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Results: 1-15 |
Results: 15
INACTIVATION OF THE LUTEINIZING HORMONE CHORIONIC GONADOTROPIN RECEPTOR BY AN INSERTIONAL MUTATION IN LEYDIG-CELL HYPOPLASIA/
Authors: WU SM HALLERMEIER KM LAUE L BRAIN C BERRY AC GRANT DB GRIFFIN JE WILSON JD CUTLER GB CHAN WY
Citation: Sm. Wu et al., INACTIVATION OF THE LUTEINIZING HORMONE CHORIONIC GONADOTROPIN RECEPTOR BY AN INSERTIONAL MUTATION IN LEYDIG-CELL HYPOPLASIA/, Molecular endocrinology, 12(11), 1998, pp. 1651-1660
EFFECTS OF FASTING ON THE GROWTH-PLATE - SYSTEMIC AND LOCAL MECHANISMS
Authors: HEINRICHS C COLLI M YANOVSKI JA LAUE L GERSTL NA KRAMER AD UYEDA JA BARON J
Citation: C. Heinrichs et al., EFFECTS OF FASTING ON THE GROWTH-PLATE - SYSTEMIC AND LOCAL MECHANISMS, Endocrinology, 138(12), 1997, pp. 5359-5365
HETEROGENEITY OF ACTIVATING MUTATIONS OF THE HUMAN LUTEINIZING-HORMONE RECEPTOR IN MALE-LIMITED PRECOCIOUS PUBERTY
Authors: LAUE L WU SM KUDO M HSUEH AJW CUTLER GB JELLY DH DIAMOND FB CHAN WY
Citation: L. Laue et al., HETEROGENEITY OF ACTIVATING MUTATIONS OF THE HUMAN LUTEINIZING-HORMONE RECEPTOR IN MALE-LIMITED PRECOCIOUS PUBERTY, Biochemical and molecular medicine, 58(2), 1996, pp. 192-198
MUTATIONS IN THE CA2-SENSING RECEPTOR GENE CAUSE AUTOSOMAL-DOMINANT AND SPORADIC HYPOPARATHYROIDISM()
Authors: BARON J WINER KK YANOVSKI JA CUNNINGHAM AW LAUE L ZIMMERMAN D CUTLER GB
Citation: J. Baron et al., MUTATIONS IN THE CA2-SENSING RECEPTOR GENE CAUSE AUTOSOMAL-DOMINANT AND SPORADIC HYPOPARATHYROIDISM(), Human molecular genetics, 5(5), 1996, pp. 601-606
TESTICULAR ADRENAL REST TISSUE IN CONGENITAL ADRENAL-HYPERPLASIA - FINDINGS AT GRAY-SCALE AND COLOR DOPPLER US
Authors: AVILA NA PREMKUMAR A SHAWKER TH JONES JV LAUE L CUTLER GB
Citation: Na. Avila et al., TESTICULAR ADRENAL REST TISSUE IN CONGENITAL ADRENAL-HYPERPLASIA - FINDINGS AT GRAY-SCALE AND COLOR DOPPLER US, Radiology, 198(1), 1996, pp. 99-104
THYROID ABNORMALITIES IN CHILDREN INFECTED WITH HUMAN-IMMUNODEFICIENCY-VIRUS
Authors: HIRSCHFELD S LAUE L CUTLER GB PIZZO PA
Citation: S. Hirschfeld et al., THYROID ABNORMALITIES IN CHILDREN INFECTED WITH HUMAN-IMMUNODEFICIENCY-VIRUS, The Journal of pediatrics, 128(1), 1996, pp. 70-74
A PRELIMINARY-STUDY OF FLUTAMIDE, TESTOLACTONE, AND REDUCED HYDROCORTISONE DOSE IN THE TREATMENT OF CONGENITAL ADRENAL-HYPERPLASIA
Authors: LAUE L MERKE DP JONES JV BARNES KM HILL S CUTLER GB
Citation: L. Laue et al., A PRELIMINARY-STUDY OF FLUTAMIDE, TESTOLACTONE, AND REDUCED HYDROCORTISONE DOSE IN THE TREATMENT OF CONGENITAL ADRENAL-HYPERPLASIA, The Journal of clinical endocrinology and metabolism, 81(10), 1996, pp. 3535-3539
A NONSENSE MUTATION OF THE HUMAN LUTEINIZING-HORMONE RECEPTOR GENE INLEYDIG-CELL HYPOPLASIA
Authors: LAUE L WU SM KUDO M HSUEH AJW CUTLER GB GRIFFIN JE WILSON JD BRAIN C BERRY AC GRANT DB CHAN WY
