Zobrazeno 1 - 10
of 23
pro vyhledávání: '"M.C. González-Fernández"'
Autor:
C Martı́nez-Bouzas, M.M. de Pancorbo, M.C. González-Fernández, A. Castro, I Fernández-Fernández, N Cuevas
Publikováno v:
International Congress Series. 1239:841-845
Biological traces that appear at the scene of a crime or on the body of the victim may be of human, animal and/or vegetable origin. Among those of animal origin, household pets are a common source, with pet hair being one of the most frequent traces
Autor:
A. Cayuela Domínguez, C. Álvarez Lacayo, M.C. González Fernández, J.M. López Chozas, A. Espino Montoro, F. Villalba Alcalá
Publikováno v:
Atención Primaria. 31:301-306
ObjetivoLos pacientes con hipertensión arterial (HTA) que no presentan un descenso nocturno de la presión arterial (PA) suelen tener un mayor grado de afección de órganos diana debido a la hipertensión mantenida. En nuestro trabajo analizamos, m
Autor:
Marian M. de Pancorbo, Juan Carlos Gómez-Esteban, Juan J. Zarranz, J. Ruiz-Martinez, Elena Lezcano, Beatriz Tijero, M.C. González-Fernández, Verónica Llorens, J. C. Cembellin
Publikováno v:
Clinical Autonomic Research. 20:267-269
Here we report the case of an asymptomatic carrier of the E46K substitution in alpha-synuclein gene where we have documented that cardiac sympathetic denervation precedes nigrostriatal dopaminergic loss.She has been followed up regularly with standar
Autor:
M.M. de Pancorbo, M.C. González-Fernández, E. Sarasola, Juan José Builes, M.A Moreno, V. Fernández del Pozo, M.L.J. Bravo, Sergio Cardoso
Publikováno v:
International Congress Series. 1288:64-66
The design of new primers with the aim to obtain minialleles of microsatellites for forensic use is an important aim nowadays. This work started with that purpose: to design primers to reduce the length of D7S820 amplification products. After sequenc
Autor:
Jessica Castro Flores, Sandra Inglés Borda, Manuel Fernández Martínez, M.C. González-Fernández, María Carrasco Zabaleta, Miryam Barandiarán Amillano, María Ángeles Gómez Beldarraín, Josefa Moraza López, Marian M. de Pancorbo, Xabier Elcoroaristizabal Martín, Begoña Indakoetxea Juanbeltz, Rocio Bereincua Gandarias, Ana Molano Salazar, Nuria Ortiz Marqués, Luis Galdos Alcelay, Juan María Uterga Valiente
Publikováno v:
BMC Neuroscience
Addi. Archivo Digital para la Docencia y la Investigación
instname
BMC Neuroscience, Vol 10, Iss 1, p 125 (2009)
Addi. Archivo Digital para la Docencia y la Investigación
instname
BMC Neuroscience, Vol 10, Iss 1, p 125 (2009)
Background: The aim of this study is to examine the influence of the catechol-O-methyltranferase (COMT) gene (polymorphism Val158 Met) as a risk factor for Alzheimer's disease (AD) and mild cognitive impairment of amnesic type (MCI), and its synergis
Autor:
Laura Valverde, Beatriz Martínez, B. Martínez Jarreta, Dora Sánchez, María Luisa Bravo, Juan José Builes, Marian M. de Pancorbo, E. Sarasola, Adrian Odriozola, Fabricio González-Andrade, Sergio Cardoso, Jose María Aznar, M.C. González-Fernández
Publikováno v:
International journal of legal medicine. 123(6)
Single nucleotide polymorphisms (SNPs) in the flanking regions of microsatellite loci (SNPSTRs) help to increase the power of discrimination of short tandem repeat (STR) loci. SNPs are positions in the genome that have been well-conserved over the co
Autor:
Renee Ribacoba, Luis M. Guisasola, Marian M. de Pancorbo, Hao Deng, Marta Blazquez, Victoria Alvarez, Cecilia Huerta, Juan Carlos Gómez-Esteban, Carlos Salvador, Jon Infante, Karen L. Edwards, Carolyn M. Hutter, Juan J. Zarranz, Ignacio F. Mata, Cyrus P. Zabetian, M.C. González-Fernández, Elena Lezcano, Joseph Jankovic
Mutations in the leucine-rich repeat kinase 2 (LRRK2) gene together represent the most common genetic determinant of Parkinson's disease (PD) identified to date. The vast majority of patients with LRRK2-related PD reported in the literature carry one
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8388035cf3b6fbdcc66d9a101d3282e4
https://europepmc.org/articles/PMC2821036/
https://europepmc.org/articles/PMC2821036/
Autor:
Elena Lezcano, Juan Carlos Gómez-Esteban, M.C. González-Fernández, Maite Alvarez-Alvarez, Owen A. Ross, Fernando Velasco, Marian M. de Pancorbo, Roberto Ciordia, Fernando Gómez-Busto, María B. Rodríguez-Martínez, Matthew J. Farrer, Juan J. Zarranz, Ignacio F. Mata
Publikováno v:
Parkinsonismrelated disorders. 13(8)
Herein we describe a comparative clinical and genetic study of Lrrk2-associated parkinsonism in Northern Spain. In our sample from the Basque region, Lrrk2 R1441G and G2019S account for 15 out of 50 kindreds (30%) with familial Parkinson’s disease.
Publikováno v:
Forensic Science International: Genetics Supplement Series. 1:589-590
Cytochrome b was used to determine the origin of hair traces contaminating food served in a hospital from the Basque Country. The same sequence was obtained for the three hairs subjected to analysis. This sequence matched exactly that for Bos taurus
Autor:
Fernando Gómez-Busto, Juan J. Zarranz, Elena Lezcano, A. López de Lapuente, M.M. de Pancorbo, M.C. González-Fernández, J.C.G. Ómez-Esteban
Publikováno v:
Parkinsonism & Related Disorders. 15:S149