Publications en collaboration avec des chercheurs de Hospital Universitari de Bellvitge (14)

2024

  1. Haemoglobinopathies and other rare anemias in Spain: ten years of a nationwide registry (REHem-AR)

    Annals of Hematology, Vol. 103, Núm. 8, pp. 2743-2755

  2. Increased Severity of Mycoplasma pneumoniae Infections in Spanish Children

    Pediatric Infectious Disease Journal

2023

  1. Immunisation schedule of the Spanish Association of Paediatrics: 2023 Recommendations

    Anales de Pediatria, Vol. 98, Núm. 1, pp. 58.e1-58.e10

2022

  1. Immunisation schedule of the Pediatric Spanish Association: 2022 recommendations

    Anales de Pediatria, Vol. 96, Núm. 1, pp. 59.e1-59.e10

  2. Incidence and Prevalence of Children's Diffuse Lung Disease in Spain

    Archivos de Bronconeumologia, Vol. 58, Núm. 1, pp. 22-29

  3. Multicentre study of magnet ingestion in Spanish paediatric emergency departments

    Anales de Pediatria, Vol. 97, Núm. 5, pp. 310-316

  4. Usefulness of lung ultrasound in the diagnosis and follow-up of respiratory diseases in neonates

    Anales de Pediatria, Vol. 96, Núm. 3, pp. 252.e1-252.e13

2020

  1. Recommendations for the diagnosis and practical management of paediatric eosinophilic oesophagitis

    Anales de Pediatria, Vol. 92, Núm. 6, pp. 376.e1-376.e10

2019

  1. Parkinsonism and spastic paraplegia type 7: Expanding the spectrum of mitochondrial Parkinsonism

    Movement Disorders, Vol. 34, Núm. 10, pp. 1547-1561

  2. Reply to: “Mitochondrial Parkinsonism due to SPG7/Paraplegin variants with secondary mtDNA depletion”

    Movement Disorders

2013

  1. A novel form of human disease

    Prion Biology: Research and Advances (Apple Academic Press), pp. 179-210

2012

  1. Coexistence of protease sensitive and resistant prion protein in 129VV homozygous sporadic Creutzfeldt-Jakob disease: A case report

    Journal of Medical Case Reports, Vol. 6

2010

  1. A Novel PRNP Y218N mutation in gerstmann-sträussler-scheinker disease with neurofibrillary degeneration

    Journal of Neuropathology and Experimental Neurology, Vol. 69, Núm. 8, pp. 789-800

  2. Somatic mosaicism in a case of apparently sporadic Creutzfeldt-Jakob disease carrying a de novo D178N mutation in the PRNP gene

    American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, Vol. 153, Núm. 7, pp. 1283-1291