Zobrazeno 1 - 10
of 19
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:
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
Akademický článek
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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
Autor:
Yeray Nóvoa-Medina, Itahisa Marcelino-Rodriguez, Nicolás M. Suárez, Marta Barreiro-Bautista, Eva Rivas-García, Santiago Sánchez-Alonso, Gema González-Martínez, Sofía Quinteiro-González, Ángela Domínguez, María Cabrera, Sara López, Svetlana Pavlovic, Carlos Flores, Gran Canarian Diabetes and Obesity Research Group, Ana M. Wägner
Publikováno v:
BMC Pediatrics, Vol 24, Iss 1, Pp 1-12 (2024)
Abstract The Canary Islands inhabitants, a recently admixed population with significant North African genetic influence, has the highest incidence of childhood-onset type 1 diabetes (T1D) in Spain and one of the highest in Europe. HLA accounts for ha
Externí odkaz:
https://doaj.org/article/e088d419d45649918f94dcbd461f893e
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:
Yeray Nóvoa Medina, Ángela Domínguez García, Sofía Quinteiro González, Loida María García Cruz, Alfredo Santana Rodríguez
Publikováno v:
Anales de Pediatría, Vol 95, Iss 2, Pp 93-100 (2021)
Resumen: Introducción: El hiperinsulinismo congénito (HC) es una patología seria caracterizada por la aparición de hipoglucemias graves. Las mutaciones patogénicas en los genes ABCC8 y KCNJ11 son la causa más frecuente, aunque también se han d
Externí odkaz:
https://doaj.org/article/9455d4a2cbcf4ccdae6c4f8ce63ee2f1