AAAAAA

   
Results: 1-7 |
Results: 7
Corneodesmosin expression in psoriasis vulgaris differs from normal skin and other inflammatory skin disorders
Authors: Allen, M Ishida-Yamamoto, A McGrath, J Davison, S Iizuka, H Simon, M Guerrin, M Hayday, A Vaughan, R Serre, G Trembath, R Barker, J
Citation: M. Allen et al., Corneodesmosin expression in psoriasis vulgaris differs from normal skin and other inflammatory skin disorders, LAB INV, 81(7), 2001, pp. 969-976
Enlarged vestibular aqueduct: a radiological marker of Pendred syndrome, and mutation of the PDS gene
Authors: Reardon, W O Mahoney, CF Trembath, R Jan, H Phelps, PD
Citation: W. Reardon et al., Enlarged vestibular aqueduct: a radiological marker of Pendred syndrome, and mutation of the PDS gene, QJM-MON J A, 93(2), 2000, pp. 99-104
PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggest a single entity with Cowden syndrome
Authors: Marsh, DJ Kum, JB Lunetta, KL Bennett, MJ Gorlin, RJ Ahmed, SF Bodurtha, J Crowe, C Curtis, MA Dasouki, M Dunn, T Feit, H Geraghty, MT Graham, JM Hodgson, SV Hunter, A Korf, BR Manchester, D Miesfeldt, S Murday, VA Nathanson, KL Parisi, M Pober, B Romano, C Tolmie, JL Trembath, R Winter, RM Zackai, EH Zori, RT Weng, LP Dahia, PLM Eng, C
Citation: Dj. Marsh et al., PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggest a single entity with Cowden syndrome, HUM MOL GEN, 8(8), 1999, pp. 1461-1472
Prevalence, age of onset, and natural history of thyroid disease in Pendred syndrome
Authors: Reardon, W Coffey, R Chowdhury, T Grossman, A Jan, H Britton, K Kendall-Taylor, P Trembath, R
Citation: W. Reardon et al., Prevalence, age of onset, and natural history of thyroid disease in Pendred syndrome, J MED GENET, 36(8), 1999, pp. 595-598
Identification of two different mutations in the PDS gene in an inbred family with Pendred syndrome
Authors: Coucke, PJ Van Hauwe, P Everett, LA Demirhan, O Kabakkaya, Y Dietrich, NL Smith, RJH Coyle, E Reardon, W Trembath, R Willems, PJ Green, ED Van Camp, G
Citation: Pj. Coucke et al., Identification of two different mutations in the PDS gene in an inbred family with Pendred syndrome, J MED GENET, 36(6), 1999, pp. 475-477
Concurrence of Pendred syndrome, autoimmune thyroiditis, and simple goiterin one family
Authors: Vaidya, B Coffey, R Coyle, B Trembath, R San Lazaro, C Reardon, W Kendall-Taylor, P
Citation: B. Vaidya et al., Concurrence of Pendred syndrome, autoimmune thyroiditis, and simple goiterin one family, J CLIN END, 84(8), 1999, pp. 2736-2738
Concerted action polyp prevention, CAPP2: A trial of aspirin and/or resistant starch in people at risk of hereditary non-polyposis colon cancer (HNPCC)
Authors: Burn, J Alonso, A Bertario, L Bishop, T Bisgaard, ML Cummings, J Davidson, R Delhanty, J Demant, P Dunlop, M Eccles, D Ellis, A Evans, G Fidalgo, P Fodde, R Haites, N Hodgson, S Hultcrantz, R Huson, S Jarvinen, H Kartheuser, A Kleibeuker, J Lenaerts, C Lucasson, A Lunt, P McDermot, K McKay, J McKeown, C Maher, E Mathers, J Mecklin, JP Moslein, G Murday, V Nagengast, F Northover, JMA Obrador, A Parks, TG Paraskeva, C Phillips, R San Roman, C Ruscheoff, J Sampson, J Shepherd, N Tempesta, A Trembath, R Turnpenny, P Vasen, HFA
Citation: J. Burn et al., Concerted action polyp prevention, CAPP2: A trial of aspirin and/or resistant starch in people at risk of hereditary non-polyposis colon cancer (HNPCC), BIOM HLTH R, 24, 1998, pp. 17-23
Risultati: 1-7 |