Publicaciones en colaboración con investigadores/as de Complexo Hospitalario Universitario de Santiago (107)

2022

  1. A Comparison between Three Different Techniques Considering Quality Skills, Fatigue and Hand Pain during a Prolonged Infant Resuscitation: A Cross-Over Study with Lifeguards

    Children, Vol. 9, Núm. 6

  2. Association of rhinitis with asthma prevalence and severity

    Scientific Reports, Vol. 12, Núm. 1

  3. Clinical and pathological features of persistent decorative tattoo reactions

    Indian Journal of Dermatology, Vol. 67, Núm. 2, pp. 152-156

  4. Clinical characteristics and prognosis of myocardial infarction with non-obstructive coronary arteries: A prospective single-center study

    Cardiology Journal, Vol. 29, Núm. 5, pp. 798-806

  5. 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

  6. Impact of a Home Telehealth Program After a Hospitalized COPD Exacerbation: A Propensity Score Analysis

    Archivos de Bronconeumologia, Vol. 58, Núm. 6, pp. 474-481

  7. Learning to resuscitate at school. Study in 8-12 year-old schoolchildren

    Anales de Pediatria, Vol. 96, Núm. 1, pp. 17-24

  8. Prevalence, Incidence, and Outcomes of Hyperkalaemia in Patients with Chronic Heart Failure and Reduced Ejection Fraction from a Spanish Multicentre Study: SPANIK-HF Design and Baseline Characteristics

    Journal of Clinical Medicine, Vol. 11, Núm. 5

  9. Quality of life and persistent symptoms after hospitalization for COVID-19. A prospective observational study comparing ICU with non-ICU patients

    Revista Espanola de Anestesiologia y Reanimacion, Vol. 69, Núm. 6, pp. 326-335

  10. Reducing Metabolic Syndrome through a Group Educational Intervention Program in Adults with Obesity: IGOBE Program

    Nutrients, Vol. 14, Núm. 5

  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