Case report: lysosomal glycogen storage disease with normal acid maltase: an unusual form of hypertrophic cardiomyopathy with rapidly progressive heart failure.
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[1] F. Cornelio,et al. Lysosomal glycogen storage with normal acid maltase: A familial study with successful heart transplant , 1994, Neuromuscular Disorders.
[2] F. Murata,et al. Cardiomyopathy, mental retardation, and autophagic vacuolar myopathy Abnormal MRI findings in the head , 1991, Journal of the Neurological Sciences.
[3] S. Dimauro,et al. Cardiomyopathy, mental retardation, and autophagic vacuolar myopathy , 1987, Neurology.
[4] H. Sybers,et al. Familial lethal cardiomyopathy with mental retardation and scapuloperoneal muscular dystrophy. , 1986, Journal of neurology, neurosurgery, and psychiatry.
[5] J. Sands,et al. Dominantly inherited cardioskeletal myopathy with lysosomal glycogen storage and normal acid maltase levels. , 1986, Brain : a journal of neurology.
[6] S. Dimauro,et al. Lysosomal glycogen storage disease without acid maltase deficiency , 1983, Neurology.
[7] S. Dimauro,et al. Lysosomal glycogen storage disease with normal acid maltase , 1981, Neurology.
[8] N. Tachi,et al. Glycogen storage disease with normal acid maltase: skeletal and cardiac muscles. , 1989, Pediatric neurology.