Zobrazeno 1 - 7
of 7
pro vyhledávání: '"David Jimenez‐Gallo"'
Autor:
Pablo Fernandez-Crehuet, Sofía Haselgruber, Alicia Padial-Gomez, Fiorella Vasquez-Chinchay, Maria Dolores Fernandez-Ballesteros, Irene López-Riquelme, David Jimenez-Gallo, Juan Manuel Segura-Palacios, Marisol Contreras-Steyls, Giovana Fernanda Osorio-Gómez, Juan Carlos Hernández-Rodríguez, Manuel Sanchez-Diaz, Carlos Cuenca-Barrales, Salvador Arias-Santiago, Alejandro Molina-Leyva
Publikováno v:
Dermatology and Therapy, Vol 13, Iss 4, Pp 1029-1038 (2023)
Abstract Introduction Hidradenitis suppurativa (HS) is a chronic inflammatory skin disease. Biologic drugs have a key role in the long-term anti-inflammatory treatment of moderate to severe patients due to their immunomodulatory properties. The aim o
Externí odkaz:
https://doaj.org/article/de1c5eaca736467a882330bcd75ad47a
Heterozygous cylindromatosis gene mutation c.1628_1629delCT in a family with brook-spiegler syndrome
Autor:
Cintia Arjona Aguilera, Raquel De la Varga Martínez, Lidia Ossorio García, David Jimenez-Gallo, Cristina Albarrán Planelles, Mario Linares Barrios
Publikováno v:
Indian Journal of Dermatology, Vol 61, Iss 5, Pp 580-580 (2016)
Brooke–Spiegler Syndrome (BSS) is a rare genodermatosis characterized by the progressive formation of adnexal skin tumors in the scalp and face, mainly trichoepitheliomas, cylindromas, and spiradenomas. It has also been associated with salivary gla
Externí odkaz:
https://doaj.org/article/a320b395916a451cbd5f054c3f7b5af9
Autor:
Myriam Viedma-Martinez, Francisco R. Dominguez-Tosso, David Jimenez-Gallo, Jesus Garcia-Palacios, Laura Riera-Tur, Natalia Montiel-Quezel, Mario Linares-Barrios
Publikováno v:
New England Journal of Medicine. 388:92-94
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce2eded24165bbb197e2cbe12abf36b3
https://doi.org/10.1056/nejmc2210823
https://doi.org/10.1056/nejmc2210823
Autor:
Gonzalo Gallo‐Pineda, Alicia Jimenez‐Anton, Irene Navarro‐Navarro, Isabel Villegas‐Romero, David Jimenez‐Gallo
Publikováno v:
Australasian Journal of Dermatology. 64
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dcccf7bd872047c492ac19d2396c7dba
https://doi.org/10.1111/ajd.13996
https://doi.org/10.1111/ajd.13996
Autor:
Antonio Tejera-Vaquerizo, Sabela Paradela, Agusti Toll, Jorge Santos-Juanes, Ane Jaka, Alba López, Javier Cañueto, Àlvaro Bernal, Isabel Villegas-Romero, Carla Fernández-Pulido, Héctor Perandones, David Moreno-Ramírez, Carolina Domínguez-Mahamud, Rafael Salido-Vallejo, Onofre Sanmartin, Francisco M. Almazán-Fernández, Pedro Rodríguez-Jiménez, José Bañuls, Sebastian Podlipnik, Alejandra Sandoval-Clavijo, Aram Boada, Beatriz García-Bracamonte, Sara Palencia, David Revilla-Nevreda, Enara Reola-Ramírez, María del Carmen Gómez-Mateo, Mario Linares-Barrios, David Jiménez-Gallo, Carlos González-Cruz, Elia Samaniego, María Navedo-de las Heras, Rosa Taberner, Teresa Ródenas-Herranz, Carmen García-Donoso, Susana Puig, Eduardo Nagore
Publikováno v:
Acta Dermato-Venereologica, Vol 101, Iss 8, p adv00525 (2021)
The aim of this study was to compare tumour burden in patients who underwent surgery for melanoma and cutaneous squamous cell carcinoma during nationwide lockdown in Spain due to COVID-19 (for the period 14 March to 13 June 2020) and during the same
Externí odkaz:
https://doaj.org/article/1f0d2388807747f097b1bcef8ff00ba8
Autor:
Uxia Esperón-Moldes, Manuel Ginarte-Val, Laura Rodríguez-Pazos, Laura Fachal, Ana Martín-Santiago, Asunción Vicente, David Jiménez-Gallo, Encarna Guillén-Navarro, Loreto Martorell Sampol, María Antonia González-Enseñat, Ana Vega
Publikováno v:
PLoS ONE, Vol 15, Iss 2, p e0229025 (2020)
Mutations in CYP4F22 cause autosomal recessive congenital ichthyosis (ARCI). However, less than 10% of all ARCI patients carry a mutation in CYP4F22. In order to identify the molecular basis of ARCI among our patients (a cohort of ninety-two Spanish
Externí odkaz:
https://doaj.org/article/0ea9eb0f0fb14027b11273ccb93e27d4
Autor:
Marta Rivas-Rivas, David Jiménez-Gallo, Natalia Navas-García, Cristina Albarrán-Planelles, Claudio Rodríguez-Ramos
Publikováno v:
Revista Espanola de Enfermedades Digestivas, Vol 105, Iss 10, Pp 624-625 (2013)
Externí odkaz:
https://doaj.org/article/d80af469fea3405cbe332da94a11f958