Differences in Motor Features of
Journal
Neurology
ISSN: 1526-632X
Titre abrégé: Neurology
Pays: United States
ID NLM: 0401060
Informations de publication
Date de publication:
13 Sep 2022
13 Sep 2022
Historique:
received:
02
11
2021
accepted:
02
05
2022
pubmed:
6
7
2022
medline:
14
10
2022
entrez:
5
7
2022
Statut:
ppublish
Résumé
Familial frontotemporal lobar degeneration (f-FTLD) is a phenotypically heterogeneous spectrum of neurodegenerative disorders most often caused by variants within chromosome 9 open reading frame 72 ( We screened the Advancing Research and Treatment in Frontotemporal Lobar Degeneration (ARTFL)/Longitudinal Evaluation of Familial Frontotemporal Dementia Subjects (LEFFTDS)/ARTFL LEFFTDS Longitudinal Frontotemporal Lobar Degeneration Consortium for symptomatic carriers of pathogenic variants in We identified 184 symptomatic participants who had a single pathogenic variant in We present a large comparative study of motor features in NCT02365922, NCT02372773, and NCT04363684.
Sections du résumé
BACKGROUND AND OBJECTIVES
Familial frontotemporal lobar degeneration (f-FTLD) is a phenotypically heterogeneous spectrum of neurodegenerative disorders most often caused by variants within chromosome 9 open reading frame 72 (
METHODS
We screened the Advancing Research and Treatment in Frontotemporal Lobar Degeneration (ARTFL)/Longitudinal Evaluation of Familial Frontotemporal Dementia Subjects (LEFFTDS)/ARTFL LEFFTDS Longitudinal Frontotemporal Lobar Degeneration Consortium for symptomatic carriers of pathogenic variants in
RESULTS
We identified 184 symptomatic participants who had a single pathogenic variant in
DISCUSSION
We present a large comparative study of motor features in
TRIAL REGISTRATION INFORMATION
NCT02365922, NCT02372773, and NCT04363684.
Identifiants
pubmed: 35790423
pii: WNL.0000000000200860
doi: 10.1212/WNL.0000000000200860
pmc: PMC9536745
doi:
Substances chimiques
C9orf72 Protein
0
C9orf72 protein, human
0
GRN protein, human
0
Granulins
0
MAPT protein, human
0
Progranulins
0
tau Proteins
0
Banques de données
ClinicalTrials.gov
['NCT04363684', 'NCT02365922', 'NCT02372773']
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Langues
eng
Sous-ensembles de citation
IM
Pagination
e1154-e1167Subventions
Organisme : NIA NIH HHS
ID : K24 AG045333
Pays : United States
Organisme : NIA NIH HHS
ID : U19 AG063911
Pays : United States
Organisme : NIA NIH HHS
ID : P30 AG062422
Pays : United States
Organisme : NIA NIH HHS
ID : P50 AG023501
Pays : United States
Organisme : NIA NIH HHS
ID : P01 AG019724
Pays : United States
Organisme : NINDS NIH HHS
ID : U54 NS092089
Pays : United States
Organisme : NIA NIH HHS
ID : P30 AG066509
Pays : United States
Organisme : NIA NIH HHS
ID : P30 AG072977
Pays : United States
Organisme : NIA NIH HHS
ID : U01 AG045390
Pays : United States
Informations de copyright
© 2022 American Academy of Neurology.
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