The clinical and electrodiagnostic characteristics of Pompe disease with post-enzyme replacement therapy findings (Q37875464)

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scientific article published on May 13, 2011

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English	The clinical and electrodiagnostic characteristics of Pompe disease with post-enzyme replacement therapy findings	scientific article published on May 13, 2011

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scholarly article

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Europe PubMed Central

PubMed publication ID

21570905

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24 August 2017

review article

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Europe PubMed Central

title

The clinical and electrodiagnostic characteristics of Pompe disease with post-enzyme replacement therapy findings (English)

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Europe PubMed Central

PubMed publication ID

21570905

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24 August 2017

main subject

enzyme replacement therapy

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author

Stephanie M DeArmey

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2

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Stephanie Dearmey

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Europe PubMed Central

PubMed publication ID

21570905

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24 August 2017

Priya S Kishnani

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Priya S Kishnani

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Europe PubMed Central

PubMed publication ID

21570905

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24 August 2017

author name string

Lisa D. Hobson-Webb

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1

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Europe PubMed Central

PubMed publication ID

21570905

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A21570905

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2 December 2024

Stephanie Dearmey

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2

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Europe PubMed Central

PubMed publication ID

21570905

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A21570905

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2 December 2024

language of work or name

English

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National Center for Biotechnology Information

PubMed publication ID

21570905

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=21570905

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publication date

13 May 2011

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Europe PubMed Central

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21570905

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24 August 2017

full work available at URL

https://api.elsevier.com/content/article/PII:S1388245711002732?httpAccept=text/xml

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Crossref

DOI

10.1016/J.CLINPH.2011.04.016

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https://api.crossref.org/works/10.1016/J.CLINPH.2011.04.016

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2 December 2024

https://api.elsevier.com/content/article/PII:S1388245711002732?httpAccept=text/plain

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Crossref

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10.1016/J.CLINPH.2011.04.016

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https://api.crossref.org/works/10.1016/J.CLINPH.2011.04.016

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2 December 2024

published in

Clinical Neurophysiology

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Europe PubMed Central

PubMed publication ID

21570905

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24 August 2017

volume

122

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Europe PubMed Central

PubMed publication ID

21570905

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24 August 2017

issue

11

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Europe PubMed Central

PubMed publication ID

21570905

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24 August 2017

page(s)

2312-2317

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Europe PubMed Central

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21570905

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cites work

Diagnostic criteria for late-onset (childhood and adult) Pompe disease

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10.1016/J.CLINPH.2011.04.016

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https://api.crossref.org/works/10.1016/J.CLINPH.2011.04.016

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2 December 2024

Adult acid maltase deficiency

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10.1016/J.CLINPH.2011.04.016

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https://api.crossref.org/works/10.1016/J.CLINPH.2011.04.016

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2 December 2024

Pompe's disease. Electromyographic, electron microscopic, and cardiovascular aspects

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10.1016/J.CLINPH.2011.04.016

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https://api.crossref.org/works/10.1016/J.CLINPH.2011.04.016

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2 December 2024

Muscle MRI findings in siblings with juvenile-onset acid maltase deficiency (Pompe disease)

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4

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10.1016/J.CLINPH.2011.04.016

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2 December 2024

Acid maltase deficiency in adults: studies in four cases of a syndrome which may mimic muscular dystrophy or other myopathies

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5

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10.1016/J.CLINPH.2011.04.016

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2 December 2024

The spectrum and diagnosis of acid maltase deficiency.

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10.1016/J.CLINPH.2011.04.016

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2 December 2024

glycogen storage disease II

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10.1016/J.CLINPH.2011.04.016

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2 December 2024

Screening for Pompe disease using a rapid dried blood spot method: experience of a clinical diagnostic laboratory

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9

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10.1016/J.CLINPH.2011.04.016

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2 December 2024

Pompe's disease

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11

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10.1016/J.CLINPH.2011.04.016

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https://api.crossref.org/works/10.1016/J.CLINPH.2011.04.016

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2 December 2024

Adult myopathy from glycogen storage disease due to acid maltase deficiency

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12

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Crossref

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10.1016/J.CLINPH.2011.04.016

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2 December 2024

Electromyography in Type II Glycogenosis

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10.1016/J.CLINPH.2011.04.016

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https://api.crossref.org/works/10.1016/J.CLINPH.2011.04.016

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2 December 2024

Late onset Pompe disease: Clinical and neurophysiological spectrum of 38 patients including long-term follow-up in 18 patients

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14

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10.1016/J.CLINPH.2011.04.016

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2 December 2024

Enzyme replacement therapy in adult-onset glycogenosis II: is quantitative muscle MRI helpful?

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15

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10.1016/J.CLINPH.2011.04.016

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2 December 2024

Muscle MRI in adult-onset acid maltase deficiency

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10.1016/J.CLINPH.2011.04.016

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2 December 2024

Muscle ultrasound: a grown-up technique for children with neuromuscular disorders

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10.1016/J.CLINPH.2011.04.016

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2 December 2024

Quantitative skeletal muscle ultrasound: diagnostic value in childhood neuromuscular disease

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Probabilistic muscle characterization using quantitative electromyography: application to facioscapulohumeral muscular dystrophy

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10.1016/J.CLINPH.2011.04.016

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2 December 2024

Investigating glycogenosis type III patients with multi-parametric functional NMR imaging and spectroscopy

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10.1016/J.CLINPH.2011.04.016

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2 December 2024

Methods for a prompt and reliable laboratory diagnosis of Pompe disease: report from an international consensus meeting

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10.1016/J.CLINPH.2011.04.016

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2 December 2024

A mild form of muscular glycogenosis in two brothers with alpha-1, 4-glucosidase deficiency

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23

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10.1016/J.CLINPH.2011.04.016

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2 December 2024

Identifiers

DOI

10.1016/J.CLINPH.2011.04.016

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21570905

retrieved

24 August 2017

PubMed publication ID

21570905

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21570905

retrieved

24 August 2017

ResearchGate publication ID

51125463

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