(Q33811161)

29 July 2017

1 reference

title

Echocardiographic features of genetic diseases: part 1. Cardiomyopathy (English)

1 reference

29 July 2017

1 reference

1 reference

Alizad A

1

1 reference

PubMed ID

10625837

29 July 2017

Seward JB

series ordinal

2

1 reference

29 July 2017

1 January 2000

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Journal of the American Society of Echocardiography

29 July 2017

1 reference

29 July 2017

13

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29 July 2017

73-86

1 reference

29 July 2017

1

1 reference

Sex dependent transmission of Beckwith-Wiedemann syndrome associated with a reciprocal translocation t(9;11)(p11.2;p15.5).

29 July 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0894-7317%2800%2990048-8

7 January 2021

Tight linkage between the Beckwith-Wiedemann syndrome and a microsatellite marker for the TH locus.

1 reference

https://api.crossref.org/works/10.1016%2FS0894-7317%2800%2990048-8

7 January 2021

Molecular investigation of familial Beckwith-Wiedemann syndrome: a model for paternal imprinting

1 reference

https://api.crossref.org/works/10.1016%2FS0894-7317%2800%2990048-8

7 January 2021

Discrete subvalvular aortic stenosis in the Beckwith-Wiedemann syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0894-7317%2800%2990048-8

7 January 2021

Systemic carnitine deficiency presenting as familial endocardial fibroelastosis: a treatable cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0894-7317%2800%2990048-8

7 January 2021

Evidence for linkage of human primary systemic carnitine deficiency with D5S436: a novel gene locus on chromosome 5q

1 reference

https://api.crossref.org/works/10.1016%2FS0894-7317%2800%2990048-8

7 January 2021

Oculopharyngeal muscular dystrophy in a northern German family linked to chromosome 14q, and presenting carnitine deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0894-7317%2800%2990048-8

7 January 2021

Molecular genetics of familial hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0894-7317%2800%2990048-8

7 January 2021

Familial hypertrophic cardiomyopathy is a genetically heterogeneous disease

1 reference

https://api.crossref.org/works/10.1016%2FS0894-7317%2800%2990048-8

7 January 2021

Prediction of the site and severity of obstruction in hypertrophic cardiomyopathy by color flow mapping and continuous wave Doppler echocardiography

1 reference

https://api.crossref.org/works/10.1016%2FS0894-7317%2800%2990048-8

7 January 2021

Transesophageal Doppler echocardiography in obstructive hypertrophic cardiomyopathy: Clarification of pathophysiology and importance in intraoperative decision making

1 reference

https://api.crossref.org/works/10.1016%2FS0894-7317%2800%2990048-8

7 January 2021

The Frequency of Familial Dilated Cardiomyopathy in a Series of Patients with Idiopathic Dilated Cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0894-7317%2800%2990048-8

7 January 2021

Familial dilated cardiomyopathy: a transverse and longitudinal clinical and echocardiographic study

1 reference

https://api.crossref.org/works/10.1016%2FS0894-7317%2800%2990048-8

7 January 2021

[Genetics of dilated cardiomyopathy]

1 reference

https://api.crossref.org/works/10.1016%2FS0894-7317%2800%2990048-8

7 January 2021

Systolic and diastolic dysfunction in patients with clinical diagnosis of dilated cardiomyopathy. Relation to symptoms and prognosis.

1 reference

https://api.crossref.org/works/10.1016%2FS0894-7317%2800%2990048-8

7 January 2021

The heart in Friedreich's ataxia. Report of a case

1 reference

https://api.crossref.org/works/10.1016%2FS0894-7317%2800%2990048-8

7 January 2021

Friedreich's ataxia 1980. An overview of the physiopathology.

1 reference

https://api.crossref.org/works/10.1016%2FS0894-7317%2800%2990048-8

7 January 2021

The heart in Friedreich's ataxia

1 reference

https://api.crossref.org/works/10.1016%2FS0894-7317%2800%2990048-8

7 January 2021

Evolution of Cardio-Pulmonary Involvement in Friedreich's Ataxia

1 reference

https://api.crossref.org/works/10.1016%2FS0894-7317%2800%2990048-8

7 January 2021

Mapping of mutation causing Friedreich's ataxia to human chromosome 9

1 reference

https://api.crossref.org/works/10.1016%2FS0894-7317%2800%2990048-8

7 January 2021

Confirmation of linkage of Friedreich ataxia to chromosome 9 and identification of a new closely linked marker

1 reference

https://api.crossref.org/works/10.1016%2FS0894-7317%2800%2990048-8

7 January 2021

Congestive heart failure and cardiac thrombus as first presentations of Friedreich ataxia

1 reference

https://api.crossref.org/works/10.1016%2FS0894-7317%2800%2990048-8

7 January 2021

Genetic data and natural history of Friedreich's disease: a study of 80 Italian patients

1 reference

https://api.crossref.org/works/10.1016%2FS0894-7317%2800%2990048-8

7 January 2021

Friedreich's ataxia presenting as cardiac disease

1 reference

https://api.crossref.org/works/10.1016%2FS0894-7317%2800%2990048-8

7 January 2021

Spectrum of cardiac involvement in Friedreich's ataxia: clinical, electrocardiographic and echocardiographic observations

1 reference

https://api.crossref.org/works/10.1016%2FS0894-7317%2800%2990048-8

7 January 2021

Cardiomyopathy in Friedreich's ataxia: a Doppler-echocardiographic study

1 reference

https://api.crossref.org/works/10.1016%2FS0894-7317%2800%2990048-8

7 January 2021

Morphologic and functional characteristics of the heart in Friedreich's ataxia

1 reference

https://api.crossref.org/works/10.1016%2FS0894-7317%2800%2990048-8

7 January 2021

Friedreich's ataxia in 13 children: presentation and evolution with neurophysiologic, electrocardiographic, and echocardiographic features

