Works matching IS 00778923 AND DT 1985 AND VI 458 AND IP 1

Results: 30

Neonatal Screening for Congenital Adrenal Hyperplasia in Japan.

Published in:

Annals of the New York Academy of Sciences, 1985, v. 458, n. 1, p. 103, doi. 10.1111/j.1749-6632.1985.tb14596.x

By:

NARUSE, H.;
SUZUKI, E.;
IRIE, M.;
TSUJI, A.;
TAKASUGI, N.;
FUKUSHI, M.;
MATSUURA, N.;
SHIMOZAWA, K.

Publication type:

Article

Deoxycorticosterone Biosynthesis in Kidney Tissue of Experimental Animals: Characterization of Steroid 21-Hydroxylase Activity in Guinea Pig Kidneya.

Published in:

Annals of the New York Academy of Sciences, 1985, v. 458, n. 1, p. 232, doi. 10.1111/j.1749-6632.1985.tb14608.x

By:

CASEY, M. LINETTE;
MacDONALD, PAUL C.;
WINKEL, CRAIG A.

Publication type:

Article

Cytochrome P-450: Physiology of Steroidogenesisa.

Published in:

Annals of the New York Academy of Sciences, 1985, v. 458, n. 1, p. 203, doi. 10.1111/j.1749-6632.1985.tb14605.x

By:

HALL, PETER F.

Publication type:

Article

Pitfalls of Prenatal Diagnosis of 21-Hydroxylase Deficiency Congenital Adrenal Hyperplasiaa.

Published in:

Annals of the New York Academy of Sciences, 1985, v. 458, n. 1, p. 111, doi. 10.1111/j.1749-6632.1985.tb14597.x

By:

PANG, SONGYA;
POLLACK, MARILYN S.;
LOO, MAY;
GREEN, ORVILLE;
NUSSBAUM, ROBERT;
CLAYTON, GEORGE;
DUPONT, BO;
NEW, MARIA I.

Publication type:

Article

Evidence that Variation among Untreated Rabbits in Hepatic Progesterone 21-Hydroxylase Activity Is Indicative of Enzyme Heterogeneity Rather than a Transient Inductive Effecta.

Published in:

Annals of the New York Academy of Sciences, 1985, v. 458, n. 1, p. 225, doi. 10.1111/j.1749-6632.1985.tb14607.x

By:

MULLER-EBERHARD, U.;
GHIZZONI, L.;
LIEM, H.H.;
NEW, M.;
FINLAYSON, M.;
JOHNSON, E.F.

Publication type:

Article

The Association Between Congenital Adrenal Hyperplasia and HLA in Southern Italy.

Published in:

Annals of the New York Academy of Sciences, 1985, v. 458, n. 1, p. 46, doi. 10.1111/j.1749-6632.1985.tb14589.x

By:

ZAPPACOSTA, SERAFINO;
MAIO, MICHELE;
FELICE, MARIO de;
VALENTINO, ROSSELLA

Publication type:

Article

Different Gene Defects in the Salt-Wasting (SW), Simple Virilizing (SV), and Nonclassical (NC) Types of Congenital Adrenal Hyperplasia (CAH).

Published in:

Annals of the New York Academy of Sciences, 1985, v. 458, n. 1, p. 71, doi. 10.1111/j.1749-6632.1985.tb14592.x

By:

KNORR, D.;
ALBERT, E. D.;
BIDLINGMAIER, F.;
HÖLLER, W.;
SCHOLZ, S.

Publication type:

Article

Structure Organization and Expression of the Major Histocompatibility Class III Genes.

Published in:

Annals of the New York Academy of Sciences, 1985, v. 458, n. 1, p. 269, doi. 10.1111/j.1749-6632.1985.tb14612.x

By:

COLTEN, HARVEY R.

Publication type:

Article

The Use of Gamma Interferon to Increase HLA Antigen Expression on Cultured Amniotic Cells Used for the Prenatal Diagnosis of 21-Hydroxylase Deficiencya.

Published in:

Annals of the New York Academy of Sciences, 1985, v. 458, n. 1, p. 148, doi. 10.1111/j.1749-6632.1985.tb14599.x

By:

MAURER, DAVID H.;
POLLACK, MARILYN S.

Publication type:

Article

HLA Associations in 21-Hydroxylase Deficiency (Congenital and Late-Onset Adrenal Hyperplasia) in France.

