Cargando…

Neocortical morphometry in Huntington's disease: Indication of the coexistence of abnormal neurodevelopmental and neurodegenerative processes

Huntington's disease (HD) is an inherited, autosomal dominant disorder that is characteristically thought of as a degenerative disorder. Despite cellular and molecular grounds suggesting HD could also impact normal development, there has been scarce systems-level data obtained from in vivo huma...

Descripción completa

Detalles Bibliográficos
Autores principales:	Mangin, Jean-Francois, Rivière, Denis, Duchesnay, Edouard, Cointepas, Yann, Gaura, Véronique, Verny, Christophe, Damier, Philippe, Krystkowiak, Pierre, Bachoud-Lévi, Anne-Catherine, Hantraye, Philippe, Remy, Philippe, Douaud, Gwenaëlle
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Elsevier 2020
Materias:	Regular Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7044794/ https://www.ncbi.nlm.nih.gov/pubmed/32113174 http://dx.doi.org/10.1016/j.nicl.2020.102211

Ejemplares similares

Alloimmunisation to Donor Antigens and Immune Rejection Following Foetal Neural Grafts to the Brain in Patients with Huntington's Disease
por: Krystkowiak, Pierre, et al.
Publicado: (2007)

Automatic segmentation of the striatum and globus pallidus using MIST: Multimodal Image Segmentation Tool
por: Visser, Eelke, et al.
Publicado: (2016)

How to Capitalize on the Retest Effect in Future Trials on Huntington’s Disease
por: Schramm, Catherine, et al.
Publicado: (2015)

Neuroendocrine Disturbances in Huntington's Disease
por: Saleh, Nadine, et al.
Publicado: (2009)

Insulin-Like Growth Factor-1 but Not Insulin Predicts Cognitive Decline in Huntington’s Disease
por: Salem, Linda, et al.
Publicado: (2016)

Effectiveness of Anti-Psychotics and Related Drugs in the Huntington French-Speaking Group Cohort
por: Désaméricq, Gaëlle, et al.
Publicado: (2014)

Longitudinal Study of Informed Consent in Innovative Therapy Research: Experience and Provisional Recommendations from a Multicenter Trial of Intracerebral Grafting
por: Cleret de Langavant, Laurent, et al.
Publicado: (2015)

International Guidelines for the Treatment of Huntington's Disease
por: Bachoud-Lévi, Anne-Catherine, et al.
Publicado: (2019)

Genetics and Function of Neocortical GABAergic Interneurons in Neurodevelopmental Disorders
por: Rossignol, E.
Publicado: (2011)

COMT Val(158)Met Polymorphism Modulates Huntington's Disease Progression
por: de Diego-Balaguer, Ruth, et al.
Publicado: (2016)

Cell therapy in Huntington's disease: Taking stock of past studies to move the field forward
por: Bachoud‐Lévi, Anne‐Catherine, et al.
Publicado: (2020)

The Neurodevelopmental Hypothesis of Huntington’s Disease
por: van der Plas, Ellen, et al.
Publicado: (2020)

A new approach to digitized cognitive monitoring: validity of the SelfCog in Huntington’s disease
por: Lunven, Marine, et al.
Publicado: (2023)

Awareness of Memory Deficits in Early Stage Huntington's Disease
por: Cleret de Langavant, Laurent, et al.
Publicado: (2013)

The specific role of the striatum in interval timing: The Huntington’s disease model
por: Lemoine, Laurie, et al.
Publicado: (2021)

One-year changes in brain microstructure differentiate preclinical Huntington's disease stages
por: Pflanz, Chris Patrick, et al.
Publicado: (2019)

Functional Changes in Neocortical Activity in Huntington's Disease Model Mice: An in vivo Intracellular Study
por: Stern, Edward A.
Publicado: (2011)

Combining Literature Review With a Ground Truth Approach for Diagnosing Huntington's Disease Phenocopy
por: Nguyen, Quang Tuan Rémy, et al.
Publicado: (2022)

