Pathophysiology of neuropathic lysosomal storage disorders

Journal of Inherited Metabolic Disease

Volumn 33, Issue 4, 2010, Pages 347-362

  Bellettato, Cinzia Maria ^a   Scarpa, Maurizio ^a  

^a UNIVERSITY OF PADOVA   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

ALZHEIMER DISEASE; APOPTOSIS; CELL ORGANELLE; CENTRAL NERVOUS SYSTEM DISEASE; CLINICAL FEATURE; DEATH; DEGENERATIVE DISEASE; DEMENTIA; DISEASE CLASSIFICATION; DISEASE COURSE; DISEASE SEVERITY; ENZYME DEFICIENCY; HUMAN; HUNTINGTON CHOREA; INFANCY; LYSOSOME; LYSOSOME STORAGE DISEASE; MENTAL DEFICIENCY; METABOLIC DISORDER; NECROSIS; NERVE CELL; NERVE DEGENERATION; PARKINSON DISEASE; REVIEW; TREATMENT INDICATION; PATHOLOGY; PATHOPHYSIOLOGY;

HUMANS; LYSOSOMAL STORAGE DISEASES, NERVOUS SYSTEM; NERVE DEGENERATION;

EID: 77956063541     PISSN: 01418955     EISSN: 15732665     Source Type: Journal    
DOI: 10.1007/s10545-010-9075-9     Document Type: Review

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