Published in:

Annals of the New York Academy of Sciences, 1985, v. 458, n. 1, p. 41, doi. 10.1111/j.1749-6632.1985.tb14588.x

By:

COUILLIN, P.;
RAPPAPORT, R.;
KUTTENN, F.;
HORS, J.;
FEINGOLD, J.;
BOUÉ, J.;
BOUÉ, A.

Publication type:

Article

HLA Associations in Late-Onset 21-Hydroxylase Deficiency in Israel.

Published in:

Annals of the New York Academy of Sciences, 1985, v. 458, n. 1, p. 52, doi. 10.1111/j.1749-6632.1985.tb14590.x

By:

LARON, Z.;
ROITMAN, A.;
PERTZELAN, A.;
KAUFMAN, H.;
ZAMIR, R.

Publication type:

Article

Neonatal Screening Program for Congenital Adrenal Hyperplasia in a Homogeneous Caucasian Population.

Published in:

Annals of the New York Academy of Sciences, 1985, v. 458, n. 1, p. 85, doi. 10.1111/j.1749-6632.1985.tb14594.x

By:

CACCIARI, E.;
BALSAMO, A.;
CASSIO, A.;
PIAZZI, S.;
BERNARDI, F.;
SALARDI, S.;
CICOGNANI, A.;
PIRAZZOLI, P.;
ZAPPULLA, F.;
CAPELLI, M.;
PAOLINI, M.;
CORDARO, C.I.

Publication type:

Article

Extended MHC Haplotypes in Salt-Losing 21-Hydroxylase Deficiencya.

Published in:

Annals of the New York Academy of Sciences, 1985, v. 458, n. 1, p. 28, doi. 10.1111/j.1749-6632.1985.tb14586.x

By:

ALPER, CHESTER A.;
FLEISCHNICK, ELLEN;
AWDEH, ZUHEIR;
RAUM, DONALD;
CRIGLER, JOHN F.;
GERALD, PARK S.;
YUNIS, EDMOND J.

Publication type:

Article

Modern Medical Therapy of Congenital Adrenal Hyperplasia A Decade of Experiencea.

Published in:

Annals of the New York Academy of Sciences, 1985, v. 458, n. 1, p. 165, doi. 10.1111/j.1749-6632.1985.tb14601.x

By:

WINTER, JEREMY S. D.;
COUCH, ROBERT M.

Publication type:

Article

Introduction.

Published in:

Annals of the New York Academy of Sciences, 1985, v. 458, n. 1, p. ix, doi. 10.1111/j.1749-6632.1985.tb14584.x

By:

BONGIOVANNI, ALFRED M.

Publication type:

Article

Clinical and Endocrinological Aspects of 21-Hydroxylase Deficiencya.

Published in:

Annals of the New York Academy of Sciences, 1985, v. 458, n. 1, p. 1, doi. 10.1111/j.1749-6632.1985.tb14585.x

By:

NEW, MARIA I.

Publication type:

Article

Regulation of Cytochrome P-45017α Activity and Synthesis in Bovine Adrenocortical Cellsa.

Published in:

Annals of the New York Academy of Sciences, 1985, v. 458, n. 1, p. 252, doi. 10.1111/j.1749-6632.1985.tb14610.x

By:

ZUBER, MAURICIO X.;
SIMPSON, EVAN R.;
WATERMAN, MICHAEL R.

Publication type:

Article

Biochemical Properties of Cytochrome P-450 in Relation to Steroid Oxygenationa.

Published in:

Annals of the New York Academy of Sciences, 1985, v. 458, n. 1, p. 216, doi. 10.1111/j.1749-6632.1985.tb14606.x

By:

COON, MINOR J.;
INOUYE, KUNIYO

Publication type:

Article

Effect of Hydrocortisone Dose Schedule on Adrenal Steroid Secretion in Congenital Adrenal Hyperplasia.

Published in:

Annals of the New York Academy of Sciences, 1985, v. 458, n. 1, p. 182, doi. 10.1111/j.1749-6632.1985.tb14603.x

By:

WINTERER, JORG;
CHROUSOS, GEORGE P.;
LORIAUX, D. LYNN;
CUTLER, GORDON B.

Publication type:

Article

Monitoring Treatment in Congenital Adrenal Hyperplasia Use of Serial Measurements of 17-OH-Progesterone in Plasma, Capillary Blood, and Salivaa.

