Hypertrophic cardiomyopathy.

This publication has 24 references indexed in Scilit:

• Arrhythmia and prognosis in infants, children and adolescents with hypertrophic cardiomyopathy
  Published by Elsevier ,2010
• Prenatal diagnosis of Pompe's disease (type ii glycogenosis) in chorionic villus biopsy using maltose as a substrate
  Prenatal Diagnosis, 1992
• Sudden death during empiric amiodarone therapy in symptomatic hypertrophic cardiomyopathy
  The American Journal of Cardiology, 1991
• A molecular basis for familial hypertrophic cardiomyopathy: A β cardiac myosin heavy chain gene missense mutation
  Published by Elsevier ,1990
• Mapping a Gene for Familial Hypertrophic Cardiomyopathy to Chromosome 14q1
  New England Journal of Medicine, 1989
• Development and Progression of Left Ventricular Hypertrophy in Children with Hypertrophic Cardiomyopathy
  New England Journal of Medicine, 1986
• Noonan syndrome: The changing phenotype
  American Journal of Medical Genetics, 1985
• Hypertrophic cardiomyopathy: an important cause of sudden death.
  Archives of Disease in Childhood, 1984
• Characterization of the cardiomyopathy in infants of diabetic mothers.
  Circulation, 1980
• Quantitative analysis of cardiac muscle cell disorganization in the ventricular septum of patients with hypertrophic cardiomyopathy.
  Circulation, 1979