High frequency of gastrointestinal manifestations in myotonic dystrophy type 1 and type 2.

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Assessing the influence of age and gender on the phenotype of myotonic dystrophy type 2.

P2860

Q47594478-017E84C6-5310-4ECA-A96E-5B5907E6472E

P2860

High frequency of gastrointestinal manifestations in myotonic dystrophy type 1 and type 2.

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http://www.wikidata.org/entity/Q38601634

description

2017 nî lūn-bûn

@nan

2017年の論文

@ja

2017年論文

@yue

2017年論文

@zh-hant

2017年論文

@zh-hk

2017年論文

@zh-mo

2017年論文

@zh-tw

2017年论文

@wuu

2017年论文

@zh

2017年论文

@zh-cn

name

High frequency of gastrointest ...... c dystrophy type 1 and type 2.

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type

Item

label

High frequency of gastrointest ...... c dystrophy type 1 and type 2.

@en

prefLabel

High frequency of gastrointest ...... c dystrophy type 1 and type 2.

@en

P1476

High frequency of gastrointestinal manifestations in myotonic dystrophy type 1 and type 2

@en

P2093

Charles A Thornton

http://www.w3.org/2001/XMLSchema#string

Elizabeth A Luebbe

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James E Hilbert

http://www.w3.org/2001/XMLSchema#string

Michael P McDermott

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National Registry Scientific Advisory Committee/Investigators

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Paula R Clemens

http://www.w3.org/2001/XMLSchema#string

Rabi Tawil

http://www.w3.org/2001/XMLSchema#string

Richard J Barohn

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Richard T Moxley

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William B Martens

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P2860

Interventions for dysphagia in long-term, progressive muscle disease

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

Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene

Update on the epidemiology of gastro-oesophageal reflux disease: a systematic review

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

If you build a rare disease registry, will they enroll and will they use it? Methods and data from the National Registry of Myotonic Dystrophy (DM) and Facioscapulohumeral Muscular Dystrophy (FSHD).

An unstable triplet repeat in a gene related to myotonic muscular dystrophy.

Gender as a Modifying Factor Influencing Myotonic Dystrophy Type 1 Phenotype Severity and Mortality: A Nationwide Multiple Databases Cross-Sectional Observational Study

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.

Correlates of tumor development in patients with myotonic dystrophy

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1348-1354

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scholarly article

P356

10.1212/WNL.0000000000004420

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English

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http://www.w3.org/2001/XMLSchema#string

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Amy L Parkhill

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2017-08-30T00:00:00Z

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28855409

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P932

5649763

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High frequency of gastrointestinal manifestations in myotonic dystrophy type 1 and type 2.

about

P2860

P2860

High frequency of gastrointestinal manifestations in myotonic dystrophy type 1 and type 2.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P932