Zobrazeno 1 - 10 of 104 pro vyhledávání: '"J. Dapena"'
1
Pneumocystis jiroveciiand cystic fibrosis
Autor: Carmen de la Horra, Francisco J. Dapena, Enrique J. Calderón, Vicente Friaza
Publikováno v: Medical Mycology. 48:S17-S21
Pneumocystis jirovecii is an atypical opportunistic fungus with lung tropism and worldwide distribution that causes pneumonia in immunosuppressed individuals. The development of sensitive molecular techniques has led to the recognition of a colonizat
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba9962527253688923fb5d5a545c1867
https://doi.org/10.3109/13693786.2010.505205
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3
[Comparative study of the efficacy of 2 respiratory physiotherapy protocols for patients with cystic fibrosis]
Autor: H, Sánchez Riera, F J, Dapena Fernández, F, Gómez Domínguez, F, Ortega Ruiz, T, Elías Hernández, T, Montemayor Rubio, J, Castillo Gómez
Publikováno v: Archivos de bronconeumologia. 35(6)
To compare the short-term efficacy of two respiratory physiotherapy protocols on sputum clearance, lung function and symptoms in patients with cystic fibrosis. Treatment A consisted of diaphragm breathing with incentive spirometry and postural draina
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::29dac3c866a7e5ed23425743f7b37c91
https://pubmed.ncbi.nlm.nih.gov/10410207
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5
Listeriosis materna y muerte fetal intraútero
Autor: J. Dapena, A. Otero, E. García-Jiménez, J.M. Cumbraos, R. Vidal
Publikováno v: Clínica e Investigación en Ginecología y Obstetricia. 32:180-181
Listeriosis is a very infrequent infectious disease, caused by Listeria monocytogenes. The prevalence of Listeriosis in Europe is 2-3 cases per million of the population. In Spain, the estimated incidence is 0.5 per million of the population per year
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::1000d81095a1f2053094a306609c20b4
https://doi.org/10.1016/s0210-573x(05)74543-3
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6
Clinical characteristics of 16 cystic fibrosis patients with the missense mutation R334W, a pancreatic insufficiency mutation with variable age of onset and interfamilial clinical differences
Autor: X. Estivill, R. Llevadot, J. Gim�nez, V. Nunes, T. Casals, L. Ortigosa, J. P�rez-Frias, J. Dapena, J. Ferrer, J. Pe�a, L. Pe�a, N. Cobos, C. V�zquez
Publikováno v: Human Genetics. 95
We present the genotype/phenotype correlation analysis for 16 cystic fibrosis (CF) patients who carry mutation R334W. Current age and age of diagnosis was significantly higher in the R334W/any-mutation group (P0.05 and P0.01), compared with the delta
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af20d2361604ae450ee3a5a70d2145b1
https://doi.org/10.1007/bf00225203
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8
[ORL pathology in cystic fibrosis]
Autor: J, Jiménez Morales, F, Delgado Moreno, S, Sánchez Gómez, J, Ceballo Pedraja, F, Mata Maderuelo, J, Dapena Fernández
Publikováno v: Acta otorrinolaringologica espanola. 44(6)
We have studied during 1991 a randomized group of 25 cystic fibrosis children whose ages were between 1 and 18 years, analyzing the disease's ENT signs. We have found polyps in the 20% of the patients points up for its high incidence, and the practic
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::55fc65ee111fe197f324bd1f2973a571
https://pubmed.ncbi.nlm.nih.gov/8155359
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