(Q87411199)

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Myotonic dystrophy

scientific article published on 06 June 2014

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scholarly article

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9 March 2020

Myotonic dystrophy (English)

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9 March 2020

author name string

Charles A Thornton

1

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9 March 2020

publication date

6 June 2014

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9 March 2020

Neurologic Clinics

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9 March 2020

32

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9 March 2020

3

1 reference

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9 March 2020

705-19, viii

1 reference

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9 March 2020

A new window on neurocognitive dysfunction in the childhood form of myotonic dystrophy type 1 (DM1).

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Foci of trinucleotide repeat transcripts in nuclei of myotonic dystrophy cells and tissues

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Somatic instability of CTG repeat in myotonic dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Aberrant regulation of insulin receptor alternative splicing is associated with insulin resistance in myotonic dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Population frequency of myotonic dystrophy: higher than expected frequency of myotonic dystrophy type 2 (DM2) mutation in Finland

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cis and trans effects of the myotonic dystrophy (DM) mutation in a cell culture model

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of the CTG repeat in skeletal muscle of young and adult myotonic dystrophy patients: when does the expansion occur?

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital myotonic dystrophy in Britain. I. Clinical aspects

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Reversal of RNA missplicing and myotonia after muscleblind overexpression in a mouse poly(CUG) model for myotonic dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recruitment of human muscleblind proteins to (CUG)(n) expansions associated with myotonic dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Premutation allele pool in myotonic dystrophy type 2.

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Transcriptome-wide regulation of pre-mRNA splicing and mRNA localization by muscleblind proteins

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Relationship between parental trinucleotide GCT repeat length and severity of myotonic dystrophy in offspring.

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Expansion of a CUG trinucleotide repeat in the 3' untranslated region of myotonic dystrophy protein kinase transcripts results in nuclear retention of transcripts

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mexiletine is an effective antimyotonia treatment in myotonic dystrophy type 1.

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Epidemiology of myotonic dystrophy in Italy: re-apprisal after genetic diagnosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Most expression and splicing changes in myotonic dystrophy type 1 and type 2 skeletal muscle are shared with other muscular dystrophies

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cancer risk among patients with myotonic muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A polysomnographic study of daytime sleepiness in myotonic dystrophy type 1.

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Splicing biomarkers of disease severity in myotonic dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Viral vector producing antisense RNA restores myotonic dystrophy myoblast functions

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Absence of a differentiation defect in muscle satellite cells from DM2 patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member.

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Muscleblind localizes to nuclear foci of aberrant RNA in myotonic dystrophy types 1 and 2.

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Randomized controlled trial of testosterone in myotonic dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A simple ligand that selectively targets CUG trinucleotide repeats and inhibits MBNL protein binding.

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Muscle chloride channel dysfunction in two mouse models of myotonic dystrophy.

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Muscle weakness in myotonic dystrophy associated with misregulated splicing and altered gating of Ca(V)1.1 calcium channel

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ethnic distribution of myotonic dystrophy gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Failure of MBNL1-dependent post-natal splicing transitions in myotonic dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The epidemiology of myotonic dystrophy in Northern Ireland

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The muscleblind gene participates in the organization of Z-bands and epidermal attachments of Drosophila muscles and is regulated by Dmef2.

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Left ventricular dysfunction and cardiac arrhythmias are frequent in type 2 myotonic dystrophy: a case control study.

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Frequency and stability of the myotonic dystrophy type 1 premutation.

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Myotonic dystrophy. Part I. A genealogical study in the northern Transvaal.

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Drug treatment for myotonia

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The brain in myotonic dystrophy 1 and 2: evidence for a predominant white matter disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cognition and adaptive skills in myotonic dystrophy type 1: a study of 55 individuals with congenital and childhood forms.

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Supine changes in lung function correlate with chronic respiratory failure in myotonic dystrophy patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Triplet-repeat oligonucleotide-mediated reversal of RNA toxicity in myotonic dystrophy.

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Muscleblind proteins regulate alternative splicing

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Intergenerational instability of the expanded CTG repeat in the DMPK gene: studies in human gametes and preimplantation embryos

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characteristics of intergenerational contractions of the CTG repeat in myotonic dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Age and causes of death in adult-onset myotonic dystrophy.

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diffusion tensor imaging reveals widespread white matter abnormalities in children and adolescents with myotonic dystrophy type 1.

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prevalence of genetic muscle disease in Northern England: in-depth analysis of a muscle clinic population

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cold extends electromyography distinction between ion channel mutations causing myotonia

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Repeat instability: mechanisms of dynamic mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Daytime sleep in myotonic dystrophy is not caused by sleep apnoea

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Modafinil for the treatment of hypersomnia associated with myotonic muscular dystrophy in adults: a multicenter, prospective, randomized, double-blind, placebo-controlled, 4-week trial

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DM2 intronic expansions: evidence for CCUG accumulation without flanking sequence or effects on ZNF9 mRNA processing or protein expression

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Abnormal liver test results in myotonic dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutant (CCTG)n expansion causes abnormal expression of zinc finger protein 9 (ZNF9) in myotonic dystrophy type 2.

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Intergenerational stability of the myotonic dystrophy protomutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Disruption of splicing regulated by a CUG-binding protein in myotonic dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

From dynamic combinatorial 'hit' to lead: in vitro and in vivo activity of compounds targeting the pathogenic RNAs that cause myotonic dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hypogonadism and erectile dysfunction in myotonic dystrophy type 1.

