Morphology of Niemann-Pick type C metabolic storage disorder
Por um escritor misterioso
Descrição
A white girl, born of nonconsanguineous parents at term by spontaneous vaginal delivery, developed neonatal hepatitis with jaundice at 2 months. Jaund
IJMS, Free Full-Text
Niemann-Pick disease type C, Orphanet Journal of Rare Diseases
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Medical School Pathology: Pathophysiology of Lysosomal Storage Diseases
Lysosomal storage diseases - IOS Press
A proposed model for the pathogenesis of Niemann-Pick disease type
Pathophysiology of neuropathic lysosomal storage disorders - Bellettato - 2010 - Journal of Inherited Metabolic Disease - Wiley Online Library
Frontiers CNS-Targeting Therapies for Lysosomal Storage Diseases: Current Advances and Challenges
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Models to study basic and applied aspects of lysosomal storage disorders - ScienceDirect
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