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Results: 1-8 |
Results: 8

Authors: Gualandri, L Cambiaghi, S Ermacora, E Tadini, G Gianotti, R Caputo, R
Citation: L. Gualandri et al., Multiple familial smooth muscle hamartomas, PEDIAT DERM, 18(1), 2001, pp. 17-20

Authors: Gardella, R Nuytinck, L Barlati, S Van Acker, P Tadini, G De Paepe, A Colombi, M
Citation: R. Gardella et al., Characterization of mutations leading to recessive dystrophic epidermolysis bullosa and Marfan syndrome in a single patient, CLIN EXP D, 26(8), 2001, pp. 710-713

Authors: Fine, JD Eady, RAJ Bauer, EA Briggaman, RA Bruckner-Tuderman, L Christiano, A Heagerty, A Hintner, H Jonkman, MF McGrath, J McGuire, J Moshell, A Shimizu, H Tadini, G Uitto, J
Citation: Jd. Fine et al., Revised classification system for inherited epidermolysis bullosa: Report of the Second International Consensus Meeting on diagnosis and classification of epidermolysis bullosa, J AM ACAD D, 42(6), 2000, pp. 1051-1066

Authors: Restano, L Cambiaghi, S Brusasco, A Tadini, G Caputo, R
Citation: L. Restano et al., A hyperkeratotic linear lesion in a girl with KID syndrome. A further example of early allelic loss?, EUR J DERM, 9(2), 1999, pp. 142-143

Authors: Gardella, R Zoppi, N Ferraboli, S Marini, D Tadini, G Barlati, S Colombi, M
Citation: R. Gardella et al., Three homozygous PTC mutations in the collagen type VII gene of patients affected by recessive dystrophic epidermolysis bullosa: Analysis of transcript levels in dermal fibroblasts, HUM MUTAT, 13(6), 1999, pp. 439-452

Authors: Restano, L Cambiaghi, S Tadini, G
Citation: L. Restano et al., The pattern of inheritance in KID syndrome, PEDIAT DERM, 16(2), 1999, pp. 164-165

Authors: Cambiaghi, S Restano, L Tadini, G
Citation: S. Cambiaghi et al., Atrophoderma vermiculata along Blaschko lines, PEDIAT DERM, 16(2), 1999, pp. 165-165

Authors: Restano, L Cambiaghi, S Tadini, G Cerri, A Caputo, R
Citation: L. Restano et al., Blaschko lines of the face: A step closer to completing the map, J AM ACAD D, 39(6), 1998, pp. 1028-1030
Risultati: 1-8 |