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Huntington disease: a single-gene degenerative disorder of the striatum

Dialogues in clinical neuroscience, 2016-03, Vol.18 (1), p.91-98

Nopoulos, Peggy C.

2016

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White matter microstructure relates to motor outcomes in myotonic dystrophy type 1 independently of disease duration and genetic burden

Scientific reports, 2021-03, Vol.11 (1), p.4886-4886, Article 4886

2021

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Cerebral cortex structure in prodromal Huntington disease

Neurobiology of disease, 2010-12, Vol.40 (3), p.544-554

2010

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Cognitive Deficits, Apathy, and Hypersomnolence Represent the Core Brain Symptoms of Adult-Onset Myotonic Dystrophy Type 1

Frontiers in neurology, 2021-07, Vol.12, p.700796-700796

2021

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Blood-Based Markers of Neuronal Injury in Adult-Onset Myotonic Dystrophy Type 1

Frontiers in neurology, 2022-01, Vol.12, p.791065-791065

2022

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Association of CAG Repeat Length in the Huntington Gene With Cognitive Performance in Young Adults

Neurology, 2021-05, Vol.96 (19), p.e2407

2021

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Behavioral features in child and adolescent huntingtin gene‐mutation carriers

Brain and behavior, 2022-07, Vol.12 (7), p.e2630-n/a

2022

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Associations between neurofilament light-chain protein, brain structure, and chronic kidney disease

Pediatric research, 2022-06, Vol.91 (7), p.1735-1740

2022

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Assisted annotation in Deep LOGISMOS: Simultaneous multi‐compartment 3D MRI segmentation of calf muscles

Medical physics (Lancaster), 2023-08, Vol.50 (8), p.4916-4929

2023

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Abnormal brain development in child and adolescent carriers of mutant huntingtin

Neurology, 2019-09, Vol.93 (10), p.e1021

2019

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Procedural and declarative memory brain systems in developmental language disorder (DLD)

Brain and language, 2020-06, Vol.205, p.104789-104789, Article 104789

2020

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Brain tissue- and region-specific abnormalities on volumetric MRI scans in 21 patients with Bardet-Biedl syndrome (BBS)

BMC medical genetics, 2011-07, Vol.12 (1), p.101-101, Article 101

2011

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Mutant Huntingtin Drives Development of an Advantageous Brain Early in Life: Evidence in Support of Antagonistic Pleiotropy

Annals of neurology, 2024-08

2024

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Neurofilament Light Protein as a Potential Blood Biomarker for Huntington's Disease in Children

Movement disorders, 2022-07, Vol.37 (7), p.1526-1531

2022

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Cognitive function and its relationship with brain structure in myotonic dystrophy type 1

Journal of neuroscience research, 2021-01, Vol.99 (1), p.190-199

2021

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Global and Regional White Matter Fractional Anisotropy in Children with Chronic Kidney Disease

The Journal of pediatrics, 2022-03, Vol.242, p.166-173.e3

2022

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Cerebral blood flow and neuropsychological functioning in elderly vascular disease patients

Journal of clinical and experimental neuropsychology, 2012-02, Vol.34 (2), p.220-225

2012

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Longitudinal change in regional brain volumes in prodromal Huntington disease

Journal of neurology, neurosurgery and psychiatry, 2011-04, Vol.82 (4), p.405-410

2011

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Striatal Development in Early‐Onset Huntington's Disease

Movement disorders, 2022-12, Vol.37 (12), p.2459-2460

2022

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Early pediatric chronic kidney disease is associated with brain volumetric gray matter abnormalities

Pediatric research, 2021-02, Vol.89 (3), p.526-532

2021

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Striatal and white matter predictors of estimated diagnosis for Huntington disease

Brain research bulletin, 2010-05, Vol.82 (3), p.201-207

2010

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Longitudinal changes in white matter as measured with diffusion tensor imaging in adult-onset myotonic dystrophy type 1

Neuromuscular disorders : NMD, 2023-08, Vol.33 (8), p.660-669

2023

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Longitudinal Clinical and Biological Characteristics in Juvenile‐Onset Huntington's Disease

Movement disorders, 2023-01, Vol.38 (1), p.113-122

2023

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Abnormal subcortical components of the corticostriatal system in young adults with DLI: A combined structural MRI and DTI study

Neuropsychologia, 2013-09, Vol.51 (11), p.2154-2161

2013

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Striatal Volume Contributes to the Prediction of Onset of Huntington Disease in Incident Cases

Biological psychiatry (1969), 2012-05, Vol.71 (9), p.822-828

2012

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Huntington disease: a single-gene degenerative disorder of the striatum

White matter microstructure relates to motor outcomes in myotonic dystrophy type 1 independently of disease duration and genetic burden

Cerebral cortex structure in prodromal Huntington disease

Cognitive Deficits, Apathy, and Hypersomnolence Represent the Core Brain Symptoms of Adult-Onset Myotonic Dystrophy Type 1

Blood-Based Markers of Neuronal Injury in Adult-Onset Myotonic Dystrophy Type 1

Association of CAG Repeat Length in the Huntington Gene With Cognitive Performance in Young Adults

Behavioral features in child and adolescent huntingtin gene‐mutation carriers

Associations between neurofilament light-chain protein, brain structure, and chronic kidney disease

Assisted annotation in Deep LOGISMOS: Simultaneous multi‐compartment 3D MRI segmentation of calf muscles

Abnormal brain development in child and adolescent carriers of mutant huntingtin

Procedural and declarative memory brain systems in developmental language disorder (DLD)

Brain tissue- and region-specific abnormalities on volumetric MRI scans in 21 patients with Bardet-Biedl syndrome (BBS)

Mutant Huntingtin Drives Development of an Advantageous Brain Early in Life: Evidence in Support of Antagonistic Pleiotropy

Neurofilament Light Protein as a Potential Blood Biomarker for Huntington's Disease in Children

Cognitive function and its relationship with brain structure in myotonic dystrophy type 1

Global and Regional White Matter Fractional Anisotropy in Children with Chronic Kidney Disease

Cerebral blood flow and neuropsychological functioning in elderly vascular disease patients

Longitudinal change in regional brain volumes in prodromal Huntington disease

Striatal Development in Early‐Onset Huntington's Disease

Early pediatric chronic kidney disease is associated with brain volumetric gray matter abnormalities

Striatal and white matter predictors of estimated diagnosis for Huntington disease

Longitudinal changes in white matter as measured with diffusion tensor imaging in adult-onset myotonic dystrophy type 1

Longitudinal Clinical and Biological Characteristics in Juvenile‐Onset Huntington's Disease

Abnormal subcortical components of the corticostriatal system in young adults with DLI: A combined structural MRI and DTI study

Striatal Volume Contributes to the Prediction of Onset of Huntington Disease in Incident Cases

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