Literature DB >> 9049131

Heart transplantation for Barth syndrome.

S S Adwani1, B F Whitehead, P G Rees, A Morris, D M Turnball, M J Elliott, M R de Leval.   

Abstract

Barth syndrome is an X-linked recessive disorder comprising dilated cardiomyopathy, muscular hypotonia, and cyclical neutropenia. Affected children usually die during infancy as a consequence of septicemia, cardiac failure, or both. We report a patient with Barth syndrome who underwent successful heart transplantation.

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Year:  1997        PMID： 9049131     DOI： 10.1007/s002469900135

Source DB:  PubMed          Journal:  Pediatr Cardiol        ISSN： 0172-0643            Impact factor:   1.655


  14 in total

1.  Heart transplantation in children with mitochondrial cardiomyopathy.

Authors:  D Bonnet; P Rustin; A Rötig; J Le Bidois; A Munnich; P Vouhé; J Kachaner; D Sidi
Journal:  Heart       Date:  2001-11       Impact factor: 5.994

2.  Sedation by physician with diazepam for DC cardioversion of atrial arrhythmias.

Authors:  P J Pugh; P Spurrell; K Kamalvand; A N Sulke
Journal:  Heart       Date:  2001-11       Impact factor: 5.994

3.  Role of conscious sedation for external cardioversion.

Authors:  R Raipancholia; L Sentinella; M Lynch
Journal:  Heart       Date:  2001-11       Impact factor: 5.994

4.  Effect of circadian rhythm on response to carotid sinus massage.

Authors:  Y Atmaca; A Alpman; M Kilickap; S Murat; D Oral
Journal:  Heart       Date:  2001-11       Impact factor: 5.994

5.  Left ventricular noncompaction cardiomyopathy in Barth syndrome: an example of an undulating cardiac phenotype necessitating mechanical circulatory support as a bridge to transplantation.

Authors:  Samuel P Hanke; Aimee B Gardner; John P Lombardi; Peter B Manning; David P Nelson; Jeffrey A Towbin; John L Jefferies; Angela Lorts
Journal:  Pediatr Cardiol       Date:  2012-03-17       Impact factor: 1.655

Review 6.  Eponym: Barth syndrome.

Authors:  Atsuhito Takeda; Akira Sudo; Masafumi Yamada; Hirokuni Yamazawa; Gaku Izumi; Ichizo Nishino; Tadashi Ariga
Journal:  Eur J Pediatr       Date:  2011-09-23       Impact factor: 3.183

7.  Differing clinical courses and outcomes in two siblings with Barth syndrome and left ventricular noncompaction.

Authors:  Nobuo Momoi; Bo Chang; Izumi Takeda; Yoshimichi Aoyagi; Kisei Endo; Fukiko Ichida
Journal:  Eur J Pediatr       Date:  2011-10-07       Impact factor: 3.183

Review 8.  TAZ encodes tafazzin, a transacylase essential for cardiolipin formation and central to the etiology of Barth syndrome.

Authors:  Anders O Garlid; Calvin T Schaffer; Jaewoo Kim; Hirsh Bhatt; Vladimir Guevara-Gonzalez; Peipei Ping
Journal:  Gene       Date:  2019-10-21       Impact factor: 3.688

Review 9.  Cardiogenetics, neurogenetics, and pathogenetics of left ventricular hypertrabeculation/noncompaction.

Authors:  Josef Finsterer
Journal:  Pediatr Cardiol       Date:  2009-01-29       Impact factor: 1.655

10.  Natural history of Barth syndrome: a national cohort study of 22 patients.

Authors:  Charlotte Rigaud; Anne-Sophie Lebre; Renaud Touraine; Blandine Beaupain; Chris Ottolenghi; Allel Chabli; Helene Ansquer; Hulya Ozsahin; Sylvie Di Filippo; Pascale De Lonlay; Betina Borm; Francois Rivier; Marie-Catherine Vaillant; Michèle Mathieu-Dramard; Alice Goldenberg; Géraldine Viot; Philippe Charron; Marlene Rio; Damien Bonnet; Jean Donadieu
Journal:  Orphanet J Rare Dis       Date:  2013-05-08       Impact factor: 4.123
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