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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 guidelineAdrenocortical hormone abnormalities in men with chronic prostatitis/chronic pelvic pain syndromeRecent advances in biochemical and molecular analysis of congenital adrenal hyperplasia due to 21-hydroxylase deficiencyEndocrine and metabolic emergencies in children: hypocalcemia, hypoglycemia, adrenal insufficiency, and metabolic acidosis including diabetic ketoacidosisPitfalls in molecular diagnosis of 21-hydroxylase deficiency in congenital adrenal hyperplasiaCongenital Adrenal HyperplasiaUse of prednisone with abiraterone acetate in metastatic castration-resistant prostate cancerManagement of adolescents with congenital adrenal hyperplasiaHypertension in infancy: diagnosis, management and outcomeHigh frequency of copy number variations and sequence variants at CYP21A2 locus: implication for the genetic diagnosis of 21-hydroxylase deficiency.Assessment of cardiac function in children with congenital adrenal hyperplasia: a case control study in Cameroon.Variations in the 3'UTR of the CYP21A2 Gene in Heterozygous Females with Hyperandrogenaemia.Genotype-phenotype correlation in 27 pediatric patients in congenital adrenal hyperplasia due to 21-hydroxylase deficiency in a single centerEffects of Adrenal Androgen Levels on Bone Age Advancement in Prepubertal Children: Using the Ewha Birth and Growth Cohort Study.Testicular adrenal rest tumors in a patient with congenital adrenal hyperplasia.Prospective and Descriptive Study on Serum Androstenedione Concentration in Healthy Children from Birth until 18 Years of Age and Its Associated Factors.Functional consequences of seven novel mutations in the CYP11B1 gene: four mutations associated with nonclassic and three mutations causing classic 11{beta}-hydroxylase deficiency.Ethnic disparity in 21-hydroxylase gene mutations identified in Pakistani congenital adrenal hyperplasia patientsReactive Arrays of Colorimetric Sensors for Metabolite and Steroid IdentificationInfluence of the A3669G Glucocorticoid Receptor Gene Polymorphism on the Metabolic Profile of Pediatric Patients with Congenital Adrenal Hyperplasia.MECHANISMS IN ENDOCRINOLOGY: The sexually dimorphic role of androgens in human metabolic disease.Management of the adult with congenital adrenal hyperplasia.Abiraterone acetate to lower androgens in women with classic 21-hydroxylase deficiency.Machine learning approaches for phenotype-genotype mapping: predicting heterozygous mutations in the CYP21B gene from steroid profilesPathogenesis, diagnosis and management of hyperkalemiaCongenital adrenal hyperplasia: classification of studies employing psychological endpoints.Bone mineral status in Egyptian children with classic congenital adrenal hyperplasia. A single-center study from Upper EgyptConsensus in Guidelines for Evaluation of DSD by the Texas Children's Hospital Multidisciplinary Gender Medicine Team.A Summary of the Endocrine Society Clinical Practice Guidelines on Congenital Adrenal Hyperplasia due to Steroid 21-Hydroxylase DeficiencyThree-dimensional structure of steroid 21-hydroxylase (cytochrome P450 21A2) with two substrates reveals locations of disease-associated variantsOut of bounds? A critique of the new policies on hyperandrogenism in elite female athletesAndrogen action on human skin -- from basic research to clinical significance.Treatment and health outcomes in adults with congenital adrenal hyperplasia.Impact of glucocorticoid receptor gene polymorphisms on the metabolic profile of adult patients with the classical form of 21-hydroxylase deficiencyAdrenal and thyroid function in the fetus and preterm infant.Ontogeny of adrenal steroid biosynthesis: why girls will be girls.Guidelines for the Development of Comprehensive Care Centers for Congenital Adrenal Hyperplasia: Guidance from the CARES Foundation InitiativeIris mammillations in two female siblings with congenital adrenal hyperplasia.Health related quality of life of children and adolescents with congenital adrenal hyperplasia in Brazil.
P2860
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P2860
description
2003 nî lūn-bûn
@nan
2003年の論文
@ja
2003年学术文章
@wuu
2003年学术文章
@zh
2003年学术文章
@zh-cn
2003年学术文章
@zh-hans
2003年学术文章
@zh-my
2003年学术文章
@zh-sg
2003年學術文章
@yue
2003年學術文章
@zh-hant
name
Congenital adrenal hyperplasia.
@en
type
label
Congenital adrenal hyperplasia.
@en
prefLabel
Congenital adrenal hyperplasia.
@en
P356
P1476
Congenital adrenal hyperplasia.
@en
P2093
Perrin C White
Phyllis W Speiser
P304
P356
10.1056/NEJMRA021561
P407
P577
2003-08-01T00:00:00Z