Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Alessio Lancioni"'
Autor:
Ida Luisa Rotundo, Stefania Faraso, Elvira De Leonibus, Gerardo Nigro, Carmen Vitiello, Alessio Lancioni, Daniele Di Napoli, Sigismondo Castaldo, Vincenzo Russo, Fabio Russo, Giulio Piluso, Alberto Auricchio, Vincenzo Nigro
Publikováno v:
PLoS ONE, Vol 6, Iss 9, p e24729 (2011)
We have previously demonstrated that gene therapy can rescue the phenotype and extend lifespan in the delta-sarcoglycan deficient cardiomyopathic hamster. In patients with similar genetic defects, steroids have been largely used to slow down disease
Externí odkaz:
https://doaj.org/article/485dd427309145caaa4e304473e3957c
Autor:
Giulio Piluso, Michele Iacomino, Ida Luisa Rotundo, Alberto Auricchio, Gerardo Nigro, Alessio Lancioni, Vincenzo Nigro, Marco Savarese, Luca D'Orsi
Publikováno v:
Human Gene Therapy; Vol 24
"Abstract The BIO14.6 hamster carries a mutation in the delta sarcoglycan gene causing muscular dystrophy and cardiomyopathy. The disease can be prevented by systemic delivery of delta sarcoglycan cDNA using adeno-associated viruses (AAVs). However,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a5049d29469c47e3f57f40028ed320b
Autor:
Fabio Russo, Alessio Lancioni, Elvira De Leonibus, Vincenzo Nigro, Gerardo Nigro, Ida Luisa Rotundo, Vincenzo Russo, S. Castaldo, Giulio Piluso, Carmen Vitiello, Daniele Di Napoli, Stefania Faraso, Alberto Auricchio
Publikováno v:
PLoS ONE
PLoS ONE, Vol 6, Iss 9, p e24729 (2011)
PLoS ONE; Vol 6
PLoS ONE, Vol 6, Iss 9, p e24729 (2011)
PLoS ONE; Vol 6
We have previously demonstrated that gene therapy can rescue the phenotype and extend lifespan in the delta-sarcoglycan deficient cardiomyopathic hamster. In patients with similar genetic defects, steroids have been largely used to slow down disease
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ecdbb6c4616a376a18971bc9cd321b0
http://europepmc.org/articles/PMC3170375
http://europepmc.org/articles/PMC3170375
Autor:
Giulio Piluso, Alessio Lancioni, Kevin P. Campbell, Luca D'Orsi, Gerardo Nigro, Mafalda Cacciottolo, Ida Luisa Rotundo, S. Aurino, Yvonne M. Kobayashi, Dario Acampora, Vincenzo Nigro
Publikováno v:
Human Molecular Genetics; Vol 20
Human Molecular Genetics
Human Molecular Genetics
Cardiomyopathy is a puzzling complication in addition to skeletal muscle pathology for patients with mutations in β-, γ- or δ-sarcoglycan (SG) genes. Patients with mutations in α-SG rarely have associated cardiomyopathy, or their cardiac patholog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48a1d862722ba474ae537c019b64270a
http://hdl.handle.net/11591/190438
http://hdl.handle.net/11591/190438
Autor:
Germana Meroni, Elvira De Leonibus, Luisa M. Napolitano, Bianca Fontanella, Alessio Lancioni, Rosa Ferrentino, Mariateresa Pizzo
Opitz G/BBB syndrome (OS) is a genetic disorder characterized by midline developmental defects. Male patients with the X-linked form of OS, caused by loss-of-function mutations in theMID1gene, show high variability of the clinical signs.MID1encodes a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eae37e304e96b1c65802b2cad995119a
https://hdl.handle.net/11368/2847689
https://hdl.handle.net/11368/2847689
Autor:
Ida Luisa Rotundo, Alessio Lancioni, Marco Savarese, Luca D'Orsi, Michele Iacomino, Gerardo Nigro, Giulio Piluso, Alberto Auricchio, Vincenzo Nigro
Publikováno v:
Human Gene Therapy; Apr2013, Vol. 24 Issue 4, p424-430, 7p