Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Evelia, Ojeda"'
Autor:
Ángel Cosme, Evelia Ojeda, Ana I. Muñagorri, Eduardo Gaminde, Luis Bujanda, Mikel Larzabal, Inés Gil
Publikováno v:
Revista Espanola de Enfermedades Digestivas, Vol 103, Iss 4, Pp 213-217 (2011)
extraintestinal manifestations, species-specific PCR using different sequences of the T. whippleii genome from different tissue types and biological fluids is recommended. The diagnosis of Whipple's disease (WD) is based on the existence of clinical
Externí odkaz:
https://doaj.org/article/f8f5e031af96403b831069b0c1638a37
Autor:
Angel, Cosme, Mariano, Alvarez, Adolfo, Beguiristain, Ana María, Cobo, Mercedes, Robledo, María Jesús, Aranzadi, Evelia, Ojeda, Luis, Bujanda, Unai, Goikoetxea
Publikováno v:
Gastroenterologia y hepatologia. 31(10)
The clinical features of multiple endocrine neoplasia type-1 (MEN-1) syndrome are hyperplasia or adenoma of the parathyroid glands, pituitary adenoma and gastroenteropancreatic endocrine tumors. This syndrome is due to mutations in the MEN1 gene, loc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8be33af40b970d6e38014eec5e80e67c
https://pubmed.ncbi.nlm.nih.gov/19174080
https://pubmed.ncbi.nlm.nih.gov/19174080
Autor:
Angel, Cosme, Ana María, Cobo, Michèle, Meunier-Rotival, Michelle, Hadchouel, Paloma, Jara, Evelia, Ojeda, Luis, Bujanda, Javier, Orbegozo
Publikováno v:
Medicina clinica. 130(1)
The Alagille syndrome (AS) is characterized by biliary ductopenia and abnormalities of heart, eyes, face, bones, kidneys and brain with a dominant inheritability. Mutations of Jagged 1 gene are observed in individuals with the full syndrome and/or re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::bb2c98e270d29b9633099e279793c775
https://pubmed.ncbi.nlm.nih.gov/18221641
https://pubmed.ncbi.nlm.nih.gov/18221641
Autor:
Angel, Cosme Jiménez, Evelia, Ojeda Pérez, Fernando, Neira, Manuel, Vaquero Pérez, Luis, Bujanda Fernández de Piérola, Isabel, Montalvo, Nerea, Muro Carral
Publikováno v:
Gastroenterologia y hepatologia. 30(7)
Whipple's disease is an infrequent chronic infection caused by Tropheryma whipplei, identified in 1992. Intestinal, articular, central nervous system and cardiac involvement is common. The presence of abdominal adenopathies, especially mesenteric ade
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b2fca001662eaf811a5b5524e15186dd
https://pubmed.ncbi.nlm.nih.gov/17692197
https://pubmed.ncbi.nlm.nih.gov/17692197
Autor:
Angel, Cosme, Evelia, Ojeda, Montserrat, Poch, Luis, Bujanda, Agustín, Castiella, Javier, Fernández
Publikováno v:
Journal of clinical ultrasound : JCU. 31(7)
The aim of this retrospective study was to analyze the sonographic features of hepatic lesions in patients with fascioliasis to help determine the utility of sonography in diagnosing this disorder in patients from areas in which Fasciola hepatica inf
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2d61970f2c920ded6ddbbe186e099044
https://pubmed.ncbi.nlm.nih.gov/12923880
https://pubmed.ncbi.nlm.nih.gov/12923880
Publikováno v:
Enfermedades Infecciosas y Microbiología Clínica. 28:330-331
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e6d7b3b7eed49d4fee98d7b4db90cd18
https://doi.org/10.1016/j.eimc.2009.04.011
https://doi.org/10.1016/j.eimc.2009.04.011
Autor:
Francisco Loyola Echaniz, Fernando Mugica Aguinaga, Eva Zapata Morcillo, José Alberto Arriola Manchola, Evelia Ojeda Pérez, Ángel Cosme Jiménez
Publikováno v:
Gastroenterología y Hepatología. 29:377-378
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7efe01e8f01a21eacaf5afbcbf98d17c
https://doi.org/10.1157/13089722
https://doi.org/10.1157/13089722
Publikováno v:
Medicina Clínica. 116:118-119
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4216fef96e53f9dc8bed9f02a0788d5e
https://doi.org/10.1016/s0025-7753(01)71742-3
https://doi.org/10.1016/s0025-7753(01)71742-3