Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Alberto Conde Ferreirós"'
Autor:
Rubén García Castro, Ana María González Pérez, María Concepción Román Curto, Javier Cañueto Álvarez, Alberto Conde Ferreirós, Alex Viñolas Cuadros, David Moyano Bueno, Antonio Javier Chamorro Fernández
Publikováno v:
European Journal of Case Reports in Internal Medicine (2019)
Lysosomal storage disorders (LSDs) are a group of genetic disorders caused by mutations in genes encoding enzymes involved in lysosomal function. Schindler disease is an autosomal recessive, inherited LSD caused by defective or non-existent activity
Externí odkaz:
https://doaj.org/article/6936c6b82af5404b8facec06ccd7907c
Autor:
Natalia García-Sancha, Concepción Román-Curto, Javier Cañueto, Laura Puebla-Tornero, Alberto Conde-Ferreirós, Roberto Corchado-Cobos, Luis A. Corchete
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
instname
[Background]: Although the eighth edition of the American Joint Committee on Cancer staging system (AJCC8) provides improved prognosis stratification of cutaneous squamous cell carcinoma (CSCC) over AJCC7, T3 has a variable prognosis.
[Objective
[Objective
Autor:
Javier Cañueto, David Revilla-Nebreda, Alberto Conde-Ferreirós, Angel Santos-Briz, Concepción Román-Curto, David Moyano-Bueno, Leonor Revelles-Peñas, Sara Becerril-Andrés
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
instname
[Background]: Acantholytic cutaneous squamous cell carcinomas (aCSCCs) have been classically considered as a high-risk variant of CSCC. However, more recent studies show that aCSCC does not confer more aggressiveness. This study aims to establish whe
Autor:
Concepción Román-Curto, Natalia García-Sancha, Luis A. Corchete-Sánchez, Laura Puebla-Tornero, Javier Cañueto, Roberto Corchado-Cobos, Alberto Conde-Ferreirós
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
instname
[Introduction]: The Brigham and Women's Hospital and the Tübingen cutaneous squamous cell carcinoma (SCC) stratification systems propose different criteria from the American Joint Committee on Cancer, eighth edition. Our group identified prognostic
Autor:
Alberto Conde-Ferreirós, Rubén Garcia Castro, David Moyano-Bueno, Esther Cardeñoso, Angel Santos-Briz, Alex Viñolas-Cuadros
Publikováno v:
The American Journal of Dermatopathology. 42:972-976
Atypical fibroxanthoma is a rare mesenchymal skin tumor of intermediate malignancy that typically occurs on sun-damaged skin of elderly patients. Histologically, it is composed of pleomorphic cells with hyperchromatic nuclei and abundant cytoplasm, c
Publikováno v:
Piel. 34:427-435
Publikováno v:
Piel. 34:134-137
Autor:
Concepción Román-Curto, Laura Puebla-Tornero, Daniel Rodríguez-Baeza, Alberto Conde-Ferreirós, José María García Dompablo, Leonor Revelles-Peñas, Javier Cañueto, David Revilla-Nebreda
Background: Skin cancer is a serious health problem in our society, and UV radiation is the most significant agent in its development. Photoprotection and awareness of the risks of developing skin cancer are the basic pillars in its prevention. As fu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cc45926b938cfe54bbd9f3f93a3bbc0d
https://doi.org/10.21203/rs.3.rs-227739/v1
https://doi.org/10.21203/rs.3.rs-227739/v1
Autor:
Luis A. Corchete, Laura Pons, Sebastian Podlipnik, M José Fuente, R.M. Pujol, Ángel Santos-Briz, Ane Jaka, Alberto Conde-Ferreirós, R. Posada, Agustí Toll, Javier Cañueto, Concepción Román-Curto
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
instname
To the Editor: Perineural invasion (PNI) is rare and usually incidental in cutaneous squamous cell carcinoma (SCC), with an incidence of 2.5% to 14%.1 Incidental PNI is associated with poor prognosis in cutaneous SCC,2 and some evidence suggests its
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d36dc3f03f690598d32461adb7b228f
http://hdl.handle.net/10261/261961
http://hdl.handle.net/10261/261961
Autor:
María Concepción Román Curto, Javier Cañueto Álvarez, Alberto Conde Ferreirós, Ana María González Pérez, Alex Viñolas Cuadros, Antonio Javier Chamorro Fernández, Rubén García Castro, David Moyano Bueno
Publikováno v:
European Journal of Case Reports in Internal Medicine
European Journal of Case Reports in Internal Medicine (2019)
European Journal of Case Reports in Internal Medicine (2019)
Lysosomal storage disorders (LSDs) are a group of genetic disorders caused by mutations in genes encoding enzymes involved in lysosomal function. Schindler disease is an autosomal recessive, inherited LSD caused by defective or non-existent activity