Huntington's disease. Part 2: treatment and management issues in juvenile HD. (Q37139113)

18 August 2017

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title

Huntington's disease. Part 2: treatment and management issues in juvenile HD. (English)

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18 August 2017

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Aimee Aubeeluck

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18 August 2017

Helen Brewer

series ordinal

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18 August 2017

publication date

1 February 2008

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British Journal of Nursing

18 August 2017

published in

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18 August 2017

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18 August 2017

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18 August 2017

page(s)

260-263

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Trinucleotide repeat length and clinical progression in Huntington's disease

18 August 2017

cites work

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https://api.crossref.org/works/10.12968%2FBJON.2008.17.4.28715

Caring for a child with Juvenile Huntington's Disease: helpful and unhelpful support.

21 January 2018

1 reference

https://api.crossref.org/works/10.12968%2FBJON.2008.17.4.28715

The impact of Juvenile Huntington's Disease on the family: the case of a rare childhood condition.

21 January 2018

1 reference

https://api.crossref.org/works/10.12968%2FBJON.2008.17.4.28715

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

21 January 2018

1 reference

https://api.crossref.org/works/10.12968%2FBJON.2008.17.4.28715

Caring for a child with a progressive illness during the complex chronic phase: parents' experience of facing adversity

21 January 2018

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https://api.crossref.org/works/10.12968%2FBJON.2008.17.4.28715

A polymorphic DNA marker genetically linked to Huntington's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.12968%2FBJON.2008.17.4.28715

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

21 January 2018

1 reference

https://api.crossref.org/works/10.12968%2FBJON.2008.17.4.28715

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

https://api.crossref.org/works/10.12968%2FBJON.2008.17.4.28715

Speech and language delay are early manifestations of juvenile-onset Huntington disease

21 January 2018

1 reference

https://api.crossref.org/works/10.12968%2FBJON.2008.17.4.28715

Palliative care management of a child with juvenile onset Huntington's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.12968%2FBJON.2008.17.4.28715

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

21 January 2018

1 reference

https://api.crossref.org/works/10.12968%2FBJON.2008.17.4.28715

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

21 January 2018

1 reference

https://api.crossref.org/works/10.12968%2FBJON.2008.17.4.28715

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

21 January 2018

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https://api.crossref.org/works/10.12968%2FBJON.2008.17.4.28715

Huntington disease in children: genotype-phenotype correlation

21 January 2018

1 reference

https://api.crossref.org/works/10.12968%2FBJON.2008.17.4.28715

Psychiatric and cognitive difficulties as indicators of juvenile huntington disease onset in 29 patients

21 January 2018

1 reference

https://api.crossref.org/works/10.12968%2FBJON.2008.17.4.28715

The personal experience of juvenile Huntington's disease: an interpretative phenomenological analysis of parents' accounts of the primary features of a rare genetic condition

21 January 2018

1 reference

https://api.crossref.org/works/10.12968%2FBJON.2008.17.4.28715

Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.12968%2FBJON.2008.17.4.28715

Laboratory Guidelines for Huntington Disease Genetic Testing

21 January 2018

1 reference

https://api.crossref.org/works/10.12968%2FBJON.2008.17.4.28715

10.12968/BJON.2008.17.4.28715

21 January 2018

Identifiers

DOI

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