Zobrazeno 1 - 10
of 17
pro vyhledávání: '"María Joao Yubero"'
Autor:
Cristian De Gregorio, Evelyng Catalán, Gabriel Garrido, Pilar Morandé, Jimena Castillo Bennett, Catalina Muñoz, Glenda Cofré, Ya-Lin Huang, Bárbara Cuadra, Paola Murgas, Margarita Calvo, Fernando Altermatt, María Joao Yubero, Francis Palisson, Andrew P. South, Marcelo Ezquer, Ignacia Fuentes
Publikováno v:
Biological Research, Vol 56, Iss 1, Pp 1-16 (2023)
Abstract Background Recessive Dystrophic Epidermolysis Bullosa (RDEB) is a rare inherited skin disease caused by variants in the COL7A1 gene, coding for type VII collagen (C7), an important component of anchoring fibrils in the basement membrane of t
Externí odkaz:
https://doaj.org/article/a8dd191f66034a75a30a05ba91bc6a46
Autor:
Blanca Urzúa, Susanne Krämer, Irene Morales-Bozo, Claudia Camacho, María Joao Yubero, Francis Palisson, Ignacia Fuentes, Ana Ortega-Pinto
Publikováno v:
Frontiers in Dental Medicine, Vol 2 (2021)
Background: Epidermolysis bullosa (EB) corresponds to a series of conditions characterized by extreme fragility of the skin and/or mucous membranes. Of the four main types of EB, junctional EB (JEB) is the most associated with alterations in the teet
Externí odkaz:
https://doaj.org/article/f0f53c89356e44b18e66a736faf2e308
Autor:
Ignacia Fuentes, María Joao Yubero, Pilar Morandé, Carmen Varela, Karen Oróstica, Francisco Acevedo, Boris Rebolledo‐Jaramillo, Esteban Arancibia, Lorena Porte, Francis Palisson
Publikováno v:
International Wound Journal. 20:774-783
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5e756c29bc1fa0adb0cd392d6451f9da
https://doi.org/10.1111/iwj.13922
https://doi.org/10.1111/iwj.13922
Autor:
Elena Pope, Anes Yang, Anna E. Martinez, María Joao Yubero, Dedee F. Murrell, Carmen Liy-Wong, Mauricio Torres-Pradilla, Anne W. Lucky, Jemima E. Mellerio, Maria Berseneva, Francis Palisson, Ignacia Fuentes, Mark Mansour, Irene Lara-Corrales, Julio Salas
Publikováno v:
Journal of Pediatric Gastroenterology & Nutrition. 71:310-314
Background Esophageal strictures are the common gastrointestinal complications in patients with epidermolysis bullosa (EB) requiring dilation. There is limited information on the best type of intervention, outcomes, and predictors for re-stenosis. Ob
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::47816651e888e595f2d693e332bd70b6
https://doi.org/10.1097/mpg.0000000000002820
https://doi.org/10.1097/mpg.0000000000002820
Autor:
Anne W. Lucky, Anita N. Haggstrom, Laura Huilaja, Francis Palisson, Cristina Has, Alain Hovnanian, Gianluca Tadini, Leah Lalor, Ignacia Fuentes, María Joao Yubero, Kaisa Tasanen, Matthias Titeux
Publikováno v:
Pediatric Dermatology. 36:132-138
Background/objectives Epidermolysis bullosa is a group of diseases caused by mutations in skin structural proteins. Availability of genetic sequencing makes identification of causative mutations easier, and genotype-phenotype description and correlat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::679c5316235f70345da9a21526383957
https://doi.org/10.1111/pde.13722
https://doi.org/10.1111/pde.13722
Autor:
Luis H. Eraso, Alfred Klausegger, Raymond J. Cho, Heather I Rishel, Andrew P. South, Josefina Piñón Hofbauer, Boris Rebolledo-Jaramillo, Francis Palisson, Anja Diem, María Joao Yubero, Yessia Hidalgo, B. Tockner, Ignacia Fuentes, M. Peter Marinkovich, P. Morandé, Olga Figuera, Marco Prisco, Glenda Cofré-Araneda, T.G. Webster, Christina Guttmann-Gruber, Joyce M.C. Teng
Publikováno v:
Scientific Reports
Scientific Reports, Vol 10, Iss 1, Pp 1-10 (2020)
Scientific Reports, Vol 10, Iss 1, Pp 1-10 (2020)
Impaired wound healing complicates a wide range of diseases and represents a major cost to healthcare systems. Here we describe the use of discarded wound dressings as a novel, cost effective, accessible, and non-invasive method of isolating viable h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e2fb2f64b7c860ef74107c14235d6118
http://europepmc.org/articles/PMC7492213
http://europepmc.org/articles/PMC7492213
Autor:
Fatimah Alsayer, Ignacia Fuentes, Hinrich Huber, María Joao Yubero, Sebastián Véliz, Susanne M. Krämer
Publikováno v:
Special care in dentistry : official publication of the American Association of Hospital Dentists, the Academy of Dentistry for the Handicapped, and the American Society for Geriatric DentistryREFERENCES. 40(6)
Objectives To present early teeth extractions as a treatment option in severe dental crowding in patients with generalized recessive dystrophic epidermolysis bullosa (RDEB). Materials and methods Three patients with generalized RDEB were treated with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1956044e5f3d1cf3db63dd04efcfeea6
https://pubmed.ncbi.nlm.nih.gov/32880999
https://pubmed.ncbi.nlm.nih.gov/32880999
Publikováno v:
Journal of the American Academy of Dermatology. 83(6)
Fondo Nacional de Desarrollo Cientifico y Tecnologico (FONDECYT) Initiation into Research grant, Chile 11140440
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1676da90d951101be6698731462431f1
https://pubmed.ncbi.nlm.nih.gov/32565209
https://pubmed.ncbi.nlm.nih.gov/32565209
Autor:
Gisela Zillmann, María Elena McNab, Constanza Fuentes, María Joao Yubero, Marcelo Valle, Ignacia Fuentes, Jimena Castillo Bennett, Susanne M. Krämer, Anne W. Lucky, José Farfán, Ignacio Araya, Francis Palisson, Carolina Encina
Publikováno v:
Journal of the American Academy of Dermatology. 83:1815-1816
Comision Nacional de Investigacion Cientifica y Tecnologica (CONICYT) CONICYT FONDECYT 11140440
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a98f000f28c35568991cf631a4e94bc2
https://doi.org/10.1016/j.jaad.2020.03.117
https://doi.org/10.1016/j.jaad.2020.03.117
Publikováno v:
International Journal of Clinical Medicine. :433-436
Epidermolysis bullosa (EB) is an inherited connective tissue disease causing blisters in the skin and mucosal membranes. In severe cases, EB may be associated with renal damage through several mechanisms, mainly immunological ones. The present case d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::52ff1e0dc849973ed77dbc703eb412c3
https://doi.org/10.4236/ijcm.2016.77045
https://doi.org/10.4236/ijcm.2016.77045