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201. Postnatal virilization mimicking 21-hydroxylase deficiency in 3 very premature infants.

202. [Determination of serum steroids in monitoring therapy of congenital adrenal hyperplasia].

203. A competitive immunochromatographic strip assay for 17-α-hydroxy progesterone using colloidal gold nanoparticles.

204. Clinical features suggestive of non-classical 21-hydroxylase deficiency in children presenting with precocious pubarche.

205. Replication of clinical associations with 17-hydroxyprogesterone in preterm newborns.

206. Out of bounds? A critique of the new policies on hyperandrogenism in elite female athletes.

207. Neonatal screening: identification of children with 11β-hydroxylase deficiency by second-tier testing.

208. Gender related differences in glucocorticoid therapy and growth outcomes among pubertal children with 21-hydroxylase deficiency congenital adrenal hyperplasia (CAH).

209. Rapid steroid hormone quantification for congenital adrenal hyperplasia (CAH) in dried blood spots using UPLC liquid chromatography-tandem mass spectrometry.

210. Correlation between androstenedione and 17-hydroxyprogesterone levels in the saliva and plasma of patients with congenital adrenal hyperplasia.

211. Summary of the workshop "Management of CAH: the relevance of steroids in plasma, saliva and urine".

212. Gendered occupational interests: prenatal androgen effects on psychological orientation to Things versus People.

213. Relationship of CYP21A2 genotype and serum 17-hydroxyprogesterone and cortisol levels in a large cohort of Italian children with premature pubarche.

214. IGF-I-IGFBP-3-acid-labile subunit (ALS) complex in children and adolescents with classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency (CAH).

215. Correlation between genotype and hormonal levels in heterozygous mutation carriers and non-carriers of 21-hydroxylase deficiency.

216. Confirmation of congenital adrenal hyperplasia by adrenal steroid profiling of filter paper dried blood samples using ultra-performance liquid chromatography-tandem mass spectrometry.

217. [Usefulness of molecular analysis in the differential diagnosis of congenital 21-hidroxylase deficiency detected in neonatal screening].

218. Monitoring medical treatment in adolescents and young adults with congenital adrenal hyperplasia: utility of salivary 17α-hydroxyprogesterone day profiles.

219. Incremental cost of non-invasive prenatal diagnosis versus invasive prenatal diagnosis of fetal sex in England.

220. Precocious puberty in an eight-year-old girl.

221. The effect on the fetal pituitary-adrenal axis of dexamethasone administration early in the second trimester of pregnancy.

222. Comparison of multiple steroid concentrations in serum and dried blood spots throughout the day of patients with congenital adrenal hyperplasia.

223. Adrenarche and puberty in children with classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

224. A woman with salt-wasting congenital adrenal hyperplasia presenting with a mucinous ovarian cystadenoma during pregnancy.

225. Adult patients with congenital adrenal hyperplasia have elevated blood pressure but otherwise a normal cardiovascular risk profile.

226. Neonatal screening for congenital adrenal hyperplasia: transitory elevation of 17-hydroxyprogesterone.

227. Superior discriminating value of ACTH-stimulated serum 21-deoxycortisol in identifying heterozygote carriers for 21-hydroxylase deficiency.

228. Six new cases confirm the clinical molecular profile of complete combined 17α-hydroxylase/ 17,20-lyase deficiency in Brazil.

229. Possible andrologic markers in elevated neonatal 17-hydroxyprogesterone.

230. A 2-year-old boy with a testicular mass. Diagnosis: testicular tumor of adrenogenital syndrome due to 11-beta-hydroxylase deficiency.

231. [Corticosterone, deoxycorticosterone].

232. Adrenomedullary function in patients with nonclassic congenital adrenal hyperplasia.

233. [11-Deoxycortisol].

234. [DHEA, DHEA-S].

235. Non-classical 21-hydroxylase deficiency: prevalence in males with unexplained abnormal sperm analysis.

236. Impact of different diagnostic criteria during adrenal vein sampling on reproducibility of subtype diagnosis in patients with primary aldosteronism.

237. Sex typing for sport.

238. Identification of steroid biosynthetic defects in genotype-proven heterozygous individuals for 17alpha-hydroxylase/17,20-lyase deficiency.

239. Proteomic profiles in hyperandrogenic syndromes.

240. Serum steroid profiling for congenital adrenal hyperplasia using liquid chromatography-tandem mass spectrometry.

241. Clinical characteristics of Taiwanese children with congenital adrenal hyperplasia caused by 21-hydroxylase deficiency in the pre-screening era.

242. Insulin sensitivity and body composition in children with classical and nonclassical congenital adrenal hyperplasia.

243. Ovarian adrenal rest tumor in a congenital adrenal hyperplasia patient with adrenocorticotropin hypersecretion following adrenalectomy.

244. Three novel CYP11B1 mutations in congenital adrenal hyperplasia due to steroid 11Beta-hydroxylase deficiency in a moroccan population.

245. Quantitation of 17-OH-progesterone (OHPG) for diagnosis of congenital adrenal hyperplasia (CAH).

246. Molecular analysis of CYP21A2 can optimize the follow-up of positive results in newborn screening for congenital adrenal hyperplasia.

247. Neonatal screening for congenital adrenal hyperplasia.

248. [Search of prostatic tissue in 46,XX congenital adrenal hyperplasia].

249. Precocious pubarche: distinguishing late-onset congenital adrenal hyperplasia from premature adrenarche.

250. Transient hyper-17-hydroxyprogesteronemia: a clinical subgroup of patients diagnosed at neonatal screening for congenital adrenal hyperplasia.

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