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Respiratory therapy / Rare diseases / Inborn errors of carbohydrate metabolism / Glycogen storage disease type II / Hepatology / Lysosomal storage disease / Physical therapy / Alglucosidase alfa / Spirometry / Medicine / Health / Pulmonary function testing


Neuromuscular Disorders xxx[removed]xxx–xxx Contents lists available at ScienceDirect Neuromuscular Disorders journal homepage: www.elsevier.com/locate/nmd
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Document Date: 2011-01-02 22:37:30

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City

Groningen / New York / Rotterdam / Leuven / Cambridge / Neudorf / London / /

Company

IgG / Vulto AG / Genzyme Europe BV / M.L.C. / Slonim AE / Genzyme Corporation / McGraw-Hill / Winkel LP / Engel AG / Ó 2010 Elsevier B.V. / /

Country

Netherlands / Belgium / France / United States / United Kingdom / /

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Facility

Children’s Hospital Radboud University Medical Center / Erasmus MC University Medical Center / Sophia Children’s Hospital / University Hospital Gasthuisberg / National Hospital / Erasmus University Medical Center / /

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IndustryTerm

healthcare research / energy / therapy for patients with Pompe disease / therapy for infantile glycogen storage disease / treatment of Pompe disease / therapy for Pompe disease / /

MedicalCondition

Neuromuscular Disorders / muscular dystrophy / slowly progressive disease / hypertrophic cardiomyopathy / limb muscle weakness / ScienceDirect Neuromuscular Disorders / late-onset Pompe’s disease / pulmonary function declines / Voit T. Respiratory failure / Dysfunction / muscle weakness / fatigue / Pulmonary function Pulmonary / Pulmonary / Glycogen storage disease / moderate muscle weakness / lysosomal storage disease / Introduction Pompe disease / infantile-onset Pompe disease / Pompe disease / nonclassic Pompe’s disease / classical infantile pompe disease / only one patient pulmonary function measurements / cardiac hypertrophy / Demonstrable muscle weakness / cardiomyopathy / disease / Respiratory failure / rare neuromuscular disorder / Severe fatigue / late-onset Pompe disease / pulmonary function / progressive cardiac hypertrophy / classic infantile Pompe disease / glycogenosis / late onset glycogen storage disease type II / infantile glycogen storage disease / muscle pain / late-onset glycogen storage disease type / Pompe’s disease / inherited disease / minimal tricuspid regurgitation / Lysosomal Storage Diseases / Regular headaches / hypotonia / untreated late-onset Pompe disease / infantile Pompe’s disease / limb-girdle muscle weakness / /

MedicalTreatment

premedication / surgery / Enzyme Replacement Therapy / /

Organization

Prinses Beatrix Fund / Children’s Hospital Radboud University Medical Center / Department of Clinical Genetics / Department of Pediatrics / Erasmus University Medical Center / Department of Neurology / Charles Dent Metabolic Unit / Erasmus MC-Sophia Children’s Hospital / National Hospital for Neurology and Neurosurgery / Center for Lysosomal and Metabolic Diseases / Medical Research Council / American Thoracic Society / Division of Pediatric Cardiology / MC University Medical Center / Division of Metabolic Diseases and Genetics / Centre for Metabolic Disease / European Union / Department of Pediatric Neurology / Institutional Review Board of the Erasmus MC-Sophia Children / Department of Epidemiology and Biostatistics / /

Person

Vries Lentsch / Ann Neurol / Arch Phys Med / Charles Dent / Van Doorn / Van den Hout / Ned Tijdschr Geneeskd / /

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Position

Corresponding author / evaluator / /

Technology

alpha / antibodies / ultrasound / Neurosurgery / genotype / /

URL

www.pompecenter.nl / www.elsevier.com/locate/nmd / /

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