Zobrazeno 1 - 10
of 61
pro vyhledávání: '"Julián Solís, García Del Pozo"'
Autor:
Isabel María Soler-Moratalla, Sergio Salmerón, Silvia Lozoya-Moreno, Ana María Hermosilla-Pasamar, Antonio Henández-Martínez, Julián Solís-García del Pozo, Margarita Escribano-Talaya, Maria Antonia Font-Payeras, Francisco García-Alcaraz
Publikováno v:
Geriatrics, Vol 9, Iss 4, p 97 (2024)
Background: This work aims to establish the relationship between depression and epidemiological or imaging variables, frailty, and cognitive status in patients who suffered hospital admission for COVID-19. Methods: A longitudinal observational study
Externí odkaz:
https://doaj.org/article/c5614a02504f4517a02b988fbea4442b
Autor:
Samuel Blas Gómez, Fernando Mateos Rodríguez, María Luisa Illescas Fernández-Bermejo, Syonghyun Nam Cha, Julián Solís García del Pozo
Publikováno v:
Nefrología (English Edition), Vol 43, Iss 5, Pp 645-647 (2023)
Externí odkaz:
https://doaj.org/article/4ce84ce5629245b48960590b572e6390
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-14 (2020)
Abstract Background Satoyoshi syndrome (SS) [OMIM 600705; ORFHA 3130] is a multisystemic disease with a probable autoimmune basis, whose main symptoms are muscle spasms, alopecia, diarrhea and skeletal alterations. Chronic diarrhea may be severe and
Externí odkaz:
https://doaj.org/article/e3c7528991bd4493aae92bc945c7c67d
Autor:
Massimiliano Guillermo Trinidad Pereira, Consuelo Martínez Antolinos, Adriana Canosa Fernandez, Elisa Martinez Alfaro, Julián Solís García del Pozo
Publikováno v:
European Journal of Case Reports in Internal Medicine (2021)
We present the case of an HIV-positive patient admitted because of costal pain secondary to neoplasia. During investigations, a colonoscopy showed non-specific ulcerations. Histological examination resulted in a diagnosis of intestinal spirochetosis.
Externí odkaz:
https://doaj.org/article/b293db630747441d8a5d912a8ddfa32d
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-13 (2019)
Abstract Background Satoyoshi syndrome is a multisystemic rare disease of unknown etiology, although an autoimmune basis is presumed. Its main symptoms are: painful muscle spasms, diarrhea, alopecia and skeletal abnormalities. Clinical course without
Externí odkaz:
https://doaj.org/article/d5da23e6360a44d3ae8826014c737039
Autor:
Sergio Guillén Martínez, Yulema Rodríguez Marín, Enrique Marcos Naranjo, Julián Solís García del Pozo
Publikováno v:
Medicina Clínica Práctica, Vol 4, Iss 2, Pp 100162- (2021)
Externí odkaz:
https://doaj.org/article/54c96f281ce14e0d8306b52472399e2c
Autor:
Marta Guzmán Pérez, José Javier Blanch Sancho, Juan Carlos Segura Luque, Fernando Mateos Rodriguez, Elisa Martínez Alfaro, Julián Solís García del Pozo
Publikováno v:
Pathogens, Vol 10, Iss 9, p 1125 (2021)
Background: Leptospirosis is a worldwide zoonotic infection, and its management needs to be refined. This study aims to discern which antibiotic would be the best option to treat leptospirosis disease and analyze the efficacy of chemoprophylaxis regi
Externí odkaz:
https://doaj.org/article/a308af84dc6a4423af7142f46fcc6be9
Autor:
Nuria Monteagudo‐Martínez, Julián Solís García del Pozo, Ichiro Ikuta, Maria Francisca Galindo, Joaquín Jordán
Publikováno v:
Journal of Clinical Pharmacy and Therapeutics. 47:1299-1311
WHAT IS KNOWN AND OBJECTIVE?: Dalbavancin is used against gram-positive pathogens such as Staphylococcus aureus in acute bacterial skin and skin-structure infections. METHODS: Our main goal was to identify the key articles sustaining the current know
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::59b4941d779a90fb39077cd1e98785c3
https://doi.org/10.1111/jcpt.13719
https://doi.org/10.1111/jcpt.13719
Autor:
Vinícius Viana Abreu Montanaro, Julián Solís-García del Pozo, Thiago Falcão Hora, Beatriz H León, Carlos de Cabo, Javier Solera
Publikováno v:
Rheumatology.
ObjectivesSatoyoshi syndrome is a rare multisystem disease of presumed autoimmune aetiology. We carried out a systematic review to evaluate the available evidence to support that autoimmune hypothesis.MethodsWe searched for Satoyoshi syndrome cases i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a023133c840955aa585dcbb9370295d9
https://doi.org/10.1093/rheumatology/kead067
https://doi.org/10.1093/rheumatology/kead067
Autor:
Irene García Cuartero, Mónica Rodríguez Galdeano, Montserrat Pérez Pinar, Julián Solís García del Pozo
Publikováno v:
European Journal of Case Reports in Internal Medicine, Vol 5, Iss 3 (2018)
We present the case of a 57-year-old man with ataxia and clinical and radiological features of cerebellar degeneration. A computed tomography showed a mediastinal mass. The patient was diagnosed of thymic carcinoma. paraneoplastic cerebellar degenera
Externí odkaz:
https://doaj.org/article/76a7411aa49847c287bc9991dcee3bf0