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Results: 1-25 | 26-50 | 51-59
Results: 26-50/59
Pigmented lesions of the conjunctiva in Carney's complex
Authors: Cohen, C Turner, ML Stratakis, CA
Citation: C. Cohen et al., Pigmented lesions of the conjunctiva in Carney's complex, J AM ACAD D, 42(1), 2000, pp. 145-145
Premature adrenal cortical dysfunction in mandibuloacral dysplasia: A progeroid-like syndrome
Authors: Ng, D Stratakis, CA
Citation: D. Ng et Ca. Stratakis, Premature adrenal cortical dysfunction in mandibuloacral dysplasia: A progeroid-like syndrome, AM J MED G, 95(3), 2000, pp. 293-295
Familial hyperaldosteronism
Authors: Torpy, DJ Stratakis, CA Chrousos, GP
Citation: Dj. Torpy et al., Familial hyperaldosteronism, BRAZ J MED, 33(10), 2000, pp. 1149-1155
Adrenocorticotropin-independent macronodular adrenal hyperplasia: An uncommon cause of primary adrenal hypercortisolism
Authors: Doppman, JL Chrousos, GP Papanicolaou, DA Stratakis, CA Alexander, HR Nieman, LK
Citation: Jl. Doppman et al., Adrenocorticotropin-independent macronodular adrenal hyperplasia: An uncommon cause of primary adrenal hypercortisolism, RADIOLOGY, 216(3), 2000, pp. 797-802
Laparoscopic diagnosis and clinical management of a solitary nonpalpable cryptorchid testicle in a postpubertal male
Authors: Enquist, EG Stratakis, CA Rushton, HG Walther, MM
Citation: Eg. Enquist et al., Laparoscopic diagnosis and clinical management of a solitary nonpalpable cryptorchid testicle in a postpubertal male, J UROL, 163(3), 2000, pp. 959-960
A novel genetic locus for low renin hypertension: familial hyperaldosteronism type II maps to chromosome 7 (7p22)
Authors: Lafferty, AR Torpy, DJ Stowasser, M Taymans, SE Lin, JP Huggard, P Gordon, RD Stratakis, CA
Citation: Ar. Lafferty et al., A novel genetic locus for low renin hypertension: familial hyperaldosteronism type II maps to chromosome 7 (7p22), J MED GENET, 37(11), 2000, pp. 831-835
Anisomastia associated with interstitial duplication of chromosome 16, mental retardation, obesity, dysmorphic facies, and digital anomalies: Molecular mapping of a new syndrome by fluorescent in situ hybridization and microsatellites to 16q13 (D16S419-D16S503)
Authors: Stratakis, CA Lafferty, A Taymans, SE Gafni, RI Meck, JM Blancato, J
Citation: Ca. Stratakis et al., Anisomastia associated with interstitial duplication of chromosome 16, mental retardation, obesity, dysmorphic facies, and digital anomalies: Molecular mapping of a new syndrome by fluorescent in situ hybridization and microsatellites to 16q13 (D16S419-D16S503), J CLIN END, 85(9), 2000, pp. 3396-3401
Pituitary macroadenoma in a 5-year-old: An early expression of multiple endocrine neoplasia type 1
Authors: Stratakis, CA Schussheim, DH Freedman, SM Keil, MF Pack, SD Agarwal, SK Skarulis, MC Weil, RJ Lubensky, IA Zhuang, ZP Oldfield, EH Marx, SJ
Citation: Ca. Stratakis et al., Pituitary macroadenoma in a 5-year-old: An early expression of multiple endocrine neoplasia type 1, J CLIN END, 85(12), 2000, pp. 4776-4780
Isolated familial somatotropinomas: Does the disease map to 11q13 or to 2p16?
Authors: Stratakis, CA Kirschner, LS
Citation: Ca. Stratakis et Ls. Kirschner, Isolated familial somatotropinomas: Does the disease map to 11q13 or to 2p16?, J CLIN END, 85(12), 2000, pp. 4920-4920
Ovarian lesions in Carney complex: Clinical genetics and possible predisposition to malignancy
Authors: Stratakis, CA Papageorgiou, T Premkumar, A Pack, S Kirschner, LS Taymans, SE Zhuang, ZP Oelkers, WH Carney, JA
Citation: Ca. Stratakis et al., Ovarian lesions in Carney complex: Clinical genetics and possible predisposition to malignancy, J CLIN END, 85(11), 2000, pp. 4359-4366
Genetic and histologic studies of somatomammotropic pituitary tumors in patients with the "complex of spotty skin pigmentation, myxomas, endocrine overactivity and schwannomas" (Carney complex)
Authors: Pack, SD Kirschner, LS Pak, E Zhuang, ZP Carney, JA Stratakis, CA
Citation: Sd. Pack et al., Genetic and histologic studies of somatomammotropic pituitary tumors in patients with the "complex of spotty skin pigmentation, myxomas, endocrine overactivity and schwannomas" (Carney complex), J CLIN END, 85(10), 2000, pp. 3860-3865
Structure of the human ubiquitin fusion gene Uba80 (RPS27a) and one of itspseudogenes
Authors: Kirschner, LS Stratakis, CA
Citation: Ls. Kirschner et Ca. Stratakis, Structure of the human ubiquitin fusion gene Uba80 (RPS27a) and one of itspseudogenes, BIOC BIOP R, 270(3), 2000, pp. 1106-1110
Cushing syndrome and Addison disease
Authors: Stratakis, CA
