1998
DOI: 10.1017/s1047951100004601
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From Maude to Claude: the musings of an insomniac in the era of evidence-based medicine

Abstract: nurtured this interest and became my mentors. I remember so well the reading list they suggested to provide a firm and solid background in paediatric cardiovascular medicine: Helen Taussig's two volume text 1 (Fig. 1); Alexander Nadas' Pediatric Cardiology 2 (Fig. 2); and the book emanating from the Karolinska Institute, of which Edgar Mannheimer was a co-editor 3 (Fig. 3). I devoured those wonderful books, savoring the clinical descriptions. I was particularly intrigued even then by the wonderful angiography … Show more

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Cited by 8 publications
(5 citation statements)
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References 188 publications
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“…135,138,140 We suggested some years ago, in the Mannheimer lecture, that the development of pulmonary arteriovenous malformations following the classic cavopulmonary shunt or bidirectional cavopulmonary shunt is a wonderful paradigm for bed-to-bench research. 141 Such observations have now evolved, especially in the past decade, from those of a clinical nature or concern to resonate in more fundamental or basic investigations. This evolution was certainly stimulated in large part by the observations of Srivastava et al, with their appreciation of the development of pulmonary arteriovenous malformations secondary to hepatic venous exclusion, 66 and also from observations in the liverlung interface.…”
Section: Pulmonary Arteriovenous Fistulas and Angiogensismentioning
confidence: 99%
“…135,138,140 We suggested some years ago, in the Mannheimer lecture, that the development of pulmonary arteriovenous malformations following the classic cavopulmonary shunt or bidirectional cavopulmonary shunt is a wonderful paradigm for bed-to-bench research. 141 Such observations have now evolved, especially in the past decade, from those of a clinical nature or concern to resonate in more fundamental or basic investigations. This evolution was certainly stimulated in large part by the observations of Srivastava et al, with their appreciation of the development of pulmonary arteriovenous malformations secondary to hepatic venous exclusion, 66 and also from observations in the liverlung interface.…”
Section: Pulmonary Arteriovenous Fistulas and Angiogensismentioning
confidence: 99%
“…In those patients with previous banding and a restrictive ventricular septal defect, myocardial hypertrophy can be impressive, as the ventricular afterload is very much increased (Figs 2 and 3). 24,33,[35][36][37][38][39][40][41][42][43][44][45][46][47][48][49][50] The other concern about and the subsequent development of important obstruction in the systemic ventricular outflow tract, of course, is that this increased pressure and blood flow is transmitted to the pulmonary circulation, possibly jeopardizing the outcome of creation of the Fontan circulation. 42 We suggested nearly three decades ago several reasons for the "spontaneous" diminution in the size of the ventricular septal defect in these patients, 35 extending these observations in numerous publications.…”
Section: The Aetiology Of Myocardial Hypertrophy As a Risk Factormentioning
confidence: 99%
“…42 We suggested nearly three decades ago several reasons for the "spontaneous" diminution in the size of the ventricular septal defect in these patients, 35 extending these observations in numerous publications. 12,15,24,29,33,36,37,[39][40][41]44,50 Firstly, in those patients without obstruction to the pulmonary outflow tract, the ventricular septal defect tended to be small, often smaller than the aortic root, and thus a defect that was predisposed to spontaneous diminution in size. This notion has subsequently been confirmed by others.…”
Section: The Aetiology Of Myocardial Hypertrophy As a Risk Factormentioning
confidence: 99%
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