Published in:

Annals of the New York Academy of Sciences, 1985, v. 458, n. 1, p. 193, doi. 10.1111/j.1749-6632.1985.tb14604.x

By:

HUGHES, I. A.;
DYAS, J.;
ROBINSON, J.;
WALKER, R. F.;
FAHMY, D. R.

Publication type:

Article

An Approach to the Molecular Biology of Congenital Adrenal Hyperplasiaa.

Published in:

Annals of the New York Academy of Sciences, 1985, v. 458, n. 1, p. 238, doi. 10.1111/j.1749-6632.1985.tb14609.x

By:

CHUNG, BON-CHU;
MATTESON, KARLA J.;
MORIN, JOHN E.;
MELLON, SYNTHIA H.;
MILLER, WALTER L.

Publication type:

Article

Newborn Screening for Congenital Adrenal Hyperplasia with Special Reference to Screening in Alaskaa.

Published in:

Annals of the New York Academy of Sciences, 1985, v. 458, n. 1, p. 90, doi. 10.1111/j.1749-6632.1985.tb14595.x

By:

PANG, SONGYA;
SPENCE, DAVID A.;
NEW, MARIA I.

Publication type:

Article

The Human Major Histocompatibility Complex Genes and Proteinsa.

Published in:

Annals of the New York Academy of Sciences, 1985, v. 458, n. 1, p. 262, doi. 10.1111/j.1749-6632.1985.tb14611.x

By:

STROMINGER, JACK L.

Publication type:

Article

Pitfalls in Prenatal Diagnosis of 21-Hydroxylase Deficiency by Amniotic Fluid Steroid Analysis? A Six Years Experience in 102 Pregnancies at Riska.

Published in:

Annals of the New York Academy of Sciences, 1985, v. 458, n. 1, p. 130, doi. 10.1111/j.1749-6632.1985.tb14598.x

By:

FOREST, MAGUELONE G.

Publication type:

Article

HLA-B14 and Nonclassical 21-Hydroxylase Deficiency in a Heterogeneous New York Populationa.

Published in:

Annals of the New York Academy of Sciences, 1985, v. 458, n. 1, p. 65, doi. 10.1111/j.1749-6632.1985.tb14591.x

By:

LEVINE, LENORE S.

Publication type:

Article

The HLA Associations in Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency in a Yugoslav Population.

Published in:

Annals of the New York Academy of Sciences, 1985, v. 458, n. 1, p. 36, doi. 10.1111/j.1749-6632.1985.tb14587.x

By:

KAŠTELAN, A.;
BRKLJAČIĆ-ŠURKALOVIĆ, L. J.;
DUMIČ, M.

Publication type:

Article

The Coexistence of IgA Deficiency and 21-Hydroxylase Deficiency Marked by Specific MHC Supratypes.

Published in:

Annals of the New York Academy of Sciences, 1985, v. 458, n. 1, p. 76, doi. 10.1111/j.1749-6632.1985.tb14593.x

By:

COBAIN, T. J.;
STUCKEY, M. S.;
McCLUSKEY, J.;
WILTON, A. N.;
GEDEON, A.;
GARLEPP, M. J.;
CHRISTIANSEN, F. T.;
DAWKINS, R. L.

Publication type:

Article

LHRH Analog Treatment of Central Precocious Puberty Complicating Congenital Adrenal Hyperplasia.

Published in:

Annals of the New York Academy of Sciences, 1985, v. 458, n. 1, p. 174, doi. 10.1111/j.1749-6632.1985.tb14602.x

By:

PESCOVITZ, ORA HIRSCH;
CASSORLA, FERNANDO;
COMITE, FLORENCE;
LORIAUX, D. LYNN;
CUTLER, GORDON B.

Publication type:

Article

Prenatal Therapy in Congenital Adrenal Hyperplasia Attempted Prevention of Abnormal External Genital Masculinization by Pharmacologic Suppression of the Fetal Adrenal Gland in Utero.

Published in:

Annals of the New York Academy of Sciences, 1985, v. 458, n. 1, p. 156, doi. 10.1111/j.1749-6632.1985.tb14600.x

By:

CHROUSOS, GEORGE P.;
EVANS, MARK I.;
LORIAUX, D. LYNN;
McCLUSKEY, JAMES;
FLETCHER, JOHN C.;
SCHULMAN, JOSEPH D.