Citation: Ca. Stratakis, Cushing syndrome and Addison disease, ENDOCR DEV, 2, 2000, pp. 150-173
Mutation analyses of North American APS-1 patients
Authors: Heino, M Scott, HS Chen, QY Peterson, P Maenpaa, U Papasavvas, MP Mittaz, L Barras, C Rossier, C Chrousos, GP Stratakis, CA Nagamine, K Kudoh, J Shimizu, N Maclaren, N Antonarakis, SE Krohn, K
Citation: M. Heino et al., Mutation analyses of North American APS-1 patients, HUM MUTAT, 13(1), 1999, pp. 69-74
Congenital adrenal hyperplasia: Molecular genetics and alternative approaches to treatment
Authors: Stratakis, CA Rennert, OM
Citation: Ca. Stratakis et Om. Rennert, Congenital adrenal hyperplasia: Molecular genetics and alternative approaches to treatment, CR R CL LAB, 36(4), 1999, pp. 329-363
Genomic mapping of chromosomal region 2p15-p21 (D2S378-D2S391): Integration of Genemap'98 within a framework of yeast and bacterial artificial chromosomes
Authors: Kirschner, LS Taymans, SE Pack, S Pak, E Pike, BL Chandrasekharappa, SC Zhuang, ZP Stratakis, CA
Citation: Ls. Kirschner et al., Genomic mapping of chromosomal region 2p15-p21 (D2S378-D2S391): Integration of Genemap'98 within a framework of yeast and bacterial artificial chromosomes, GENOMICS, 62(1), 1999, pp. 21-33
Radiation hybrid mapping of chromosomal region 2p15-p16: Integration of expressed and polymorphic sequences maps at the Carney complex (CNC) and Doyne honeycomb retinal dystrophy (DHRD) loci
Authors: Taymans, SE Kirschner, LS Giatzakis, C Stratakis, CA
Citation: Se. Taymans et al., Radiation hybrid mapping of chromosomal region 2p15-p16: Integration of expressed and polymorphic sequences maps at the Carney complex (CNC) and Doyne honeycomb retinal dystrophy (DHRD) loci, GENOMICS, 56(3), 1999, pp. 344-349
The human vitamin D receptor gene (VDR) is localized to region 12cen-q12 by fluorescent in situ hybridization and radiation hybrid mapping: Genetic and physical VDR map
Authors: Taymans, SE Pack, S Pak, E Orban, Z Barsony, J Zhuang, ZP Stratakis, CA
Citation: Se. Taymans et al., The human vitamin D receptor gene (VDR) is localized to region 12cen-q12 by fluorescent in situ hybridization and radiation hybrid mapping: Genetic and physical VDR map, J BONE MIN, 14(7), 1999, pp. 1163-1166
Large-scale preparation of sequence-ready bacterial artificial chromosome DNA using QIAGEN (R) columns
Authors: Kirschner, LS Stratakis, CA
Citation: Ls. Kirschner et Ca. Stratakis, Large-scale preparation of sequence-ready bacterial artificial chromosome DNA using QIAGEN (R) columns, BIOTECHNIQU, 27(1), 1999, pp. 72
Small deletions in the type II collagen triple helix produce Kniest dysplasia
Authors: Wilkin, DJ Artz, AS South, S Lachman, RS Rimoin, DL Wilcox, WR McKusick, VA Stratakis, CA Francomano, CA Cohn, DH
Citation: Dj. Wilkin et al., Small deletions in the type II collagen triple helix produce Kniest dysplasia, AM J MED G, 85(2), 1999, pp. 105-112
Hyper- and hypoaldosteronism
Authors: Torpy, DJ Stratakis, CA Chrousos, GP
Citation: Dj. Torpy et al., Hyper- and hypoaldosteronism, VITAM HORM, 57, 1999, pp. 177-216
Carney complex and related syndromes and their genetic loci - Response
Authors: Stratakis, CA
Citation: Ca. Stratakis, Carney complex and related syndromes and their genetic loci - Response, J CLIN END, 84(4), 1999, pp. 1491-1492
Androgen receptor-mediated hypersensitivity to androgens in women with nonhyperandrogenic hirsutism: Skewing of X-chromosome inactivation
Authors: Vottero, A Stratakis, CA Ghizzoni, L Longui, CA Karl, M Chrousos, GP
Citation: A. Vottero et al., Androgen receptor-mediated hypersensitivity to androgens in women with nonhyperandrogenic hirsutism: Skewing of X-chromosome inactivation, J CLIN END, 84(3), 1999, pp. 1091-1095
Comparative genomic hybridization analysis of adrenocortical tumors of childhood
Authors: Figueiredo, BC Stratakis, CA Sandrini, R DeLacerda, L Pianovsky, MAD Giatzakis, C Young, HM Haddad, BR
Citation: Bc. Figueiredo et al., Comparative genomic hybridization analysis of adrenocortical tumors of childhood, J CLIN END, 84(3), 1999, pp. 1116-1121
Synaptophysin immunoreactivity in primary pigmented nodular adrenocorticaldisease: Neuroendocrine properties of tumors associated with Carney complex
Authors: Stratakis, CA Carney, JA Kirschner, LS Willenberg, HS Brauer, S Ehrhart-Bornstein, M Bornstein, SR
Citation: Ca. Stratakis et al., Synaptophysin immunoreactivity in primary pigmented nodular adrenocorticaldisease: Neuroendocrine properties of tumors associated with Carney complex, J CLIN END, 84(3), 1999, pp. 1122-1128
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