Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Cognitive impairment in myotonic dystrophy type 1 (DM1): a longitudinal follow-up study.

Journal of neurology - 1 Nov 2008

Modoni A, Silvestri G, Vita M Gabriella, Quaranta D, Tonali P A, Marra C

Abstract excerpt

OBJECTIVE: To characterize the progression of the cognitive involvement in patients affected by myotonic dystrophy type 1 (DM1) by a longitudinal neuropsychological follow-up study. METHODS: In a previous study we documented an ageing-related decline of frontal and temporal cognitive functions in juvenile/adult forms of DM1, irrespectively of the n(CTG) in leukocytes and the severity of muscle weakness. Here we...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Aging
Share to Cognition Disorders
Share to Language Disorders

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Leukocytes

Share to Longitudinal Studies

Share to Multivariate Analysis

Share to Myotonic Dystrophy

Share to Neuropsychological Tests

Source

Identifiers

PMID: 18821050
DOI: 10.1007/s00415-008-0017-5

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Cognitive impairment in myotonic dystrophy type 1 (DM1): a longitudinal follow-up study.PMID 18821050Read ↗

Cognitive phenotype of childhood myotonic dystrophy type 1: A multicenter pooled analysis.Semantic proximity Read ↗

Clusters of cognitive impairment among different phenotypes of myotonic dystrophy type 1 and type 2.Semantic proximity Read ↗

Cognitive impairment and (CTG)n expansion in myotonic dystrophy patientsSemantic proximity Read ↗

Cognitive function in myotonic dystrophy: a follow-up study.Semantic proximity Read ↗

Comparisons of intellectual capacities between mild and classic adult-onset phenotypes of myotonic dystrophy type 1 (DM1).Semantic proximity Read ↗

Congenital muscular dystrophies with cognitive impairment. A population study.Semantic proximity Read ↗

Longitudinal data of neuropsychological profile in a cohort of Duchenne muscular dystrophy boys without cognitive impairment.Semantic proximity Read ↗

Cognitive impairment in the preclinical stage of dementia in FTD-3 CHMP2B mutation carriers: a longitudinal prospective study.Semantic proximity Read ↗

Neuropsychological profile of adult patients with Niemann-Pick C1 (NPC1) mutations.Semantic proximity Read ↗

Variant repeats within the DMPK CTG expansion protect function in myotonic dystrophy type 1Semantic proximity Read ↗

Neuropsychological impairments and the impact of dystrophin mutations on general cognitive functioning of patients with Duchenne muscular dystrophy.Semantic proximity Read ↗

Neuropathology does not Correlate with Regional Differences in the Extent of Expansion of CTG Repeats in the Brain with Myotonic Dystrophy Type 1Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.