Literature DB >> 7488469

Probable right ventricular dysplasia and patent foramen ovale presenting with cyanosis and clubbing in a patient with characteristics of Noonan syndrome.

P Wilmshurst1, P Da Costa.   

Abstract

Probable right ventricular dysplasia and a patent foramen ovale resulted in cyanotic heart disease in a patient with some characteristics of Noonan syndrome.

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Mesh：

Year:  1995        PMID： 7488469      PMCID： PMC484061          DOI： 10.1136/hrt.74.4.471

Source DB:  PubMed          Journal:  Br Heart J        ISSN： 0007-0769


  18 in total

1.  Familial restrictive cardiomyopathy with atrioventricular block and skeletal myopathy.

Authors:  A P Fitzpatrick; L M Shapiro; A F Rickards; P A Poole-Wilson
Journal:  Br Heart J       Date:  1990-02

2.  Familial restrictive cardiomyopathy.

Authors:  C Aroney; N Bett; D Radford
Journal:  Aust N Z J Med       Date:  1988-12

3.  Hemodynamic and myocyte mitochondrial ultrastructural abnormalities in arrhythmogenic right ventricular dysplasia.

Authors:  D C Blankenship; G Hug; G Balko; J van der Bel-Kann; R L Coith; P J Engel
Journal:  Am Heart J       Date:  1993-10       Impact factor: 4.749

4.  Effects of a patent foramen ovale on arterial saturation during exercise and on cardiovascular responses to deep breathing, Valsalva manoeuvre, and passive tilt: relation to history of decompression illness in divers.

Authors:  P T Wilmshurst; D F Treacher; A Crowther; S E Smith
Journal:  Br Heart J       Date:  1994-03

5.  Noonan's cardiomyopathy: a non-hypertrophic variant.

Authors:  R A Cooke; J B Chambers; P V Curry
Journal:  Br Heart J       Date:  1994-06

6.  Left ventricular involvement in right ventricular dysplasia.

Authors:  B Pinamonti; G Sinagra; A Salvi; A Di Lenarda; T Morgera; F Silvestri; R Bussani; F Camerini
Journal:  Am Heart J       Date:  1992-03       Impact factor: 4.749

7.  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 Society and Federation of Cardiology.

Authors:  W J McKenna; G Thiene; A Nava; F Fontaliran; C Blomstrom-Lundqvist; G Fontaine; F Camerini
Journal:  Br Heart J       Date:  1994-03

8.  Dysplastic conditions of the right ventricular myocardium: Uhl's anomaly vs arrhythmogenic right ventricular dysplasia.

Authors:  L M Gerlis; S C Schmidt-Ott; S Y Ho; R H Anderson
Journal:  Br Heart J       Date:  1993-02

9.  Right ventricular dysplasia: a clinical and pathological study of two families with left ventricular involvement.

Authors:  D Miani; B Pinamonti; R Bussani; F Silvestri; G Sinagra; F Camerini
Journal:  Br Heart J       Date:  1993-02

10.  Primary restrictive cardiomyopathy: clinical and pathologic characteristics.

Authors:  D Katritsis; P T Wilmshurst; J A Wendon; M J Davies; M M Webb-Peploe
Journal:  J Am Coll Cardiol       Date:  1991-11-01       Impact factor: 24.094
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  3 in total

1.  Probable right ventricular dysplasia and patent foramen ovale presenting with cyanosis and clubbing in a patient with characteristics of Noonan syndrome.

Authors:  P Wilmshurst
Journal:  Heart       Date:  1997-03       Impact factor: 5.994

2.  Restrictive and hypertrophic cardiomyopathies in Noonan syndrome: the overlap syndromes.

Authors:  P T Wilmshurst; D Katritsis
Journal:  Heart       Date:  1996-01       Impact factor: 5.994

3.  Mediating ERK 1/2 signaling rescues congenital heart defects in a mouse model of Noonan syndrome.

Authors:  Tomoki Nakamura; Melissa Colbert; Maike Krenz; Jeffery D Molkentin; Harvey S Hahn; Gerald W Dorn; Jeffrey Robbins
Journal:  J Clin Invest       Date:  2007-08       Impact factor: 14.808
  3 in total

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