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Results: 1-13 |
Results: 13
Clear cell papulosis (pagetoid papulosis) in a non-Asian patient
Authors: Gianotti, R Cambiaghi, S Locatelli, A Gelmetti, C
Citation: R. Gianotti et al., Clear cell papulosis (pagetoid papulosis) in a non-Asian patient, DERMATOLOGY, 203(3), 2001, pp. 260-261
Multiple familial smooth muscle hamartomas
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
Heterochromia of the scalp hair: A result of pigmentary mosaicism?
Authors: Restano, L Barbareschi, M Cambiaghi, S Gelmetti, C Ghislanzoni, M Caputo, R
Citation: L. Restano et al., Heterochromia of the scalp hair: A result of pigmentary mosaicism?, J AM ACAD D, 45(1), 2001, pp. 136-139
Nail lichen planus in children - Clinical features, response to treatment,and long-term follow-up
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
Delleman syndrome: report of a case with a mild phenotype
Authors: Cambiaghi, S Levet, PS Guala, G Baldini, D Gianotti, R
Citation: S. Cambiaghi et al., Delleman syndrome: report of a case with a mild phenotype, EUR J DERM, 10(8), 2000, pp. 623-626
Fingertip calcinosis cutis
Authors: Cambiaghi, S Imondi, D Gangi, S Vegni, C
Citation: S. Cambiaghi et al., Fingertip calcinosis cutis, CUTIS, 66(6), 2000, pp. 465-467
Clinical findings in mosaic carriers of hypohidrotic ectodermal dysplasia
Authors: Cambiaghi, S Restano, L Paakkonen, K Caputo, R Kere, J
Citation: S. Cambiaghi et al., Clinical findings in mosaic carriers of hypohidrotic ectodermal dysplasia, ARCH DERMAT, 136(2), 2000, pp. 217-224
A hyperkeratotic linear lesion in a girl with KID syndrome. A further example of early allelic loss?
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
A missense mutation in connexin26, D66H, causes mutilating keratoderma with sensorineural deafness (Vohwinkel's syndrome) in three unrelated families
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
A sporadic case of congenital hypotrichosis simplex of the scalp: Difficulties in diagnosis and classification
Authors: Cambiaghi, S Barbareschi, M
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
The pattern of inheritance in KID syndrome
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
Atrophoderma vermiculata along Blaschko lines
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
Blaschko lines of the face: A step closer to completing the map
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: 1-13 |