New York / Rotterdam / Interacoustics / Cambridge / Copenhagen / /
Company
Normal Normal N.A. N.A. / V (data are represented by z-scores >1.96 is considered abnormal) N.A. / Normal Normal Normal Prolonged Normal Prolonged Prolonged N.A. N.A. N.A. / Erasmus MC / Genzyme Corp / McGraw-Hill / Winkel LP / Engel AG / Normal Normal Prolonged Prolonged Prolonged Prolonged Normal N.A. N.A. / Creative Commons / SPSS / Geneva Winkel LP / Normal Normal Normal Prolonged Normal Prolonged Normal N.A. N.A. N.A. / performed using SPSS / /
Country
Netherlands / United States / United Kingdom / Denmark / / /
Event
Business Partnership / /
Facility
Erasmus Medical Center / Erasmus MC University Medical Center / Sophia Children’s Hospital / Children’s Hospital / /
IndustryTerm
persistent otitis media / healthcare research / treatment of Pompe’s disease / chronic otitis media / consulting services / recurrent bilateral otitis media / treatment of Pompe disease / early otitis media / therapy for Pompe disease / technology transfer / /
MedicalCondition
slowly progressive disease / hypertrophic cardiomyopathy / early otitis media / recurrent bilateral otitis media / ORIGINAL ARTICLE Hearing loss / recurrent conductive hearing loss / JE / dysarthria / conductive hearing loss / infantile Pompe disease / lysosomal storage disorders / middle ear dysfunction / Axial hypotonia / muscle weakness / also called glycogen storage disease / cochlear hearing loss / Fabry’s disease / sensorineural hearing loss / chronic middle ear dysfunction / chronic otitis media / persistent otitis media / hearing disorders / infectious middle ear problems / middle ear effusion / Hearing loss / paresis / infantile-onset Pompe disease / Pompe disease / hearing impairment / cochlear dysfunction / enzyme deficiency / prox weak Paresis / Mucopolysaccharidoses / rapidly progressive disease / Oropharyngeal dysphagia / disease / Hurler’s disease / mild bilateral hearing loss / non-classic Pompe’s disease / dysphagia / pulmonary function / F Axial hypotonia / mild unilateral conductive hearing loss / classic infantile Pompe disease / Gaucher disease / late-onset glycogen storage disease type / Pompe’s disease / F Paralysis / Fabry disease / M Axial hypotonia / acid maltase deficiency / Lysosomal Storage Diseases / several lysosomal storage disorders / deficiency / Eustachian tube dysfunction / retrocochlear dysfunction / infantile Gaucher’s disease / infantile Pompe’s disease / /
Institutional Review Board / World Health Organization / Erasmus Medical Center / A. J. Reuser Department of Clinical Genetics / Department of Pediatrics / MC Sophia Children’s hospital / Children’s Hospital / Center for Lysosomal and Metabolic Diseases / MC University Medical Center / Sophia Children’s Hospital / Division of Metabolic Diseases and Genetics / ZonMw-Dutch / H. L. J. Hoeve Department of Otorhinolaryngology / European Union / /
Person
H.W. Paerl / Arnold J. Reuser / Carine I. van Capelle / Ann Otol Rhinol Laryngol / Van den Hout / Hans L. J. Hoeve / Andre Goedegebure / Sophia Children / Beatrix Fonds / T. van der Ploeg / /
J Inherit Metab Dis[removed]:597–602 DOI[removed]s10545[removed]ORIGINAL ARTICLE Hearing loss in Pompe disease revisited: results from a study