1 reference

https://api.crossref.org/works/10.1016%2FS0894-7317%2800%2990048-8

7 January 2021

Cardiac involvement in Friedreich's ataxia: a clinical study of 75 patients

1 reference

https://api.crossref.org/works/10.1016%2FS0894-7317%2800%2990048-8

7 January 2021

Accumulation of membrane-bound melanosomes occurs in Langerhans cells of patients with the Leopard syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0894-7317%2800%2990048-8

7 January 2021

Hypertrophic obstructive cardiomyopathy and lentiginosis: a little known neural ectodermal syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0894-7317%2800%2990048-8

7 January 2021

Constrictive pericarditis simulating intestinal lymphangiectasia in a patient with the Noonan syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0894-7317%2800%2990048-8

7 January 2021

Cerebral arteriovenous malformation in Noonan's syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0894-7317%2800%2990048-8

7 January 2021

Ocular manifestations of Noonan syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0894-7317%2800%2990048-8

7 January 2021

Partial atrioventricular canal with left-sided obstruction in patients with Noonan syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0894-7317%2800%2990048-8

7 January 2021

Cardiologic abnormalities in Noonan syndrome: phenotypic diagnosis and echocardiographic assessment of 118 patients

1 reference

https://api.crossref.org/works/10.1016%2FS0894-7317%2800%2990048-8

7 January 2021

Myocardial dysgenesis with persistent sinusoids in a neonate with Noonan's phenotype

1 reference

https://api.crossref.org/works/10.1016%2FS0894-7317%2800%2990048-8

7 January 2021

Intrauterine diagnosis and evolution of a cardiomyopathy in a fetus with Noonan's syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0894-7317%2800%2990048-8

7 January 2021

Arrhythmogenic right ventricular cardiomyopathy: a survey of the investigations at the University of Padua.

1 reference

https://api.crossref.org/works/10.1016%2FS0894-7317%2800%2990048-8

7 January 2021

A new locus for arrhythmogenic right ventricular dysplasia on the long arm of chromosome 14.

1 reference

https://api.crossref.org/works/10.1016%2FS0894-7317%2800%2990048-8

7 January 2021

ARVD4, a new locus for arrhythmogenic right ventricular cardiomyopathy, maps to chromosome 2 long arm

1 reference

https://api.crossref.org/works/10.1016%2FS0894-7317%2800%2990048-8

7 January 2021

Localization of a gene responsible for arrhythmogenic right ventricular dysplasia to chromosome 3p23.

1 reference

https://api.crossref.org/works/10.1016%2FS0894-7317%2800%2990048-8

7 January 2021

Contribution of cross-sectional echocardiography to the diagnosis of right ventricular dysplasia at the asymptomatic stage

1 reference

https://api.crossref.org/works/10.1016%2FS0894-7317%2800%2990048-8

7 January 2021

Echocardiographic features of right ventricular dilated cardiomyopathy and Uhl's anomaly

1 reference

https://api.crossref.org/works/10.1016%2FS0894-7317%2800%2990048-8

7 January 2021

Right ventricular dysplasia: a report of 24 adult cases

1 reference

https://api.crossref.org/works/10.1016%2FS0894-7317%2800%2990048-8

7 January 2021

Usefulness of noninvasive studies for diagnosis of right ventricular dysplasia

1 reference

https://api.crossref.org/works/10.1016%2FS0894-7317%2800%2990048-8

7 January 2021

Diagnosis of arrhythmogenic right ventricular dysplasia/cardiomyopathy. Task Force of the Working Group Myocardial and Pericardial Disease of the European Society of Cardiology and of the Scientific Council on Cardiomyopathies of the International S

1 reference

https://api.crossref.org/works/10.1016%2FS0894-7317%2800%2990048-8

7 January 2021

Isolated noncompaction of left ventricular myocardium. A study of eight cases

1 reference

https://api.crossref.org/works/10.1016%2FS0894-7317%2800%2990048-8

7 January 2021

https://api.crossref.org/works/10.1016%2FS0894-7317%2800%2990048-8

1 reference

7 January 2021

Isolated noncompaction of the myocardium in adults

1 reference

https://api.crossref.org/works/10.1016%2FS0894-7317%2800%2990048-8

7 January 2021

Xq28-linked noncompaction of the left ventricular myocardium: prenatal diagnosis and pathologic analysis of affected individuals

1 reference

https://api.crossref.org/works/10.1016%2FS0894-7317%2800%2990048-8

7 January 2021

Echocardiographic assessment of left ventricular hypertrophy: comparison to necropsy findings.

1 reference

https://api.crossref.org/works/10.1016%2FS0894-7317%2800%2990048-8

7 January 2021

Identification of a rare congenital anomaly of the myocardium by two-dimensional echocardiography: persistence of isolated myocardial sinusoids

1 reference

https://api.crossref.org/works/10.1016%2FS0894-7317%2800%2990048-8

7 January 2021

Persisting myocardial sinusoids of both ventricles as an isolated anomaly: echocardiographic, angiographic, and pathologic anatomical findings

1 reference

https://api.crossref.org/works/10.1016%2FS0894-7317%2800%2990048-8

7 January 2021

10.1016/S0894-7317(00)90048-8

Identifiers

DOI

1 reference

29 July 2017

1 reference

PubMed ID

10625837