Dystonia in ATP Synthase Defects: Reconnecting Mitochondria and Dopamine.

Indelicato, Elisabetta; Boesch, Sylvia; Mencacci, Niccolo' E; Ghezzi, Daniele; Prokisch, Holger; Winkelmann, Juliane; Zech, Michael

Indelicato, Elisabetta; Boesch, Sylvia; Mencacci, Niccolo' E; Ghezzi, Daniele; Prokisch, Holger; Winkelmann, Juliane; Zech, Michael.

Afiliación

Indelicato E; Center for Rare Movement Disorders Innsbruck, Department of Neurology, Medical University Innsbruck, Innsbruck, Austria.
Boesch S; Institute of Neurogenomics, Helmholtz Munich, Neuherberg, Germany.
Mencacci NE; Institute of Human Genetics, Technical University of Munich, School of Medicine, Munich, Germany.
Ghezzi D; Center for Rare Movement Disorders Innsbruck, Department of Neurology, Medical University Innsbruck, Innsbruck, Austria.
Prokisch H; Ken and Ruth Davee Department of Neurology and Simpson Querrey Center for Neurogenetics, Northwestern University, Feinberg School of Medicine, Chicago, Illinois, USA.
Winkelmann J; Unit of Medical Genetics and Neurogenetics, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
Zech M; Department of Pathophysiology and Transplantation (DEPT), University of Milan, Milan, Italy.

Mov Disord ; 39(1): 29-35, 2024 Jan.

Article en En | MEDLINE | ID: mdl-37964479

Asunto(s)

Distonía; Trastornos Distónicos; Humanos; Dopamina; Mitocondrias; Trastornos Distónicos/genética; Adenosina Trifosfato

Palabras clave

ATP synthase; dystonia; mitochondrial diseases; movement disorder

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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Trastornos Distónicos / Distonía Límite: Humans Idioma: En Revista: Mov Disord Asunto de la revista: NEUROLOGIA Año: 2024 Tipo del documento: Article País de afiliación: Austria

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