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G Tadini

Showing results (41-50 of 73) with videos related to

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Archives of Dermatology|August 1, 1994
Ichthyosis Curth-Macklin: a new sporadic case with immunohistochemical study of keratin expressionA Brusasco, R Cavalli, S Cambiaghi, et al.
American Journal of Orthodontics and Dentofacial Orthopedics : Official Publication of the American Association of Orthodontists, Its Constituent Societies, and the American Board of Orthodontics|May 1, 1992
A mathematical model for the computation of the forces exerted by the facial orthopedic maskF Grandori, C Merlini, C Amelotti, et al.
Clinical Genetics|October 24, 2007
De novo occurrence of the 730insG recurrent mutation in an Italian family with the ichthyotic variant of Vohwinkel syndrome, loricrin keratodermaB Drera, G Tadini, F Balbo, et al.
Archives of Dermatological Research|January 1, 1995
Altered expression of a new antigen of the dermal-epidermal junction (NU-T2 DEJ Ag) in junctional epidermolysis bullosaG Tadini, J Kanitakis, R Cavalli, et al.
American Journal of Medical Genetics|May 17, 1996
Cardio-facio-cutaneous (CFC) syndrome: report of an adult without mental retardationS Manoukian, F Lalatta, A Selicorni, et al.
Archives of Dermatology|December 1, 1991
Primary cutaneous cryptococcosis in a patient with the acquired immunodeficiency syndromeM Cusini, P Cagliani, R Grimalt, et al.
Pediatric Dermatology|February 24, 2001
Multiple familial smooth muscle hamartomasL Gualandri, S Cambiaghi, E Ermacora, et al.
Chronobiologia|April 1, 1982
Circadian temporal structure in psoriasisA Radaelli, F Carandente, G Tadini, et al.
Dermatology (Basel, Switzerland)|May 29, 2013
Anemic nevus in neurofibromatosis type 1G Tadini, M Brena, L Pezzani, et al.
Human Mutation|July 17, 1999
Three homozygous PTC mutations in the collagen type VII gene of patients affected by recessive dystrophic epidermolysis bullosa: analysis of transcript levels in dermal fibroblastsR Gardella, N Zoppi, S Ferraboli, et al.
Pageof 8

Showing results (41-50 of 73) with videos related to

Sort By:
Pageof 8
Archives of Dermatology|August 1, 1994
Ichthyosis Curth-Macklin: a new sporadic case with immunohistochemical study of keratin expressionA Brusasco, R Cavalli, S Cambiaghi, et al.
American Journal of Orthodontics and Dentofacial Orthopedics : Official Publication of the American Association of Orthodontists, Its Constituent Societies, and the American Board of Orthodontics|May 1, 1992
A mathematical model for the computation of the forces exerted by the facial orthopedic maskF Grandori, C Merlini, C Amelotti, et al.
Clinical Genetics|October 24, 2007
De novo occurrence of the 730insG recurrent mutation in an Italian family with the ichthyotic variant of Vohwinkel syndrome, loricrin keratodermaB Drera, G Tadini, F Balbo, et al.
Archives of Dermatological Research|January 1, 1995
Altered expression of a new antigen of the dermal-epidermal junction (NU-T2 DEJ Ag) in junctional epidermolysis bullosaG Tadini, J Kanitakis, R Cavalli, et al.
American Journal of Medical Genetics|May 17, 1996
Cardio-facio-cutaneous (CFC) syndrome: report of an adult without mental retardationS Manoukian, F Lalatta, A Selicorni, et al.
Archives of Dermatology|December 1, 1991
Primary cutaneous cryptococcosis in a patient with the acquired immunodeficiency syndromeM Cusini, P Cagliani, R Grimalt, et al.
Pediatric Dermatology|February 24, 2001
Multiple familial smooth muscle hamartomasL Gualandri, S Cambiaghi, E Ermacora, et al.
Chronobiologia|April 1, 1982
Circadian temporal structure in psoriasisA Radaelli, F Carandente, G Tadini, et al.
Dermatology (Basel, Switzerland)|May 29, 2013
Anemic nevus in neurofibromatosis type 1G Tadini, M Brena, L Pezzani, et al.
Human Mutation|July 17, 1999
Three homozygous PTC mutations in the collagen type VII gene of patients affected by recessive dystrophic epidermolysis bullosa: analysis of transcript levels in dermal fibroblastsR Gardella, N Zoppi, S Ferraboli, et al.
Pageof 8