Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Sofia Quinteiro"'
Autor:
Yeray Nóvoa-Medina, Alicia Pérez-Lemes, Nerea Suárez-Ramírez, Marta Barreiro-Bautista, Himar Fabelo, Sara López-López, Sofia Quinteiro, Angela Domínguez, Marta León, María A. González, Elisabeth Caballero, Ana M. Wägner
Publikováno v:
Frontiers in Nutrition, Vol 10 (2024)
AimsTo evaluate the synergistic impact of diet, lifestyle and technology on glycemic control in children with type 1 diabetes (T1D).MethodsThis cross-sectional study included 112 randomly selected patients with T1D from Gran Canaria (median age 12 ye
Externí odkaz:
https://doaj.org/article/aff705a617464685ac0f16ee87f4a26c
Autor:
Immaculada Argemí-Armengol, Javier Álvarez-Rodríguez, Marc Tor, Laura Salada, Ana Leite, Lia Vasconcelos, Alfredo Teixeira, Sandra Sofia Quinteiro Rodrigues
Publikováno v:
Animals, Vol 14, Iss 5, p 739 (2024)
Two of the main issues related to cured meat products are castration to avoid boar taint and the hefty reliance on soybean meal to feed pigs. However, data on the effects of immunocastration in pigs and alternative crop protein feeds on the sensory t
Externí odkaz:
https://doaj.org/article/3f59af6301d9452aaaab358d98bfd6dd
Akademický článek
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Autor:
Atilano Carcavilla, Larisa Suárez-Ortega, Amparo Rodríguez Sánchez, Isabel Gonzalez-Casado, Marta Ramón-Krauel, Jose Ignacio Labarta, Sofia Quinteiro Gonzalez, Isolina Riaño Galán, Begoña Ezquieta Zubicaray, Juan Pedro López-Siguero
Publikováno v:
Anales de Pediatría, Vol 93, Iss 1, Pp 61.e1-61.e14 (2020)
Resumen: El síndrome de Noonan (SN) es una enfermedad de origen genético relativamente frecuente cuyas manifestaciones fundamentales son la talla baja, la cardiopatía congénita y un fenotipo facial característico.La causa del síndrome de Noonan
Externí odkaz:
https://doaj.org/article/f267a6eea3c144beb49f90861a49602d
Autor:
Atilano Carcavilla, Larisa Suárez-Ortega, Amparo Rodríguez Sánchez, Isabel Gonzalez-Casado, Marta Ramón-Krauel, Jose Ignacio Labarta, Sofia Quinteiro Gonzalez, Isolina Riaño Galán, Juan Pedro López-Siguero
Publikováno v:
Anales de Pediatría (English Edition), Vol 93, Iss 1, Pp 61.e1-61.e14 (2020)
Noonan syndrome (NS) is a relatively common genetic condition characterised by short stature, congenital heart defects, and distinctive facial features.NS and other clinically overlapping conditions such as NS with multiple lentigines (formerly calle
Externí odkaz:
https://doaj.org/article/ce8e4e98ecbe44edab1281cbf753c299
Autor:
Carcavilla, Atilano, Suárez-Ortega, Larisa, Sánchez, Amparo Rodríguez, Gonzalez-Casado, Isabel, Ramón-Krauel, Marta, Labarta, Jose Ignacio, Gonzalez, Sofia Quinteiro, Galán, Isolina Riaño, López-Siguero, Juan Pedro *
Publikováno v:
In Anales de Pediatría (English Edition) July 2020 93(1):61-61
Dissertação de Mestrado em Gestão e Economia da Saúde apresentada à Faculdade de Economia Health literacy is essential for health promotion, disease prevention and the effective and efficient use of available healthcare services. Besides that, i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1271::e349c78a1d03b0a44362ae081f251ad0
https://hdl.handle.net/10316/100724
https://hdl.handle.net/10316/100724
Autor:
Tanja Bogdanović, Luis Patarata, Maria Leticia Miranda Fernandes Estevinho, Nevijo Zdolec, Sandra Petričević, Daniel Franco, Igor Tomasevic, Bojana Danilovic, Maria João Fraqueza, Spiros Paramithiotis, Ilija Djekic, Alfredo Teixeira, Sandra Sofia Quinteiro Rodrigues, Jose Manuel Lorenzo Rodriguez
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c1690f98522cd60d982a4b134eeff8b7
https://doi.org/10.1201/9781315369846
https://doi.org/10.1201/9781315369846
Autor:
Luciano Tato, John Raelson, Peter E. Clayton, Clement Olivier, Alicia Belgorosky, Pascale Croteau, Han-Wook Yoo, Sofia Quinteiro, Adam Stevens, Benoit Destenaves, Cheri Deal, Pierre Chatelain, Geoffrey R Ambler
Publikováno v:
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
European Journal of Endocrinology
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
European Journal of Endocrinology
Objective: Individual sensitivity to recombinant human GH (r-hGH) is variable. Identification of genetic factors contributing to this variability has potential use for individualization of treatment. The objective of this study was to identify geneti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aaf40f106e3e15c42b0dde67f856daa1
http://www.eje-online.org/content/169/3/277.long
http://www.eje-online.org/content/169/3/277.long
Autor:
Ruiz-Capillas, Claudia, Herrero, Ana M., Pintado, Tatiana, Delgado-Pando, Gonzalo, Rodrigues, Sandra Sofia Quinteiro
Publikováno v:
Foods; Feb2021, Vol. 10 Issue 2, p429-429, 1p