Zobrazeno 1 - 10
of 178
pro vyhledávání: '"J.M. Fraga"'
Autor:
Cristina Fernández-Pérez, Olalla López-Suárez, Pilar Bermejo-Barrera, María L. Couce, Natalia Mandiá, J.M. Fraga, Paloma Herbello
Publikováno v:
Nutrients
Volume 13
Issue 6
Nutrients, Vol 13, Iss 1885, p 1885 (2021)
Volume 13
Issue 6
Nutrients, Vol 13, Iss 1885, p 1885 (2021)
This study aims to quantify concentrations of minerals and trace elements in human milk (HM) and infant formula (IF) and evaluate associations with medical, social, environmental, and demographic variables. A prospective, case series study of 170 nur
Akademický článek
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Publikováno v:
Food Chemistry. 151:133-140
In this work, different types of gofio produced in the Canary Islands were characterized on the basis of physico-chemical parameters as well as spectral features. An overall of 7 physico-chemical parameters (moisture, ash, pH, Cu, Fe, Mn and Zn) were
Autor:
Pamela Cabarcos, Ana María Bermejo, Olalla López-Suárez, María Jesús Tabernero, Alejandro Pérez-Muñuzuri, María L. Couce, Ana Baña, J.M. Fraga, S. Dosil
Publikováno v:
Journal of Neonatal-Perinatal Medicine. 7:47-54
BACKGROUND: Alcohol consumption during pregnancy, even when moderate, implies a risk of impaired neurodevelopment, physical impairments and malformations. Its early identification is essential for establishing preventive measures to diminish disabili
Autor:
J.M. Fraga, Inmaculada Vives, María L. Couce, C. García-Jimémez, Daisy E. Castiñeiras, E. Balmaseda, Fernando J. Corrales, S. H. Mudd, Ana Fernández-Marmiesse, Bóveda
Publikováno v:
Molecular Genetics and Metabolism. 110:218-221
Persistent hypermethioninemia due to mutations in the MAT1A gene is often found during newborn screening (NBS) for homocystinuria due to cystathionine beta-synthase deficiency, however, outcomes and optimal management for these patients are not well
Autor:
J.M. Fraga, M.D. Bóveda, Lourdes R. Desviat, Belén Pérez, Alicia Mirás, María L. Couce, Ana Fernández-Marmiesse
Publikováno v:
Gene. 521:100-104
Knowledge of hyperphenylalaninemia (HPA) mutational spectrum in a population allows in many cases an accurate prediction of the phenotype and tetrahydrobiopterin (BH4) responsiveness, thus selecting an adequate treatment. In this work, we have perfor
Autor:
Magdalena Ugarte, Mercè Pineda, María L. Couce, J.M. Fraga, Celia Pérez-Cerdá, Belén Pérez, Jaume Campistol, María Teresa García Silva, Daisy E. Castiñeiras, Elena Martín-Hernández, Angels Garcia Cazorla, Rosa Navarrete
Publikováno v:
Medicina Clínica. 137:500-503
Resumen Fundamento y objetivo Comparar los datos clinicos, bioquimicos y geneticos de dos series de pacientes con deficiencia de biotinidasa. Pacientes y metodos Quince casos detectados en el cribado neonatal y seis en el cribado selectivo para sorde
Autor:
Alejandro Pérez-Muñuzuri, M.J. Blanco-Teijeiro, M.L. Couce-Pico, J.R. Fernández-Lorenzo, J.M. Fraga-Bermúdez
Publikováno v:
Journal of Neonatal-Perinatal Medicine. 2:163-167
Autor:
M. Luz Luis, O. Hernández, Juan J. Arias, J.M. Fraga, A.I. Jiménez, Francisco Jiménez Jiménez
Publikováno v:
Analytical Letters. 40:257-280
A procedure for selection of wavelength range and number of factors to be used in partial least square calibration that involves the calculation of prediction residual sum of squares (PRESS) in different conditions is proposed. The best model takes i
Autor:
José A. Cocho, María L. Couce, José Ramón Fernández-Lorenzo, J.M. Fraga, Alejandro Pérez-Muñuzuri, Paula Sánchez-Pintos
Publikováno v:
The journal of maternal-fetalneonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians. 29(6)
To verify whether small-for-gestational-age (SGA) preterm newborns represent a special risk group for carnitine deficiency. Secondary outcome includes assessment of longitudinal differences of total carnitine (TC), free carnitine (FC) and acylcarniti