Cognitive processes of apathy in Huntington’s disease show high sensitivity to disease progression
por: Hare, Emily, et al.
Publicado: (2022)

Corrigendum: Combining Literature Review With a Ground Truth Approach for Diagnosing Huntington's Disease Phenocopy
por: Nguyen, Quang Tuan Rémy, et al.
Publicado: (2022)

IntrAnat Electrodes: A Free Database and Visualization Software for Intracranial Electroencephalographic Data Processed for Case and Group Studies
por: Deman, Pierre, et al.
Publicado: (2018)

Voxel-based morphometry with templates and validation in a mouse model of Huntington’s disease()
por: Sawiak, Stephen J., et al.
Publicado: (2013)

Coexistence of Gait Disturbances and Chorea in Experimental Huntington's Disease
por: Casaca-Carreira, João, et al.
Publicado: (2015)

Planning deficits in Huntington’s disease: A brain structural correlation by voxel-based morphometry
por: Calderon-Villalon, Jesus, et al.
Publicado: (2021)

Behavioral and Neural Correlates of Communication via Pointing
por: Cleret de Langavant, Laurent, et al.
Publicado: (2011)

Self-Reported Social Relationship Capacities Predict Motor, Functional and Cognitive Decline in Huntington’s Disease
por: Lemercier, Pablo, et al.
Publicado: (2022)

Default-Mode Network Changes in Huntington’s Disease: An Integrated MRI Study of Functional Connectivity and Morphometry
por: Quarantelli, Mario, et al.
Publicado: (2013)

Brain-Derived Neurotrophic Factor in Patients with Huntington's Disease
por: Zuccato, Chiara, et al.
Publicado: (2011)

A validation dataset for Macaque brain MRI segmentation
por: Balbastre, Yaël, et al.
Publicado: (2017)

Predicting clinical scores in Huntington’s disease: a lightweight speech test
por: Riad, Rachid, et al.
Publicado: (2022)

Neocortical development /
por: Bayer, Shirley A. 1940- (Shirley Ann)
Publicado: (1991)

The Neocortical Column
por: DeFelipe, Javier, et al.
Publicado: (2012)

In vivo expression of polyglutamine-expanded huntingtin by mouse striatal astrocytes impairs glutamate transport: a correlation with Huntington's disease subjects
por: Faideau, Mathilde, et al.
Publicado: (2010)

Failure of the Nemo Trial: Bumetanide Is a Promising Agent to Treat Many Brain Disorders but Not Newborn Seizures
por: Ben-Ari, Yehezkel, et al.
Publicado: (2016)

Cognitive decline in Huntington’s disease in the Digitalized Arithmetic Task (DAT)
por: Lunven, Marine, et al.
Publicado: (2021)

Huntington Disease as a Neurodevelopmental Disorder and Early Signs of the Disease in Stem Cells
por: Wiatr, Kalina, et al.
Publicado: (2017)

Perinatal insults and neurodevelopmental disorders may impact Huntington's disease age of diagnosis
por: Barkhuizen, Melinda, et al.
Publicado: (2018)

Loss of the thyroid hormone-binding protein Crym renders striatal neurons more vulnerable to mutant huntingtin in Huntington's disease
por: Francelle, Laetitia, et al.
Publicado: (2015)

Connectivity-Based Parcellation of the Cortical Mantle Using q-Ball Diffusion Imaging
por: Perrin, Muriel, et al.
Publicado: (2008)

Effects of Human Alpha-Synuclein A53T-A30P Mutations on SVZ and Local Olfactory Bulb Cell Proliferation in a Transgenic Rat Model of Parkinson Disease
por: Lelan, Faustine, et al.
Publicado: (2011)

Cannot write session to /tmp/vufind_sessions/sess_cv77ip5ffmjfda36fv3tfc39qo