Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

M Paradisi

Showing results (31-40 of 48) with videos related to

Pageof 5
Sort By:
Clinical and Experimental Dermatology|September 3, 2003
Atrichia with papular lesions resulting from a novel homozygous missense mutation in the hairless geneM Paradisi, G S Chuang, C Angelo, et al.
Allergy|August 10, 2002
Circulating interleukin 16 (IL-16) in children with atopic/eczema dermatitis syndrome (AEDS): a novel serological marker of disease activityA Frezzolini, M Paradisi, A Zaffiro, et al.
Journal of Neurochemistry|September 3, 2010
A single prenatal exposure to the endocrine disruptor 2,3,7,8-tetrachlorodibenzo-p-dioxin alters developmental myelination and remyelination potential in the rat brainM Fernández, M Paradisi, G D'Intino, et al.
Cutis|October 1, 1995
Lipoid proteinosis: clinical, histologic, and ultrastructural investigationsA O Muda, M Paradisi, C Angelo, et al.
The Journal of Investigative Dermatology|April 1, 1996
A common insertion mutation in COL7A1 in two Italian families with recessive dystrophic epidermolysis bullosaA M Christiano, M D'Alessio, M Paradisi, et al.
Minerva Pediatrica|June 23, 2001
[A Pediatric case of lupoid leishmaniasis diagnosed by PCR]M Paradisi, M G Grosso, C Angelo, et al.
The Journal of Investigative Dermatology|March 1, 1995
A glycine-to-arginine substitution in the triple-helical domain of type VII collagen in a family with dominant dystrophic epidermolysis bullosaA M Christiano, A Morricone, M Paradisi, et al.
Pediatric Dermatology|June 1, 1992
Infantile condylomata of the oral cavityM Paradisi, S Mostaccioli, G Celano, et al.
Cutis|September 6, 2001
Becker's nevus syndromeC Angelo, M G Grosso, P Stella, et al.
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.
Pageof 5

Showing results (31-40 of 48) with videos related to

Sort By:
Pageof 5
Clinical and Experimental Dermatology|September 3, 2003
Atrichia with papular lesions resulting from a novel homozygous missense mutation in the hairless geneM Paradisi, G S Chuang, C Angelo, et al.
Allergy|August 10, 2002
Circulating interleukin 16 (IL-16) in children with atopic/eczema dermatitis syndrome (AEDS): a novel serological marker of disease activityA Frezzolini, M Paradisi, A Zaffiro, et al.
Journal of Neurochemistry|September 3, 2010
A single prenatal exposure to the endocrine disruptor 2,3,7,8-tetrachlorodibenzo-p-dioxin alters developmental myelination and remyelination potential in the rat brainM Fernández, M Paradisi, G D'Intino, et al.
Cutis|October 1, 1995
Lipoid proteinosis: clinical, histologic, and ultrastructural investigationsA O Muda, M Paradisi, C Angelo, et al.
The Journal of Investigative Dermatology|April 1, 1996
A common insertion mutation in COL7A1 in two Italian families with recessive dystrophic epidermolysis bullosaA M Christiano, M D'Alessio, M Paradisi, et al.
Minerva Pediatrica|June 23, 2001
[A Pediatric case of lupoid leishmaniasis diagnosed by PCR]M Paradisi, M G Grosso, C Angelo, et al.
The Journal of Investigative Dermatology|March 1, 1995
A glycine-to-arginine substitution in the triple-helical domain of type VII collagen in a family with dominant dystrophic epidermolysis bullosaA M Christiano, A Morricone, M Paradisi, et al.
Pediatric Dermatology|June 1, 1992
Infantile condylomata of the oral cavityM Paradisi, S Mostaccioli, G Celano, et al.
Cutis|September 6, 2001
Becker's nevus syndromeC Angelo, M G Grosso, P Stella, et al.
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.
Pageof 5