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kw.\*:("21-Hydroxylase")

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HIRSUTISMO SIN PSEUDOHERMAFRODITISMO COMO EXPRESION SINTOMATICA DE FRACASO PARCIAL DE LA 21-HIDROXILASA = HIRSUTISME SANS PSEUDOHERMAPHRODISME COMME EXPRESSION SYMPTOMATIQUE DE DEFICIT PARTIEL EN 21-HYDROXYLASEAZNAR REIG A; ZAMORA MADARIA E; HERRERA JUSTINIANO E et al.1972; REV. IBER. ENDOCRINOL.; ESP.; DA. 1972; VOL. 19; NO 112; PP. 331-359; ABS. PORT. ANGL. ALLEM.; BIBL. 2P.Article

Functional studies of two novel and two rare mutations in the 21-hydroxylase geneBARBARO, M; BALDAZZI, L; BALSAMO, A et al.Journal of molecular medicine (Berlin. Print). 2006, Vol 84, Num 6, pp 521-528, issn 0946-2716, 8 p.Article

Les hyperandrogénies péripubertairesRICHARD-PROUST, Chloé; REYSS, Anne-Céline; JONARD-CATTEAU, Sophie et al.MT médecine de la reproduction. 2006, Vol 8, Num 5, pp 339-346, issn 1774-640X, 8 p.Article

EFFECT OF ADRENOCORTICOTROPHIN ON 21-AND 11BETA -HYDROXYLASE ACTIVITY IN THE BIOSYNTHESIS OF CORTISOL = EFFET DE LA CORTICOSTIMULINE SUR L'ACTIVITE DE LA 21- ET DE LA 11BETA -HYDROXYLASE DANS LA BIOSYNTHESE DU CORTISOLMOLINO G; CAVANNA A; MARINO M et al.1973; J. ENDOCRINOL.; G.B.; DA. 1973; VOL. 56; NO 2; PP. 333-334; BIBL. 7 REF.Article

Assessment of the one hour adrenocorticotrophic hormone test in the diagnosis of attentuated 21-hydroxylase deficiencyINNANEN, V. T; VALE, J. M.Journal of clinical pathology. 1990, Vol 43, Num 6, pp 493-495, issn 0021-9746Article

17ALPHA HYDROXYPROGESTERONE PLASMATIQUE DANS L'HYPERPLASIE CONGENITALE DES SURRENALES PAR DEFICIT EN 21 HYDROXYLASE, TRAITEE ET NON TRAITEELORAS B; ROUX H; AUDI PARERA L et al.1974; BIOMEDICINE; FR.; DA. 1974; VOL. 21; NO 7; PP. 317-322; ABS. ANGL.; BIBL. 16 REF.Article

Adrenal myelolipoma associated with congenital adrenal 21-hydroxylase deficiencyMURAKAMI, C; ISHIBASHI, M; KONDO, M et al.Internal medicine : (Tokyo). 1992, Vol 31, Num 6, pp 803-806Article

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

Pituitary-adrenal responses to corticotropin-releasing hormone in different degrees of adrenal 21- hydroxylase deficiencyMOREIRA, A. C; ELIAS, L. L. K.The Journal of clinical endocrinology and metabolism. 1992, Vol 74, Num 1, pp 198-203, issn 0021-972XArticle

Hétérogénéité du gène de la 21-hydroxylase surrénalienne = Gene heterogeneity in adrenal 21-hydroxylaseMOREL, Y.La Presse médicale (1983). 1991, Vol 20, Num 20, pp 945-949, issn 0755-4982Article

Conseil génétique et conduite à tenir avant, pendant et après la grossesse en cas de bloc surrénalien en 21-hydroxylaseTARDY, Véronique; MOREL, Yves.MTE. Médecine thérapeutique endocrinologie. 2004, Vol 6, Num 5-6, pp 281-286, issn 1295-9359, 6 p.Article

Déficits en 21-hydroxylase et fertilité féminine : Les androgènes = Steroid 21-hydroxylase deficiencies and female fertilityROBIN, Geoffroy; BAFFET, Hortense; CATTEAU-JONARD, Sophie et al.MT médecine de la reproduction. 2012, Vol 14, Num 3, pp 226-235, issn 1774-640X, 10 p.Article

