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Motor neurone disease / Glycogen storage disease type II / Hepatology / Lysosomal storage disease / Dysphagia / Swallowing / Acid alpha-glucosidase / Amyotrophic lateral sclerosis / Hypotonia / Health / Medicine / Rare diseases


J Inherit Metab Dis DOI[removed]s10545[removed]ORIGINAL ARTICLE Facial-muscle weakness, speech disorders and dysphagia
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Document Date: 2012-01-17 11:57:59


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City

New York / Rotterdam / Cambridge / Neudorf / Philadelphia Gambetti / London / Sauders / /

Company

Vulto AG / Bijvoet AG / Erasmus MC Revolving Fund / GE / Genzyme Corp / McGraw-Hill / Winkel LP / Creative Commons / Hout / Aronson AE / /

Country

Netherlands / Japan / United States / United Kingdom / /

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Event

Business Partnership / /

Facility

Erasmus MC University Medical Center / /

IndustryTerm

online version / healthcare research / treatment of Pompe’s disease / Treatment of infantile Pompe disease / Treatment of Swallowing Disorders / consulting services / food / therapy for infantile glycogen storage disease / motor systems / treatment of Pompe disease / food intake / pharyngeal food residue / therapy for infantile Pompe disease / eaten food / e-h / technology transfer / /

MedicalCondition

flaccid dysarthria / myopia / Velopharyngeal insufficiency / choking / FMW=Facial muscle weakness / hypertrophic cardiomyopathy / Pompe's disease / Diffuse Glycogenosis / JE / dysarthria / progressive muscle weakness / orofacial hypotonia / infantile Pompe disease / articulatory disorders / rare autosomal recessive lysosomal storage disorder / severe facial muscle weakness / muscle weakness / ORIGINAL ARTICLE Facial-muscle weakness / extraocular motility disorder / glycogen storage disease / Muscle Disorders / muscle contraction / recurrent respiratory infections / why obvious bulbar muscle weakness / Introduction Pompe disease / late onset Pompe disease / hearing loss / infantile-onset Pompe disease / Pompe disease / residual pharyngeal muscle weakness / bulbar muscle weakness / classical infantile Pompe disease / pneumonia / inborn lysosomal disorder / advanced Pompe disease / disease / facial-muscle weakness / dysphagia / airway infections / classic infantile Pompe disease / contraction / inherited generalized glycogen storage disorder / coughing / infantile glycogen storage disease / aspiration pneumonias / severest facial muscle weakness / Pompe’s disease / complete enzyme deficiency / inherited disease / Swallowing Disorders / recurrent airway infections / facial muscle weakness / speech disorders / infantile Pompe's disease / acid maltase deficiency / Lysosomal Storage Diseases / dysarthrias / respiratory insufficiency / respiratory muscle weakness / deficiency / disorders / dysarthria using / mild hearing loss / /

MedicalTreatment

antibiotics / tube feeding / enzyme replacement therapy / speech therapy / /

Organization

Institutional Review Board / the Netherlands A. J. J. Reuser Department of Clinical Genetics / Department of Pediatrics / Department of Neurology / Center for Lysosomal and Metabolic Diseases / MC University Medical Center / Division of Metabolic Diseases and Genetics / US Federal Reserve / European Union / MC Revolving Fund / /

Person

Van Hirtum / David Alexander / Van Capelle / Tom de Vries Lentsch / Ned Tijdschr Geneeskd / Beatrix Fonds / Neck Surg / /

Position

Curr Opin Otolaryngol Head / Swallowing function The speech therapist / speech therapist / Author / /

ProvinceOrState

New York / /

RadioStation

Rowlerson AM / /

Technology

alpha / /

SocialTag