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Atypical presentations of DYT1 dystonia with acute craniocervical onset.
Parkinsonism Relat. Disord. 83, 54-55 (2021)
DYT1 gene mutations lead to early-onset dystonia that begins with focal limb onset and spreads to other body regions within 5 years, with typical sparing of the oromandibular muscles. In the present study, we describe two patients with an unusual presentation of the disease.
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4.891
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Anmerkungen
Besondere Publikation
Auf Hompepage verbergern
Publikationstyp
Artikel: Journalartikel
Dokumenttyp
Wissenschaftlicher Artikel
Schlagwörter
Acute Onset ; Acute-onset Dystonia ; Atypical Dyt1 ; Dyt1 ; Rapid-onset Dystonia ; Tor1a; Phenotypes
Sprache
englisch
Veröffentlichungsjahr
2021
HGF-Berichtsjahr
2021
ISSN (print) / ISBN
1353-8020
e-ISSN
1873-5126
Zeitschrift
Parkinsonism & Related Disorders
Quellenangaben
Band: 83,
Seiten: 54-55
Verlag
Elsevier
Verlagsort
The Boulevard, Langford Lane, Kidlington, Oxford Ox5 1gb, Oxon, England
Begutachtungsstatus
Peer reviewed
Institut(e)
Institute of Neurogenomics (ING)
POF Topic(s)
30205 - Bioengineering and Digital Health
Forschungsfeld(er)
Genetics and Epidemiology
PSP-Element(e)
G-503200-001
Förderungen
Helmholtz Center Munich, Germany
Helmholtz Zentrum Munchen, Munich, Germany
Technische Universitat Munchen, Munich, Germany
Czech Ministry of Education
MH CZ - DRO University Hospital Motol
Ministry of Health of the Czech Republic (AZV)
Slovak Research and Development Agency
Helmholtz Zentrum Munchen, Munich, Germany
Technische Universitat Munchen, Munich, Germany
Czech Ministry of Education
MH CZ - DRO University Hospital Motol
Ministry of Health of the Czech Republic (AZV)
Slovak Research and Development Agency
WOS ID
WOS:000631818800011
Scopus ID
85100166660
PubMed ID
33476878
Erfassungsdatum
2021-02-09