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
Niemann-Pick disease types A and B (NORD): Video
IJMS, Free Full-Text
Pathophysiology of neuropathic lysosomal storage disorders - Bellettato - 2010 - Journal of Inherited Metabolic Disease - Wiley Online Library
Niemann-Pick Disease Concise Medical Knowledge
Frontiers Lysosomal and Mitochondrial Liaisons in Niemann-Pick Disease
Gaucher disease with foamy transformed macrophages and erythrophagocytic activity - Machaczka - 2011 - Journal of Inherited Metabolic Disease - Wiley Online Library
Loss of NPC1 enhances phagocytic uptake and impairs lipid trafficking in microglia
Lysosomal storage diseases - IOS Press
Morphology of Niemann-Pick type A metabolic storage disorder
TPC2 rescues lysosomal storage in mucolipidosis type IV, Niemann–Pick type C1, and Batten disease
Niemann-Pick C disease and mobilization of lysosomal cholesterol by cyclodextrin - ScienceDirect
IJMS, Free Full-Text
Models to study basic and applied aspects of lysosomal storage disorders - ScienceDirect
Lysosomal storage diseases—the horizon expands
de
por adulto (o preço varia de acordo com o tamanho do grupo)
