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G Tadini

Showing results (61-70 of 73) with videos related to

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The British Journal of Dermatology|July 20, 2007
Transglutaminase 1 deficiency and corneocyte collapse: an indication for targeted molecular screening in autosomal recessive congenital ichthyosisG Esposito, G Tadini, F Paparo, et al.
American Journal of Medical Genetics|December 1, 1993
Prenatal testing in a fetus at risk for autosomal dominant polycystic kidney disease and autosomal recessive junctional epidermolysis bullosa with pyloric atresiaA E Turco, B Peissel, S Rossetti, et al.
Clinical and Experimental Dermatology|June 25, 2016
Clinical and molecular characterization of two patients with palmoplantar keratoderma-congenital alopecia syndrome type 2M Castori, S Morlino, M E Sana, et al.
Human Molecular Genetics|October 1, 1994
A novel homozygous nonsense mutation in the LAMC2 gene in patients with the Herlitz junctional epidermolysis bullosaC Baudoin, C Miquel, L Gagnoux-Palacios, et al.
Clinical Genetics|October 5, 2017
WNT10A gene is the second molecular candidate in a cohort of young Italian subjects with ectodermal derivative impairment (EDI)L Guazzarotti, G Tadini, G E Mancini, et al.
Archives of Dermatology|May 15, 1998
Phacomatosis pigmentokeratotica: report of new cases and further delineation of the syndromeG Tadini, L Restano, R Gonzáles-Pérez, et al.
Clinical Genetics|September 13, 2006
Dystrophic epidermolysis bullosa pruriginosa in Italy: clinical and molecular characterizationB Drera, D Castiglia, N Zoppi, et al.
The British Journal of Dermatology|March 5, 2010
Identification of novel and known KRT5 and KRT14 mutations in 53 patients with epidermolysis bullosa simplex: correlation between genotype and phenotypeM J Arin, G Grimberg, H Schumann, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|March 20, 2014
Identification of a novel frameshift mutation in the EDAR gene causing autosomal dominant hypohidrotic ectodermal dysplasiaM Callea, C E Willoughby, P Nieminen, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|December 25, 2016
Birmingham epidermolysis severity score and vitamin D status are associated with low BMD in children with epidermolysis bullosaG Rodari, S Guez, F Manzoni, et al.
Pageof 8

Showing results (61-70 of 73) with videos related to

Sort By:
Pageof 8
The British Journal of Dermatology|July 20, 2007
Transglutaminase 1 deficiency and corneocyte collapse: an indication for targeted molecular screening in autosomal recessive congenital ichthyosisG Esposito, G Tadini, F Paparo, et al.
American Journal of Medical Genetics|December 1, 1993
Prenatal testing in a fetus at risk for autosomal dominant polycystic kidney disease and autosomal recessive junctional epidermolysis bullosa with pyloric atresiaA E Turco, B Peissel, S Rossetti, et al.
Clinical and Experimental Dermatology|June 25, 2016
Clinical and molecular characterization of two patients with palmoplantar keratoderma-congenital alopecia syndrome type 2M Castori, S Morlino, M E Sana, et al.
Human Molecular Genetics|October 1, 1994
A novel homozygous nonsense mutation in the LAMC2 gene in patients with the Herlitz junctional epidermolysis bullosaC Baudoin, C Miquel, L Gagnoux-Palacios, et al.
Clinical Genetics|October 5, 2017
WNT10A gene is the second molecular candidate in a cohort of young Italian subjects with ectodermal derivative impairment (EDI)L Guazzarotti, G Tadini, G E Mancini, et al.
Archives of Dermatology|May 15, 1998
Phacomatosis pigmentokeratotica: report of new cases and further delineation of the syndromeG Tadini, L Restano, R Gonzáles-Pérez, et al.
Clinical Genetics|September 13, 2006
Dystrophic epidermolysis bullosa pruriginosa in Italy: clinical and molecular characterizationB Drera, D Castiglia, N Zoppi, et al.
The British Journal of Dermatology|March 5, 2010
Identification of novel and known KRT5 and KRT14 mutations in 53 patients with epidermolysis bullosa simplex: correlation between genotype and phenotypeM J Arin, G Grimberg, H Schumann, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|March 20, 2014
Identification of a novel frameshift mutation in the EDAR gene causing autosomal dominant hypohidrotic ectodermal dysplasiaM Callea, C E Willoughby, P Nieminen, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|December 25, 2016
Birmingham epidermolysis severity score and vitamin D status are associated with low BMD in children with epidermolysis bullosaG Rodari, S Guez, F Manzoni, et al.
Pageof 8