Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Alzenira F. Costa"'
Autor:
Pablo Stiefel, Antonio Ordóñez, Alzenira F. Costa, Luis M. Beltrán, Rafael Moreno-Luna, Antonio J. Vallejo-Vaz, Luis Gómez, José Villar
Publikováno v:
Coronary Artery Disease. 23:57-61
Endothelial function can be measured by the level of reactive vasodilation due to a transient ischemia caused by a blood pressure cuff on the arm, measured using Laser-Doppler flowmetry. This device has software that provides various parameters that
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5c4e2ef08eef1ec43aab2c566b12f8b
https://doi.org/10.1097/mca.0b013e32834e4f34
https://doi.org/10.1097/mca.0b013e32834e4f34
Autor:
Miguel Lucas, Amal Chadli, Luminita Dinca, Alzenira F. Costa, Guillermo Izquierdo, Francisca Solano, Marı́a D Zayas
Publikováno v:
European Neurology. 52:12-17
We studied the association between multiple sclerosis (MS) and a novel single nucleotide polymorphism (SNP), A/T(735)G/C, localized in intron IV of the ApoI/Fas gene, which is recognized by the restrictase MaeI. Fas-MaeI genotypes were screened in ch
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::43336807b176cf0d6006630daebc6428
https://doi.org/10.1159/000079253
https://doi.org/10.1159/000079253
Autor:
Alzenira F. Costa, Francisca Solano, Marı́a D Zayas, Mariano Montori, Miguel Lucas, Guillermo Izquierdo
Publikováno v:
Annals of Neurology. 49:529-532
Mutations in the Kritl gene have been recently discovered as the cause of hereditary cerebral cavernous angioma. We sought the possibility that de novo, noninherited mutations of Kritl also cause cavernous angioma. A patient with two cerebral malform
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8b9224369d4f1b7b89b867d92c26fb8f
https://doi.org/10.1002/ana.105
https://doi.org/10.1002/ana.105
Autor:
Alzenira F. Costa, Francisco J. G. Muriana, Pablo Stiefel, Luis Jimenez-Jimenez, María Miranda, Rafael Moreno-Luna, Jose Villar, Antonio J. Vallejo-Vaz, Rocío Muñoz-Hernández
Publikováno v:
American journal of hypertension. 25(12)
BACKGROUND Olive oil polyphenols have been associated with several cardiovascular health benefits. This study aims to examine the influence of a polyphenol-rich olive oil on blood pressure (BP) and endothelial function in 24 young women with high-nor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::61b177b41f7f29d1d39641d365a4b783
https://pubmed.ncbi.nlm.nih.gov/22914255
https://pubmed.ncbi.nlm.nih.gov/22914255
Autor:
Victoria Bonilla-Henao, Alzenira F. Costa, C.Ó. Pintado, E. Pintado, Raquel Chillón Martínez, J.J. Fernández, E. Andújar, Francisco Sobrino, M. Pérez-Alegre
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
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17 páginas, 3 figuras, 2 tablas.-- et al.
Modifications in the GABA pathway are considered to be responsible for motor alterations in animal models for fragile X-associated tremor ataxia syndrome. We analyzed the expression profile in the cereb
Modifications in the GABA pathway are considered to be responsible for motor alterations in animal models for fragile X-associated tremor ataxia syndrome. We analyzed the expression profile in the cereb
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa6447d09962d53f363918d2056b28f1
https://pubmed.ncbi.nlm.nih.gov/22427040
https://pubmed.ncbi.nlm.nih.gov/22427040
Autor:
Fátima Carrillo, Pilar Gómez-Garre, José López-Barneo, Manuel Carballo, Miguel Lucas, Juan Díaz-Martín, Pablo Mir, Francisco Sobrino, Alzenira F. Costa, Elizabeth Pintado, Lin Gao, María Teresa Cáceres-Redondo
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
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instname
[Background]It is debatable whether the size of triplet repeats of the fragile X mental retardation genes FMR1 and FMR2 (found at the FRAXA and FRAXE loci) is associated with Parkinson's disease (PD). The aims of the current study were to investigate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf0864e67c8e86773dfbdcd862bd014d
http://hdl.handle.net/10261/69309
http://hdl.handle.net/10261/69309
Autor:
Manuel Conde-Sanchez, Amalia Rubio-Calvo, Elena Navarro, Hada C. Macher, Alzenira F. Costa, Juan M. Guerrero, Maria A. Martinez-Broca, Cristina Leon-Garcia
Publikováno v:
PLoS ONE
PLoS ONE, Vol 7, Iss 12, p e51024 (2012)
PLoS ONE, Vol 7, Iss 12, p e51024 (2012)
Journal Article; Research Support, Non-U.S. Gov't; The multiple endocrine neoplasia type 2A (MEN2A) is a monogenic disorder characterized by an autosomal dominant pattern of inheritance which is characterized by high risk of medullary thyroid carcino
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d148f65cb8feadeb93780939115ca981
https://doi.org/10.1371/journal.pone.0051024
https://doi.org/10.1371/journal.pone.0051024
Autor:
García-Moreno Jm, Gamero Ma, Guillermo Izquierdo, Miguel Lucas, Francisca Solano, Marı́a D Zayas, Alzenira F. Costa
Publikováno v:
Annals of Neurology. 47:836-836
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d2107ef113186766750a33a6de9f1aa2
https://doi.org/10.1002/1531-8249(200006)47:6<836::aid-ana22>3.0.co
https://doi.org/10.1002/1531-8249(200006)47:6<836::aid-ana22>3.0.co