(Q24679142)

hypertrophic cardiomyopathy

inferred from title

1 reference

familial hypertrophic cardiomyopathy

inferred from title

1 reference

inferred from title

author

Hugh Christian Watkins

object named as

H C Watkins

6

0 references

Sinéad Donnelly

4

object named as

S Donnelly

0 references

author name string

C A MacRae

1

0 references

N Ghaisas

2

0 references

S Kass

3

0 references

C T Basson

5

0 references

R Anan

7

0 references

L H Thierfelder

8

0 references

K McGarry

9

0 references

E Rowland

Journal of Clinical Investigation

10

0 references

language of work or name

English

0 references

publication date

September 1995

0 references

published in

0 references

volume

96

0 references

issue

3

0 references

page(s)

1216-20

0 references

cites work

Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomere

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=185741

Mapping of a novel gene for familial hypertrophic cardiomyopathy to chromosome 11

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=185741

Comparative mapping of the actin-binding protein 280 genes in human and mouse

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=185741

The 1993-94 Généthon human genetic linkage map

7 April 2017

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=185741

A familial hypertrophic cardiomyopathy locus maps to chromosome 15q2.

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=185741

Isolation and chromosomal localization of the human endothelial nitric oxide synthase (NOS3) gene

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=185741

Familial cardiomyopathy. A review of 11 families

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=185741

Syncope in hypertrophic cardiomyopathy. II. Coexistence of atrioventricular block and Wolff-Parkinson-White syndrome

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=185741

Electrophysiologic abnormalities in patients with hypertrophic cardiomyopathy. A consecutive analysis in 155 patients

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=185741

Usefulness of adenosine in augmenting ventricular preexcitation for noninvasive localization of accessory pathways

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=185741

The gene responsible for familial hypocalciuric hypercalcemia maps to chromosome 3q in four unrelated families

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=185741

Familial occurrence of accessory atrioventricular pathways (preexcitation syndrome).

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=185741

A disease locus for familial hypertrophic cardiomyopathy maps to chromosome 1q3.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=185741

Polymorphism and phylogeny of dinucleotide repeats in human T-cell receptor Vb6 genes

19 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=185741

Structure and chromosomal localization of the human constitutive endothelial nitric oxide synthase gene

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=185741

Familial Wolff-Parkinson-White syndrome with cardiomyopathy

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=185741

Wolff-Parkinson-White syndrome and familial cardiomegaly.

28 November 2018

1 reference

12 December 2020

A proposed autosomal dominant method of inheritance of the Wolff-Parkinson-White syndrome and supraventricular tachycardia.

1 reference

12 December 2020

Anatomic substrate for preexcitation in idiopathic myocardial hypertrophy with fibroelastosis of the left ventricle

1 reference

12 December 2020

Familial Wolff-Parkinson-White syndrome

1 reference

12 December 2020

Familial sudden death in preexcitation syndrome. Surgical interruption of the anomalous pathways in two brothers (author's transl)

1 reference

12 December 2020

Pre-excitation syndrome and hypertrophic cardiomyopathy

1 reference

12 December 2020

1 reference

12 December 2020

An unusual variant of familial preexcitation

1 reference

12 December 2020

Mapping a gene for familial hypertrophic cardiomyopathy to chromosome 14q1

1 reference

12 December 2020

Use of intravenous adenosine in sinus rhythm as a diagnostic test for latent preexcitation

1 reference

12 December 2020

Left ventricular hypertrophy and morphology in familial hypertrophic cardiomyopathy associated with mutations of the beta-myosin heavy chain gene

1 reference

12 December 2020

Report and abstracts of the First International Workshop on Human Chromosome 7 Mapping 1993

1 reference

12 December 2020

Hereditary occurrence of the pre-excitation (Wolff-Parkinson-White) syndrome with re-entry mechanism and concealed conduction.

1 reference

12 December 2020

Familial occurrence of Wolff-Parkinson-White syndrome

1 reference

12 December 2020