Las enfermedades minoritarias en Galicia. Un reto, una oportunidad y una obligación para el médico internista

by Alvaro Hermida Amejeiras
Published 2021-03-01

Varón de 30 años con hiperamonemia de 24 horas de evolución

by Álvaro Hermida Ameijeiras, Gemma Rodríguez Carnero, Miguel Ángel Martínez
Published 2021-03-01

Prevalencia de prescripción: indicación de protectores gástricos en pacientes hospitalizados A survey of gastroprotective drugs: prescription-indication in hospitalized patients

by Vicente Lorenzo Zúñiga, Belén Cabana González, Álvaro Hermida Ameijeiras
Published 2007-10-01

Medida no invasiva de la presión arterial central mediante tonometría por aplanamiento. Análisis de la onda de pulso

by Dr. Alvaro Hermida Amejeiras, Dr. Jose Enrique Lopez Paz, Dr Carlos Calvo Gómez
Published 2012-12-01

Variable Expressivity in Type 2 Familial Partial Lipodystrophy Related to R482 and N466 Variants in the LMNA Gene

by David Araújo-Vilar, Sofía Sánchez-Iglesias, Ana I. Castro, Silvia Cobelo-Gómez, Álvaro Hermida-Ameijeiras, Gemma Rodríguez-Carnero, Felipe F. Casanueva, Antía Fernández-Pombo
Published 2021-03-01

Clinical characteristics and prognosis of heart failure in elderly patients

by Lucía Martínez-Braña, Lara Mateo-Mosquera, María Bermúdez-Ramos, María de los Ángeles Valcárcel García, Lorena Fernández Hernández, Álvaro Hermida Ameijeiras, Francisco Luis Lado Lado
Published 2015-07-01

Clinical characteristics and prognosis of heart failure in elderly patients

by Lucía Martínez-Braña, Lara Mateo-Mosquera, María Bermúdez-Ramos, María de los Ángeles Valcárcel García, Lorena Fernández Hernández, Álvaro Hermida Ameijeiras, Francisco Luis Lado Lado
Published 2015-07-01

Identification of a Novel Variant in <i>EARS2</i> Associated with a Severe Clinical Phenotype Expands the Clinical Spectrum of LTBL

by Sofia Barbosa-Gouveia, Emiliano González-Vioque, Álvaro Hermida, María Unceta Suarez, María Jesús Martínez-González, Filipa Borges, Liesbeth Wintjes, Antonia Kappen, Richard Rodenburg, María-Luz Couce
Published 2020-09-01

Variable Expressivity and Allelic Heterogeneity in Type 2 Familial Partial Lipodystrophy: The p.(Thr528Met) LMNA Variant

by David Araújo-Vilar, Antía Fernández-Pombo, Berta Victoria-Martínez, Adrián Mosquera-Orgueira, Silvia Cobelo-Gómez, Ana Castro-Pais, Álvaro Hermida-Ameijeiras, Lourdes Loidi, Sofía Sánchez-Iglesias
Published 2021-04-01

Celia’s Encephalopathy (<i>BSCL2</i>-Gene-Related): Current Understanding

by Sofía Sánchez-Iglesias, Antía Fernández-Pombo, Silvia Cobelo-Gómez, Álvaro Hermida-Ameijeiras, Helena Alarcón-Martínez, Rosario Domingo-Jiménez, Alejandro Iván Ruíz Riquelme, Jesús R. Requena, David Araújo-Vilar
Published 2021-04-01

Carbohydrate status in patients with phenylketonuria

by María L. Couce, Paula Sánchez-Pintos, Isidro Vitoria, María-José De Castro, Luís Aldámiz-Echevarría, Patricia Correcher, Ana Fernández-Marmiesse, Iria Roca, Alvaro Hermida, Miguel Martínez-Olmos, Rosaura Leis
Published 2018-06-01

LipoDDx: a mobile application for identification of rare lipodystrophy syndromes

by David Araújo-Vilar, Antía Fernández-Pombo, Gemma Rodríguez-Carnero, Miguel Ángel Martínez-Olmos, Ana Cantón, Rocío Villar-Taibo, Álvaro Hermida-Ameijeiras, Alicia Santamaría-Nieto, Carmen Díaz-Ortega, Carmen Martínez-Rey, Antonio Antela, Elena Losada, Andrés E. Muy-Pérez, Blanca González-Méndez, Sofía Sánchez-Iglesias
Published 2020-04-01