Smaller intracranial volume in prodromal Huntington's disease: evidence for abnormal neurodevelopment. - Wikidata - wikimedia - TriplyDB

Smaller intracranial volume in prodromal Huntington's disease: evidence for abnormal neurodevelopment.

Smaller intracranial volume in prodromal Huntington's disease: evidence for abnormal neurodevelopment.

http://www.wikidata.org/entity/Q34514619

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Iron dysregulation in Huntington's disease Huntington's disease: the past, present, and future search for disease modifiers.PGC-1α, mitochondrial dysfunction, and Huntington's disease Modeling Huntington's disease with induced pluripotent stem cells Polyglutamine neurodegeneration: expanded glutamines enhance native functions Dominant-Negative Effects of Adult-Onset Huntingtin Mutations Alter the Division of Human Embryonic Stem Cells-Derived Neural Cells Neuroimaging evidence of deficient axon myelination in Wolfram syndrome.Abnormal subcortical components of the corticostriatal system in young adults with DLI: a combined structural MRI and DTI study.Tractography of the corpus callosum in Huntington's disease.Stable Atlas-based Mapped Prior (STAMP) machine-learning segmentation for multicenter large-scale MRI data.Regionally selective atrophy of subcortical structures in prodromal HD as revealed by statistical shape analysis.Early brain vulnerability in Wolfram syndrome.Spinal cord atrophy in early Huntington's disease.Striatal neurons expressing full-length mutant huntingtin exhibit decreased N-cadherin and altered neuritogenesis.Indexing disease progression at study entry with individuals at-risk for Huntington disease Early white matter abnormalities, progressive brain pathology and motor deficits in a novel knock-in mouse model of Huntington's disease.Characterization of Behavioral, Neuropathological, Brain Metabolic and Key Molecular Changes in zQ175 Knock-In Mouse Model of Huntington's Disease Language deficits in pre-symptomatic Huntington's disease: evidence from Hungarian.Delayed identification and diagnosis of Huntington's disease due to psychiatric symptoms.Measures of growth in children at risk for Huntington disease Depressive symptoms in prodromal Huntington's Disease correlate with Stroop-interference related functional connectivity in the ventromedial prefrontal cortex The dynamics of early-state transcriptional changes and aggregate formation in a Huntington's disease cell model Neurodevelopmental model of schizophrenia: update 2012 Characterization of forebrain neurons derived from late-onset Huntington's disease human embryonic stem cell lines.Cognitive impairment in Huntington disease: diagnosis and treatment.C9ORF72 expansion in a family with bipolar disorder Plasma 24S-hydroxycholesterol correlation with markers of Huntington disease progression.Selective expression of mutant huntingtin during development recapitulates characteristic features of Huntington's disease Abnormal Weight and Body Mass Index in Children with Juvenile Huntington's Disease.8OHdG as a marker for Huntington disease progression Loss of corticostriatal and thalamostriatal synaptic terminals precedes striatal projection neuron pathology in heterozygous Q140 Huntington's disease mice.Patterns of Co-Occurring Gray Matter Concentration Loss across the Huntington Disease Prodrome.Interregional compensatory mechanisms of motor functioning in progressing preclinical neurodegeneration The biological function of the Huntingtin protein and its relevance to Huntington's Disease pathology Huntington disease: a single-gene degenerative disorder of the striatum.Long Term Aggresome Accumulation Leads to DNA Damage, p53-dependent Cell Cycle Arrest, and Steric Interference in Mitosis.Embryonic Mutant Huntingtin Aggregate Formation in Mouse Models of Huntington's Disease.Juvenile Huntington disease in Argentina.Peroxisome-proliferator-activated receptor gamma coactivator 1 α contributes to dysmyelination in experimental models of Huntington's disease.Postnatal and adult consequences of loss of huntingtin during development: Implications for Huntington's disease.

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P2860

Smaller intracranial volume in prodromal Huntington's disease: evidence for abnormal neurodevelopment.

http://www.wikidata.org/entity/Q34514619

description

2010 nî lūn-bûn

@nan

2010 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի հոտեմբերին հրատարակված գիտական հոդված

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2010年の論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年论文

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Smaller intracranial volume in ...... for abnormal neurodevelopment.

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Smaller intracranial volume in ...... for abnormal neurodevelopment.

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Smaller intracranial volume in ...... for abnormal neurodevelopment.

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Smaller intracranial volume in ...... for abnormal neurodevelopment.

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Smaller intracranial volume in ...... for abnormal neurodevelopment.

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Smaller intracranial volume in ...... for abnormal neurodevelopment.

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Smaller intracranial volume in ...... for abnormal neurodevelopment.

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Elizabeth H Aylward

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James A Mills

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Leigh J Beglinger

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Martha A Nance

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PREDICT-HD Investigators and Coordinators of the Huntington Study Group

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Ronald K Pierson

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P2860

RORalpha-mediated Purkinje cell development determines disease severity in adult SCA1 mice

Growth of the normal skull vault and its alteration in craniosynostosis: insights from human genetics and experimental studies

Normal huntingtin function: an alternative approach to Huntington's disease

Targeted disruption of the Huntington's disease gene results in embryonic lethality and behavioral and morphological changes in heterozygotes

Increased apoptosis and early embryonic lethality in mice nullizygous for the Huntington's disease gene homologue

Expression of normal and mutant huntingtin in the developing brain

Huntingtin is required for neurogenesis and is not impaired by the Huntington's disease CAG expansion

AFNI: software for analysis and visualization of functional magnetic resonance neuroimages

Sex differences in behavior and striatal ascorbate release in the 140 CAG knock-in mouse model of Huntington's disease.

Impairment of developmental stem cell-mediated striatal neurogenesis and pluripotency genes in a knock-in model of Huntington's disease

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137-142

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10.1093/BRAIN/AWQ280

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P433

Pt 1

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P478

134

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P50

Jane S. Paulsen

Vincent Magnotta

Douglas R Langbehn

Peggy C Nopoulos

Roger A. Barker

Christopher A Ross

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2010-10-04T00:00:00Z

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47349260

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20923788

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Huntington disease

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3025719

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