Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Helena Higelmo Gómez"'
Publikováno v:
Anales de Pediatría, Vol 90, Iss 2, Pp 134-135 (2019)
Externí odkaz:
https://doaj.org/article/300699650fdb4fd4969c9f9afa792ac1
Publikováno v:
Revista Alergia México, Vol 66, Iss 3, Pp 375-378 (2019)
Background: DRESS syndrome (rash with eosinophilia and systemic symptoms) is an uncommon and severe drug-induced reaction. Clinical case: An 8-year-old boy was diagnosed with tonsillopharyngitis, and treatment with amoxicillin was started. One day l
Externí odkaz:
https://doaj.org/article/f9870fbc487d4c6bb3aa65589e2d20ef
Autor:
Elisa García-García, Laura Calle-Miguel, David Pérez-Solís, Ignacio Carvajal Urueña, Águeda García Merino, Helena Higelmo Gómez, María Morán Poladura, Mercedes Rodríguez-Pérez
Publikováno v:
Pediatric Infectious Disease Journal. 42:226-231
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eeac38cdcb9b13361b00c2c721507867
https://doi.org/10.1097/inf.0000000000003790
https://doi.org/10.1097/inf.0000000000003790
Publikováno v:
Revista Alergia México, Vol 66, Iss 3, Pp 375-378 (2019)
DRESS syndrome (rash with eosinophilia and systemic symptoms) is an uncommon and severe drug-induced reaction.An 8-year-old boy was diagnosed with tonsillopharyngitis, and treatment with amoxicillin was started. One day later, he presented bilateral
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ae031ea5b02698f815c5cab0cd06e7d
https://doi.org/10.29262/ram.v66i3.540
https://doi.org/10.29262/ram.v66i3.540
Autor:
Helena Higelmo-Gómez, Laura Míguez-Martín, Igor Vázquez-Osorio, Eloy Rodríguez-Díaz, M Elena Reimunde Seoane
Publikováno v:
Dermatology online journal. 26(5)
Lipedematous scalp is an uncommon entity of unknown etiology, rarely described in the pediatric age. It is characterized by boggy thickening of the scalp predominantly located at the vertex and occiput, which acquires a cotton-like consistency. This
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f26b3091cef2c776b3ebd4a07ba832c3
https://pubmed.ncbi.nlm.nih.gov/32621703
https://pubmed.ncbi.nlm.nih.gov/32621703
Autor:
Eloy Rodríguez-Díaz, M Elena Reimunde-Seoane, M Teresa González-Martínez, Laura Míguez-Martín, Jennifer Carolina Barbato-Mateos, Helena Higelmo-Gómez, Igor Vázquez-Osorio
Publikováno v:
Higelmo-Gómez, Helena; Míguez-Martín, Laura; Barbato-Mateos, Jennifer Carolina; González-Martínez, M Teresa; Reimunde-Seoane, M Elena; Rodríguez-Díaz, Eloy; et al.(2018). Aplasia cutis congénita con defecto óseo subyacente: evolución favorable tras manejo conservador. Dermatology Online Journal, 24(9). Retrieved from: http://www.escholarship.org/uc/item/1bq5z51v
La aplasia cutis congenita es una rara alteracion caracterizada por la ausencia de areas localizadas de piel en el momento del nacimiento. Suele manifestarse como una lesion solitaria localizada principalmente en el cuero cabelludo, que puede estar a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::33981d9c2526a2746ddcb2eb6ac3d43c
https://pubmed.ncbi.nlm.nih.gov/30677836
https://pubmed.ncbi.nlm.nih.gov/30677836
Publikováno v:
Anales de Pediatría, Vol 90, Iss 2, Pp 134-135 (2019)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::737498f74aab488b6055f97c6e9aa4b8
http://www.sciencedirect.com/science/article/pii/S1695403318305290
http://www.sciencedirect.com/science/article/pii/S1695403318305290