Publication type:

Article

Molecular Cloning of Steroid 21-Hydroxylasea.

Published in:

Annals of the New York Academy of Sciences, 1985, v. 458, n. 1, p. 277, doi. 10.1111/j.1749-6632.1985.tb14613.x

By:

WHITE, PERRIN C.;
NEW, MARIA I.;
DUPONT, BO

Publication type:

Article

Works matching IS 00778923 AND DT 1985 AND VI 458 AND IP 1

Neonatal Screening for Congenital Adrenal Hyperplasia in Japan.

Deoxycorticosterone Biosynthesis in Kidney Tissue of Experimental Animals: Characterization of Steroid 21-Hydroxylase Activity in Guinea Pig Kidney<sup>a</sup>.

Cytochrome P-450: Physiology of Steroidogenesis<sup>a</sup>.

Pitfalls of Prenatal Diagnosis of 21-Hydroxylase Deficiency Congenital Adrenal Hyperplasia<sup>a</sup>.

Evidence that Variation among Untreated Rabbits in Hepatic Progesterone 21-Hydroxylase Activity Is Indicative of Enzyme Heterogeneity Rather than a Transient Inductive Effect<sup>a</sup>.

The Association Between Congenital Adrenal Hyperplasia and HLA in Southern Italy.

Different Gene Defects in the Salt-Wasting (SW), Simple Virilizing (SV), and Nonclassical (NC) Types of Congenital Adrenal Hyperplasia (CAH).

Structure Organization and Expression of the Major Histocompatibility Class III Genes.

The Use of Gamma Interferon to Increase HLA Antigen Expression on Cultured Amniotic Cells Used for the Prenatal Diagnosis of 21-Hydroxylase Deficiency<sup>a</sup>.

HLA Associations in 21-Hydroxylase Deficiency (Congenital and Late-Onset Adrenal Hyperplasia) in France.

HLA Associations in Late-Onset 21-Hydroxylase Deficiency in Israel.

Neonatal Screening Program for Congenital Adrenal Hyperplasia in a Homogeneous Caucasian Population.

Extended MHC Haplotypes in Salt-Losing 21-Hydroxylase Deficiency<sup>a</sup>.

Modern Medical Therapy of Congenital Adrenal Hyperplasia A Decade of Experience<sup>a</sup>.

Introduction.

Clinical and Endocrinological Aspects of 21-Hydroxylase Deficiency<sup>a</sup>.

Regulation of Cytochrome P-450<sub>17</sub>α Activity and Synthesis in Bovine Adrenocortical Cells<sup>a</sup>.

Biochemical Properties of Cytochrome P-450 in Relation to Steroid Oxygenation<sup>a</sup>.

Effect of Hydrocortisone Dose Schedule on Adrenal Steroid Secretion in Congenital Adrenal Hyperplasia.

Monitoring Treatment in Congenital Adrenal Hyperplasia Use of Serial Measurements of 17-OH-Progesterone in Plasma, Capillary Blood, and Saliva<sup>a</sup>.

An Approach to the Molecular Biology of Congenital Adrenal Hyperplasia<sup>a</sup>.

Newborn Screening for Congenital Adrenal Hyperplasia with Special Reference to Screening in Alaska<sup>a</sup>.

The Human Major Histocompatibility Complex Genes and Proteins<sup>a</sup>.

Pitfalls in Prenatal Diagnosis of 21-Hydroxylase Deficiency by Amniotic Fluid Steroid Analysis? A Six Years Experience in 102 Pregnancies at Risk<sup>a</sup>.

HLA-B14 and Nonclassical 21-Hydroxylase Deficiency in a Heterogeneous New York Population<sup>a</sup>.

The HLA Associations in Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency in a Yugoslav Population.

The Coexistence of IgA Deficiency and 21-Hydroxylase Deficiency Marked by Specific MHC Supratypes.

LHRH Analog Treatment of Central Precocious Puberty Complicating Congenital Adrenal Hyperplasia.

Prenatal Therapy in Congenital Adrenal Hyperplasia Attempted Prevention of Abnormal External Genital Masculinization by Pharmacologic Suppression of the Fetal Adrenal Gland in Utero.

Molecular Cloning of Steroid 21-Hydroxylase<sup>a</sup>.