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2004, ISBN 0198508786, xxvii. 447
Lysosomal storage diseases are inherited metabolic disorders characterized by severe pathology, typically involving the brain... 
Brain | Lysosomal storage diseases | Treatment | Metabolism | Disorders | Disorders of the Nervous System
Book
Autophagy, ISSN 1554-8635, 10/2014, Volume 6, Issue 8, pp. 1078 - 1089
Journal Article
Nature reviews. Neurology, ISSN 1759-4766, 08/2013, Volume 9, Issue 10, pp. 583 - 598
.... The concept of lysosomal storage diseases (LSDs)-disorders characterized by aberrant, excessive storage of cellular material in lysosomes-developed following the discovery of a-glucosidase deficiency as the cause of Pompe disease in 1963... 
Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Neuronal Ceroid-Lipofuscinoses - therapy | Lysosomal Storage Diseases - therapy | Humans | Lysosomal Storage Diseases - metabolism | Neuronal Ceroid-Lipofuscinoses - metabolism | Lysosomal Storage Diseases - etiology | Neuronal Ceroid-Lipofuscinoses - etiology | Metabolism, Inborn errors of | Care and treatment | Neuronal ceroid-lipofuscinosis | Research | Risk factors | Index Medicus
Journal Article
Autophagy, ISSN 1554-8635, 11/2014, Volume 8, Issue 5, pp. 719 - 730
Journal Article
Physiology (Bethesda, Md.), ISSN 1548-9221, 04/2010, Volume 25, Issue 2, pp. 102 - 115
... between the storage material and disease pathogenesis. However, the accumulation of undegraded substrate... 
Life Sciences & Biomedicine | Physiology | Science & Technology | Lysosomes - pathology | Lysosomal Storage Diseases - physiopathology | Lysosomes - physiology | Humans | Lysosomal Storage Diseases - pathology | Index Medicus
Journal Article