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Severity, type, and distribution of myotonic discharges are different in type 1 and type 2 myotonic dystrophy.

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The hypocretin neurotransmission system in myotonic dystrophy type 1.

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

RNA-dominant diseases

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Confirmation of the type 2 myotonic dystrophy (CCTG)n expansion mutation in patients with proximal myotonic myopathy/proximal myotonic dystrophy of different European origins: a single shared haplotype indicates an ancestral founder effect

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Variant CCG and GGC repeats within the CTG expansion dramatically modify mutational dynamics and likely contribute toward unusual symptoms in some myotonic dystrophy type 1 patients.

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Increased cancer risks in myotonic dystrophy.

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Compound loss of muscleblind-like function in myotonic dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Patient-reported impact of symptoms in myotonic dystrophy type 1 (PRISM-1)

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

140th ENMC International Workshop: Myotonic Dystrophy DM2/PROMM and other myotonic dystrophies with guidelines on management

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Proximal myotonic myopathy: evidence for anticipation in families with linkage to chromosome 3q.

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification, tissue-specific expression, and subcellular localization of the 80- and 71-kDa forms of myotonic dystrophy kinase protein

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Metabolic and clinical response to recombinant human insulin-like growth factor I in myotonic dystrophy--a clinical research center study

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Myotonic dystrophy type 1 is associated with nuclear foci of mutant RNA, sequestration of muscleblind proteins and deregulated alternative splicing in neurons

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Myotonic dystrophy patients have larger CTG expansions in skeletal muscle than in leukocytes.

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Electrocardiographic abnormalities and sudden death in myotonic dystrophy type 1

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

PKC inhibition ameliorates the cardiac phenotype in a mouse model of myotonic dystrophy type 1.

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Laboratory abnormalities in ambulatory patients with myotonic dystrophy type 1.

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prenatal diagnosis in myotonic dystrophy type 1. Thirteen years of experience: implications for reproductive counselling in DM1 families.

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rationally designed small molecules targeting the RNA that causes myotonic dystrophy type 1 are potently bioactive

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cerebral involvement in myotonic dystrophies

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Anatomy of a founder effect: myotonic dystrophy in Northeastern Quebec

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Increased mortality with left ventricular systolic dysfunction and heart failure in adults with myotonic dystrophy type 1

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Correlation between CTG trinucleotide repeat length and frequency of severe congenital myotonic dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Histopathological differences of myotonic dystrophy type 1 (DM1) and PROMM/DM2

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Reduction of the rate of protein translation in patients with myotonic dystrophy 2

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Targeting nuclear RNA for in vivo correction of myotonic dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Increased steady-state levels of CUGBP1 in myotonic dystrophy 1 are due to PKC-mediated hyperphosphorylation

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nuclear RNA foci in the heart in myotonic dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A putative role of ribonuclear inclusions and MBNL1 in the impairment of gallbladder smooth muscle contractility with cholelithiasis in myotonic dystrophy type 1.

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

RNA-mediated neurodegeneration in repeat expansion disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The exercise test distinguishes proximal myotonic myopathy from myotonic dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Myotonic dystrophy type 2: molecular, diagnostic and clinical spectrum

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ribonuclear inclusions in skeletal muscle in myotonic dystrophy types 1 and 2

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Quantifying cancer absolute risk and cancer mortality in the presence of competing events after a myotonic dystrophy diagnosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Epidemiological and genetic studies of myotonic dystrophy type 1 in Taiwan

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Misregulated alternative splicing of BIN1 is associated with T tubule alterations and muscle weakness in myotonic dystrophy.

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Reducing levels of toxic RNA with small molecules

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital myotonic dystrophy: prenatal ultrasound findings and pregnancy outcome

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sudden cardiac death in myotonic dystrophy type 2.

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Modafinil reduces excessive somnolence and enhances mood in patients with myotonic dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Decreased insulin sensitivity of forearm muscle in myotonic dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Expanded CUG repeat RNAs form hairpins that activate the double-stranded RNA-dependent protein kinase PKR

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Open-label trial of recombinant human insulin-like growth factor 1/recombinant human insulin-like growth factor binding protein 3 in myotonic dystrophy type 1.

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mechanisms and management of the heart in myotonic dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital myotonic dystrophy: Canadian population-based surveillance study.

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Psychiatric and cognitive phenotype of childhood myotonic dystrophy type 1.

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Daytime sleepiness and REM sleep characteristics in myotonic dystrophy: a case-control study

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Expanded CUG repeats trigger aberrant splicing of ClC-1 chloride channel pre-mRNA and hyperexcitability of skeletal muscle in myotonic dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Non-ATG-initiated translation directed by microsatellite expansions

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Consensus on cerebral involvement in myotonic dystrophy: workshop report: May 24-27, 2013, Ferrere (AT), Italy

1 reference

https://pubmed.ncbi.nlm.nih.gov/25037086

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1016/J.NCL.2014.04.011

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25037086%20AND%20SRC:MED&resulttype=core&format=json

9 March 2020

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25037086%20AND%20SRC:MED&resulttype=core&format=json

9 March 2020

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25037086%20AND%20SRC:MED&resulttype=core&format=json

9 March 2020

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