Expanding the Allelic and Clinical Heterogeneity of Movement Disorders Linked to Defects of Mitochondrial Adenosine Triphosphate Synthase.
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| Title: | Expanding the Allelic and Clinical Heterogeneity of Movement Disorders Linked to Defects of Mitochondrial Adenosine Triphosphate Synthase. |
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| Authors: | Harrer P; Institute of Human Genetics, School of Medicine and Health, Technical University of Munich, Munich, Germany.; Institute of Neurogenomics, Helmholtz Zentrum München, Munich, Germany., Krygier M; Department of Developmental Neurology, Medical University of Gdansk, Gdansk, Poland., Krenn M; Department of Neurology, Medical University of Vienna, Vienna, Austria.; Comprehensive Center for Clinical Neurosciences & Mental Health, Medical University of Vienna, Vienna, Austria., Kittke V; Institute of Human Genetics, School of Medicine and Health, Technical University of Munich, Munich, Germany.; Institute of Neurogenomics, Helmholtz Zentrum München, Munich, Germany., Danis M; Neurological Clinic of Faculty Hospital Trnava and Slovak Health University Bratislava, Bratislava, Slovakia., Krastev G; Neurological Clinic of Faculty Hospital Trnava and Slovak Health University Bratislava, Bratislava, Slovakia., Saparov A; Institute of Human Genetics, School of Medicine and Health, Technical University of Munich, Munich, Germany.; Institute of Neurogenomics, Helmholtz Zentrum München, Munich, Germany.; Institute for Advanced Study, Technical University of Munich, Garching, Germany., Pichon V; CRMR Neurogenetique, Service de Neurologie, Centre Hospitalier, Universitaire d'Angers, Angers, France., Malbos M; CRMRs 'Anomalies du Développement et syndromes malformatifs' et 'Déficiences Intellectuelles de causes rares,' FHU-TRANSLAD, CHU Dijon Bourgogne, Dijon, France.; Laboratoire de Génomique Médicale, UF Innovation en diagnostic génomique des maladies rares, CHU Dijon Bourgogne, Dijon, France., Scherer C; CRMR Neurogenetique, Service de Neurologie, Centre Hospitalier, Universitaire d'Angers, Angers, France., Dzinovic I; Institute of Human Genetics, School of Medicine and Health, Technical University of Munich, Munich, Germany.; Institute of Neurogenomics, Helmholtz Zentrum München, Munich, Germany., Skorvanek M; Department of Neurology, P.J. Safarik University, Kosice, Slovakia.; Department of Neurology, University Hospital of L. Pasteur, Kosice, Slovakia., Kopajtich R; Institute of Human Genetics, School of Medicine and Health, Technical University of Munich, Munich, Germany.; Institute of Neurogenomics, Helmholtz Zentrum München, Munich, Germany., Prokisch H; Institute of Human Genetics, School of Medicine and Health, Technical University of Munich, Munich, Germany.; Institute of Neurogenomics, Helmholtz Zentrum München, Munich, Germany., Silvaieh S; Department of Neurology, Medical University of Vienna, Vienna, Austria.; Comprehensive Center for Clinical Neurosciences & Mental Health, Medical University of Vienna, Vienna, Austria., Grisold A; Department of Neurology, Medical University of Vienna, Vienna, Austria.; Comprehensive Center for Clinical Neurosciences & Mental Health, Medical University of Vienna, Vienna, Austria., Mazurkiewicz-Bełdzińska M; Department of Developmental Neurology, Medical University of Gdansk, Gdansk, Poland., de Sainte Agathe JM; Department of Medical Genetics, Sorbonne Université, AP-HP Sorbonne Université, Paris, France.; Laboratoire de Biologie Médicale Multi-Site SeqOIA, Sorbonne Université, Paris, France., Winkelmann J; Institute of Human Genetics, School of Medicine and Health, Technical University of Munich, Munich, Germany.; Institute of Neurogenomics, Helmholtz Zentrum München, Munich, Germany.; DZPG (German Center for Mental Health), Munich, Germany.; Munich Cluster for Systems Neurology, SyNergy, Munich, Germany., Necpal J; Department of Neurology, Zvolen Hospital, Zvolen, Slovakia.; Parkinsonism and Movement Disorders Treatment Center, Zvolen Hospital, Zvolen, Slovakia., Jech R; Department of Neurology and Center of Clinical Neuroscience, First Faculty of Medicine Charles University and General University Hospital in Prague, Prague, Czech Republic., Zech M; Institute of Human Genetics, School of Medicine and Health, Technical University of Munich, Munich, Germany.; Institute of Neurogenomics, Helmholtz Zentrum München, Munich, Germany.; Institute for Advanced Study, Technical University of Munich, Garching, Germany. |
