227 related articles for article (PubMed ID: 21981961)
1. Steroid 21 hydroxylase deficiency congenital adrenal hyperplasia.
Nimkarn S; Lin-Su K; New MI
Pediatr Clin North Am; 2011 Oct; 58(5):1281-300, xii. PubMed ID: 21981961
[TBL] [Abstract][Full Text] [Related]
2. Steroid 21 hydroxylase deficiency congenital adrenal hyperplasia.
Nimkarn S; Lin-Su K; New MI
Endocrinol Metab Clin North Am; 2009 Dec; 38(4):699-718. PubMed ID: 19944288
[TBL] [Abstract][Full Text] [Related]
3. Genetic disorders of adrenal hormone synthesis.
New MI
Horm Res; 1992; 37 Suppl 3():22-33. PubMed ID: 1427638
[TBL] [Abstract][Full Text] [Related]
4. 21-hydroxylase deficiency congenital adrenal hyperplasia.
New MI
J Steroid Biochem Mol Biol; 1994 Jan; 48(1):15-22. PubMed ID: 8136301
[TBL] [Abstract][Full Text] [Related]
5. An update of congenital adrenal hyperplasia.
New MI
Ann N Y Acad Sci; 2004 Dec; 1038():14-43. PubMed ID: 15838095
[TBL] [Abstract][Full Text] [Related]
6. Update on adrenal steroid hormone biosynthesis and clinical implications.
Bacila IA; Elder C; Krone N
Arch Dis Child; 2019 Dec; 104(12):1223-1228. PubMed ID: 31175123
[TBL] [Abstract][Full Text] [Related]
7. Steroid 21-hydroxylase deficiency in congenital adrenal hyperplasia.
Parsa AA; New MI
J Steroid Biochem Mol Biol; 2017 Jan; 165(Pt A):2-11. PubMed ID: 27380651
[TBL] [Abstract][Full Text] [Related]
8. [Congenital adrenal hyperplasia].
Stanić M; Nesović M
Med Pregl; 1999; 52(11-12):447-54. PubMed ID: 10748766
[TBL] [Abstract][Full Text] [Related]
9. Non-Classic Disorder of Adrenal Steroidogenesis and Clinical Dilemmas in 21-Hydroxylase Deficiency Combined with Backdoor Androgen Pathway. Mini-Review and Case Report.
Sumińska M; Bogusz-Górna K; Wegner D; Fichna M
Int J Mol Sci; 2020 Jun; 21(13):. PubMed ID: 32610579
[TBL] [Abstract][Full Text] [Related]
10. Congenital adrenal hyperplasia due to 21 hydroxylase deficiency: from birth to adulthood.
White PC; Bachega TA
Semin Reprod Med; 2012 Oct; 30(5):400-9. PubMed ID: 23044877
[TBL] [Abstract][Full Text] [Related]
11. Congenital adrenal hyperplasia: clinical symptoms and diagnostic methods.
Podgórski R; Aebisher D; Stompor M; Podgórska D; Mazur A
Acta Biochim Pol; 2018; 65(1):25-33. PubMed ID: 29543924
[TBL] [Abstract][Full Text] [Related]
12. [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]
13. Congenital adrenal hyperplasia due to 21-hydroxylase deficiency: A paradigm for prenatal diagnosis and treatment.
Nimkarn S; New MI
Ann N Y Acad Sci; 2010 Mar; 1192():5-11. PubMed ID: 20392211
[TBL] [Abstract][Full Text] [Related]
14. Recent advances in the diagnosis and management of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
Forest MG
Hum Reprod Update; 2004; 10(6):469-85. PubMed ID: 15514016
[TBL] [Abstract][Full Text] [Related]
15. Congenital adrenal hyperplasia due to 21-hydroxylase deficiency - management in adults.
Ambroziak U; Bednarczuk T; Ginalska-Malinowska M; Małunowicz EM; Grzechocińska B; Kamiński P; Bablok L; Przedlacki J; Bar-Andziak E
Endokrynol Pol; 2010; 61(1):142-55. PubMed ID: 20205117
[TBL] [Abstract][Full Text] [Related]
16. [Congenital adrenal hyperplasia].
Bouvattier C; Chatelain P
Rev Prat; 2008 May; 58(9):990-4. PubMed ID: 18672665
[TBL] [Abstract][Full Text] [Related]
17. The management of congenital adrenal hyperplasia during preconception, pregnancy, and postpartum.
Maher JY; Gomez-Lobo V; Merke DP
Rev Endocr Metab Disord; 2023 Feb; 24(1):71-83. PubMed ID: 36399318
[TBL] [Abstract][Full Text] [Related]
18. Diagnosis and management of classical congenital adrenal hyperplasia.
Marumudi E; Khadgawat R; Surana V; Shabir I; Joseph A; Ammini AC
Steroids; 2013 Aug; 78(8):741-6. PubMed ID: 23624029
[TBL] [Abstract][Full Text] [Related]
19. Inborn errors of adrenal steroidogenesis.
New MI
Mol Cell Endocrinol; 2003 Dec; 211(1-2):75-83. PubMed ID: 14656479
[TBL] [Abstract][Full Text] [Related]
20. Combined homozygous 21 hydroxylase with heterozygous P450 oxidoreductase mutation in a Saudi boy presented with hypertension.
Aljabri A; Alnaim F; Alsaleh Y
BMJ Case Rep; 2020 Sep; 13(9):. PubMed ID: 32994263
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
