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

Non-dystrophic myotonia: 2-year clinical and patient reported outcomes.

Muscle & nerve - 1 Aug 2022

Fullam Timothy R, Chandrashekhar Swathy, Farmakidis Constantine, Jawdat Omar, Pasnoor Mamatha, Dimachkie Mazen M, Statland Jeffrey M

Abstract excerpt

INTRODUCTION/AIMS: Consistency of differences between non-dystrophic myotonias over time measured by standardized clinical/patient-reported outcomes is lacking. Evaluation of longitudinal data could establish clinically relevant endpoints for future research. METHODS: Data from prospective observational study of 95 definite/clinically suspected non-dystrophic myotonia participants (six sites in the United States,...

Read the complete abstract on PubMed

Topics

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

Share to Channelopathies
Share to Chloride Channels

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Hand Strength

Share to Myotonia

Share to Myotonia Congenita

Share to Myotonic Dystrophy

Share to NAV1.4 Voltage-Gated Sodium Channel

Share to Patient Reported Outcome Measures

Source

Open in PubMed Open full text

Identifiers

PMID: 35644941
DOI: 10.1002/mus.27649
PMCID: PMC9308727

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Non-dystrophic myotonia: 2-year clinical and patient reported outcomes.PMID 35644941Read ↗

Non-dystrophic myotonia: prospective study of objective and patient reported outcomes.Semantic proximity Read ↗

Core Clinical Phenotypes in Myotonic DystrophiesSemantic proximity Read ↗

Redefining the clinical phenotypes of non-dystrophic myotonic syndromes.Semantic proximity Read ↗

Data from the European registry for patients with McArdle disease and other muscle glycogenoses (EUROMAC)Semantic proximity Read ↗

Primary mitochondrial myopathy: 12-month follow-up results of an Italian cohortSemantic proximity Read ↗

Long-term Evaluation Parameters in GNE Myopathy: A Five-year Observational Follow-up Natural History StudySemantic proximity Read ↗

Diagnosis and Management of Myotonic Dystrophy Type 1.Semantic proximity Read ↗

Exploring Outcome Measures for Mitochondrial Myopathies; Insights From a Longitudinal Study on TK2 Deficiency.Semantic proximity Read ↗

The myotubular and centronuclear myopathy patient registry: a multifunctional tool for translational research.Semantic proximity Read ↗

Non-dystrophic myotonias: clinical and mutation spectrum of 70 German patients.Semantic proximity Read ↗

A quantitative measure of handgrip myotonia in non-dystrophic myotonia.Semantic proximity Read ↗

Andersen-Tawil syndrome.Semantic proximity Read ↗

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