Detalhe da pesquisa
1.
Loss of Function of the Nuclear Receptor NR2F2, Encoding COUP-TF2, Causes Testis Development and Cardiac Defects in 46,XX Children.
Am J Hum Genet
; 102(3): 487-493, 2018 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29478779
2.
[Steroid 21-hydroxylase deficiency, the most frequent cause of congenital adrenal hyperplasia]. / Szteroid-21-hidroxiláz-deficientia, a congenitalis adrenalis hyperplasia leggyakoribb oka.
Orv Hetil
; 159(7): 269-277, 2018 Feb.
Artigo
em Húngaro
| MEDLINE | ID: mdl-29429350
3.
Implant-Related Complications and Mortality After Use of Short or Long Gamma Nail for Intertrochanteric and Subtrochanteric Fractures: A Prospective Study with Minimum 13-Year Follow-up.
JB JS Open Access
; 2(3): e0026, 2017 Sep 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-30229225
4.
[Incomplete androgen insensitivity]. / Inkomplett androgéninszenzitivitás szindróma.
Orv Hetil
; 147(37): 1805-7, 2006 Sep 17.
Artigo
em Húngaro
| MEDLINE | ID: mdl-17131800
5.
[Nucleotide sequence variants of the glucocorticoid receptor gene and their significance in determining glucocorticoid sensitivity]. / A glükokortikoidreceptor gén szekvenciavariánsai és jelentoségük a glükokortikoidok iráinti érzékenység meghatározásában.
Orv Hetil
; 147(44): 2107-15, 2006 Nov 05.
Artigo
em Húngaro
| MEDLINE | ID: mdl-17209299
6.
Estimation of the false-negative rate in newborn screening for congenital adrenal hyperplasia.
Eur J Endocrinol
; 152(6): 869-74, 2005 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-15941926
7.
Mutational analysis of Hungarian patients with androgen insensitivity syndrome.
J Pediatr Endocrinol Metab
; 16(3): 367-73, 2003 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-12705360
8.
[Identification of congenital adrenal hyperplasia by measurement of blood-spot 17-hydroxyprogesterone]. / Congenitalis adrenalis hyperplasia azonosítása vérfolt-17-hidroxiprogeszteron mérésével
Orv Hetil
; 145(40): 2051-6, 2004 Oct 03.
Artigo
em Húngaro
| MEDLINE | ID: mdl-15559532
9.
Hyperthyroidism caused by a germline activating mutation of the thyrotropin receptor gene: difficulties in diagnosis and therapy.
Thyroid
; 20(3): 327-32, 2010 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-20146656
10.
High prevalence of PROP1 gene mutations in Hungarian patients with childhood-onset combined anterior pituitary hormone deficiency.
Endocrine
; 30(3): 255-60, 2006 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-17526936
11.
Twenty years experience in rapid identification of congenital adrenal hyperplasia in Hungary.
Eur J Pediatr
; 162(12): 844-9, 2003 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-14648216
12.
Stability of 17alpha-hydroxyprogesterone in dried blood spots after autoclaving and prolonged storage.
Clin Chem
; 48(2): 370-2, 2002 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-11805024