Anatomo-functional origins of the cortical silent period: spotlight on the basal ganglia
D Zeugin, S Ionta - Brain sciences, 2021 - mdpi.com
The so-called cortical silent period (CSP) refers to the temporary interruption of
electromyographic signal from a muscle following a motor-evoked potential (MEP) triggered …
electromyographic signal from a muscle following a motor-evoked potential (MEP) triggered …
Amyloid-Induced Neurodegeneration: A Comprehensive Review through Aggregomics Perception of Proteins in Health and Pathology
Amyloidosis of protein caused by fibrillation and aggregation are some of the most exciting
new edges not only in protein sciences but also in molecular medicines. The present review …
new edges not only in protein sciences but also in molecular medicines. The present review …
Cerebellar degeneration correlates with motor symptoms in Huntington disease
MK Singh‐Bains, NF Mehrabi, T Sehji… - Annals of …, 2019 - Wiley Online Library
Objective Huntington disease (HD) is an autosomal dominant neurodegenerative disorder
characterized by variable motor and behavioral symptoms attributed to major …
characterized by variable motor and behavioral symptoms attributed to major …
Beta-boswellic acid reverses 3-nitropropionic acid-induced molecular, mitochondrial, and histopathological defects in experimental rat model of Huntington's disease
Huntington's disease (HD) is distinguished by a triple repeat of CAG in exon 1, an increase
in poly Q in the Htt gene, and a loss of GABAergic medium spiny neurons (MSN) in the …
in poly Q in the Htt gene, and a loss of GABAergic medium spiny neurons (MSN) in the …
Apathy in Huntington's Disease: A review of the current conceptualization
Apathy is one of the most common psychiatric symptoms experienced by patients with
Huntington's disease (HD). It appears early, progresses with the disease course and has …
Huntington's disease (HD). It appears early, progresses with the disease course and has …
Neuropathology and pathogenesis of extrapyramidal movement disorders: a critical update. II. Hyperkinetic disorders
KA Jellinger - Journal of Neural Transmission, 2019 - Springer
Extrapyramidal movement disorders comprise hypokinetic-rigid and hyperkinetic or mixed
forms, most of them originating from dysfunction of the basal ganglia (BG) and their …
forms, most of them originating from dysfunction of the basal ganglia (BG) and their …
Intellectual curiosity and action initiation are subtypes of apathy affected in Huntington disease gene expansion carriers
RK Hendel, MNN Hellem, LE Hjermind… - Cognitive and …, 2021 - journals.lww.com
Background: Apathy is a prevalent behavioral syndrome of Huntington disease (HD) that
can result in severe loss of function for the individual with HD and substantial caregiver …
can result in severe loss of function for the individual with HD and substantial caregiver …
Endophenotypical drift in Huntington's disease: a 5-year follow-up study
MNN Hellem, RK Hendel, T Vinther-Jensen… - Orphanet Journal of …, 2021 - Springer
Background Huntington's disease (HD) is clinically characterized by progressing motor,
cognitive and psychiatric symptoms presenting as varying phenotypes within these three …
cognitive and psychiatric symptoms presenting as varying phenotypes within these three …
Investigating altered limbic reward system in Huntington's Disease: Implications for apathy
V Bikou, I de Vicente, AE De Paepe, C Garcia-Gorro… - bioRxiv, 2024 - biorxiv.org
Huntington's disease (HD) is an inherited neurodegenerative condition characterized by
motor, cognitive, and behavioral impairments. Apathy, marked by reduced motivation and …
motor, cognitive, and behavioral impairments. Apathy, marked by reduced motivation and …
[PDF][PDF] Identification and characterisation of genetic variation that modifies age at onset in Huntington's disease
WB McAllister - 2019 - core.ac.uk
Huntington's disease (HD) is a progressive and ultimately fatal neurodegeneration caused
by a CAG repeat expansion in the huntingtin gene (HTT). The length of the CAG repeat is …
by a CAG repeat expansion in the huntingtin gene (HTT). The length of the CAG repeat is …