Longitudinal Observational Study of Cardiac Outcome Risk Factor Prediction in Children, Adolescents, and Adults with Barth Syndrome
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cardiology and Cardiovascular Medicine,Pediatrics, Perinatology and Child Health
Link
https://link.springer.com/content/pdf/10.1007/s00246-022-02846-8.pdf
Reference51 articles.
1. Vreken P, Valianpour F, Nijtmans LG, Grivell LA, Plecko B, Wanders RJ et al (2000) Defective remodeling of cardiolipin and phosphatidylglycerol in Barth syndrome. Biochem Biophys Res Commun 279(2):378–382
2. Barth PG, Scholte HR, Berden JA, Van der Klei-Van Moorsel JM, Luyt-Houwen IE, Van’t Veer-Korthof ET et al (1983) An X-linked mitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leucocytes. J Neurol Sci 62(1–3):327–355
3. Neustein HB, Lurie PR, Dahms B, Takahashi M (1979) An X-linked recessive cardiomyopathy with abnormal mitochondria. Pediatrics 64(1):24–29
4. Spencer CT, Bryant RM, Day J, Gonzalez IL, Colan SD, Thompson WR et al (2006) Cardiac and clinical phenotype in Barth syndrome. Pediatrics 118(2):e337–e346
5. Roberts AE, Nixon C, Steward CG, Gauvreau K, Maisenbacher M, Fletcher M et al (2012) The Barth Syndrome Registry: distinguishing disease characteristics and growth data from a longitudinal study. Am J Med Genet A 158A(11):2726–2732
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