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Journal Article
Handbook of Experimental Pharmacology, ISSN 0171-2004, 2013, Volume 216, Issue 216, pp. 405 - 419
Conference Proceeding
DMM Disease Models and Mechanisms, ISSN 1754-8403, 11/2011, Volume 4, Issue 6, pp. 746 - 752
Journal Article
Brain, ISSN 0006-8950, 2012, Volume 135, Issue 6, pp. 1724 - 1735
Gaucher's disease, the most common lysosomal storage disorder, is caused by the defective activity of glucocerebrosidase, the lysosomal hydrolase that degrades... 
neuroinflammation | lysosomal storage disorders | Gaucher's disease | CYTOKINES | MICROGLIAL ACTIVATION | NEURODEGENERATION | SANDHOFF-DISEASE | NEUROSCIENCES | MOUSE MODELS | CLINICAL NEUROLOGY | PATHOPHYSIOLOGY | HEPARAN-SULFATE | MICE | TNF-ALPHA | Enzyme-Linked Immunosorbent Assay - methods | Ibuprofen - therapeutic use | Neurons - pathology | Encephalitis - diagnosis | Nestin | Blood-Brain Barrier - physiopathology | Gene Expression Regulation, Developmental - genetics | Tyrosine - analogs & derivatives | Antigens, CD - metabolism | Dose-Response Relationship, Drug | Glucosylceramidase - deficiency | Encephalitis - drug therapy | Intermediate Filament Proteins - genetics | Microglia - pathology | Microfilament Proteins - metabolism | Cell Death - drug effects | Neurons - drug effects | Cytokines - genetics | Gaucher Disease - drug therapy | Disease Models, Animal | Animals, Newborn | Calcium-Binding Proteins - metabolism | Cytokines - metabolism | Encephalitis - pathology | Mice, Transgenic | Gaucher Disease - complications | Nerve Tissue Proteins - genetics | Magnetic Resonance Imaging | Intercellular Adhesion Molecule-1 - metabolism | Tyrosine - metabolism | Animals | Gaucher Disease - genetics | Anti-Inflammatory Agents, Non-Steroidal - therapeutic use | Antigens, Differentiation, Myelomonocytic - metabolism | TATA Box | Mice | Endothelial Cells - pathology | Vascular Cell Adhesion Molecule-1 - metabolism | Encephalitis - etiology | Immunoglobulin G - metabolism
Journal Article
VACCINES, ISSN 2076-393X, 02/2019, Volume 7, Issue 1, p. 19
Viral infections of the central nervous system (CNS) lead to a broad range of pathologies. CNS infections with Orthopox viruses have been mainly documented as... 
UNITED-STATES | MEDICINE, RESEARCH & EXPERIMENTAL | IMMUNE-RESPONSE | smallpox | IMMUNOLOGY | brain | BLOOD-BRAIN-BARRIER | METALLOPROTEINASE-1 | vaccinia | meningoencephalitis | REPLICATION | RNA-seq | GENE | neurovirulence | MATRIX-METALLOPROTEINASE-9 | SMALLPOX VACCINATION | INHIBITOR | ADVERSE EVENTS
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 04/2011, Volume 20, Issue 7, pp. 1375 - 1386
Gaucher disease (GD), the most common lysosomal storage disorder, is caused by a deficiency in the lysosomal enzyme glucocerebrosidase (GlcCerase), which... 
Brain | Animal models | Pons | lysosomal storage diseases | Neurons | Substantia nigra | Inflammation | Cochlear nuclei | Somatosensory system | Gliosis | Cell death | Lysosomal enzymes | Neurological complications | Glucosylceramidase | Gaucher's disease
Journal Article