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Acta Neuropathologica, ISSN 0001-6322, 10/2013, Volume 126, Issue 4, pp. 555 - 573
α-Synuclein (α-syn) is a protein prevalent in neural tissue and known to undergo axonal transport. Intracellular α-syn aggregates are a hallmark of Parkinson’s... 
Pathology | α-Synuclein | Neurosciences | Olfactory pathway | Medicine & Public Health | Transfer | Olfactory bulb | Parkinson’s disease | Microglia | Parkinson's disease | CLEARANCE | RAT | AXONAL-TRANSPORT | PATHOLOGY | NEUROSCIENCES | OLIGOMERS | CLINICAL NEUROLOGY | FIBRILS | NEURODEGENERATIVE-DISEASES | DYSFUNCTION | TO-NEURON TRANSMISSION | PROTEINS | alpha-Synuclein | PARKINSONS-DISEASE PATHOLOGY | Immunohistochemistry | Microglia - metabolism | Parkinson Disease - pathology | Olfactory Bulb - pathology | Cell Count | Coloring Agents | Humans | Mice, Inbred C57BL | Axonal Transport - physiology | Neural Pathways - pathology | Parkinson Disease - genetics | Recombinant Proteins - biosynthesis | Recombinant Proteins - pharmacology | Stereotaxic Techniques | Animals | Fluorescent Antibody Technique | Brain - pathology | Microglia - pathology | Female | Mice | alpha-Synuclein - genetics | Lewy Bodies - pathology | Fluorescent Dyes | Axonal transport | Brain | Axonal Transport | Neurons and Cognition | Neurobiology | Recombinant Proteins | Neural Pathways | Life Sciences | Psychology and behavior | Olfactory Bulb | Lewy Bodies | Parkinson Disease | Cognitive Sciences | Original Paper | Basic Medicine | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper | Neurovetenskaper
Journal Article
Acta Neuropathologica, ISSN 0001-6322, 9/2015, Volume 130, Issue 3, pp. 333 - 348
Parkinson disease (PD) is a neurodegenerative disorder characterized by massive loss of midbrain dopaminergic neurons. Whereas onset of motor impairments... 
Pathology | Neurosciences | Braak stages | Medicine & Public Health | Neurodegeneration | Hyposmia | Olfactory perception | Parkinson disease | Olfactory bulbectomy | ADULT NEUROGENESIS | SUBVENTRICULAR ZONE | PATHOLOGY | PARKINSONS-DISEASE PATIENTS | SUBSTANTIA-NIGRA | NEUROSCIENCES | PRECURSOR CELL-PROLIFERATION | CLINICAL NEUROLOGY | RECEPTOR STIMULATION | ALPHA-SYNUCLEINOPATHY | BULB | NEURONS | BRAIN | Immunohistochemistry | Neurons - pathology | Neural Pathways - drug effects | Rats, Wistar | Substantia Nigra - pathology | Neuroanatomical Tract-Tracing Techniques | Male | Olfactory Bulb - metabolism | Neural Pathways - pathology | Substantia Nigra - metabolism | Oxidopamine | Parkinsonian Disorders - metabolism | Olfaction Disorders - metabolism | Parkinsonian Disorders - drug therapy | Neurogenesis - drug effects | Neurons - metabolism | Neurons - drug effects | Dopamine - metabolism | Dopamine Agonists - pharmacology | Olfaction Disorders - pathology | Olfactory Bulb - pathology | Neural Stem Cells - drug effects | Thiophenes - pharmacology | Neural Stem Cells - pathology | Olfaction Disorders - drug therapy | Substantia Nigra - drug effects | Animals | Parkinsonian Disorders - pathology | Neurogenesis - physiology | Tetrahydronaphthalenes - pharmacology | Neural Pathways - metabolism | Neural Stem Cells - metabolism | Olfactory Bulb - drug effects | Neuronal Tract-Tracers | Physiological aspects | Nervous system diseases | Parkinson's disease | Index Medicus
Journal Article
Journal of Comparative Neurology, ISSN 0021-9967, 10/2003, Volume 465, Issue 1, pp. 11 - 26
Huntington's disease (HD) is caused by an abnormal expansion of CAG repeats in the gene encoding huntingtin. The development of therapies for HD requires... 
