Longitudinal psychiatric symptoms in prodromal Huntington's disease: a decade of data

EA Epping, JI Kim, D Craufurd… - American Journal of …, 2016 - Am Psychiatric Assoc
Objective: Psychiatric symptoms are a significant aspect of Huntington's disease, an
inherited neurodegenerative illness. The presentation of these symptoms is highly variable …

[HTML][HTML] Movement disorder society task force viewpoint: Huntington's disease diagnostic categories

CA Ross, R Reilmann, F Cardoso… - Movement disorders …, 2019 - ncbi.nlm.nih.gov
Huntington's disease (HD) is traditionally considered as a triad of movement, cognitive, and
emotional disorders. 1–4 According to current clinical practice,“manifest HD” is diagnosed …

Selective expression of mutant huntingtin during development recapitulates characteristic features of Huntington's disease

AE Molero, EE Arteaga-Bracho… - Proceedings of the …, 2016 - National Acad Sciences
Recent studies have identified impairments in neural induction and in striatal and cortical
neurogenesis in Huntington's disease (HD) knock-in mouse models and associated …

[HTML][HTML] Enroll-HD: an integrated clinical research platform and worldwide observational study for Huntington's disease

S Sathe, J Ware, J Levey, E Neacy… - Frontiers in …, 2021 - frontiersin.org
Established in July 2012, Enroll-HD is both an integrated clinical research platform and a
worldwide observational study designed to meet the clinical research requirements …

Striatal synaptic dysfunction and altered calcium regulation in Huntington disease

LA Raymond - Biochemical and biophysical research communications, 2017 - Elsevier
Synaptic dysfunction and altered calcium homeostasis in the brain is common to many
neurodegenerative disorders. Among these, Huntington disease (HD), which is inherited in …

A machine‐learning derived Huntington's disease progression model: insights for clinical trial design

A Mohan, Z Sun, S Ghosh, Y Li, S Sathe… - Movement …, 2022 - Wiley Online Library
Background Applying machine‐learning algorithms to large datasets such as those
available in Huntington's disease offers the opportunity to discover hidden patterns, often not …

Network topology and functional connectivity disturbances precede the onset of Huntington's disease

DL Harrington, M Rubinov, S Durgerian, L Mourany… - Brain, 2015 - academic.oup.com
Cognitive, motor and psychiatric changes in prodromal Huntington's disease have nurtured
the emergent need for early interventions. Preventive clinical trials for Huntington's disease …

[HTML][HTML] Huntington disease as a neurodevelopmental disorder and early signs of the disease in stem cells

K Wiatr, WJ Szlachcic, M Trzeciak, M Figlerowicz… - Molecular …, 2018 - Springer
Huntington disease (HD) is a dominantly inherited disorder caused by a CAG expansion
mutation in the huntingtin (HTT) gene, which results in the HTT protein that contains an …

Longitudinal imaging of regional brain volumes, SV2A, and glucose metabolism in Huntington's disease

A Delva, K Van Laere, W Vandenberghe - Movement Disorders, 2023 - Wiley Online Library
Background Development of disease‐modifying treatments for Huntington's disease (HD)
could be aided by the use of imaging biomarkers of disease progression. Positron emission …

[HTML][HTML] Neurotrophin receptor p75NTR mediates Huntington's disease–associated synaptic and memory dysfunction

V Brito, A Giralt, L Enriquez-Barreto… - The Journal of …, 2014 - Am Soc Clin Investig
Learning and memory deficits are early clinical manifestations of Huntington's disease (HD).
These cognitive impairments have been mainly associated with frontostriatal HD pathology; …