Results: 1-25 | 26-50 | 51-59
Results: 1-25/59

Authors: Tsilou, E Stratakis, CA Rubin, BI Hay, BN Patronas, N Kaiser-Kupfer, MI
Citation: E. Tsilou et al., Ophthalmic manifestations of Allgrove syndrome: report of a case, CLIN DYSMOR, 10(3), 2001, pp. 231-233

Authors: Stratakis, CA
Citation: Ca. Stratakis, Clinical genetics of multiple endocrine neoplasias, Carney complex and related syndromes, J ENDOC INV, 24(5), 2001, pp. 370-383

Authors: Marsh, DJ Stratakis, CA
Citation: Dj. Marsh et Ca. Stratakis, Hamartoma and lentiginosis syndromes: Clinical and molecular aspects, FRONT HORM, 28, 2001, pp. 167-213

Authors: Egan, CA Stratakis, CA Turner, ML
Citation: Ca. Egan et al., Multiple lentigines associated with cutaneous myxomas, J AM ACAD D, 44(2), 2001, pp. 282-284

Authors: Carney, JA Boccon-Gibod, L Jarka, DE Tanaka, Y Swee, RG Unni, KK Stratakis, CA
Citation: Ja. Carney et al., Osteochondromyxoma of bone - A congenital tumor associated with lentiginesand other unusual disorders, AM J SURG P, 25(2), 2001, pp. 164-176

Authors: Ribeiro, RC Sandrini, F Figueiredo, B Zambetti, GP Michalkiewicz, E Lafferty, AR DeLacerda, L Rabin, M Cadwell, C Sampaio, G Cat, I Stratakis, CA Sandrini, R
Citation: Rc. Ribeiro et al., A inherited p53 mutation that contributes in a tissue-specific manner to pediatric adrenal cortical carcinoma, P NAS US, 98(16), 2001, pp. 9330-9335

Authors: Stratakis, CA Turner, ML Lafferty, A Toro, JR Hill, S Meck, JM Blancato, J
Citation: Ca. Stratakis et al., A syndrome of overgrowth and acromegaloidism with normal growth hormone secretion is associated with chromosome 11 pericentric inversion, J MED GENET, 38(5), 2001, pp. 338-343

Authors: Stratakis, CA Taymans, SE Schteingart, D Haddad, BR
Citation: Ca. Stratakis et al., Segmental uniparental isodisomy (UPD) for 2p16 without clinical symptoms: implications for UPD and other genetic studies of chromosome 2, J MED GENET, 38(2), 2001, pp. 106-109

Authors: Zouboulis, CC Stratakis, CA Gollnick, HPM Orfanos, CE
Citation: Cc. Zouboulis et al., Keratosis pilaris/ulerythema ophryogenes and 18p deletion: is it possible that the LAMA1 gene is involved?, J MED GENET, 38(2), 2001, pp. 127-128

Authors: Stratakis, CA Kirschner, LS Carney, JA
Citation: Ca. Stratakis et al., Genetics of endocrine disease - Clinical and molecular features of the Carney complex: Diagnostic criteria and recommendations for patient evaluation, J CLIN END, 86(9), 2001, pp. 4041-4046

Authors: Glasow, A Horn, LC Taymans, SE Stratakis, CA Kelly, PA Kohler, U Gillespie, J Vonderhaar, BK Bornstein, SR
Citation: A. Glasow et al., Mutational analysis of the PRL receptor gene in human breast tumors with differential PRL receptor protein expression, J CLIN END, 86(8), 2001, pp. 3826-3832

Authors: Sandrini, F Farmakidis, C Kirschner, LS Wu, SM Tullio-Pelet, A Lyonnet, S Metzger, DL Bourdony, CJ Tiosano, D Chan, WY Stratakis, CA
Citation: F. Sandrini et al., Spectrum of mutations of the AAAS gene in Allgrove syndrome: Lack of mutations in six kindreds with isolated resistance to corticotropin, J CLIN END, 86(11), 2001, pp. 5433-5437

Authors: Stratakis, CA
Citation: Ca. Stratakis, Genetics of adrenocortical tumors: Carney complex, ANN ENDOCR, 62(3), 2001, pp. 180-184

Authors: Stratakis, CA
Citation: Ca. Stratakis, Micronodular adrenal disease and the syndrome of myxomas, spotty skin pigmentation, and endocrine overactivity, CONT ENDOC, 2001, pp. 283-289

Authors: Stratakis, CA
Citation: Ca. Stratakis, Genetics of Carney complex and related familial lentiginoses, and other multiple tumor syndromes, PEDIAT PATH, 19(1), 2000, pp. 41-68

Authors: Stratakis, CA
Citation: Ca. Stratakis, Genetics of Carney complex and related familial lentiginoses, and other multiple tumor syndromes, FRONT BIOSC, 5, 2000, pp. D353-D366

Authors: Kirschner, LS Carney, JA Pack, SD Taymans, SE Giatzakis, C Cho, YS Cho-Chung, YS Stratakis, CA
Citation: Ls. Kirschner et al., Mutations of the gene encoding the protein kinase A type I-alpha regulatory subunit in patients with the Carney complex, NAT GENET, 26(1), 2000, pp. 89-92

Authors: Boardman, LA Couch, FJ Burgart, LJ Schwartz, D Berry, R McDonnell, SK Schaid, DJ Hartmann, LC Schroeder, JJ Stratakis, CA Thibodeau, SN
Citation: La. Boardman et al., Genetic heterogeneity in Peutz-Jeghers syndrome, HUM MUTAT, 16(1), 2000, pp. 23-30

Authors: Kirschner, LS Sandrini, F Monbo, J Lin, JP Carney, JA Stratakis, CA
Citation: Ls. Kirschner et al., Genetic heterogeneity and spectrum of mutations of the PRKAR1A gene in patients with the Carney complex, HUM MOL GEN, 9(20), 2000, pp. 3037-3046

Authors: Stratakis, CA Chrousos, GP
Citation: Ca. Stratakis et Gp. Chrousos, Adrenal cancer, END METAB C, 29(1), 2000, pp. 15

Authors: Koch, CA Bornstein, SR Chrousos, GP Stratakis, CA
Citation: Ca. Koch et al., Primary pigmented adrenocortical dysplasia (PPNAD) in the context of the Carney complex causing Cushing syndrome, MED KLIN, 95(4), 2000, pp. 224-230

Authors: Stratakis, CA Rusovici, DE Kulin, HE Finkelstein, JW
Citation: Ca. Stratakis et al., Dysregulation of the hypothalamic-pituitary-adrenal axis in short childrenwith and without growth hormone deficiency, J PED END M, 13(8), 2000, pp. 1095-1100

Authors: Stratakis, CA Ball, DW
Citation: Ca. Stratakis et Dw. Ball, A concise genetic and clinical guide to multiple endocrine neoplasias and related syndromes, J PED END M, 13(5), 2000, pp. 457-465

Authors: Raff, SB Carney, JA Krugman, D Doppman, JL Stratakis, CA
Citation: Sb. Raff et al., Prolactin secretion abnormalities in patients with the "syndrome of spottyskin pigmentation, myxomas, endocrine overactivity and schwannomas" (Carney complex), J PED END M, 13(4), 2000, pp. 373-379

Authors: Stratakis, CA
Citation: Ca. Stratakis, Genetics of Peutz-Jeghers syndrome, Carney complex and other familial lentiginoses, HORMONE RES, 54(5-6), 2000, pp. 334-343
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