(Q35438487)

8 August 2017

title

Genetic testing and genetic counselling in hypertrophic cardiomyopathy: the French experience (English)

1 reference

hypertrophic cardiomyopathy

8 August 2017

main subject

1 reference

M Gargiulo

3

0 references

Philippe Charron

object named as

P Charron

1

0 references

Michel Komajda

12

object named as

M Komajda

1 reference

8 August 2017

D Héron

2

1 reference

8 August 2017

P Richard

4

1 reference

8 August 2017

O Dubourg

5

1 reference

8 August 2017

M Desnos

6

1 reference

8 August 2017

J B Bouhour

7

1 reference

8 August 2017

J Feingold

8

1 reference

8 August 2017

L Carrier

9

1 reference

8 August 2017

B Hainque

10

1 reference

8 August 2017

K Schwartz

11

1 reference

8 August 2017

language of work or name

English

0 references

publication date

1 October 2002

1 reference

Journal of Medical Genetics

8 August 2017

published in

1 reference

8 August 2017

volume

39

1 reference

8 August 2017

issue

10

1 reference

8 August 2017

page(s)

741-746

1 reference

Hypertrophic cardiomyopathy: a systematic review

8 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735000

Tissue Doppler imaging consistently detects myocardial abnormalities in patients with hypertrophic cardiomyopathy and provides a novel means for an early diagnosis before and independently of hypertrophy

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735000

The molecular genetic basis for hypertrophic cardiomyopathy

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735000

Psychological consequences of predictive genetic testing: a systematic review

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735000

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735000

A new mutation of the cardiac troponin T gene causing familial hypertrophic cardiomyopathy without left ventricular hypertrophy

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735000

The new genetics. Psychological responses to genetic testing

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735000

Diagnostic value of electrocardiography and echocardiography for familial hypertrophic cardiomyopathy in a genotyped adult population.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735000

The management of hypertrophic cardiomyopathy

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735000

Hypertrophic cardiomyopathy. Clinical spectrum and treatment.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735000

Should we test children for "adult" genetic diseases?

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735000

The psychological complexity of predictive testing for late onset neurogenetic diseases and hereditary cancers: implications for multidisciplinary counselling and for genetic education.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735000

Experience in prenatal testing for Huntington's disease in The Netherlands: procedures, results and guidelines (1987-1997).

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735000

Sudden death in young competitive athletes. Clinical, demographic, and pathological profiles.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735000

Task force 3: clinical research in a molecular era and the need to expand its ethical imperatives

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735000

AHA journals lead with definitive new online site

15 November 2018

1 reference

12 December 2020

Genetic testing for hypertrophic cardiomyopathy

1 reference

12 December 2020

Efficacy of Implantable Cardioverter–Defibrillators for the Prevention of Sudden Death in Patients with Hypertrophic Cardiomyopathy

1 reference

12 December 2020

A De Novo Mutation in α-Tropomyosin That Causes Hypertrophic Cardiomyopathy

1 reference

12 December 2020

Impact of laboratory molecular diagnosis on contemporary diagnostic criteria for genetically transmitted cardiovascular diseases: hypertrophic cardiomyopathy, long-QT syndrome, and marfan syndrome : A statement for healthcare professionals from the

1 reference

12 December 2020

Identifiers

DOI

10.1136/JMG.39.10.741

1 reference

8 August 2017

1 reference

8 August 2017

1 reference