Authors:
Tosti, A
Piraccini, BM
Cambiaghi, S
Jorizzo, M
Citation: A. Tosti et al., Nail lichen planus in children - Clinical features, response to treatment,and long-term follow-up, ARCH DERMAT, 137(8), 2001, pp. 1027-1032
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:
Maestrini, E
Korge, BP
Ocana-Sierra, J
Calzolari, E
Cambiaghi, S
Scudder, PM
Hovnanian, A
Monaco, AP
Munro, CS
Citation: E. Maestrini et al., A missense mutation in connexin26, D66H, causes mutilating keratoderma with sensorineural deafness (Vohwinkel's syndrome) in three unrelated families, HUM MOL GEN, 8(7), 1999, pp. 1237-1243
Citation: S. Cambiaghi et M. Barbareschi, A sporadic case of congenital hypotrichosis simplex of the scalp: Difficulties in diagnosis and classification, PEDIAT DERM, 16(4), 1999, pp. 301-304