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A Novel Phenotype of Junctional Epidermolysis Bullosa with Transient Skin Fragility and Predominant Ocular Involvement Responsive to Human Amniotic Membrane Eyedrops.
Castiglia, Daniele; Fortugno, Paola; Condorelli, Angelo Giuseppe; Barresi, Sabina; De Luca, Naomi; Pizzi, Simone; Neri, Iria; Graziano, Claudio; Trojan, Diletta; Ponzin, Diego; Rossi, Sabrina; Zambruno, Giovanna; Tartaglia, Marco.
Afiliación
  • Castiglia D; Laboratory of Molecular and Cell Biology, IDI-IRCCS, 00167 Rome, Italy.
  • Fortugno P; Laboratory of Molecular and Cell Biology, IDI-IRCCS, 00167 Rome, Italy.
  • Condorelli AG; Genodermatosis Unit, Genetics and Rare Diseases Research Division, Bambino Gesù Children's Hospital, IRCCS, 00165 Rome, Italy.
  • Barresi S; Genetics and Rare Diseases Research Division, Bambino Gesù Children's Hospital, IRCCS, 00146 Rome, Italy.
  • De Luca N; Laboratory of Molecular and Cell Biology, IDI-IRCCS, 00167 Rome, Italy.
  • Pizzi S; Genetics and Rare Diseases Research Division, Bambino Gesù Children's Hospital, IRCCS, 00146 Rome, Italy.
  • Neri I; Department of Experimental, Diagnostic and Specialty Medicine, Division of Dermatology, S. Orsola-Malpighi University Hospital, 40138 Bologna, Italy.
  • Graziano C; Medical Genetics, S. Orsola-Malpighi University Hospital, 40138 Bologna, Italy.
  • Trojan D; Treviso Tissue Bank Foundation, 31100 Treviso, Italy.
  • Ponzin D; The Veneto Eye Bank Foundation, 30174 Venice, Italy.
  • Rossi S; Pathology Unit, Department of Laboratories, Bambino Gesù Children's Hospital, IRCCS, 00165 Rome, Italy.
  • Zambruno G; Genodermatosis Unit, Genetics and Rare Diseases Research Division, Bambino Gesù Children's Hospital, IRCCS, 00165 Rome, Italy.
  • Tartaglia M; Genetics and Rare Diseases Research Division, Bambino Gesù Children's Hospital, IRCCS, 00146 Rome, Italy.
Genes (Basel) ; 12(5)2021 05 11.
Article en En | MEDLINE | ID: mdl-34064633
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Soluciones Oftálmicas / Fenotipo / Distrofias Hereditarias de la Córnea / Epidermólisis Ampollosa de la Unión / Epitelio Corneal Tipo de estudio: Prognostic_studies Límite: Child, preschool / Female / Humans Idioma: En Revista: Genes (Basel) Año: 2021 Tipo del documento: Article País de afiliación: Italia
Texto completo
Añadir a Mi BVS
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XML
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Soluciones Oftálmicas / Fenotipo / Distrofias Hereditarias de la Córnea / Epidermólisis Ampollosa de la Unión / Epitelio Corneal Tipo de estudio: Prognostic_studies Límite: Child, preschool / Female / Humans Idioma: En Revista: Genes (Basel) Año: 2021 Tipo del documento: Article País de afiliación: Italia