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Journal Article
Journal Article
Neurology, ISSN 0028-3878, 01/2018, Volume 90, Issue 4, pp. e264 - e272
OBJECTIVETo investigate the feasibility of microRNA (miRNA) levels in CSF as biomarkers for prodromal Huntington disease (HD). METHODSmiRNA levels were... 
CLINICAL NEUROLOGY | MicroRNAs - cerebrospinal fluid | Humans | Middle Aged | Huntington Disease - genetics | Adult | Female | Heterozygote | Male | Biomarkers - cerebrospinal fluid | Prodromal Symptoms | Huntington Disease - cerebrospinal fluid | Feasibility Studies | 319 | 164
Journal Article
Journal Article
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 12/2017, Volume 114, Issue 52, pp. E11293 - E11302
The neurodegenerative disorder Huntington's disease (HD) is typically characterized by extensive loss of striatal neurons and the midlife onset of debilitating... 
Urea | Sheep | Huntington's disease | Metabolism | Prodromal | MOLECULAR CHARACTERIZATION | LIVING RAT | TRANSPORTER | MULTIDISCIPLINARY SCIENCES | WEIGHT-LOSS | IDENTIFICATION | prodromal | urea | GENE | metabolism | INTRANUCLEAR INCLUSIONS | EXPRESSION | sheep | TRINUCLEOTIDE REPEAT | Diagnosis | Huntington's chorea | Health aspects
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 12/2017, Volume 114, Issue 52, pp. E11293 - E11302
The neurodegenerative disorder Huntington’s disease (HD) is typically characterized by extensive loss of striatal neurons and the midlife onset of debilitating... 
Biological Sciences | PNAS Plus | Huntington’s disease | metabolism | prodromal | sheep | urea
Journal Article
Human Brain Mapping, ISSN 1065-9471, 10/2018, Volume 39, Issue 10, pp. 3871 - 3883
Huntington's disease (HD) is an inherited neurodegenerative disorder that causes progressive breakdown of striatal neurons. Standard white matter integrity... 
diffusion MRI | cortico‐striatal pathways | CAG‐repeats | isotropic volume fraction | prodromal‐HD | prodromal-HD | cortico-striatal pathways | CAG-repeats | TRACK-HD | WHITE-MATTER | AT-RISK | EXTRACELLULAR FREE-WATER | PREMANIFEST | NEUROSCIENCES | NEUROIMAGING | CEREBRAL-CORTEX | LONGITUDINAL CHANGE | BASAL GANGLIA VOLUME | CORTICOSTRIATAL PATHWAY | RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING | PROGRESSION | Putamen - pathology | Humans | Huntington Disease - pathology | Middle Aged | Atrophy - pathology | Caudate Nucleus - pathology | Male | Neural Pathways - pathology | Prodromal Symptoms | Trinucleotide Repeats - genetics | Diffusion Tensor Imaging - methods | Young Adult | Genetic Load | Aged, 80 and over | Adult | Female | Putamen - diagnostic imaging | Motor Cortex - pathology | White Matter - pathology | Huntington Disease - diagnostic imaging | Motor Cortex - diagnostic imaging | Caudate Nucleus - diagnostic imaging | White Matter - diagnostic imaging | Neural Pathways - diagnostic imaging | Adolescent | Huntington Disease - genetics | Aged | Longitudinal Studies | Genetic research | Brain | Nervous system diseases | Diagnostic imaging | Algorithms | Anisotropy | Huntingtons disease | Neuroimaging | Diffusion rate | Genetic load | Motors | Atrophy | Confidence intervals | Pathways | Neostriatum | Diffusion | Medical imaging | Statistical analysis | Polyglutamine | Neurodegenerative diseases | Trinucleotide repeats | Regression analysis | Huntington's disease | Substantia alba | Hand | Putamen | Magnetic resonance imaging | Diagnostic systems | Integrity
Journal Article