Myotonic dystrophy type 2 found in two of sixty-three persons diagnosed as having fibromyalgia. - Wikidata - wikimedia - TriplyDB

Myotonic dystrophy type 2 found in two of sixty-three persons diagnosed as having fibromyalgia.

Myotonic dystrophy type 2 found in two of sixty-three persons diagnosed as having fibromyalgia.

http://www.wikidata.org/entity/Q36979268

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Myotonic disorders: A review article Predominantly myalgic phenotype caused by the c.3466G>A p.A1156T mutation in SCN4A gene Diagnostic odyssey of patients with myotonic dystrophy Differences in aberrant expression and splicing of sarcomeric proteins in the myotonic dystrophies DM1 and DM2.Population frequency of myotonic dystrophy: higher than expected frequency of myotonic dystrophy type 2 (DM2) mutation in Finland.Sleep disturbances in myotonic dystrophy type 2.The Overlap between Fibromyalgia Syndrome and Myotonia Congenita Multidimensional aspects of pain in myotonic dystrophies.A Molecular Signature of Myalgia in Myotonic Dystrophy 2 Altered expression and splicing of Ca(2+) metabolism genes in myotonic dystrophies DM1 and DM2.Clinical aspects, molecular pathomechanisms and management of myotonic dystrophies.Sleep-Wake Cycle and Daytime Sleepiness in the Myotonic Dystrophies Myotonic Dystrophy Type 2: An Update on Clinical Aspects, Genetic and Pathomolecular Mechanism.Myotonic dystrophy type 2 and modifier genes: an update on clinical and pathomolecular aspects.Validation of sensitivity and specificity of tetraplet-primed PCR (TP-PCR) in the molecular diagnosis of myotonic dystrophy type 2 (DM2).Pain in patients with myotonic dystrophy type 2: a postal survey in Finland.Generalized epilepsy in a patient with myotonic dystrophy type 2.Screening for the presence of FMR1 premutation alleles in a Spanish population with fibromyalgia.Diagnostic confounders of chronic widespread pain: not always fibromyalgia.Pain in SCN4A Mutated P.A1156T muscle sodium channelopathy-a postal survey.Electromyography and muscle biopsy in chronic isolated Myalgia: A prospective study.

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P2860

Myotonic dystrophy type 2 found in two of sixty-three persons diagnosed as having fibromyalgia.

http://www.wikidata.org/entity/Q36979268

description

2008 nî lūn-bûn

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2008年の論文

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2008年論文

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2008年論文

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2008年論文

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2008年論文

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2008年論文

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2008年论文

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2008年论文

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2008年论文

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Myotonic dystrophy type 2 foun ...... gnosed as having fibromyalgia.

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Myotonic dystrophy type 2 foun ...... gnosed as having fibromyalgia.

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Myotonic dystrophy type 2 foun ...... gnosed as having fibromyalgia.

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Arthritis & Rheumatology

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Myotonic dystrophy type 2 foun ...... gnosed as having fibromyalgia.

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Bjarne Udd

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Linda L Bachinski

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Pekka Hannonen

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Ralf Krahe

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Satu Auvinen

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Tiina Suominen

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P2860

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

Myotonic dystrophy type 2: molecular, diagnostic and clinical spectrum

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

The American College of Rheumatology 1990 Criteria for the Classification of Fibromyalgia. Report of the Multicenter Criteria Committee

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.

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

Therapy Insight: fibromyalgia--a different type of pain needing a different type of treatment.

A family with an unusual myotonic and myopathic phenotype and no CTG expansion (proximal myotonic myopathy syndrome): a challenge for future molecular studies.

Report of the 115th ENMC workshop: DM2/PROMM and other myotonic dystrophies. 3rd Workshop, 14-16 February 2003, Naarden, The Netherlands.

Proximal myotonic dystrophy--a family with autosomal dominant muscular dystrophy, cataracts, hearing loss and hypogonadism: heterogeneity of proximal myotonic syndromes?

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10.1002/ART.24037

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