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Systemic immune profile in Prader-Willi syndrome: elevated matrix metalloproteinase and myeloperoxidase and reduced macrophage inhibitory factor.
Hope, Sigrun; Nærland, Terje; Olav Kolset, Svein; Ueland, Thor; Andreassen, Ole A; Nordstrøm, Marianne.
Afiliación
  • Hope S; K.G. Jebsen Centre for Neurodevelopmental disorders, Institute of Clinical Medicine, University of Oslo, Oslo, Norway. sigrun.hope@ous-hf.no.
  • Nærland T; Department of Neurohabilitation, Division of Clinical Neuroscience, Oslo University Hospital, Oslo, Norway. sigrun.hope@ous-hf.no.
  • Olav Kolset S; Nevsom, Department of Rare Diagnoses and Disabilities, Pediatric and Adolescent Medicine, Oslo University Hospital, Oslo, Norway. sigrun.hope@ous-hf.no.
  • Ueland T; K.G. Jebsen Centre for Neurodevelopmental disorders, Institute of Clinical Medicine, University of Oslo, Oslo, Norway.
  • Andreassen OA; Nevsom, Department of Rare Diagnoses and Disabilities, Pediatric and Adolescent Medicine, Oslo University Hospital, Oslo, Norway.
  • Nordstrøm M; Department of Nutrition, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway.
Orphanet J Rare Dis ; 18(1): 185, 2023 07 10.
Article en En | MEDLINE | ID: mdl-37430349

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndrome de Prader-Willi / Enfermedades Cardiovasculares Tipo de estudio: Observational_studies / Prevalence_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Orphanet J Rare Dis Asunto de la revista: MEDICINA Año: 2023 Tipo del documento: Article País de afiliación: Noruega Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndrome de Prader-Willi / Enfermedades Cardiovasculares Tipo de estudio: Observational_studies / Prevalence_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Orphanet J Rare Dis Asunto de la revista: MEDICINA Año: 2023 Tipo del documento: Article País de afiliación: Noruega Pais de publicación: Reino Unido