INSTITUTO UNIVERSITARIO DE INTEGRACIÓN EN LA COMUNIDAD
Institut
University of Edinburgh
Edimburgo, Reino UnidoPublikationen in Zusammenarbeit mit Forschern von University of Edinburgh (13)
2023
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Randomised trial of genetic testing and targeted intervention to prevent the development and progression of Paget’s disease of bone
Annals of the Rheumatic Diseases, Vol. 83, Núm. 4, pp. 529-536
2020
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Characteristics of Early Paget's Disease in SQSTM1 Mutation Carriers: Baseline Analysis of the ZiPP Study Cohort
Journal of Bone and Mineral Research, Vol. 35, Núm. 7, pp. 1246-1252
2019
2018
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Evaluating Sex and Age Differences in ADI-R and ADOS Scores in a Large European Multi-site Sample of Individuals with Autism Spectrum Disorder
Journal of Autism and Developmental Disorders, Vol. 48, Núm. 7, pp. 2490-2505
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Identification of a novel locus on chromosome 2q13, which predisposes to clinical vertebral fractures independently of bone density
Annals of the rheumatic diseases, Vol. 77, Núm. 3, pp. 378-385
2017
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Attitudes of the autism community to early autism research
Autism
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Bisphosphonates for Paget's disease of bone in adults
Cochrane Database of Systematic Reviews, Vol. 2017, Núm. 12
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Clinical and Genetic Advances in Paget’s Disease of Bone: a Review
Clinical Reviews in Bone and Mineral Metabolism, Vol. 15, Núm. 1, pp. 37-48
2016
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Use of early intervention for young children with autism spectrum disorder across Europe
Autism, Vol. 20, Núm. 2, pp. 233-249
2013
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Common susceptibility alleles and SQSTM1 mutations predict disease extent and severity in a multinational study of patients with Paget's disease
Journal of Bone and Mineral Research, Vol. 28, Núm. 11, pp. 2338-2346
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Epidemiology of Paget's disease of bone: A systematic review and meta-analysis of secular changes
Bone, Vol. 55, Núm. 2, pp. 347-352
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Secular changes in Paget's disease: Contrasting changes in the number of new referrals and in disease severity in two neighboring regions of Spain
Osteoporosis International, Vol. 24, Núm. 2, pp. 443-450
2010
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Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone
Nature Genetics, Vol. 42, Núm. 6, pp. 520-524