Antenatal diagnosis of pompe disease by fetal echocardiography: impact on outcome after early initiation of enzyme replacement therapy
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/s10545-010-9179-2
Reference32 articles.
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2. Allan L (2000) Antenatal diagnosis of heart disease. Heart 83:367–370
3. Ansong AK, Li JS, Nozik-Grayck E et al (2006) Electrocardiographic response to enzyme replacement therapy for Pompe disease. Genet Med 8:297–301
4. Bhat AH, Corbett V, Carpenter N et al (2004) Fetal ventricular mass determination on three-dimensional echocardiography: studies in normal fetuses and validation experiments. Circulation 110:1054–1060
5. Chen LR, Chen CA, Chiu SN et al (2009) Reversal of cardiac dysfunction after enzyme replacement in patients with infantile-onset Pompe disease. J Pediatr 155:271–275
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2. The Importance of Early Treatment of Inherited Neuromuscular Conditions;Journal of Neuromuscular Diseases;2024-03-05
3. Efficacy and safety of enzyme replacement therapy with alglucosidase alfa for the treatment of patients with infantile-onset Pompe disease: a systematic review and metanalysis;Frontiers in Pediatrics;2024-02-15
4. Advances in Fetal Cardiac Imaging and Intervention;CJC Pediatric and Congenital Heart Disease;2023-11
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