(Q45289285)

11 December 2017

Predictive, pre-natal and diagnostic genetic testing for Huntington's disease: the experience in Canada from 1987 to 2000. (English)

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11 December 2017

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25

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11 December 2017

30

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11 December 2017

Creighton S

1

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11 December 2017

Almqvist EW

2

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11 December 2017

MacGregor D

3

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11 December 2017

Fernandez B

4

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11 December 2017

Hogg H

5

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11 December 2017

Beis J

6

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11 December 2017

Welch JP

7

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11 December 2017

Riddell C

8

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11 December 2017

Lokkesmoe R

9

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11 December 2017

Khalifa M

10

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11 December 2017

MacKenzie J

11

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11 December 2017

Sajoo A

12

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11 December 2017

Farrell S

13

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11 December 2017

Robert F

14

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11 December 2017

Shugar A

15

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11 December 2017

Summers A

16

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11 December 2017

Meschino W

17

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11 December 2017

Allingham-Hawkins D

18

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11 December 2017

Chiu T

19

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11 December 2017

Hunter A

20

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11 December 2017

Allanson J

21

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11 December 2017

Hare H

22

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11 December 2017

Schween J

23

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11 December 2017

Collins L

24

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11 December 2017

Greenberg C

26

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11 December 2017

Cardwell S

27

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11 December 2017

Lemire E

28

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11 December 2017

MacLeod P

29

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11 December 2017

1 June 2003

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11 December 2017

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11 December 2017

63

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11 December 2017

462-475

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11 December 2017

6

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Presymptomatic testing in Huntington's disease and autosomal dominant cerebellar ataxias

11 December 2017

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00093.X

DNA analysis of Huntington's disease: five years of experience in Germany, Austria, and Switzerland

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00093.X

Incidence and prevalence of Huntington's disease in Olmsted County, Minnesota (1950 through 1989).

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00093.X

CAG/CTG repeat expansions at the Huntington's disease-like 2 locus are rare in Huntington's disease patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00093.X

A polymorphic DNA marker genetically linked to Huntington's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00093.X

7 January 2021

Predictive testing for Huntington disease: I. Description of a pilot project in British Columbia

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00093.X

7 January 2021

Presymptomatic diagnosis of delayed-onset disease with linked DNA markers. The experience in Huntington's disease

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00093.X

7 January 2021

Predictive testing for Huntington's disease with use of a linked DNA marker

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00093.X

7 January 2021

Presymptomatic testing for Huntington's disease: a world wide survey. The World Federation of Neurology Research Group on Huntington's Disease

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00093.X

7 January 2021

The psychological consequences of predictive testing for Huntington's disease. Canadian Collaborative Study of Predictive Testing

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00093.X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00093.X

7 January 2021

Molecular analysis of new mutations for Huntington's disease: intermediate alleles and sex of origin effects.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00093.X

7 January 2021

Increased instability of intermediate alleles in families with sporadic Huntington disease compared to similar sized intermediate alleles in the general population

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00093.X

7 January 2021

To test or not to test: an ethical conflict with presymptomatic testing of individuals at 25% risk for Huntington's disorder

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00093.X

7 January 2021

United Kingdom experience with presymptomatic testing of individuals at 25% risk for Huntington's disease

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00093.X

7 January 2021

Predictive testing of 25 percent at-risk individuals for Huntington disease (1987-1997).

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00093.X

7 January 2021

International Huntington Association and the World Federation of Neurology Research Group on Huntington's Chorea. Guidelines for the molecular genetics predictive test in Huntington's disease

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00093.X

7 January 2021

Attitudes towards predictive testing in Huntington's disease: a recent survey in Belgium

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00093.X

7 January 2021

Attitudes of persons at risk for Huntington disease toward predictive testing

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00093.X

7 January 2021

Attitudes toward direct predictive testing for the Huntington disease gene. Relevance for other adult-onset disorders. The Canadian Collaborative Group on Predictive Testing for Huntington Disease

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00093.X

7 January 2021

Ten years of presymptomatic testing for Huntington's disease: the experience of the UK Huntington's Disease Prediction Consortium

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00093.X

7 January 2021

Paradox of a better test for Huntington's disease

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00093.X

7 January 2021

Attitudes toward presymptomatic testing in Huntington disease

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00093.X

7 January 2021

Predictive testing for Huntington disease: II. Demographic characteristics, life-style patterns, attitudes, and psychosocial assessments of the first fifty-one test candidates

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00093.X

7 January 2021

Presymptomatic DNA-testing for Huntington disease: pretest attitudes and expectations of applicants and their partners in the Dutch program

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00093.X

7 January 2021

Self-selection in predictive testing for Huntington's disease

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00093.X

7 January 2021

Predictive testing for Huntington's disease: the calm after the storm

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00093.X

7 January 2021

A worldwide assessment of the frequency of suicide, suicide attempts, or psychiatric hospitalization after predictive testing for Huntington disease.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00093.X

7 January 2021

Causes of death in patients with Huntington's disease and in unaffected first degree relatives

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00093.X

7 January 2021

Suicide risk in Huntington's disease

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00093.X

7 January 2021

Accurate determination of the number of CAG repeats in the Huntington disease gene using a sequence-specific internal DNA standard

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00093.X

7 January 2021

Risk reversals in predictive testing for Huntington disease.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00093.X

7 January 2021

Caspases and neurodegeneration: on the cutting edge of new therapeutic approaches.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00093.X

7 January 2021

Family history and DNA analysis in patients with suspected Huntington's disease

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00093.X

7 January 2021

Measurement of mutational flow implies both a high new-mutation rate for Huntington disease and substantial underascertainment of late-onset cases.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00093.X

7 January 2021

Prenatal testing for Huntington's disease: experience within the UK 1994-1998.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00093.X

7 January 2021

Prenatal testing for Huntington's disease: a European collaborative study.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00093.X

7 January 2021

Predictive DNA-testing for Huntington's disease and reproductive decision making: a European collaborative study.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00093.X

7 January 2021

Five year study of prenatal testing for Huntington's disease: demand, attitudes, and psychological assessment

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00093.X

7 January 2021

The genetic testing of children. Working Party of the Clinical Genetics Society (UK)

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00093.X

7 January 2021

High incidence rate and absent family histories in one quarter of patients newly diagnosed with Huntington disease in British Columbia

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00093.X

7 January 2021

Rethinking genotype and phenotype correlations in polyglutamine expansion disorders

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00093.X

7 January 2021

Late-onset Huntington's disease: a clinical and molecular study

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00093.X

7 January 2021

Mutation size and age at onset in Huntington's disease

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00093.X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00093.X

7 January 2021

Huntington disease phenocopy is a familial prion disease

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00093.X

7 January 2021

10.1034/J.1399-0004.2003.00093.X

Identifiers

DOI

1 reference

11 December 2017

1 reference