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Fluorescence enzyme immunoassay of 17α-hydroxyprogesterone in dried blood samples on filter paper and its application to mass screening for congenital adrenal hyperplasiaARAKAWA, H; MAEDA, M; TSUJI, A et al.Chemical and pharmaceutical bulletin. 1983, Vol 31, Num 8, pp 2724-2731, issn 0009-2363Article

Neonatal screening for congenital adrenal hyperplasiaCACCIARI, E; BALSAMO, A; PAOLINI, M et al.Archives of disease in childhood. 1983, Vol 58, Num 10, pp 803-806, issn 0003-9888Article

Dermatoglyphics in congenital adrenal hyperplasia (CAH)BÖRGER, D; HELD, K. R; LÜTTGEN, S et al.Clinical genetics. 1986, Vol 30, Num 3, pp 173-176, issn 0009-9163Article

L'hyperplasie congénitale des surrénales (21-OH) en France: génétique des populations = Populations genetics of congenital Achenal Hyperplasia (21-OH) in FranceBOIS, E; MORNET, E; CHOMPRET, A et al.Archives françaises de pédiatrie. 1985, Vol 42, Num 3, pp 175-179, issn 0003-9764Article

Atrial natriuretic peptide and fludrocortisone therapy in congenital adrenal hyperplasiaARISAKA, O; HOSAKA, A; ARISAKA, M et al.Acta paediatrica (Oslo). 1992, Vol 81, Num 3, pp 268-269, issn 0803-5253Conference Paper

Computed tomography in untreated congenital adrenal hyperplasiaHARINARAYANA, C. V; RENU, G; AMMINI, A. C et al.Pediatric radiology. 1991, Vol 21, Num 2, pp 103-105, issn 0301-0449Article

The urinary excretion of 17 ketosteroids and Δ5 pregnane-3α,17α,20α-triol in infancy, childhood, adolescence and congenital adrenal hyperplasiaSHEN-HUI CHEN.Acta paediatrica sinica. 1984, Vol 25, Num 1, pp 20-26Article

Classical and late-onset forms of congenital adrenal hyperplasia caused by 21-OH deficiency reveal different alterations in the C4/21-OH gene regionNOEHM, B. O; ROSAK, C; BOEHM, T. L. J et al.Molecular biology & medicine. 1986, Vol 3, Num 5, pp 437-448, issn 0735-1313Article

Delayed diagnosis in congenital adrenal hyperplasiaLEBOVITZ, R. M; PAULI, R. M; LAXOVA, R et al.American journal of diseases of children (1960). 1984, Vol 138, Num 6, pp 571-573, issn 0002-922XArticle

Hyperplasie surrénale congénitale et grossesse: un cas de bloc de la 21-hydroxylase avec ambiguïté sexuelle de type III, traité tardivement = Congenital adrenocortical hyperplasia and pregnancy: a case report of 21-hydroxylase deficiency, with type III sexual ambiguity, treated lateMARTINAND, A; BEGUE, R. J; DESGRES, J et al.Revue française d'endocrinologie clinique, nutrition et métabolisme. 1983, Vol 24, Num 2, pp 113-120, issn 0048-8062Article

Mineralocorticoid in congenital adrenal hyperplasiaBIGLIERI, E. G; KATER, C. E.Journal of steroid biochemistry and molecular biology. 1991, Vol 40, Num 4-6, pp 493-499, issn 0960-0760Conference Paper

Le conseil génétique et le diagnostic prénatal de ĺhyperplasie des surrénales par déficit en 21-hydroxylase = Prenatal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency and genetic counsellingCOUILLIN, P.La Presse médicale (1983). 1984, Vol 13, Num 17, pp 1087-1090, issn 0755-4982Article

Salt loss in congenital adrenal hyperplasia due to 11 β-hydroxylase deficiencyHOCHBERG, Z; BENDERLY, A; ZADIK, Z et al.Archives of disease in childhood. 1984, Vol 59, Num 11, pp 1092-1094, issn 0003-9888Article

Workshop on screening for congenital adrenal hyperplasia (steroid 21-hydroxylase deficiency)ADDISON, G. M.Journal of inherited metabolic disease. 1986, Vol 9, pp 111-114, issn 0141-8955, Suppl. 1Article

Plasma renin activity in the management of congenital adrenal hyperplasiaGRIFFITHS, K. D; ANDERSON, J. M; RUDD, B. T et al.Archives of disease in childhood. 1984, Vol 59, Num 4, pp 360-365, issn 0003-9888Article

URINARY AND SERUM STEROID CONCENTRATIONS IN THE MANAGEMENT OF CONGENITAL ADRENAL HYPERPLASIA. LACK OF PHYSIOLOGIC CORRELATIONSHENDRICKS SA; LIPPE BM; KAPLAN SA et al.1982; AM. J. DIS. CHILD. (1960); ISSN 0002-922X; USA; DA. 1982; VOL. 136; NO 3; PP. 229-232; BIBL. 20 REF.Article

Congenital adrenal hyperplasiaMERKE, Deborah P; BORNSTEIN, Stefan R.Lancet (British edition). 2005, Vol 365, Num 9477, pp 2125-2136, issn 0140-6736, 12 p.Article

Prenatal diagnosis/treatment in families at risk for infants with steroid 21-hydroxylase deficiency (congenital adrenal hyperplasia)KARAVITI, L. P; MERCADO, A. B; MERCADO, M. B et al.Journal of steroid biochemistry and molecular biology. 1992, Vol 41, Num 3-8, pp 445-451, issn 0960-0760Conference Paper

Plasma insulin-like growth factor I levels during treatment of congenital adrenal hyperplasiaCAVALLO, A; FURLANETTO, R. W; MEYER, W. J et al.Hormone research. 1990, Vol 34, Num 1, pp 23-26, issn 0301-0163, 4 p.Article

Computed tomography in the early detection of congenital lipoid adrenal hyperplasiaOGATA, T; ISHIKAWA, K; KOHDA, E et al.Pediatric radiology. 1988, Vol 18, Num 4, pp 360-361, issn 0301-0449Article

The relationship of endogenous ACTH levels to visual. Attentional functioning in patients with congenital adrenal hyperplasiaVEITH, J. L; SANDMAN, C. A; GEORGE, J. M et al.Psychoneuroendocrinology. 1985, Vol 10, Num 1, pp 33-48, issn 0306-4530Article

Growth and pubertal development in patients with congenital adrenal hyperplasia due to 11-β-hydroxylase deficiencyHOCHBERG, Z; SCHECHTER, J; BENDERLY, A et al.American journal of diseases of children (1960). 1985, Vol 139, Num 8, pp 771-776, issn 0002-922XArticle

Proceedings/Symposium on advances in congenital adrenal hyperplasia: Satellite meeting: VIIth international congress of endocrinology, July 7-9, 1984NEW, M. I.Annals of the New York Academy of Sciences. 1985, Vol 458, issn 0077-8923, X-290 pConference Proceedings

Genetic basis of endocrine disease 2 : congenital adrenal hyperplasia due to 21-hydroxylase deficiencyWHITE, P. C; NEW, M. I.The Journal of clinical endocrinology and metabolism. 1992, Vol 74, Num 1, pp 6-11, issn 0021-972XArticle

Adrenal steroidogenic defects in children with precocious pubarcheDEL BALZO, P; BORRELLI, P; CAMBIASO, P et al.Hormone research. 1992, Vol 37, Num 4-5, pp 180-184, issn 0301-0163Article

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