The clinical and electrodiagnostic characteristics of Pompe disease with post-enzyme replacement therapy findings
- 13 May 2011
- journal article
- case report
- Published by Elsevier in Clinical Neurophysiology
- Vol. 122 (11) , 2312-2317
- https://doi.org/10.1016/j.clinph.2011.04.016
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- Diagnostic criteria for late‐onset (childhood and adult) pompe diseaseMuscle & Nerve, 2009
- Screening for pompe disease using a rapid dried blood spot method: Experience of a clinical diagnostic laboratoryMuscle & Nerve, 2009
- Muscle MRI findings in siblings with juvenile-onset acid maltase deficiency (Pompe disease)Neuromuscular Disorders, 2008
- Late onset Pompe disease: Clinical and neurophysiological spectrum of 38 patients including long-term follow-up in 18 patientsNeuromuscular Disorders, 2007
- Adult acid maltase deficiencyMuscle & Nerve, 1993
- Electromyography in Type II GlycogenosisNeuropediatrics, 1974
- The spectrum and diagnosis of acid maltase deficiencyNeurology, 1973
- Pompe's DiseaseArchives of Neurology, 1970
- ACID MALTASE DEFICIENCY IN ADULTS: STUDIES IN FOUR CASES OF A SYNDROME WHICH MAY MIMIC MUSCULAR DYSTROPHY OR OTHER MYOPATHIESBrain, 1970
- Pompe's diseaseNeurology, 1969