Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Carolina Sánchez-Malo"'
Autor:
María José Martínez Ramírez, Piedad Santiago Fernández, Carolina Sánchez-Malo, Carmen Gutiérrez Alcántara, Tomás Ureña Fernández, Manuela Gassó Campos, Eduardo García Fuentes, Pablo Olmedo Carrillo
Publikováno v:
Endocrinología, Diabetes y Nutrición. 64:417-423
Resumen Antecedentes y objetivos Las guias de tratamiento de disfuncion tiroidea recomiendan definir los intervalos de referencia de las hormonas tiroideas de cada area mediante la evaluacion de datos de poblacion local considerando el grado de nutri
Autor:
Pablo Olmedo Carrillo, Piedad Santiago Fernández, Tomás Ureña Fernández, María José Martínez Ramírez, Eduardo García Fuentes, Manuela Gassó Campos, Carolina Sánchez-Malo, Carmen Gutiérrez Alcántara
Publikováno v:
Endocrinologia, diabetes y nutricion. 64(8)
Background and objectives The treatment guidelines for thyroid dysfunction recommend defining reference ranges for thyroid hormones in each area through assessment of local population data considering the iodine nutritional status. The aim of this st
Autor:
Piedad Santiago Fernández, Carolina Sánchez Malo, Cristina Montes Castillo, Carmen Gutiérrez Alcántara, María Macarena Moreno Martínez
Publikováno v:
Endocrinología y Nutrición. 61:548-550
Autor:
Massimo Mannelli, Alberto Cascón, Aguirre A. de Cubas, Álvaro Gómez-Graña, Carmen Bernal, Iñaki Comino-Méndez, César L. Ramírez-Tortosa, Alessandra Bacca, Veronika Mancikova, Guillermoó Pita, Cristina Rodríguez-Antona, Elena Rapizzi, Susana Pedrinaci, Mercedes Robledo, Giampaolo Bernini, Carolina Sánchez-Malo, Cristina Álvarez-Escolá, Tonino Ercolino, Luis J Leandro-García, María R Alonso, Lucía Inglada-Pérez, Rocío Letón
Publikováno v:
Human Molecular Genetics; Vol 22
Pheochromocytomas (PCCs) and paragangliomas (PGLs) are chromaffin-cell tumors that arise from the adrenal medulla and extra-adrenal paraganglia, respectively. The dysfunction of genes involved in the cellular response to hypoxia, such as VHL, EGL nin
Autor:
Francisco Fernandez-Rosado, Carmen Entrala-Bernal, Maria Jesus Alvarez-Cubero, Esther Martinez-Espίn, Piedad Santiago-Fernández, Cristina Montes-Castillo, Carmen Gutiérrez-Alcántara, Carolina Sánchez-Malo
Publikováno v:
Hormones (Athens, Greece). 13(2)
Kallmann Syndrome (KS) is a genetic disease of embryonic development which is characterized by the association of hypogonadotropic hypogonadism (HH) due to a deficit of the gonadotropin-releasing hormone (GnRH) and a hypo/anosmia (including a hypopla
Autor:
Alicia Serraclara, Alberto Garcia-Hernandez, Elda Castro, Maria M. Campos, Manuel Aguilar-Diosdado, Fernando Escobar-Jiménez, Federico Hawkins, Alberto Moreno, J.L. Herrera-Pombo, Lourdes G. García-Doncel, Carolina Sánchez-Malo
Publikováno v:
Nephron. Clinical practice. 101(3)
Aims: The aims of the study were to evaluate the prevalence of increased urinary albumin excretion (UAE) and associated cardiovascular risk factors and vascular diabetes complications in patients with type 2 diabetes mellitus (DM). Methods: We studie