Clinical Characteristics and Outcomes of Cardiomyopathy in Barth Syndrome: The UK Experience-Reference-Cited by-同舟云学术

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Clinical Characteristics and Outcomes of Cardiomyopathy in Barth Syndrome: The UK Experience

Published:2015-09-04 Issue:1 Volume:37 Page:167-176
ISSN:0172-0643
Container-title:Pediatric Cardiology
language:en
Short-container-title:Pediatr Cardiol

Author:

Kang Sok-Leng,Forsey Jonathan,Dudley Declan,Steward Colin G.,Tsai-Goodman Beverly

Funder

none

Publisher

Springer Science and Business Media LLC

Subject

Cardiology and Cardiovascular Medicine,Pediatrics, Perinatology, and Child Health

Link

http://link.springer.com/content/pdf/10.1007/s00246-015-1260-z.pdf

Reference32 articles.

1. Al-Naami GH (2010) Torsion of young hearts: a speckle tracking study of normal infants, children, and adolescents. Eur J Echocardiogr 11(10):853–862

2. Amundsen BH, Crosby J, Steen PA, Torp H, Slørdahl SA, Støylen A (2009) Regional myocardial long-axis strain and strain rate measured by different tissue Doppler and speckle tracking echocardiography methods: a comparison with tagged magnetic resonance imaging. Eur J Echocardiogr 10(2):229–237

3. Bione S, Adamo P, Maestrini E, Gedeon AK, Bolhuis PA, Toniolo D (1996) A novel X-linked gene, G4.5. is responsible for Barth Syndrome. Nat Genet 12(4):385–389

4. Bleyl SB, Mumford BR, Thompson V, Carey JC, Pysher TJ, Chin TK, Ward K (1997) Neonatal, lethal noncompaction of the left ventricular myocardium is allelic with Barth Syndrome. Am J Hum Genet 61(4):868–872

5. Bowron A, Frost R, Powers VE, Thomas PH, Heales SJ, Steward CG (2013) Diagnosis of Barth Syndrome using a novel LC-MS/MS method for leukocyte cardiolipin analysis. J Inherit Metab Dis 36(5):741–746

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