AAAAAA
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