Late onset Pompe disease: Clinical and neurophysiological spectrum of 38 patients including long-term follow-up in 18 patients

This publication has 30 references indexed in Scilit:

• Autophagy and Lysosomes in Pompe Disease
  Autophagy, 2006
• The natural course of non–classic Pompe’s disease; a review of 225 published cases
  Zeitschrift für Neurologie, 2005
• Respiratory failure in Pompe disease: Treatment with noninvasive ventilation
  Neurology, 2005
• Enzyme Replacement Therapy in Classical Infantile Pompe Disease: Results of a Ten-Month Follow-Up Study
  Neuropediatrics, 2005
• Safety and efficacy of recombinant acid alpha-glucosidase (rhGAA) in patients with classical infantile Pompe disease: results of a phase II clinical trial
  Neuromuscular Disorders, 2005
• Enzyme replacement therapy in late‐onset Pompe's disease: A three‐year follow‐up
  Annals of Neurology, 2004
• Recombinant human α-glucosidase from rabbit milk in Pompe patients
  The Lancet, 2000
• Carrier frequency for glycogen storage disease type II in New York and estimates of affected individuals born with the disease
  American Journal of Medical Genetics, 1998
• Decompensated Cor pulmonaleas the First Manifestation of Ad ult-Onset Myopathy
  Respiration, 1998
• Clinical Variability in Adult-Onset Acid Maltase Deficiency: Report of Affected Sibs and Review of the Literature
  Medicine, 1995