AndreJ.CodispotiMD

PubMed

• Connexin 26 (GJB2) mutations as a cause of the KID syndrome with hearing loss.
  Terrinoni, A., Codispoti, A., Serra, V., Bruno, E., Didona, B., Paradisi, M., Nisticò, S., Campione, E., Napolitano, B., Diluvio, L., Melino, G.> ;Biochem Biophys Res Commun. 2010 Apr 23
• Connexin 26 (GJB2) mutations, causing KID Syndrome, are associated with cell death due to calcium gating deregulation.
  Terrinoni, A., Codispoti, A., Serra, V., Didona, B., Bruno, E., Nisticò, R., Giustizieri, M., Alessandrini, M., Campione, E., Melino, G.> ;Biochem Biophys Res Commun. 2010 Apr 16
• Transglutaminases expression in human supraspinatus tendon ruptures and in mouse tendons.
  Oliva, F., Zocchi, L., Codispoti, A., Candi, E., Celi, M., Melino, G., Maffulli, N., Tarantino, U.> ;Biochem Biophys Res Commun. 2009 Feb 20
• Knuckle pads, in an epidermal palmoplantar keratoderma patient with Keratin 9 R163W transgrediens expression.
  Codispoti, A., Colombo, E., Zocchi, L., Serra, V., Pertusi, G., Leigheb, G., Tiberio, R., Bornacina, G., Zuccoli, R., Ramponi, A., Campione, E., Melino, G., Terrinoni, A.> ;Eur J Dermatol. 2008 Dec 25
• Scotin: A new p63 target gene expressed during epidermal differentiation.
  Zocchi, L., Bourdon, J. C., Codispoti, A., Knight, R., Lane, D. P., Melino, G., Terrinoni, A.> ;Biochem Biophys Res Commun. 2008 Mar 7
• Novel and recurrent ALDH3A2 mutations in Italian patients with Sjögren-Larsson syndrome.
  Didona, B., Codispoti, A., Bertini, E., Rizzo, W. B., Carney, G., Zambruno, G., Dionisi-Vici, C., Paradisi, M., Pedicelli, C., Melino, G., Terrinoni, A.> ;J Hum Genet. 2007
• Cerebral cavernomas in a family with multiple cutaneous and uterine leiomyomas associated with a new mutation in the fumarate hydratase gene.
  Campione, E., Terrinoni, A., Orlandi, A., Codispoti, A., Melino, G., Bianchi, L., Mazzotta, A., Garaci, F. G., Ludovici, A., Chimenti, S.> ;J Invest Dermatol. 2007 Sep
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