Publicacións (118) Publicacións de Miguel Ángel Martínez Olmos

2022

  1. A telephone support program for patients with home enteral nutrition contributes to nutrition status and quality of life maintenance and reduces health resource use

    Nutrition in Clinical Practice, Vol. 37, Núm. 4, pp. 878-886

  2. Adipose tissue and blood leukocytes ACE2 DNA methylation in obesity and after weight loss

    European Journal of Clinical Investigation, Vol. 52, Núm. 2

  3. Aetiological diagnosis of hyponatraemia in non-critical patients on total parenteral nutrition: A prospective multicentre study

    Endocrinologia, Diabetes y Nutricion, Vol. 69, Núm. 3, pp. 160-167

  4. At-admission HbA1c levels in hospitalized COVID-19 participants with and without known diabetes

    Clinica Chimica Acta, Vol. 532, pp. 188-192

  5. Cognitive Status and Nutritional Markers in a Sample of Institutionalized Elderly People

    Frontiers in Aging Neuroscience, Vol. 14

  6. Epigenetic Effects of Healthy Foods and Lifestyle Habits from the Southern European Atlantic Diet Pattern: A Narrative Review

    Advances in nutrition (Bethesda, Md.), Vol. 13, Núm. 5, pp. 1725-1747

  7. Gestational weight gain influences neonatal outcomes in women with obesity and gestational diabetes

    Endocrinologia, Diabetes y Nutricion, Vol. 69, Núm. 10, pp. 852-858

  8. Multidisciplinary consensus on nutritional and metabolic therapy in enhanced recovery after abdominal surgery programs: NutRICA Project

    Endocrinologia, Diabetes y Nutricion, Vol. 69, Núm. 2, pp. 98-111

  9. Prevención de los trastornos de la conducta alimentaria en la atención sanitaria especializada

    Nutricion hospitalaria, Vol. 39, Núm. 2, pp. 129-137

  10. Registro del Grupo NADYA-SENPE de Nutrición Enteral Domiciliaria en España: años 2018 y 2019

    Nutricion hospitalaria, Vol. 39, Núm. 1, pp. 223-229

  11. Transcriptomic analysis of patients with clinical suspicion of maturity-onset diabetes of the young (MODY) with a negative genetic diagnosis

    Orphanet journal of rare diseases, Vol. 17, Núm. 1, pp. 105