Huntington’s disease (HD) is a hereditary disorder characterized by personality changes, chorea, dementia and weight loss. The cause of this weight loss is unknown. The aim of this study was to examine body weight changes and weight-regulating factors in HD using the R6/2 mouse model as a tool. We found that R6/2 mice started losing weight at 9 weeks of age. Total locomotor activity was unaltered and caloric intake was not decreased until 11 weeks of age, which led us to hypothesize that increased metabolism might underlie the weight loss. Indeed, oxygen consumption in R6/2 mice was elevated from 6 weeks of age, indicative of an increased metabolism. Several organ systems that regulate weight and metabolism, including the hypothalamus, the ...
Psychiatric and metabolic features appear several years before motor disturbances in the neurodegene...
Huntington's disease (HD) is characterized by a triad of motor, psychiatric and cognitive symptoms. ...
Huntington's disease (HD) is caused by the expansion of a CAG repeat in the huntingtin (HTT) gene. T...
Huntington’s disease (HD) is a hereditary disorder characterized by personality changes, chorea, dem...
OBJECTIVE: In Huntington's disease (HD), the disease-causing huntingtin (HTT) protein is ubiquitousl...
Huntington´s disease (HD) is a fatal inherited neurodegenerative disorder caused by a CAG triplet re...
Body weight has been shown to be a predictor of clinical progression in Huntington's disease (HD). A...
Huntington’s disease (HD) is a fatal, hereditary disorder caused by a mutation in the gene encoding ...
Huntington disease (HD) is a hereditary neurodegenerative disorder caused by an expanded number of C...
Accumulating evidence suggests altered energy metabolism as a key feature in Huntington's disease (H...
Huntington Disease (HD) is an autosomal dominant neurodegenerative disorder caused by a trinucleotid...
Huntington's disease (HD) is a fatal neurodegenerative disorder caused by an expanded polyglutamine ...
Huntington’s disease (HD) is caused by the expansion of a CAG repeat in the huntingtin (HTT) gene. T...
Huntington’s disease is a progressive neurodegenerative disease caused by a mutation in the huntingt...
Huntington's disease (HD) is a fatal, autosomal dominantly inherited neurodegenerative disorder, cha...
Psychiatric and metabolic features appear several years before motor disturbances in the neurodegene...
Huntington's disease (HD) is characterized by a triad of motor, psychiatric and cognitive symptoms. ...
Huntington's disease (HD) is caused by the expansion of a CAG repeat in the huntingtin (HTT) gene. T...
Huntington’s disease (HD) is a hereditary disorder characterized by personality changes, chorea, dem...
OBJECTIVE: In Huntington's disease (HD), the disease-causing huntingtin (HTT) protein is ubiquitousl...
Huntington´s disease (HD) is a fatal inherited neurodegenerative disorder caused by a CAG triplet re...
Body weight has been shown to be a predictor of clinical progression in Huntington's disease (HD). A...
Huntington’s disease (HD) is a fatal, hereditary disorder caused by a mutation in the gene encoding ...
Huntington disease (HD) is a hereditary neurodegenerative disorder caused by an expanded number of C...
Accumulating evidence suggests altered energy metabolism as a key feature in Huntington's disease (H...
Huntington Disease (HD) is an autosomal dominant neurodegenerative disorder caused by a trinucleotid...
Huntington's disease (HD) is a fatal neurodegenerative disorder caused by an expanded polyglutamine ...
Huntington’s disease (HD) is caused by the expansion of a CAG repeat in the huntingtin (HTT) gene. T...
Huntington’s disease is a progressive neurodegenerative disease caused by a mutation in the huntingt...
Huntington's disease (HD) is a fatal, autosomal dominantly inherited neurodegenerative disorder, cha...
Psychiatric and metabolic features appear several years before motor disturbances in the neurodegene...
Huntington's disease (HD) is characterized by a triad of motor, psychiatric and cognitive symptoms. ...
Huntington's disease (HD) is caused by the expansion of a CAG repeat in the huntingtin (HTT) gene. T...