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Medical terms / Glycogen storage disease type II / Hepatology / Quality of life / Medical home / Home care / Intensive-care medicine / Medicine / Health / Healthcare


J Inherit Metab Dis DOI[removed]s10545[removed]x ORIGINAL ARTICLE Burden of illness of Pompe disease in patients
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Document Date: 2011-05-07 19:36:05

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City

New York / Rotterdam / The Hague / Cambridge / /

Company

Clague AE / Vulto AG / Tim A. Kanters & Marloes L. C. / The Netherlands N. A. / Erasmus MC / M. L. C. / GE / Genzyme Corp / McGraw-Hill / Winkel LP / Oxford University Press / The Netherlands M. L. C. / Creative Commons / SPSS / Microsoft / EuroQol Group / J Inherit Metab Dis Franke LC / /

Continent

Europe / /

Country

Netherlands / France / United States / /

Currency

USD / EUR / /

Event

Business Partnership / /

Facility

Erasmus Medical Center / Erasmus MC University Medical Center / Erasmus University / /

IndustryTerm

healthcare innovation / respiratory devices / consulting services / Lower utilities / ambulatory support equipment / treatment of Pompe disease / health care systems / social network / technology transfer / /

MedicalCondition

neuromuscular and lysosomal storage disorder / muscular dystrophy / rare diseases / adult Pompe disease / COPD / lysosomal storage disorders / ankylosing spondylitis / late-onset Pompe’s disease / rheumatoid arthritis / average disease / Springerlink.com Abstract Background Pompe disease / Muscle weakness / inherited enzyme deficiency / rare illness / Fabry’s disease / glycogen storage disease / Maroteaux-Lamy syndrome / multiple sclerosis / U.S. as a disease / Lysosomal storage disease / Introduction Pompe disease / inheritable muscle disorder / illness / infantile-onset Pompe disease / Pompe disease / orphan diseases / asthma / orphan disease / mucopolysaccharidosis VI / chronic condition / Disease / different diseases / Late-onset Pompe disease / Gaucher disease / Pompe’s disease / pain / Fabry disease / mucopolysaccharidosis I / inherited disease / neuromuscular disorder / Gaucher’s disease / Longer disease / anxiety/depression / acid maltase deficiency / Conclusions Adult Pompe disease / few other lysosomal storage disorders / deficiency / infantile Pompe’s disease / adultonset acid maltase deficiency / /

MedicalTreatment

counseling / Physiotherapy / mechanical ventilation / enzyme replacement therapy / self-care / /

MusicGroup

Excel / performed using Microsoft Excel / /

Organization

Central Committee on Research Involving Human Subjects in the Netherlands / Erasmus Medical Center / Erasmus University Rotterdam / Department of Pediatrics / MC University Medical Center Rotterdam / Department of Neurology / Center for Lysosomal and Metabolic Diseases / Institute for Medical Technology Assessment / Department of Health Policy & Management / MC University Medical Center / national referral center / Division of Metabolic Diseases and Genetics / Health Care Insurance Board / Oxford University / Source Hospital / /

Person

Van Roijen / Van Ineveld / Jaap de Boer / Judy Kempf / Robin Lachmann / Jan Meerding / Leona Hakkaart / Ken Redekop / Ann Rheum Dis / /

Position

general practitioner / den Hout WB / neurologist / Author / representative / /

Product

Intensive care Nursing home Ambulatory care Home care Medication / /

ProvinceOrState

New York / /

Technology

alpha / MRI / genotype / /

SocialTag