| Source: | Movement disorders : official journal of the Movement Disorder Society [Mov Disord] 2025 Jul; Vol. 40 (7), pp. 1388-1400. Date of Electronic Publication: 2025 Apr 25. |
| Publication Type: | Journal Article; Case Reports |
| Journal Info: | Publisher: Wiley-Liss Country of Publication: United States NLM ID: 8610688 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1531-8257 (Electronic) Linking ISSN: 08853185 NLM ISO Abbreviation: Mov Disord Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 40276935 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Expanding the Allelic and Clinical Heterogeneity of Movement Disorders Linked to Defects of Mitochondrial Adenosine Triphosphate Synthase. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Harrer+P%22">Harrer P</searchLink>; Institute of Human Genetics, School of Medicine and Health, Technical University of Munich, Munich, Germany.; Institute of Neurogenomics, Helmholtz Zentrum München, Munich, Germany.<br /><searchLink fieldCode="AU" term="%22Krygier+M%22">Krygier M</searchLink>; Department of Developmental Neurology, Medical University of Gdansk, Gdansk, Poland.<br /><searchLink fieldCode="AU" term="%22Krenn+M%22">Krenn M</searchLink>; Department of Neurology, Medical University of Vienna, Vienna, Austria.; Comprehensive Center for Clinical Neurosciences & Mental Health, Medical University of Vienna, Vienna, Austria.<br /><searchLink fieldCode="AU" term="%22Kittke+V%22">Kittke V</searchLink>; Institute of Human Genetics, School of Medicine and Health, Technical University of Munich, Munich, Germany.; Institute of Neurogenomics, Helmholtz Zentrum München, Munich, Germany.<br /><searchLink fieldCode="AU" term="%22Danis+M%22">Danis M</searchLink>; Neurological Clinic of Faculty Hospital Trnava and Slovak Health University Bratislava, Bratislava, Slovakia.<br /><searchLink fieldCode="AU" term="%22Krastev+G%22">Krastev G</searchLink>; Neurological Clinic of Faculty Hospital Trnava and Slovak Health University Bratislava, Bratislava, Slovakia.<br /><searchLink fieldCode="AU" term="%22Saparov+A%22">Saparov A</searchLink>; Institute of Human Genetics, School of Medicine and Health, Technical University of Munich, Munich, Germany.; Institute of Neurogenomics, Helmholtz Zentrum München, Munich, Germany.; Institute for Advanced Study, Technical University of Munich, Garching, Germany.<br /><searchLink fieldCode="AU" term="%22Pichon+V%22">Pichon V</searchLink>; CRMR Neurogenetique, Service de Neurologie, Centre Hospitalier, Universitaire d'Angers, Angers, France.<br /><searchLink fieldCode="AU" term="%22Malbos+M%22">Malbos M</searchLink>; CRMRs 'Anomalies du Développement et syndromes malformatifs' et 'Déficiences Intellectuelles de causes rares,' FHU-TRANSLAD, CHU Dijon Bourgogne, Dijon, France.; Laboratoire de Génomique Médicale, UF Innovation en diagnostic génomique des maladies rares, CHU Dijon Bourgogne, Dijon, France.<br /><searchLink fieldCode="AU" term="%22Scherer+C%22">Scherer C</searchLink>; CRMR Neurogenetique, Service de Neurologie, Centre Hospitalier, Universitaire d'Angers, Angers, France.<br /><searchLink fieldCode="AU" term="%22Dzinovic+I%22">Dzinovic I</searchLink>; Institute of Human Genetics, School of Medicine and Health, Technical University of Munich, Munich, Germany.; Institute of Neurogenomics, Helmholtz Zentrum München, Munich, Germany.<br /><searchLink fieldCode="AU" term="%22Skorvanek+M%22">Skorvanek M</searchLink>; Department of Neurology, P.J. 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Pasteur, Kosice, Slovakia.<br /><searchLink fieldCode="AU" term="%22Kopajtich+R%22">Kopajtich R</searchLink>; Institute of Human Genetics, School of Medicine and Health, Technical University of Munich, Munich, Germany.; Institute of Neurogenomics, Helmholtz Zentrum München, Munich, Germany.<br /><searchLink fieldCode="AU" term="%22Prokisch+H%22">Prokisch H</searchLink>; Institute of Human Genetics, School of Medicine and Health, Technical University of Munich, Munich, Germany.; Institute of Neurogenomics, Helmholtz Zentrum München, Munich, Germany.<br /><searchLink fieldCode="AU" term="%22Silvaieh+S%22">Silvaieh S</searchLink>; Department of Neurology, Medical University of Vienna, Vienna, Austria.; Comprehensive Center for Clinical Neurosciences & Mental Health, Medical University of Vienna, Vienna, Austria.