Back to Results
First PageMeta Content
Glycogen storage disease type II / Enzyme replacement therapy / Lysosomal storage disease / Spirometry / Amyotrophic lateral sclerosis / Fabry disease / Alglucosidase alfa / ERT / Health / Medicine / Rare diseases


Evidence for decline in the incidence of cystic fibrosis: a 35-year observational study in Brittany, France
Add to Reading List

Document Date: 2013-05-26 18:38:43


Open Document

File Size: 500,86 KB

Share Result on Facebook

City

Utrecht / Maastricht / Nijmegen / Groningen / Shapira / Chen / New York / Kroos / Worden / Rotterdam / Beaudet / Cambridge / Neudorf / Amsterdam / Cary / Bengur / London / Chicago / Florence / /

Company

SPSS Inc. / Vulto AG / Zivkovic SA / Erasmus MC Revolving Fund / GE / Erasmus MC University Medical Center / Google / Genzyme Corp / McGraw-Hill / Winkel LP / Engel AG / Miller AE / Creative Commons / BioMed Central Ltd. / /

Country

Netherlands / France / United States / /

/

Event

Business Partnership / /

Facility

Maastricht University Medical Center / Leiden University Medical Center / University Medical Center Utrecht / Rudolf Magnus Institute of Neurosciences / Radboud University Nijmegen Medical Center / University Medical Center Groningen / Academic Medical Center / Institute Inc. / /

IndustryTerm

study protocol / therapy for infantile glycogen storage disease / therapy for Pompe disease / online submission / steel / /

MedicalCondition

allergies / Pompe's disease / late-onset Pompe's disease / Rare Diseases / JE / measurable muscle weakness / myopathy / infantile glycogen storage disease type II / Glycogen storage disease type II / Dysfunction / muscle weakness / progressive neuromuscular disorder / severe muscle weakness / pulmonary / Glycogen storage disease / mild muscle weakness / moderate muscle weakness / limb-girdle myopathy / lysosomal storage disease / Background Pompe disease / Pompe disease / sepsis / glycogenosis type II / Lysosomal storage disorder / respiratory failure / disease / Metabolic Diseases / late-onset Pompe disease / pulmonary function / Pulmonary function Forced / chronic / Lysosomal Storage Diseases / respiratory insufficiency / mild and moderate muscle weakness / deficiency / disorders / /

MedicalTreatment

premedication / intravenous infusions / mechanical ventilation / Enzyme replacement therapy / /

Organization

Leiden University / Department of Pediatrics / Medical Research Council / Majesty's Stationary Office / American Thoracic Society/European Respiratory Society / Center for Lysosomal / Dutch national referral center / European Union / Medical Ethical Committee / /

Person

Van Hirtum / Van Hove / Ann Neurol / Vital Capacity / David Alexander / Van Doorn / Hester Lingsma / Van den Hout / Van Diggelen / Ewout Steyerberg / Van Corven / /

Position

RT / Princess / author / Leshner RT / Major / /

ProgrammingLanguage

ML / /

ProvinceOrState

Bali / Alabama / Saskatchewan / YT / Pennsylvania / Massachusetts / Arkansas / /

Technology

alpha / study protocol / /

URL

www.biomedcentral.com/submit / www.pompecenter.nl / http /

SocialTag