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PLoS ONE, ISSN 1932-6203, 2011, Volume 6, Issue 10, p. e26317
Journal Article
PLoS ONE, ISSN 1932-6203, 09/2009, Volume 4, Issue 9, p. e6951
Journal Article
Neurobiology of Learning and Memory, ISSN 1074-7427, 2018, p. 106867
Christianson syndrome (CS) is a recently described rare neurogenetic disorder presenting early in life with a broad range of neurological symptoms, including... 
Nociception | Autism | Lysosomal disease | Ganglioside | Neurodegeneration
Journal Article
Cerebral cortex (New York, N.Y. : 1991), ISSN 1047-3211, 09/2019
In mice, terminal differentiation of subpopulations of interneurons occurs in late postnatal stages, paralleling the emergence of the adult cortical... 
Journal Article
International Journal of Cancer, ISSN 0020-7136, 02/2015, Volume 136, Issue 4, pp. 982 - 988
Journal Article
Cell Reports, ISSN 2211-1247, 01/2015, Volume 10, Issue 3, pp. 346 - 358
Polymorphisms that alter serotonin transporter SERT expression and functionality increase the risks for autism and psychiatric traits. Here, we investigate how... 
MONOAMINE-OXIDASE | PRIMARY SOMATOSENSORY CORTEX | CAENORHABDITIS-ELEGANS | TRANSPORTER | CRITICAL PERIOD | BARREL CORTEX | DEFICIENT MICE | RAT-BRAIN | EXPRESSION | PLASTICITY | CELL BIOLOGY
Journal Article
Journal Article
Cerebral cortex (New York, N.Y. : 1991), ISSN 1047-3211, 03/2019
Preterm-born children suffer from neurological and behavioral disorders. Herein, we hypothesized that premature birth and non-maternal care of preterm newborns... 
Journal Article
Neurobiology of Disease, ISSN 0969-9961, 2017, Volume 105, pp. 257 - 270
Abstract Mucolipidosis type IV (MLIV) is a lysosomal storage disease exhibiting progressive intellectual disability, motor impairment, and premature death.... 
Neurology | small molecule therapy | mucolipidosis type IV | lysosomal storage disease | Purkinje cells | glycosphingolipids | miglustat | mucolipin-1
Journal Article
Annals of Clinical and Translational Neurology, ISSN 2328-9503, 05/2016, Volume 3, Issue 5, pp. 366 - 380
Objective Niemann–Pick type C (NPC) disease is a fatal, neurodegenerative, lysosomal storage disorder characterized by intracellular accumulation of... 
STORAGE | TRANSPORT | CHOLESTEROL ACCUMULATION | BETA-CYCLODEXTRIN | NEURONS | GANGLIOSIDES | 2-HYDROXYPROPYL-BETA-CYCLODEXTRIN | MICE | MODEL | CYTOTOXICITY | NEUROSCIENCES | CLINICAL NEUROLOGY | Proteins | Disease | Homeostasis | Lipids | Design of experiments | Age | Cholesterol | Pharmaceuticals
Journal Article