Correction of glycogenstoragediseasetypeII by an adeno-associated virus vector containing a muscle-specific...Hydrocephalus associated with glycogenstoragediseasetypeII (Pompe's disease)....
Pompe disease, or acid maltase deficiency, is an autosomal recessive disorder ...Late-onset Pompe disease is characterized by onset of symptoms ...Disease by Ray Sahelian, M.D. ...New Medication for Pompe Disease ...
Pompe disease (glycogenstoragediseasetypeII) in Argentineans: Clinical manifestations and identification of...Two clinical forms of glycogen-storagediseasetypeII in two generations of the same...
Congenital Disorder of Glycosylation Type Ia...Glucose Transporter Type 1 Deficiency Syndrome...Inclusion Body Myopathy with Paget Disease of Bone and/or Frontotemporal Dementia...Parkin Type of Juvenile Parkinson...
genetic disorders known as lysosomal storage diseases, and Pompe disease is one of them....It is also classified as glycogenstoragediseasetypeII (GSD II)....