Recent advances in the diagnosis and management of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
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The molecular biology, biochemistry, and physiology of human steroidogenesis and its disordersCongenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency: an Endocrine Society clinical practice guidelinePrenatal Dexamethasone for Congenital Adrenal HyperplasiaRecent advances in biochemical and molecular analysis of congenital adrenal hyperplasia due to 21-hydroxylase deficiencyReproductive outcomes of female patients with congenital adrenal hyperplasia due to 21-hydroxylase defi ciencyCYP21A2 gene mutations in congenital adrenal hyperplasia: genotype-phenotype correlation in Turkish childrenEarly dexamethasone treatment induces placental apoptosis in sheepConcurrence of Meningomyelocele and Salt-Wasting Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency.Effects of maternal dexamethasone treatment early in pregnancy on glucocorticoid receptors in the ovine placenta.Dried blood spot testing for seven steroids using liquid chromatography-tandem mass spectrometry with reference interval determination in the Korean population.Evolution of siglec-11 and siglec-16 genes in homininsMolecular Diagnosis of Congenital Adrenal Hyperplasia in Iran: Focusing on CYP21A2 Gene.Sperm retrieval and concomitant tumor resection in azoospermic men with congenital adrenal hyperplasia and bilateral testicular adrenal rest tumors: a case report.Transgenic GATA-4 expression induces adrenocortical tumorigenesis in C57Bl/6 mice.Prenatal treatment of mothers with fetuses at risk for congenital adrenal hyperplasia: How relevant is it to Indian context?The clinical and biochemical spectrum of congenital adrenal hyperplasia secondary to 21-hydroxylase deficiency.Surgical Treatment after Failed Primary Correction of Urogenital Sinus in Female Patients with Virilizing Congenital Adrenal Hyperplasia: Are Good Results Possible?Testicular adrenal rest tumours in congenital adrenal hyperplasia.An update to 21-hydroxylase deficient congenital adrenal hyperplasia.Prenatal treatment of congenital adrenal hyperplasia-not standard of care.Perspectives in Pediatric Pathology, Chapter 22. Testicular Involvement in Systemic Diseases.Using SILAC proteomics to investigate the effect of the mycotoxin, alternariol, in the human H295R steroidogenesis model.High frequency of splice site mutation in 21-hydroxylase deficiency children.Premature pubarche in Mediterranean girls: high prevalence of heterozygous CYP21 mutation carriers.Novel Use of Tolvaptan in a Pediatric Patient With Congestive Heart Failure Due to Duchenne Muscular Dystrophy and Congenital Adrenal Hyperplasia.The spectrum of clinical, hormonal and molecular findings in 280 individuals with nonclassical congenital adrenal hyperplasia caused by mutations of the CYP21A2 gene.Comparison of different glucocorticoid regimens in the management of classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency.CYP21-catalyzed production of the long-term urinary metandienone metabolite 17beta-hydroxymethyl-17 alpha-methyl-18-norandrosta-1,4,13-trien-3-one: a contribution to the fight against doping.Prevalence of non classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency in Greek women with acne: a hospital-based cross-sectional study.Development of CYP21A2 Genotyping Assay for the Diagnosis of Congenital Adrenal Hyperplasia.Still concerned.Identification of a novel compound heterozygous mutation of the CYP21A2 gene causing 21‑hydroxylase deficiency in a Chinese pedigree.High carrier frequency of 21-hydroxylase deficiency in Cyprus.Sonography and Magnetic Resonance Imaging Characteristics of Testicular Adrenal Rest Tumors.Trophoblast Retrieval and Isolation From the Cervix for Noninvasive, First Trimester, Fetal Gender Determination in a Carrier of Congenital Adrenal Hyperplasia.Mortality in children with classic congenital adrenal hyperplasia and 21-hydroxylase deficiency (CAH) in Germany.
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P2860
Recent advances in the diagnosis and management of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
2004年论文
@zh
2004年论文
@zh-cn
name
Recent advances in the diagnos ...... to 21-hydroxylase deficiency.
@ast
Recent advances in the diagnos ...... to 21-hydroxylase deficiency.
@en
type
label
Recent advances in the diagnos ...... to 21-hydroxylase deficiency.
@ast
Recent advances in the diagnos ...... to 21-hydroxylase deficiency.
@en
prefLabel
Recent advances in the diagnos ...... to 21-hydroxylase deficiency.
@ast
Recent advances in the diagnos ...... to 21-hydroxylase deficiency.
@en
P356
P1476
Recent advances in the diagnos ...... to 21-hydroxylase deficiency.
@en
P2093
Maguelone G Forest
P304
P356
10.1093/HUMUPD/DMH047
P577
2004-11-01T00:00:00Z