Zobrazeno 1 - 10
of 192
pro vyhledávání: '"Luis Garcia, Alonso"'
Publikováno v:
L'Antiquité Classique, 2011 Jan 01. 80, 445-446.
Externí odkaz:
https://www.jstor.org/stable/antiqclassi.80.445
Autor:
Emma Velasquez, Jose A Gomez-Sanchez, Emmanuelle Donier, Carmen Grijota-Martinez, Hugo Cabedo, Luis Garcia-Alonso
Publikováno v:
PLoS Genetics, Vol 18, Iss 6, p e1010224 (2022)
How cell to cell interactions control local tissue growth to attain a species-specific organ size is a central question in developmental biology. The Drosophila Neural Cell Adhesion Molecule, Fasciclin 2, is expressed during the development of neural
Externí odkaz:
https://doaj.org/article/d77ce66930e7458088ea807289777148
Publikováno v:
Frontiers in Psychology, Vol 13 (2022)
Externí odkaz:
https://doaj.org/article/c3b6e3dc074c4fc58f918b7f2914c981
Publikováno v:
Frontiers in Psychology, Vol 12 (2021)
Introduction: The high degree of religious/spiritual involvement that brings meaning and purpose to a patients’ life, especially when they are weakened by pain, is among the various reasons to consider the spiritual dimension in clinical practice.
Externí odkaz:
https://doaj.org/article/8eefe10a48c94bdc9d59277999c43c3b
Autor:
Carla Sustek D’Angelo, Monica Castro Varela, Claudia Irene Emílio de Castro, Paulo Alberto Otto, Ana Beatriz Alvarez Perez, Charles Marques Lourenço, Chong Ae Kim, Debora Romeo Bertola, Fernando Kok, Luis Garcia-Alonso, Celia Priszkulnik Koiffmann
Publikováno v:
Molecular Cytogenetics, Vol 11, Iss 1, Pp 1-18 (2018)
Abstract Background Syndromic obesity is an umbrella term used to describe cases where obesity occurs with additional phenotypes. It often arises as part of a distinct genetic syndrome with Prader-Willi syndrome being a classical example. These rare
Externí odkaz:
https://doaj.org/article/612e42939b5e4293892f748d59d04e3e
Autor:
Rodrigo Barbosa de Souza, Luis Ernesto Farinha-Arcieri, Marcia Helena Braga Catroxo, Ana Maria Cristina Rebelo Pinto da Fonseca Martins, Roberto Carlos Tedesco, Luis Garcia Alonso, Ivan Hong Jun Koh, Lygia V Pereira
Publikováno v:
PLoS ONE, Vol 14, Iss 11, p e0224581 (2019)
AIMS:Cardiovascular manifestations are a major cause of mortality in Marfan syndrome (MFS). Animal models that mimic the syndrome and its clinical variability are instrumental for understanding the genesis and risk factors for cardiovascular disease
Externí odkaz:
https://doaj.org/article/3193b52c28544e259f2eb877a53c28b8
Autor:
Claudia Branco Battistella, Thatiana Bastos Guimarães, Camila Leite Quaglio, Mariana Brandão Ferreira-Cabrini, Dinamar Aparecida Gaspar-Martins, Neil Ferreira Novo, Yara Juliano, Deusvenir de Souza Carvalho, Antonio Sérgio Guimarães, Luis Garcia Alonso
Publikováno v:
Revista Dor, Vol 17, Iss 1, Pp 19-23 (2016)
RESUMO JUSTIFICATIVA E OBJETIVOS: Relacionar as variáveis biopsicossociais do Research Diagnostic Criteria for Temporomandibular Disorders com os grupos de pacientes com disfunção temporomandibular, com disfunção temporomandibular e migrânea e
Externí odkaz:
https://doaj.org/article/cb55f328a0234fee880b352769c71186
Autor:
Juan Luis Garcia Alonso
Publikováno v:
Вопросы Ономастики. 19:45-65
Рукопись поступила в редакцию 28.08.2021. Received on 28 August 2021. Определение языков, на которых говорили на юге Иберийского полуострова в древности,
Autor:
Emma Velasquez, Jose A. Gomez-Sanchez, Emmanuelle Donier, Carmen Grijota-Martinez, Hugo Cabedo, Luis Garcia-Alonso
Publikováno v:
PLoS genetics. 18(6)
How cell to cell interactions control local tissue growth to attain a species-specific organ size is a central question in developmental biology. The Drosophila Neural Cell Adhesion Molecule, Fasciclin 2, is expressed during the development of neural
Autor:
Luis Garcia Alonso, Luiz Felipe Palma, Fábio Redivo Lodi, Luís Otávio Carvalho de Moraes, Nathalia C de Victo
Publikováno v:
Cardiology in the Young. 30:238-242
Hypoplastic left heart syndrome consists of several structural abnormalities in the left side of the heart and may be associated with a hereditary genetic cause, possibly related to the connexin gene GJA1; however, only a few studies have investigate