neurodegenerative disease | immunohistochemistry | behavior | huntingtin protein | Immunohistochemistry | Huntingtin protein | Neurodegenerative disease | Behavior | CATECHOLAMINE INNERVATION | NEUROSCIENCES | CELL-DEATH | NEURONAL INTRANUCLEAR INCLUSIONS | NUCLEAR-LOCALIZATION | ZOOLOGY | INTRASTRIATAL INJECTION | TERMINAL FRAGMENTS | BASAL FOREBRAIN | STRIATAL NEURONS | TRANSGENIC MICE | Neurons - pathology | Neuropil - pathology | Huntington Disease - pathology | Nerve Tissue Proteins - deficiency | Nucleus Accumbens - metabolism | Cerebral Cortex - pathology | Male | Trinucleotide Repeats - genetics | Corpus Striatum - metabolism | Cerebral Cortex - metabolism | Cerebral Cortex - physiopathology | Brain - metabolism | Olfactory Pathways - physiopathology | Time Factors | Nuclear Proteins - deficiency | Female | Neurons - metabolism | Inclusion Bodies - metabolism | Nuclear Proteins - genetics | Corpus Striatum - pathology | Olfactory Pathways - pathology | Huntington Disease - physiopathology | Disease Models, Animal | Nucleus Accumbens - pathology | Grooming - physiology | Nucleus Accumbens - physiopathology | Olfactory Pathways - metabolism | Corpus Striatum - physiopathology | Brain - physiopathology | Mice, Transgenic | Lameness, Animal - pathology | Nerve Tissue Proteins - genetics | Lameness, Animal - physiopathology | Motor Activity - genetics | Inclusion Bodies - genetics | Neuropil - metabolism | Animals | Brain - pathology | Huntington Disease - genetics | Inclusion Bodies - pathology | Recombinant Fusion Proteins - genetics | Mice | Lameness, Animal - genetics
Journal Article
Journal Article
Brain, ISSN 0006-8950, 2013, Volume 136, Issue 10, pp. 3028 - 3037
Journal Article
Journal Article
Neurobiology of Disease, ISSN 0969-9961, 2011, Volume 46, Issue 3, pp. 527 - 552
Abstract Olfactory dysfunction is an early ‘pre-clinical’ sign of Parkinson's disease (PD). The present review is a comprehensive and up-to-date assessment of... 
Neurology | Parkinson's disease | Dopamine | Neurodegenerative diseases | Serotonin | Lewy body disease | Electrophysiology | Psychophysics | Olfaction | Aging | Genetics | Acetylcholine | Norepinephrine | Dystonia | Functional imaging | PRIMATE ORBITOFRONTAL CORTEX | MULTIPLE SYSTEM ATROPHY | SMELL IDENTIFICATION TEST | G2019S MUTATION CARRIERS | NIGROSTRIATAL DOPAMINERGIC DENERVATION | AMYOTROPHIC-LATERAL-SCLEROSIS | ODOR DETECTION PERFORMANCE | NEUROSCIENCES | 1-METHYL-4-PHENYL-1,2,3,6-TETRAHYDROPYRIDINE RAT MODEL | DRUG-INDUCED PARKINSONISM | PROGRESSIVE SUPRANUCLEAR PALSY | Parkinson Disease - complications | Parkinsonian Disorders - physiopathology | Diagnosis, Differential | Olfactory Bulb - physiopathology | Parkinsonian Disorders - complications | Humans | Parkinsonian Disorders - psychology | Neurotransmitter Agents - metabolism | Olfactory Mucosa - physiopathology | Parkinson Disease - genetics | Parkinson Disease - physiopathology | Parkinson Disease - psychology | Neuropsychological Tests | Olfactory Pathways - physiopathology | Smell - physiology | Phenotype | Animals | Olfaction Disorders - physiopathology | Olfactory Mucosa - pathology | Parkinsonian Disorders - genetics | Olfaction Disorders - etiology | Olfactory Pathways - pathology | Index Medicus | Oxidative stress | Animal models | Data processing | Nervous system | Inflammation | Dysautonomia | Olfactory thresholds | Olfactory system | Reviews | Sleep | Olfactory bulb | Brain injury | Movement disorders
Journal Article