<br /><searchLink fieldCode="AU" term="%22Grisold+A%22">Grisold A</searchLink>; Department of Neurology, Medical University of Vienna, Vienna, Austria.; Comprehensive Center for Clinical Neurosciences & Mental Health, Medical University of Vienna, Vienna, Austria.<br /><searchLink fieldCode="AU" term="%22Mazurkiewicz-Bełdzińska+M%22">Mazurkiewicz-Bełdzińska M</searchLink>; Department of Developmental Neurology, Medical University of Gdansk, Gdansk, Poland.<br /><searchLink fieldCode="AU" term="%22de+Sainte+Agathe+JM%22">de Sainte Agathe JM</searchLink>; Department of Medical Genetics, Sorbonne Université, AP-HP Sorbonne Université, Paris, France.; Laboratoire de Biologie Médicale Multi-Site SeqOIA, Sorbonne Université, Paris, France.<br /><searchLink fieldCode="AU" term="%22Winkelmann+J%22">Winkelmann J</searchLink>; Institute of Human Genetics, School of Medicine and Health, Technical University of Munich, Munich, Germany.; Institute of Neurogenomics, Helmholtz Zentrum München, Munich, Germany.; DZPG (German Center for Mental Health), Munich, Germany.; Munich Cluster for Systems Neurology, SyNergy, Munich, Germany.<br /><searchLink fieldCode="AU" term="%22Necpal+J%22">Necpal J</searchLink>; Department of Neurology, Zvolen Hospital, Zvolen, Slovakia.; Parkinsonism and Movement Disorders Treatment Center, Zvolen Hospital, Zvolen, Slovakia.<br /><searchLink fieldCode="AU" term="%22Jech+R%22">Jech R</searchLink>; Department of Neurology and Center of Clinical Neuroscience, First Faculty of Medicine Charles University and General University Hospital in Prague, Prague, Czech Republic.<br /><searchLink fieldCode="AU" term="%22Zech+M%22">Zech M</searchLink>; Institute of Human Genetics, School of Medicine and Health, Technical University of Munich, Munich, Germany.; Institute of Neurogenomics, Helmholtz Zentrum München, Munich, Germany.; Institute for Advanced Study, Technical University of Munich, Garching, Germany. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%228610688%22">Movement disorders : official journal of the Movement Disorder Society</searchLink> [Mov Disord] 2025 Jul; Vol. 40 (7), pp. 1388-1400. <i>Date of Electronic Publication: </i>2025 Apr 25. – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article; Case Reports – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Wiley-Liss%22">Wiley-Liss </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>8610688 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1531-8257 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2208853185%22">08853185 </searchLink><i>NLM ISO Abbreviation: </i>Mov Disord <i>Subsets: </i>MEDLINE |
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| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1002/mds.30209 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 1388 Titles: – TitleFull: Expanding the Allelic and Clinical Heterogeneity of Movement Disorders Linked to Defects of Mitochondrial Adenosine Triphosphate Synthase. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Harrer P – PersonEntity: Name: NameFull: Krygier M – PersonEntity: Name: NameFull: Krenn M – PersonEntity: Name: NameFull: Kittke V – PersonEntity: Name: NameFull: Danis M – PersonEntity: Name: NameFull: Krastev G – PersonEntity: Name: NameFull: Saparov A – PersonEntity: Name: NameFull: Pichon V – PersonEntity: Name: NameFull: Malbos M – PersonEntity: Name: NameFull: Scherer C – PersonEntity: Name: NameFull: Dzinovic I – PersonEntity: Name: NameFull: Skorvanek M – PersonEntity: Name: NameFull: Kopajtich R – PersonEntity: Name: NameFull: Prokisch H – PersonEntity: Name: NameFull: Silvaieh S – PersonEntity: Name: NameFull: Grisold A – PersonEntity: Name: NameFull: Mazurkiewicz-Bełdzińska M – PersonEntity: Name: NameFull: de Sainte Agathe JM – PersonEntity: Name: NameFull: Winkelmann J – PersonEntity: Name: NameFull: Necpal J – PersonEntity: Name: NameFull: Jech R – PersonEntity: Name: NameFull: Zech M IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 07 Text: 2025 Jul Type: published Y: 2025 Identifiers: – Type: issn-electronic Value: 1531-8257 Numbering: – Type: volume Value: 40 – Type: issue Value: 7 Titles: – TitleFull: Movement disorders : official journal of the Movement Disorder Society Type: main |
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