Morphology of Niemann-Pick type A metabolic storage disorder
Por um escritor misterioso
Descrição
An Italian girl, of nonconsanguineous parents, had normal growth and development but at 1 year, hepatosplenomegaly was noted. An older sister was norm
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Niemann–Pick disease - Wikipedia
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Frontiers Pre-clinical Mouse Models of Neurodegenerative Lysosomal Storage Diseases
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IJMS, Free Full-Text
Neiman pick disease Type C – Classical morphology
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Glycosphingolipid catabolism and associated lysosomal storage diseases.
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The value of axillary skin electron microscopic analysis in the diagnosis of lysosomal storage disorders - Modern Pathology
Niemann Pick Disease Type C - Symptoms, Causes, Treatment
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Lysosomal Storage Disease: Revealing Lysosomal Function and Physiology
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Frontiers Lysosomal and Mitochondrial Liaisons in Niemann-Pick Disease
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Loss of NPC1 enhances phagocytic uptake and impairs lipid trafficking in microglia
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Models to study basic and applied aspects of lysosomal storage disorders - ScienceDirect
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