungary--clinical characteristics and disease course of 44 patients with juvenile dermatomyositis.

Constantin T, Ponyi A, Orbán I, Molnár K, Dérfalvi B, Dicso F, Kálovics T, Müller J, Garami M, Sallai A, Balogh Z, Szalai Z, Fekete G, Dankó K. Constantin T, et al. Among authors: fekete g. Autoimmunity. 2006 May;39(3):223-32. doi: 10.1080/08916930600622819. Autoimmunity. 2006. PMID: 16769656

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