Morphology of Niemann-Pick type A metabolic storage disorder
Por um escritor misterioso
Last updated 18 janeiro 2025
An Italian girl, of nonconsanguineous parents, had normal growth and development but at 1 year, hepatosplenomegaly was noted. An older sister was norm
Adenosine A2A receptor stimulation restores cell functions and differentiation in Niemann-Pick type C-like oligodendrocytes
Morphology of Niemann-Pick type A metabolic storage disorder
PDF) A therapy with miglustat, 2-hydroxypropyl-ß-cyclodextrin and allopregnanolone restores splenic cholesterol homeostasis in Niemann-pick disease type C1
Frontiers Reproduction in Animal Models of Lysosomal Storage Diseases: A Scoping Review
JCM, Free Full-Text
Classification of lysosomal storage diseases according to the
Selected Lysosomal Storage Disorders (LSD).
IJMS, Free Full-Text
Finding pathogenic commonalities between Niemann-Pick type C and other lysosomal storage disorders: Opportunities for shared therapeutic interventions - ScienceDirect
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