(Q45301042)

11 December 2017

Atypical movement disorders in the early stages of Huntington's disease: clinical and genetic analysis (English)

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11 December 2017

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2

Berardelli A

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ORCID Public Data File 2021

11 December 2017

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author name string

Squitieri F

1

1 reference

11 December 2017

Nargi E

3

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11 December 2017

Castellotti B

4

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11 December 2017

Mariotti C

5

1 reference

11 December 2017

Cannella M

6

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11 December 2017

Lavitrano ML

7

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11 December 2017

de Grazia U

8

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11 December 2017

Gellera C

9

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11 December 2017

Ruggieri S

10

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11 December 2017

1 July 2000

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11 December 2017

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11 December 2017

58

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11 December 2017

50-56

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11 December 2017

1

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A worldwide study of the Huntington's disease mutation. The sensitivity and specificity of measuring CAG repeats

11 December 2017

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.580108.X

Onset symptoms in 510 patients with Huntington's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.580108.X

Differences in duration of Huntington's disease based on age at onset

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.580108.X

Tourettism associated with Huntington's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.580108.X

Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.580108.X

A new polymerase chain reaction (PCR) assay for the trinucleotide repeat that is unstable and expanded on Huntington's disease chromosomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.580108.X

A CCG repeat polymorphism adjacent to the CAG repeat in the Huntington disease gene: implications for diagnostic accuracy and predictive testing

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.580108.X

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/10.1034%2FJ.1399-0004.2000.580108.X

Huntington's disease in Venezuela: 7 years of follow-up on symptomatic and asymptomatic individuals

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.580108.X

Subtle involuntary movements are not reliable indicators of incipient Huntington's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.580108.X

Motor changes in presymptomatic Huntington disease gene carriers

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.580108.X

CAG repeat size and clinical presentation in Huntington's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.580108.X

Mutation analysis in patients with possible but apparently sporadic Huntington's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.580108.X

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/10.1034%2FJ.1399-0004.2000.580108.X

Pathophysiology of chorea and bradykinesia in Huntington's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.580108.X

The coexistence of bradykinesia and chorea in Huntington's disease and its implications for theories of basal ganglia control of movement

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.580108.X

Huntington disease and childhood-onset Tourette syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.580108.X

Repetitive belching, aerophagia, and torticollis in Huntington's disease: a case report

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.580108.X

Relationship between trinucleotide repeats and neuropathological changes in Huntington's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.580108.X

CAG repeat number governs the development rate of pathology in Huntington's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.580108.X

[11C]raclopride-PET studies of the Huntington's disease rate of progression: relevance of the trinucleotide repeat length

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.580108.X

The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.580108.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.580108.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.580108.X

DNA analysis in hereditary dentatorubral-pallidoluysian atrophy: correlation between CAG repeat length and phenotypic variation and the molecular basis of anticipation

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.580108.X

Genetic polymorphisms adjacent to the CAG repeat influence clinical features at onset in Huntington's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.580108.X

Ancestral differences in the distribution of the delta 2642 glutamic acid polymorphism is associated with varying CAG repeat lengths on normal chromosomes: insights into the genetic evolution of Huntington disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.580108.X

DNA haplotype analysis of Huntington disease reveals clues to the origins and mechanisms of CAG expansion and reasons for geographic variations of prevalence

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.580108.X

Evidence for the GluR6 gene associated with younger onset age of Huntington's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.580108.X

Neuro-psychiatric aspects of Huntington's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.580108.X

inferred from DOI database lookup

7 January 2021

based on heuristic

Unstable mutations and neurodegenerative disorders

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.580108.X

inferred from DOI database lookup

7 January 2021

based on heuristic

Dentatorubral-pallidoluysian atrophy: clinical features are closely related to unstable expansions of trinucleotide (CAG) repeat

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.580108.X

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1034/J.1399-0004.2000.580108.X

1 reference

11 December 2017

1 reference