Publicaciones en colaboración con investigadores/as de Hospital Universitario La Paz (265)

2024

  1. Assessing coagulopathy and endothelial dysfunction in pediatric venous malformation: A thromboelastometry and syndecan-1 study

    Pediatric Blood and Cancer, Vol. 71, Núm. 5

  2. Clinical features and prognosis of prosthetic valve endocarditis due to Staphylococcus aureus

    European Journal of Clinical Microbiology and Infectious Diseases, Vol. 43, Núm. 10, pp. 1989-2000

  3. Genetic and phenotypic findings in 34 novel Spanish patients with DDX3X neurodevelopmental disorder

    Clinical Genetics, Vol. 105, Núm. 2, pp. 140-149

  4. Heart Failure Knowledge Assessment and Perceived Patient Satisfaction in Heart Failure Units: A Multicenter Observational Survey

    Reviews in Cardiovascular Medicine, Vol. 25, Núm. 9

  5. Identification of copy-number variants in patients with overgrowth disorders

    Clinical Genetics, Vol. 106, Núm. 5, pp. 614-624

  6. Rationale and design of the artificial intelligence scalable solution for acute myocardial infarction (ASSIST) study

    Journal of Electrocardiology, Vol. 86

  7. The Human Phenotype Ontology in 2024: phenotypes around the world

    Nucleic acids research, Vol. 52, Núm. D1, pp. D1333-D1346

  8. Zoonosis screening in Spanish immunocompromised children and their pets

    Frontiers in Veterinary Science, Vol. 11

2023

  1. A Spanish Family with Gordon Syndrome Due to a Variant in the Acidic Motif of WNK1

    Genes, Vol. 14, Núm. 10

  2. Cardiogenic shock code 2023. Expert document for a multidisciplinary organization that allows quality care

    Revista Espanola de Cardiologia, Vol. 76, Núm. 4, pp. 261-269

  3. Chromosomal Microarray in Patients with Non-Syndromic Autism Spectrum Disorders in the Clinical Routine of a Tertiary Hospital

    Genes, Vol. 14, Núm. 4

  4. Clinical Heterogeneity and Different Phenotypes in Patients with SETD2 Variants: 18 New Patients and Review of the Literature

    Genes, Vol. 14, Núm. 6

  5. Cognitive–Behavioral Profile in Pediatric Patients with Syndrome 5p-; Genotype–Phenotype Correlationships

    Genes, Vol. 14, Núm. 8

  6. Consensus recommendations on organization of care for individuals with Phelan-McDermid syndrome

    European Journal of Medical Genetics, Vol. 66, Núm. 7

  7. Contemporary use of cefazolin for MSSA infective endocarditis: analysis of a national prospective cohort

    International Journal of Infectious Diseases, Vol. 137, pp. 134-143

  8. Early approach to LDL-related risk after acute coronary syndrome: the OPTA project

    Expert Review of Cardiovascular Therapy, Vol. 21, Núm. 6, pp. 373-378

  9. Genetic counselling and testing in pulmonary arterial hypertension: a consensus statement on behalf of the International Consortium for Genetic Studies in PAH

    European Respiratory Journal, Vol. 61, Núm. 2

  10. Map of use of parenteral analgesic admixtures in Spain. MEDPAIN project

    Farmacia Hospitalaria, Vol. 47, Núm. 4, pp. 161-167

  11. NGS Custom Panel Implementation in Patients with Non-Syndromic Autism Spectrum Disorders in the Clinical Routine of a Tertiary Hospital

    Genes, Vol. 14, Núm. 11

  12. Systematic influenza screening in cardiac intensive care units during the influenza season: A prospective study in Spain

    International Journal of Infectious Diseases, Vol. 136, pp. 37-42