Citation: L. Laue et al., A NONSENSE MUTATION OF THE HUMAN LUTEINIZING-HORMONE RECEPTOR GENE INLEYDIG-CELL HYPOPLASIA, Human molecular genetics, 4(8), 1995, pp. 1429-1433
GAIN-OF-FUNCTION MUTATIONS OF THE CA2-SENSING RECEPTOR CAUSE AUTOSOMAL-DOMINANT HYPOPARATHYROIDISM()
Authors: BARON J WINER KK YANOVSKI JA CUNNINGHAM AW LAUE L ZIMMERMAN D CUTLER GB
Citation: J. Baron et al., GAIN-OF-FUNCTION MUTATIONS OF THE CA2-SENSING RECEPTOR CAUSE AUTOSOMAL-DOMINANT HYPOPARATHYROIDISM(), Pediatric research, 37(4), 1995, pp. 84-84
GENETIC-HETEROGENEITY OF CONSTITUTIVELY ACTIVATING MUTATIONS OF THE HUMAN LUTEINIZING-HORMONE RECEPTOR IN FAMILIAL MALE-LIMITED PRECOCIOUS PUBERTY
Authors: LAUE L CHAN WY HSUEH AJW KUDO M HSU SY WU SM BLOMBERG LA CUTLER GB
Citation: L. Laue et al., GENETIC-HETEROGENEITY OF CONSTITUTIVELY ACTIVATING MUTATIONS OF THE HUMAN LUTEINIZING-HORMONE RECEPTOR IN FAMILIAL MALE-LIMITED PRECOCIOUS PUBERTY, Proceedings of the National Academy of Sciences of the United Statesof America, 92(6), 1995, pp. 1906-1910
MISSENSE MUTATIONS IN EXON-10 AND EXON-11 OF THE HUMAN LUTEINIZING-HORMONE RECEPTOR GENE ARE ASSOCIATED WITH LEYDIG-CELL HYPOPLASIA
Authors: LAUE L WU SM KUDO M HSUEH AJW CUTLER GB CHAN WY
Citation: L. Laue et al., MISSENSE MUTATIONS IN EXON-10 AND EXON-11 OF THE HUMAN LUTEINIZING-HORMONE RECEPTOR GENE ARE ASSOCIATED WITH LEYDIG-CELL HYPOPLASIA, American journal of human genetics, 57(4), 1995, pp. 1252-1252
CONSTITUTIVELY ACTIVATING MUTATIONS AT MULTIPLE SITES WITHIN THE HUMAN LUTEINIZING-HORMONE RECEPTOR (HLHR) IN FAMILIAL MALE PRECOCIOUS PUBERTY (FMPP)
Authors: LAUE L HSUEH A CUTLER GB CHAN WY
Citation: L. Laue et al., CONSTITUTIVELY ACTIVATING MUTATIONS AT MULTIPLE SITES WITHIN THE HUMAN LUTEINIZING-HORMONE RECEPTOR (HLHR) IN FAMILIAL MALE PRECOCIOUS PUBERTY (FMPP), The FASEB journal, 8(7), 1994, pp. 10001320-10001320
SEX-DIFFERENCES IN SENSITIVITY OF THE HYPOTHALAMIC-PITUITARY-ADRENAL AXIS
Authors: GALLUCCI WT BAUM A LAUE L RABIN DS CHROUSOS GP GOLD PW KLING MA
Citation: Wt. Gallucci et al., SEX-DIFFERENCES IN SENSITIVITY OF THE HYPOTHALAMIC-PITUITARY-ADRENAL AXIS, Health psychology, 12(5), 1993, pp. 420-425
A CONSTITUTIVELY ACTIVATING MUTATION OF THE LUTEINIZING-HORMONE RECEPTOR IN FAMILIAL MALE PRECOCIOUS PUBERTY
Authors: SHENKER A LAUE L KOSUGI S MERENDINO JJ MINEGISHI T CUTLER GB
Citation: A. Shenker et al., A CONSTITUTIVELY ACTIVATING MUTATION OF THE LUTEINIZING-HORMONE RECEPTOR IN FAMILIAL MALE PRECOCIOUS PUBERTY, Nature, 365(6447), 1993, pp. 652-654
TREATMENT OF FAMILIAL MALE PRECOCIOUS PUBERTY WITH SPIRONOLACTONE, TESTOLACTONE, AND DESLORELIN
Authors: LAUE L JONES J BARNES KM CUTLER GB
Citation: L. Laue et al., TREATMENT OF FAMILIAL MALE PRECOCIOUS PUBERTY WITH SPIRONOLACTONE, TESTOLACTONE, AND DESLORELIN, The Journal of clinical endocrinology and metabolism, 76(1), 1993, pp. 151-155
Risultati: 1-15 |