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Cellular processes / Autophagy / Programmed cell death / Rare diseases / Inborn errors of carbohydrate metabolism / Glycogen storage disease type II / Lysosomal storage disease / Lysosome / Acid alpha-glucosidase / Biology / Anatomy / Muscular system


[Autophagy 3:6, [removed]; November/December 2007]; ©2007 Landes Bioscience Research Paper ©2007 LANDES BIOSCIENCE.BiDO NOT DISTRIBUTE.
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Document Date: 2010-08-10 22:44:52


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City

Carlsbad / Burlingame / Bedford / Washington DC / Munich / Framingham / Diego / San Paolo / Bethesda / Bonn / Washington / Trieste / Durham / /

Company

Kalamidas SA / Vector Laboratories / Genzyme Corp. / Engel AG / Eurobiobank / /

Country

Taiwan / Germany / Italy / Japan / United States / Brazil / /

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Event

FDA Phase / Product Issues / /

Facility

National Institute of Arthritis / Ludwig Maximilian University / Washington University / Hospital Burlo Garofolo / National Taiwan University Hospital / Rockville Pike / Fort Washington / FriedrichBaur Institute / Ludwig-Maximilians University / Duke University Medical Center / /

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IndustryTerm

Pompe disease therapy / energy homeostasis / molecular machinery / therapy for Pompe disease / cytoplasmic degradation products / /

MedicalCondition

muscular dystrophy / Infantile acid maltase deficiency / JE / early neonatal starvation / myopathy / neurodegenerative disease / Pompe Disease C / Raben N. Dysfunction / lysosomal dysfunction / muscle weakness / PAN nephrosis / severe hypotonia / starvation / glycogen storage disease / II glycogenosis / lysosomal storage disease / Adult-onset glycogen storage disease / Hypoglycemia / Infantile-Onset Pompe disease / adult-onset disease / Pompe Disease / myopathies / Raben N. Acid Alpha-Glucosidase Deficiency / lysosomal storage disorder / Alzheimer’s disease / typical vacuolar myopathy / lysosomal glycogen storage disorder / disease / adult lysosomal storage disease / symptomatic disease / glycogenosis / sickness / Inherited Disease / Acid maltase deficiency / muscular dystrophies / deficiency / metabolic disorder / Skin Diseases / syndrome / human disease / /

MedicalTreatment

enzyme replacement therapy / /

Organization

Washington University / St. Louis / North Carolina USA Department of Neurology / Department of Pediatrics / office of Science and Technology / Department of Neurology / Ludwig-Maximilians University / Munich / San Paolo Medical School / German Ministry of Education / National Taiwan University Hospital / Ludwig Maximilian University / Juntendo University School of Medicine / National Institute of Arthritis and Musculoskeletal / FriedrichBaur Institute / Duke University Medical Center / /

Person

T. Ueno / William Blake / Ann Neurol / Alexa Fluor / Acta Neuropathol / Stuart Kornfeld / Nina Raben / /

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Position

Mathews PM / /

Product

Balanced Salt / pathophysiology / Recombinant Human Acid / /

ProgrammingLanguage

EC / ML / /

ProvinceOrState

Bali / /

RadioStation

Cataldo AM / Cuervo AM / /

Technology

alpha / antibodies / /

URL

http /

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