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D Castiglia

Showing results (21-30 of 43) with videos related to

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Biochemical and Biophysical Research Communications|March 17, 1998
Compound heterozygosity for an out-of-frame deletion and a splice site mutation in the LAMB3 gene causes nonlethal junctional epidermolysis bullosaP Posteraro, S Sorvillo, L Gagnoux-Palacios, et al.
The Journal of Investigative Dermatology|November 6, 1998
Compound heterozygosity for a recessive glycine substitution and a splice site mutation in the COL7A1 gene causes an unusually mild form of localized recessive dystrophic epidermolysis bullosaM Terracina, P Posteraro, M Schubert, et al.
The British Journal of Dermatology|March 23, 2010
Lethal autosomal recessive epidermolytic ichthyosis due to a novel donor splice-site mutation in KRT10C Covaciu, M Castori, N De Luca, et al.
The British Journal of Dermatology|May 22, 2016
Childhood epidermolysis bullosa acquisita during squaric acid dibutyl ester immunotherapy for alopecia areataL Guerra, V Pacifico, V Calabresi, et al.
Ecotoxicology and Environmental Safety|January 26, 2015
Effects of heavy metals on ultrastructure and Hsp70 induction in Lemna minor L. exposed to water along the Sarno River, ItalyA Basile, S Sorbo, M Cardi, et al.
The British Journal of Dermatology|June 1, 2017
Lack of K140 immunoreactivity in junctional epidermolysis bullosa skin and keratinocytes associates with misfolded laminin epidermal growth factor-like motif 2 of the β3 short armA G Condorelli, P Fortugno, F Cianfarani, et al.
The British Journal of Dermatology|May 18, 2011
A founder synonymous COL7A1 mutation in three Danish families with dominant dystrophic epidermolysis bullosa pruriginosa identifies exonic regulatory sequences required for exon 87 splicingC Covaciu, F Grosso, E Pisaneschi, et al.
The British Journal of Dermatology|July 24, 2009
Quality of life in patients with epidermolysis bullosaS Tabolli, F Sampogna, C Di Pietro, et al.
Il Giornale Di Chirurgia|October 1, 1994
[Gastric angiodysplasia: a rare cause of bleeding from the upper digestive tract]G D'Elia, G Lucandri, E Di Giulio, et al.
Neurochemical Research|February 1, 1995
Expression of synapsin I gene in primary cultures of differentiating rat cortical neuronsI Di Liegro, G Savettieri, M Coppolino, et al.
Pageof 5

Showing results (21-30 of 43) with videos related to

Sort By:
Pageof 5
Biochemical and Biophysical Research Communications|March 17, 1998
Compound heterozygosity for an out-of-frame deletion and a splice site mutation in the LAMB3 gene causes nonlethal junctional epidermolysis bullosaP Posteraro, S Sorvillo, L Gagnoux-Palacios, et al.
The Journal of Investigative Dermatology|November 6, 1998
Compound heterozygosity for a recessive glycine substitution and a splice site mutation in the COL7A1 gene causes an unusually mild form of localized recessive dystrophic epidermolysis bullosaM Terracina, P Posteraro, M Schubert, et al.
The British Journal of Dermatology|March 23, 2010
Lethal autosomal recessive epidermolytic ichthyosis due to a novel donor splice-site mutation in KRT10C Covaciu, M Castori, N De Luca, et al.
The British Journal of Dermatology|May 22, 2016
Childhood epidermolysis bullosa acquisita during squaric acid dibutyl ester immunotherapy for alopecia areataL Guerra, V Pacifico, V Calabresi, et al.
Ecotoxicology and Environmental Safety|January 26, 2015
Effects of heavy metals on ultrastructure and Hsp70 induction in Lemna minor L. exposed to water along the Sarno River, ItalyA Basile, S Sorbo, M Cardi, et al.
The British Journal of Dermatology|June 1, 2017
Lack of K140 immunoreactivity in junctional epidermolysis bullosa skin and keratinocytes associates with misfolded laminin epidermal growth factor-like motif 2 of the β3 short armA G Condorelli, P Fortugno, F Cianfarani, et al.
The British Journal of Dermatology|May 18, 2011
A founder synonymous COL7A1 mutation in three Danish families with dominant dystrophic epidermolysis bullosa pruriginosa identifies exonic regulatory sequences required for exon 87 splicingC Covaciu, F Grosso, E Pisaneschi, et al.
The British Journal of Dermatology|July 24, 2009
Quality of life in patients with epidermolysis bullosaS Tabolli, F Sampogna, C Di Pietro, et al.
Il Giornale Di Chirurgia|October 1, 1994
[Gastric angiodysplasia: a rare cause of bleeding from the upper digestive tract]G D'Elia, G Lucandri, E Di Giulio, et al.
Neurochemical Research|February 1, 1995
Expression of synapsin I gene in primary cultures of differentiating rat cortical neuronsI Di Liegro, G Savettieri, M Coppolino, et al.
Pageof 5