A study of glycogen storage disease with 99Tcm-MIBI gated myocardial perfusion imaging.

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Multimodality imaging in restrictive cardiomyopathies: an EACVI expert consensus document: In collaboration with the 'Working Group on myocardial and pericardial diseases' of the European Society of Cardiology Endorsed by the Indian Academy of Echoc

P2860

Q38782767-FB2E1232-69F6-4332-AEFC-F8BF2458D84B

P2860

A study of glycogen storage disease with 99Tcm-MIBI gated myocardial perfusion imaging.

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http://www.wikidata.org/entity/Q43848564

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2013 nî lūn-bûn

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2013年の論文

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2013年学术文章

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2013年学术文章

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2013年学术文章

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2013年学术文章

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A study of glycogen storage disease with 99Tcm-MIBI gated myocardial perfusion imaging.

@en

A study of glycogen storage disease with 99Tcm-MIBI gated myocardial perfusion imaging.

@nl

type

Item

label

A study of glycogen storage disease with 99Tcm-MIBI gated myocardial perfusion imaging.

@en

A study of glycogen storage disease with 99Tcm-MIBI gated myocardial perfusion imaging.

@nl

prefLabel

A study of glycogen storage disease with 99Tcm-MIBI gated myocardial perfusion imaging.

@en

A study of glycogen storage disease with 99Tcm-MIBI gated myocardial perfusion imaging.

@nl

P1476

A study of glycogen storage disease with 99Tcm-MIBI gated myocardial perfusion imaging.

@en

P2093

J M Huang

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J Q Gao

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L G Wei

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X M Liu

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

X Z Li

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P2860

Glycogen storage disease type III diagnosis and management guidelines

Glycogen storage diseases: new perspectives.

Pompe disease diagnosis and management guideline.

Lysosomal dysfunction in muscle with special reference to glycogen storage disease type II.

Glycogen storage disease: clinical, biochemical, and molecular heterogeneity.

Myocardial late gadolinium enhancement in specific cardiomyopathies by cardiovascular magnetic resonance: a preliminary experience.

Echocardiographic manifestations of Glycogen Storage Disease III: increase in wall thickness and left ventricular mass over time.

Clinical and histologic ocular findings in pompe disease.

A new mutation in PRKAG2 gene causing hypertrophic cardiomyopathy with conduction system disease and muscular glycogenosis.

The electrodiagnostic characteristics of Glycogen Storage Disease Type III.

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s11845-013-0939-5

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615-620

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scholarly article

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10.1007/S11845-013-0939-5

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182

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2013-04-25T00:00:00Z

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23616069

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A study of glycogen storage disease with 99Tcm-MIBI gated myocardial perfusion imaging.

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P2860

P2860

A study of glycogen storage disease with 99Tcm-MIBI gated myocardial perfusion imaging.

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P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P433

P478

P577

P698

P356

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P433

P478

P577

P698