Screening for late onset congenital adrenal hyperplasia due to 21-hydroxylase deficiencyKHANDEKAR, S; LATA, V; DASH, R. J et al.Indian journal of medical research. 1990, Vol 92, pp 79-82, issn 0019-5340, 4 p.Article

Refractory Acne and 21-Hydroxylase Deficiency in a Selected Group of Female PatientsCAPUTO, Valentina; FIORELLA, Santi; CURIALE, Salvatrice et al.Dermatology (Basel). 2010, Vol 220, Num 2, pp 121-127, issn 1018-8665, 7 p.Article

Multiple gene-like sequences related to the rabbit hepatic progesterone 21-hydroxylase cytochrome P-450 1TUKEY, R. H; OKINO, S; BARNES, H et al.The Journal of biological chemistry (Print). 1985, Vol 260, Num 24, pp 13347-13354, issn 0021-9258Article

UN CAS D'ADENOME CORTICOSURRENALIEN VIRILISANT PRESENTANT LE PROFIL HORMONAL D'UN DEFICIT PARTIEL EN 21-HYDROXYLASE.LINCK DUBOST M; RIFLE C; BEGUE RJ et al.1977; ANN. ENDOCRINOL.; FR.; DA. 1977; VOL. 38; NO 6; PP. 397-398; ABS. ANGL.; BIBL. 3 REF.Article

A new CYP21A2 nonsense mutation causing severe 21-hydroxylase deficiencyCONCOLINO, Paola; MINUCCI, Angelo; MELLO, Enrica et al.Clinical chemistry and laboratory medicine. 2009, Vol 47, Num 7, pp 824-825, issn 1434-6621, 2 p.Article

The activities of 5α-reductase and 17,20-lyase determine the direction through androgen synthesis pathways in patients with 21-hydroxylase deficiencyKAMRATH, Clemens; HARTMANN, Michaela F; REMER, Thomas et al.Steroids. 2012, Vol 77, Num 13, pp 1391-1397, issn 0039-128X, 7 p.Article

A PCR strategy that differentiates two alleles for a single base insertion within a T repeatLANGU, O; SILVERSTEIN, S.BioTechniques. 1993, Vol 14, Num 1, pp 62-64, issn 0736-6205, 2 p.Article

Molecular heterogeneity of complement component C4-null and 21-hydroxylase genes in systemic lupus erythematosusGOLDSTEIN, R; ARNETT, F. C; MCLEAN, R. H et al.Arthritis and rheumatism. 1988, Vol 31, Num 6, pp 736-744, issn 0004-3591Article

Dépistage des blocages enzymatiques incomplets de la 21-hydroxylase. Etude de la 17 OH progestérone sous tétracosactide en phases folliculaire et lutéale chez la femme hirsute = Screening for incomplete 21-hydroxylase enzyme blocks. A study of 17-hydroxyprogesterone before and after the administration of tetracosactide in the luteal and follicular phases in hirsute womenHEIM, J; MASSART, C.Journal de gynécologie obstétrique et biologie de la reproduction. 1983, Vol 12, Num 8, pp 861-864, issn 0368-2315Article

Abnormalities of 21-hydroxylase gene ratio and adrenal steroidogenesis in hyperandrogenic women with an exaggerated 17-hydroxyprogesterone response to acute adrenal stimulationAZZIZ, R; WELLS, G; ZACUR, H. A et al.The Journal of clinical endocrinology and metabolism. 1991, Vol 73, Num 6, pp 1327-1331, issn 0021-972XArticle

C4 null phenotypes among lupus erythematosus patients are predominantly the result of deletions covering C4 and closely linked 21-hydroxylase A genesPARTANEN, J; KOSKIMIES, S; JOHANSSON, E et al.Journal of medical genetics. 1988, Vol 25, Num 6, pp 387-391, issn 0022-2593Article

DRB1*04 and DQ alleles : Expression of 21-hydroxylase autoantibodies and risk of progression to Addison's diseaseLIPING YU; BREWER, K. W; REWERS, M. J et al.The Journal of clinical endocrinology and metabolism. 1999, Vol 84, Num 1, pp 328-335, issn 0021-972XArticle

Early growth is not increased in untreated moderately severe 21-hydroxylase deficiencyTHILEN, A; WOODS, K. A; PERRY, L. A et al.Acta paediatrica (Oslo). 1995, Vol 84, Num 8, pp 894-898, issn 0803-5253Article

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