Juvenile onset Huntington's disease--clinical and research perspectives. (Q34091006)

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11 November 2019

review article

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title

Juvenile onset Huntington's disease--clinical and research perspectives (English)

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11 November 2019

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11 November 2019

M A Nance

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11 November 2019

publication date

1 January 2001

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Mental Retardation and Developmental Disabilities Research Reviews

11 November 2019

published in

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11 November 2019

volume

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11 November 2019

issue

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11 November 2019

page(s)

153-157

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Ethical issues policy statement on Huntington's disease molecular genetics predictive test. International Huntington Association. World Federation of Neurology

11 November 2019

cites work

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Guidelines for the molecular genetics predictive test in Huntington's disease

21 January 2018

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Intranuclear neuronal inclusions in Huntington's disease and dentatorubral and pallidoluysian atrophy: correlation between the density of inclusions and IT15 CAG triplet repeat length

21 January 2018

1 reference

Formation of neuronal intranuclear inclusions underlies the neurological dysfunction in mice transgenic for the HD mutation

21 January 2018

1 reference

Aggregation of huntingtin in neuronal intranuclear inclusions and dystrophic neurites in brain

21 January 2018

1 reference

Trinucleotide repeat length instability and age of onset in Huntington's disease

21 January 2018

1 reference

Inactivation of the mouse Huntington's disease gene homolog Hdh

21 January 2018

1 reference

Huntingtin interacts with a family of WW domain proteins

21 January 2018

1 reference

A polymorphic DNA marker genetically linked to Huntington's disease

21 January 2018

1 reference

The neurogenetics genie: testing for the Huntington's disease mutation

21 January 2018

1 reference

A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes.

21 January 2018

1 reference

The expanded CAG repeat associated with juvenile Huntington disease shows a common origin of most or all neurons and glia in human cerebrum.

21 January 2018

1 reference

Single sperm analysis of the trinucleotide repeats in the Huntington's disease gene: quantification of the mutation frequency spectrum

21 January 2018

1 reference

Exon 1 of the HD gene with an expanded CAG repeat is sufficient to cause a progressive neurological phenotype in transgenic mice

21 January 2018

1 reference

Clinical and neuropathologic assessment of severity in Huntington's disease

21 January 2018

1 reference

Factors associated with slow progression in Huntington's disease

21 January 2018

1 reference

Genetic testing of children at risk for Huntington's disease. US Huntington Disease Genetic Testing Group

21 January 2018

1 reference

Analysis of a very large trinucleotide repeat in a patient with juvenile Huntington's disease

21 January 2018

1 reference

Behavioural abnormalities and selective neuronal loss in HD transgenic mice expressing mutated full-length HD cDNA.

21 January 2018

1 reference

Transgenic models of Huntington's disease

21 January 2018

1 reference

Axonal transport of N-terminal huntingtin suggests early pathology of corticostriatal projections in Huntington disease

21 January 2018

1 reference

Molecular analysis of juvenile Huntington disease: the major influence on (CAG)n repeat length is the sex of the affected parent.

21 January 2018

1 reference

Presymptomatic testing for Huntington's disease in Wales 1987-90

21 January 2018

1 reference

Long glutamine tracts cause nuclear localization of a novel form of huntingtin in medium spiny striatal neurons in HdhQ92 and HdhQ111 knock-in mice

21 January 2018

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

21 January 2018

1 reference

Mitotic stability and meiotic variability of the (CAG)n repeat in the Huntington disease gene

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1002/MRDD.1022

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11 November 2019

1 reference

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