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Results: 1-15 |
Results: 15
EVALUATION OF BOYS WITH MARKED BREAST DEVELOPMENT AT PUBERTY
Authors: SHER ES MIGEON CJ BERKOVITZ GD
Citation: Es. Sher et al., EVALUATION OF BOYS WITH MARKED BREAST DEVELOPMENT AT PUBERTY, Clinical pediatrics, 37(6), 1998, pp. 367-371
ABNORMAL GONADAL DIFFERENTIATION IN 2 SUBJECTS WITH AMBIGUOUS GENITALIA, MULLERIAN STRUCTURES, AND NORMALLY DEVELOPED TESTES - EVIDENCE FORA DEFECT IN GONADAL RIDGE DEVELOPMENT
Authors: FUQUA JS SHER ES PERLMAN EJ URBAN MD GHAHREMANI M PELLETIER J MIGEON CJ BROWN TR BERKOVITZ GD
Citation: Js. Fuqua et al., ABNORMAL GONADAL DIFFERENTIATION IN 2 SUBJECTS WITH AMBIGUOUS GENITALIA, MULLERIAN STRUCTURES, AND NORMALLY DEVELOPED TESTES - EVIDENCE FORA DEFECT IN GONADAL RIDGE DEVELOPMENT, Human genetics, 97(4), 1996, pp. 506-511
THE USE OF ADRENALECTOMY AS A TREATMENT FOR CONGENITAL ADRENAL-HYPERPLASIA
Authors: VANWYK JJ GUNTHER DF RITZEN EM WEDELL A CUTLER GB MIGEON CJ NEW MI
Citation: Jj. Vanwyk et al., THE USE OF ADRENALECTOMY AS A TREATMENT FOR CONGENITAL ADRENAL-HYPERPLASIA, The Journal of clinical endocrinology and metabolism, 81(9), 1996, pp. 3180-3182
CAN THE LONG-RANGE RESULTS OF THE TREATMENT OF CONGENITAL ADRENAL-HYPERPLASIA BE IMPROVED
Authors: MIGEON CJ
Citation: Cj. Migeon, CAN THE LONG-RANGE RESULTS OF THE TREATMENT OF CONGENITAL ADRENAL-HYPERPLASIA BE IMPROVED, The Journal of clinical endocrinology and metabolism, 81(9), 1996, pp. 3187-3189
LINKAGE ANALYSIS OF A KINDRED WITH INHERITED 46,XY PARTIAL GONADAL-DYSGENESIS
Authors: FUQUA JS SHER ES FECHNER PY OSTRER H ODDEUX C SCHAFER AJ ROSALES TO MIGEON CJ BERKOVITZ GD
Citation: Js. Fuqua et al., LINKAGE ANALYSIS OF A KINDRED WITH INHERITED 46,XY PARTIAL GONADAL-DYSGENESIS, The Journal of clinical endocrinology and metabolism, 81(12), 1996, pp. 4479-4483
HUMAN ANDROGEN INSENSITIVITY DUE TO POINT MUTATIONS ENCODING AMINO-ACID SUBSTITUTIONS IN THE ANDROGEN RECEPTOR STEROID-BINDING DOMAIN
Authors: MURONO K MENDONCA BB ARNHOLD IJP RIGON ACMM MIGEON CJ BROWN TR
Citation: K. Murono et al., HUMAN ANDROGEN INSENSITIVITY DUE TO POINT MUTATIONS ENCODING AMINO-ACID SUBSTITUTIONS IN THE ANDROGEN RECEPTOR STEROID-BINDING DOMAIN, Human mutation, 6(2), 1995, pp. 152-162
IS THERE A TRIGGER FOR PUBERTY IN THE MALE - SHOULD EARLY OR DELAYED PUBERTY BE TREATED - IF SO, HOW
Authors: MIGEON CJ
Citation: Cj. Migeon, IS THERE A TRIGGER FOR PUBERTY IN THE MALE - SHOULD EARLY OR DELAYED PUBERTY BE TREATED - IF SO, HOW, Journal of andrology, 1995, pp. 46-47
ASSAY OF PLASMA TESTOSTERONE DURING THE FIRST 6 MONTHS OF LIFE - IMPORTANCE OF CHROMATOGRAPHIC PURIFICATION OF STEROIDS
Authors: FUQUA JS SHER ES MIGEON CJ BERKOVITZ GD
Citation: Js. Fuqua et al., ASSAY OF PLASMA TESTOSTERONE DURING THE FIRST 6 MONTHS OF LIFE - IMPORTANCE OF CHROMATOGRAPHIC PURIFICATION OF STEROIDS, Clinical chemistry, 41(8), 1995, pp. 1146-1149
