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dc.contributorVall d'Hebron Barcelona Hospital Campus
dc.contributor.authorDe Giorgis, Valentina
dc.contributor.authorBhatia, Kailash
dc.contributor.authorboespflug-tanguy, odile
dc.contributor.authorgras, domitille
dc.contributor.authorDella Marina, Adela
dc.contributor.authorDesurkar, Archana
dc.contributor.authorToledo, Manuel
dc.date.accessioned2024-10-01T09:56:26Z
dc.date.available2024-10-01T09:56:26Z
dc.date.issued2024-08
dc.identifier.citationDe Giorgis V, Bhatia KP, Boespflug-Tanguy O, Gras D, Marina AD, Desurkar A, et al. Triheptanoin Did Not Show Benefit versus Placebo for the Treatment of Paroxysmal Movement Disorders in Glut1 Deficiency Syndrome: Results of a Randomized Phase 3 Study. Mov Disord. 2024 Aug;39(8):1386–96.
dc.identifier.issn1531-8257
dc.identifier.urihttps://hdl.handle.net/11351/11994
dc.descriptionSíndrome de deficiencia del transportador de glucosa tipo 1; Trastorno del movimiento paroxístico; Triheptanoína
dc.language.isoeng
dc.publisherWiley
dc.relation.ispartofseriesMovement Disorders;39(8)
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.sourceScientia
dc.subjectTrastorns motors - Tractament
dc.subjectTriglicèrids - Ús terapèutic
dc.subjectMetabolisme, Errors congènits del
dc.subject.meshMovement Disorders
dc.subject.mesh/drug therapy
dc.subject.meshTriglycerides
dc.subject.meshGlucose Transporter Type 1
dc.subject.mesh/deficiency
dc.titleTriheptanoin Did Not Show Benefit versus Placebo for the Treatment of Paroxysmal Movement Disorders in Glut1 Deficiency Syndrome: Results of a Randomized Phase 3 Study
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1002/mds.29822
dc.subject.decstrastornos del movimiento
dc.subject.decs/farmacoterapia
dc.subject.decstriglicéridos
dc.subject.decstransportador de glucosa de tipo 1
dc.subject.decs/deficiencia
dc.relation.publishversionhttps://doi.org/10.1002/mds.29822
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dc.audienceProfessionals
dc.contributor.organismesInstitut Català de la Salut
dc.contributor.authoraffiliation[De Giorgis V] Department of Child Neurology and Psychiatry, Mondino Foundation, Pavia, Italy. [Bhatia KP] Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology, National Hospital for Neurology and Neurosurgery, Queen Square, London, United Kingdom. [Boespflug-Tanguy O, Gras D] Service de Neurologie Pédiatrique, Centre de Référence Leucodystrophies et Leucoencephalopathies de Cause Rare (LEUKOFRANCE), APHP Robert-Debré, Paris, France. [Marina AD] Department of Pediatric Neurology, Centre for Neuromuscular Disorders, Centre for Translational Neuro- and Behavioral Sciences, University Hospital Essen, University Duisburg-Essen, Essen, Germany. [Desurkar A] Neurology Department, Sheffield Children’s National Health Service Foundation Trust, Sheffield, United Kingdom. [Toledo M] Unitat d’Epilèpsia, Servei de Neurologia, Vall d’Hebron Hospital Universitari, Barcelona, Spain
dc.identifier.pmid38725190
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess


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