Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Begoña Sánchez Albisua"'
Autor:
Kevin, Díez-Madueño, Begoña Sánchez, Albisua, Ana Burdaspal, Moratilla, Jose Luis Galán, Sanchez, Mónica González, Olivares, Pablo, de la Cueva Dobao
Publikováno v:
Cutis. 109
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::96632e47c96b9e0baa416ee1fedc9b8a
https://doi.org/10.12788/cutis.0457
https://doi.org/10.12788/cutis.0457
Autor:
Elena, Conde Montero, Begoña, Sánchez-Albisua, Soledad, Guisado, María, Ángeles Martín-Díaz, Eva, Balbín-Carrero, Marta, Valdivelso-Ramos, Pablo, de la Cueva Dobao
Publikováno v:
Wounds : a compendium of clinical research and practice. 28(2)
Dermatitis artefacta may represent a real challenge for the clinician. As the patient does not admit self-inflicting the lesions, misdiagnosis with other diseases, such as pyoderma gangrenosum, is common. Consequently, these patients normally go thro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::08fcdc0a047fc7a31184fdc510718959
https://pubmed.ncbi.nlm.nih.gov/26891139
https://pubmed.ncbi.nlm.nih.gov/26891139
Autor:
Berta Pérez-Tato, Silvia Marinero, Paloma Fernández-López, Begoña Sánchez-Albisua, Isabel Polimón
Publikováno v:
International Journal of Dermatology. 52:897-899
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::66d60ba5ba7dc3362de5bd0f92c499a3
https://doi.org/10.1111/j.1365-4632.2011.05055.x
https://doi.org/10.1111/j.1365-4632.2011.05055.x
Autor:
Berta Pérez Tato, Begoña Sánchez Albisua, Silvia Marinero Escobedo, Paloma Fernández López, Yosmar Carolina Pérez González, Isabel Polimón Olabarrieta, Beatriz Encabo Mayoral
Publikováno v:
The American Journal of Dermatopathology. 34:746-748
Granulomatous pigmented purpuric dermatosis is a rare entity. Historically, it has been seen in Asians. In this article, we report the case of a white man with this unusual variant. A 65-year-old, white man presented with a 1-year history of asymptom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f90e7dacda4451eefc4589bc2ee1545
https://doi.org/10.1097/dad.0b013e31823f616a
https://doi.org/10.1097/dad.0b013e31823f616a
Autor:
Yosmar Carolina Pérez González, Silvia Marinero Escobedo, Berta Pérez Tato, Begoña Sánchez Albisua, Paloma Fernández López, Elena Zamora Martínez, Isabel Polimón Olabarrieta
Publikováno v:
Tato, Berta Pérez; Martínez, Elena Zamora; Albisua, Begoña Sánchez; González, Yosmar C Pérez; Olabarrieta, Isabel Polimón; Escobedo, Silvia Marinero; et al.(2012). Facial and axillary apocrine chromhidrosis. Dermatology Online Journal, 18(3). Retrieved from: http://www.escholarship.org/uc/item/4md22376
Apocrine chromhidrosis is a rare, chronic, idiopathic disorder, characterized by the excretion of pigmented sweat. A 26-year-old woman presented with a 3-year history of dark blue secretions on bilateral malar cheeks. On examination, upon pressure on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bdf59d7a936ca02e668ebae8a71dc607
http://www.escholarship.org/uc/item/4md22376
http://www.escholarship.org/uc/item/4md22376
