Zobrazeno 1 - 10
of 13
pro vyhledávání: '"José M. Cabezas"'
Autor:
Christine Judt, Gema Guzmán, José A. Gómez, José M. Cabezas, José A. Entrenas, Silvia Winter, Johann G. Zaller, Daniel Paredes
Publikováno v:
Insects, Vol 10, Iss 10, p 320 (2019)
Land use at landscape and field scales can increase the diversity and abundance of natural enemies for pest control. In this study, we investigated interactions between landscape elements (semi-natural vegetation, olive orchards, vineyards, other agr
Externí odkaz:
https://doaj.org/article/3013dd501970445383d508d6ede1b622
Autor:
Katjana Wiederkehr, Caroline Mai, José M. Cabezas, Teresita Rocha-Jiménez, Tamara Otzen, Nicolás Montalva, Esteban Calvo, Alvaro Castillo-Carniglia
Publikováno v:
International Journal of Environmental Research and Public Health; Volume 19; Issue 19; Pages: 12791
Background: Despite its enormous health and social burden, there are limited published studies describing the epidemiology of violent deaths in Chile. We described violent mortality rate trends in Chile between 2001 and 2018, its current spatial dist
Publikováno v:
Electoral Studies. 72:102362
This article revisits the debate over Chile's binomial electoral rules and its consequences and examines how the new electoral system conceived by a democratic congress altered political competition. It utilizes a seat-vote model of multiparty compet
Autor:
Patricio Navia, José M. Cabezas
Publikováno v:
Revista Latinoamericana de Opinión Pública. 8:63
Studies on presidential approval in consolidated and emerging democracies identify similar determinants of popular support and show a common U-shaped cyclical pattern, with higher levels of support during the honeymoon period and in the last year of
Autor:
David Araújo-Vilar, Samuel I. Pascual-Pascual, José M. Cabezas-Agrícola, Angel Díaz-Pérez, Ana M. Ramos-Leví, María-Jesús Sobrido, Patricia Blanco-Arias, Sergio Piñeiro-Hermida
Publikováno v:
Muscle & Nerve. 46:957-961
Introduction: Multiple endocrine neoplasia type 2 (MEN 2) is an uncommon autosomal dominant cancer syndrome which can be associated with nerve conduction abnormalities. Methods: A 14-year-old boy with a family history of consanguinity developed progr
Autor:
José, Cameselle-Teijeiro, Carmen, Fachal, José M, Cabezas-Agrícola, Natividad, Alfonsín-Barreiro, Ihab, Abdulkader, Ana, Vega-Gliemmo, José Antonio, Hermo
Publikováno v:
American journal of clinical pathology. 144(2)
PTEN hamartoma tumor syndrome (PHTS) is a hereditary disorder caused by germline inactivating mutations of the PTEN gene. PHTS includes Cowden syndrome and Bannayan-Riley-Ruvalcaba syndrome. We describe how the peculiar pathologic and immunohistochem
Autor:
José M Cabezas-Agrícola, José L Otero-Cepeda, Maria J. López-Valladares, C. Capeans, Rogelio Conde-Freire, Rosario Touriño, Teresa Rodríguez-Aves
Publikováno v:
International Ophthalmology. 25:101-112
Several kinds of congenital hypertrophy of the retinal pigment epithelium (CHRPE) have been described in patients with familial adenomatous polyposis (FAP). This study aims to assess which properties of CHRPE better predict FAP and investigate whethe
Autor:
Patricio Navia, José M. Cabezas
Publikováno v:
Revista Política. 45
Pese a haber sido alegadamente establecido con ese objetivo, el sistema binominal no ha contribuido a reducir el numero de partidos politicos desde que fue utilizado por primera vez en 1989. Al analizar los resultados electorales por distritos de las
Autor:
Ana M, Ramos-Leví, Angel, Díaz-Pérez, María-Jesús, Sobrido, Sergio, Piñeiro-Hermida, Patricia, Blanco-Arias, José M, Cabezas-Agrícola, Samuel I, Pascual-Pascual, David, Araújo-Vilar
Publikováno v:
Musclenerve. 46(6)
Multiple endocrine neoplasia type 2 (MEN 2) is an uncommon autosomal dominant cancer syndrome which can be associated with nerve conduction abnormalities.A 14-year-old boy with a family history of consanguinity developed progressive gait clumsiness,
Autor:
José M, Cabezas Agrícola
Publikováno v:
Endocrinologia y nutricion : organo de la Sociedad Espanola de Endocrinologia y Nutricion. 56
Gastroenteropancreatic neuroendocrine tumors are relatively rare neoplasms but their incidence has significantly increased in the last 30 years. These tumors are usually sporadic but can also occur as part of certain endocrine tumor susceptibility sy