298 related articles for article (PubMed ID: 23539930)
1. Diagnosis and management of congenital adrenal hyperplasia: 20-year experience in Songklanagarind Hospital.
Jaruratanasirikul S; Thongseiratch T
J Med Assoc Thai; 2013 Mar; 96(3):288-93. PubMed ID: 23539930
[TBL] [Abstract][Full Text] [Related]
2. Obesity among children and adolescents with classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
Völkl TM; Simm D; Beier C; Dörr HG
Pediatrics; 2006 Jan; 117(1):e98-105. PubMed ID: 16396852
[TBL] [Abstract][Full Text] [Related]
3. [Congenital adrenal hyperplasia].
Stanić M; Nesović M
Med Pregl; 1999; 52(11-12):447-54. PubMed ID: 10748766
[TBL] [Abstract][Full Text] [Related]
4. [Screening for congenital adrenal hyperplasia in Hungary].
Sólyom J
Orv Hetil; 1989 Sep; 130(37):1979-82, 1985-6. PubMed ID: 2780047
[TBL] [Abstract][Full Text] [Related]
5. Assessment of the 21-hydroxylase deficiency and the adrenal functions in young females with Turner syndrome.
Onder A; Aycan Z; Cetinkaya S; Kendirci HN; Bas VN; Agladioglu SY
J Pediatr Endocrinol Metab; 2012; 25(7-8):681-5. PubMed ID: 23155693
[TBL] [Abstract][Full Text] [Related]
6. Newly proposed hormonal criteria via genotypic proof for type II 3beta-hydroxysteroid dehydrogenase deficiency.
Lutfallah C; Wang W; Mason JI; Chang YT; Haider A; Rich B; Castro-Magana M; Copeland KC; David R; Pang S
J Clin Endocrinol Metab; 2002 Jun; 87(6):2611-22. PubMed ID: 12050224
[TBL] [Abstract][Full Text] [Related]
7. Androgens concentrations and second-to fourth-digit ratio (2D:4D) in girls with congenital adrenal hyperplasia (21-hydroxylase deficiency).
Oswiecimska JM; Ksiazek A; Sygulla K; Pys-Spychala M; Roczniak GR; Roczniak W; Stojewska M; Ziora K
Neuro Endocrinol Lett; 2012; 33(8):787-91. PubMed ID: 23391972
[TBL] [Abstract][Full Text] [Related]
8. [Determination of serum steroids in monitoring therapy of congenital adrenal hyperplasia].
Xiao HW; Ma HM; Su Z; Du ML; Li YH; Chen HS; Chen QL
Zhonghua Er Ke Za Zhi; 2012 Apr; 50(4):301-7. PubMed ID: 22801236
[TBL] [Abstract][Full Text] [Related]
9. Congenital adrenal hyperplasia: neonatal mass screening compared with clinical diagnosis only in the Emilia-Romagna region of Italy, 1980-1995.
Balsamo A; Cacciari E; Piazzi S; Cassio A; Bozza D; Pirazzoli P; Zappulla F
Pediatrics; 1996 Sep; 98(3 Pt 1):362-7. PubMed ID: 8784357
[TBL] [Abstract][Full Text] [Related]
10. Detection of late-onset adrenal hyperplasia in girls with peripubertal virilization.
Sólyom J; Gács G; Keszei K; Láng K; Orley J; Petheö I; Ságodi L
Acta Endocrinol (Copenh); 1987 Jul; 115(3):413-8. PubMed ID: 3039770
[TBL] [Abstract][Full Text] [Related]
11. Adrenocorticotropin stimulation test in congenital adrenal hyperplasia: comparison between standard and low dose test.
Panamonta O; Thinkhamrop B; Kirdpon W; Pudtawaro LO; Sungsahachart D
J Med Assoc Thai; 2003 Jul; 86(7):634-40. PubMed ID: 12948258
[TBL] [Abstract][Full Text] [Related]
12. Transient hyper-17-hydroxyprogesteronemia: a clinical subgroup of patients diagnosed at neonatal screening for congenital adrenal hyperplasia.
Cavarzere P; Samara-Boustani D; Flechtner I; Dechaux M; Elie C; Tardy V; Morel Y; Polak M
Eur J Endocrinol; 2009 Aug; 161(2):285-92. PubMed ID: 19451212
[TBL] [Abstract][Full Text] [Related]
13. [Contemporary diagnosis and therapy in women with congenital adrenal hyperplasia].
Maciejewska-Jeske M; Meczekalski B
Pol Merkur Lekarski; 2013 Nov; 35(209):297-9. PubMed ID: 24575652
[TBL] [Abstract][Full Text] [Related]
14. Delayed diagnosis of congenital adrenal hyperplasia with salt wasting due to type II 3beta-hydroxysteroid dehydrogenase deficiency.
Johannsen TH; Mallet D; Dige-Petersen H; Müller J; Main KM; Morel Y; Forest MG
J Clin Endocrinol Metab; 2005 Apr; 90(4):2076-80. PubMed ID: 15671104
[TBL] [Abstract][Full Text] [Related]
15. Persistent testicular delta5-isomerase-3beta-hydroxysteroid dehydrogenase (delta5-3beta-HSD) deficiency in the delta5-3beta-HSD form of congenital adrenal hyperplasia.
Schneider G; Genel M; Bongiovanni AM; Goldman AS; Rosenfield RL
J Clin Invest; 1975 Apr; 55(4):681-90. PubMed ID: 164481
[TBL] [Abstract][Full Text] [Related]
16. Diagnosis of adrenal cortical dysfunction by liquid chromatography-tandem mass spectrometry.
Kao PC; Machacek DA; Magera MJ; Lacey JM; Rinaldo P
Ann Clin Lab Sci; 2001 Apr; 31(2):199-204. PubMed ID: 11337910
[TBL] [Abstract][Full Text] [Related]
17. Adiponectin levels are high in children with classic congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency.
Völkl TM; Simm D; Körner A; Kiess W; Kratzsch J; Dörr HG
Acta Paediatr; 2009 May; 98(5):885-91. PubMed ID: 19236311
[TBL] [Abstract][Full Text] [Related]
18. Monitoring congenital adrenal hyperplasia using blood spot 17-hydroxyprogesterone assay.
Santos CM; Abad LR; Cua SC; Domingo CF
Southeast Asian J Trop Med Public Health; 2003; 34 Suppl 3():174-8. PubMed ID: 15906729
[TBL] [Abstract][Full Text] [Related]
19. Clinical characteristics of Taiwanese children with congenital adrenal hyperplasia caused by 21-hydroxylase deficiency in the pre-screening era.
Lee CT; Tung YC; Hsiao PH; Lee JS; Tsai WY
J Formos Med Assoc; 2010 Feb; 109(2):148-55. PubMed ID: 20206839
[TBL] [Abstract][Full Text] [Related]
20. Raised 17-hydroxyprogesterone levels in congenital adrenal hyperplasia.
Iqbal S; Khan AH
J Coll Physicians Surg Pak; 2013 May; 23(5):373-4. PubMed ID: 23673184
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]