Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Eliana Cella"'
Autor:
Mónica Inés Natale, Graciela Beatriz Manzur, Silvina Beatriz Lusso, Eliana Cella, María Elsa Giovo, Romina Andrada, Juana Goitia, María Florencia Fernández, Patricia Silvia Della Giovanna, María José Guillamondegui, Mariángeles Domínguez, Olga Gutiérrez, Agustín Izquierdo, Heliana Hernández Herrera, Luz Graciela Velázquez Perdomo, Alicia Susana Mistchenko, Laura Elena Valinotto
Publikováno v:
American journal of medical genetics. Part AREFERENCES. 188(11)
Dystrophic epidermolysis bullosa (DEB) is a clinically heterogeneous heritable skin disorder, characterized by blistering of the skin and mucous membranes following minor trauma. Dominant (DDEB) and recessive (RDEB) forms are caused by pathogenic var
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::90cf32db219d635cf5240550af91c966
https://pubmed.ncbi.nlm.nih.gov/35979658
https://pubmed.ncbi.nlm.nih.gov/35979658
Autor:
Maria Laura Bageta, Eliana Cella, Andrea Bettina Cervini, María Del Valle Centeno, Liliana Roquel, John B. Mee, Richard W. Groves, Eduardo Calonje, Richard G. Goodwin, Jemima E. Mellerio, Gabriela Petrof, Anna E. Martinez
Publikováno v:
Clinical and experimental dermatologyReferences. 47(7)
Epidermolysis bullosa acquisita is a highly uncommon condition in the paediatric population. This article describes three children with this disease, different clinical presentation and management. It also reviews the most relevant articles on this t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b6dc068f3a164eda0933f85fdca1f5f
https://pubmed.ncbi.nlm.nih.gov/35080258
https://pubmed.ncbi.nlm.nih.gov/35080258
Autor:
Laura Elena Valinotto, Graciela Manzur, Olga Gutierrez, Mónica I Natale, Silvina Beatriz Lusso, Eliana Cella, Fernando Sebastiani
Publikováno v:
Pediatric dermatologyREFERENCES. 37(2)
Kindler syndrome is a rare genodermatosis. Major clinical criteria include acral blistering in infancy and childhood, progressive poikiloderma, skin atrophy, abnormal photosensitivity, and gingival fragility.FERMT1 gene was sequenced in 5 patients wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f0b467074621906c25a9970b46c37079
https://pubmed.ncbi.nlm.nih.gov/31957900
https://pubmed.ncbi.nlm.nih.gov/31957900