THE HLA-A3,CW6,B47,DR7 EXTENDED HAPLOTYPES IN SALT LOSING 21-HYDROXYLASE DEFICIENCY AND IN THE OLD-ORDER AMISH, IDENTICAL CLASS-I ANTIGENS AND CLASS-II ALLELES WITH AT LEAST 2 CROSSOVER SITES IN THE CLASS-III REGION
Authors: DONOHOUE PA GUETHLEIN L COLLINS MM VANDOP C MIGEON CJ BIAS WB SCHMECKPEPER BJ
Citation: Pa. Donohoue et al., THE HLA-A3,CW6,B47,DR7 EXTENDED HAPLOTYPES IN SALT LOSING 21-HYDROXYLASE DEFICIENCY AND IN THE OLD-ORDER AMISH, IDENTICAL CLASS-I ANTIGENS AND CLASS-II ALLELES WITH AT LEAST 2 CROSSOVER SITES IN THE CLASS-III REGION, Tissue antigens, 46(3), 1995, pp. 163-172
NONRANDOM INACTIVATION OF THE Y-BEARING X-CHROMOSOME IN A 46,XX INDIVIDUAL - EVIDENCE FOR THE ETIOLOGY OF 46,XX TRUE HERMAPHRODITISM
Authors: FECHNER PY ROSENBERG C STETTEN G CARGILE CB PEARSON PL SMITH KD MIGEON CJ BERKOVITZ GD
Citation: Py. Fechner et al., NONRANDOM INACTIVATION OF THE Y-BEARING X-CHROMOSOME IN A 46,XX INDIVIDUAL - EVIDENCE FOR THE ETIOLOGY OF 46,XX TRUE HERMAPHRODITISM, Cytogenetics and cell genetics, 66(1), 1994, pp. 22-26
EMBRYONIC TESTICULAR REGRESSION SEQUENCE - A PART OF THE CLINICAL SPECTRUM OF 46,XY GONADAL-DYSGENESIS
Authors: MARCANTONIO SM FECHNER PY MIGEON CJ PERLMAN EJ BERKOVITZ GD
Citation: Sm. Marcantonio et al., EMBRYONIC TESTICULAR REGRESSION SEQUENCE - A PART OF THE CLINICAL SPECTRUM OF 46,XY GONADAL-DYSGENESIS, American journal of medical genetics, 49(1), 1994, pp. 1-5
TEMPORAL AND INDIVIDUAL VARIATIONS IN THE DOSE OF GLUCOCORTICOID USEDFOR THE TREATMENT OF SALT-LOSING CONGENITAL VIRILIZING ADRENAL-HYPERPLASIA DUE TO 21-HYDROXYLASE DEFICIENCY
Authors: SANDRINI R JOSPE N MIGEON CJ
Citation: R. Sandrini et al., TEMPORAL AND INDIVIDUAL VARIATIONS IN THE DOSE OF GLUCOCORTICOID USEDFOR THE TREATMENT OF SALT-LOSING CONGENITAL VIRILIZING ADRENAL-HYPERPLASIA DUE TO 21-HYDROXYLASE DEFICIENCY, Acta paediatrica, 82, 1993, pp. 56-61
MOLECULAR-GENETICS OF HUMAN ANDROGEN INSENSITIVITY
Authors: BROWN TR SCHERER PA CHANG YT MIGEON CJ GHIRRI P MURONO K ZHOU Z
Citation: Tr. Brown et al., MOLECULAR-GENETICS OF HUMAN ANDROGEN INSENSITIVITY, European journal of pediatrics, 152, 1993, pp. 62-69
REPORT OF A KINDRED WITH X-LINKED (OR AUTOSOMAL-DOMINANT SEX-LIMITED)46,XY PARTIAL GONADAL-DYSGENESIS
Authors: FECHNER PY MARCANTONIO SM OGATA T ROSALES TO SMITH KD GOODFELLOW PN MIGEON CJ BERKOVITZ GD
Citation: Py. Fechner et al., REPORT OF A KINDRED WITH X-LINKED (OR AUTOSOMAL-DOMINANT SEX-LIMITED)46,XY PARTIAL GONADAL-DYSGENESIS, The Journal of clinical endocrinology and metabolism, 76(5), 1993, pp. 1248-1253
NONRANDOM INACTIVATION OF THE Y-BEARING X-CHROMOSOME IN A 46,XX INDIVIDUAL - EVIDENCE FOR THE ETIOLOGY OF 46,XX TRUE HERMAPHRODITISM
Authors: FECHNER PY ROSENBERG C STETTEN G CARGILE CB PEARSON PL SMITH KD MIGEON CJ BERKOVITZ GD
Citation: Py. Fechner et al., NONRANDOM INACTIVATION OF THE Y-BEARING X-CHROMOSOME IN A 46,XX INDIVIDUAL - EVIDENCE FOR THE ETIOLOGY OF 46,XX TRUE HERMAPHRODITISM, American journal of human genetics, 53(3), 1993, pp. 545-545
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