CLINICAL PEDIATRICS AND RARE DISEASES
Hospital Universitari de Bellvitge
l'Hospitalet de Llobregat, EspañaPublications in collaboration with researchers from Hospital Universitari de Bellvitge (14)
2024
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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
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Increased Severity of Mycoplasma pneumoniae Infections in Spanish Children
Pediatric Infectious Disease Journal
2023
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Immunisation schedule of the Spanish Association of Paediatrics: 2023 Recommendations
Anales de Pediatria, Vol. 98, Núm. 1, pp. 58.e1-58.e10
2022
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Immunisation schedule of the Pediatric Spanish Association: 2022 recommendations
Anales de Pediatria, Vol. 96, Núm. 1, pp. 59.e1-59.e10
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Incidence and Prevalence of Children's Diffuse Lung Disease in Spain
Archivos de Bronconeumologia, Vol. 58, Núm. 1, pp. 22-29
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Multicentre study of magnet ingestion in Spanish paediatric emergency departments
Anales de Pediatria, Vol. 97, Núm. 5, pp. 310-316
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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
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Recommendations for the diagnosis and practical management of paediatric eosinophilic oesophagitis
Anales de Pediatria, Vol. 92, Núm. 6, pp. 376.e1-376.e10
2019
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Parkinsonism and spastic paraplegia type 7: Expanding the spectrum of mitochondrial Parkinsonism
Movement Disorders, Vol. 34, Núm. 10, pp. 1547-1561
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Reply to: “Mitochondrial Parkinsonism due to SPG7/Paraplegin variants with secondary mtDNA depletion”
Movement Disorders
2013
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A novel form of human disease
Prion Biology: Research and Advances (Apple Academic Press), pp. 179-210
2012
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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
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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
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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