Skeletal muscle glycogenosis type II: Biochemical and electron microscopic investigations of one case

[1]  D. H. Brown,et al.  Simultaneous absence of alpha-1,4-glucosidase and alpha-1,6-glucosidase activities (pH 4) in tissues of children with type II glycogen storage disease. , 1970, Biochemistry.

[2]  A. Engel Acid maltase deficiency in adults: studies in four cases of a syndrome which may mimic muscular dystrophy or other myopathies. , 1970, Brain : a journal of neurology.

[3]  A. Engel Acid maltase deficiency of adult life. , 1969, Transactions of the American Neurological Association.

[4]  P. Hudgson,et al.  Adult myopathy from glycogen storage disease due to acid maltase deficiency. , 1968, Brain : a journal of neurology.

[5]  W. Kennedy,et al.  Late infantile acid maltase deficiency. , 1968, Archives of neurology.

[6]  A. Engel,et al.  Autophagic glycogenosis of late onset with mitochondrial abnormalities: light and electron microscopic observations. , 1968, Mayo Clinic proceedings.

[7]  H. Hers,et al.  Glycogen-Storage Diseases: Type II and Type VI Glycogenosis , 1968 .

[8]  A. Afifi,et al.  Muscular form of glycogenosis, type II (Pompe) , 1967, Neurology.

[9]  J. Sidbury,et al.  Type II Glycogenosis: Report of a Case With Four-Year Survival and Absence of Acid Maltase Associated With an Abnormal Glycogen , 1966 .

[10]  R. Cardiff A histochemical and electron microscopic study of skeletal muscle in a case of Pompe's disease (glycogenosis II). , 1966, Pediatrics.

[11]  F. Thiebaut,et al.  Glycogénose musculaire à forme myopathique par déficit en maltase acide. , 1966 .

[12]  F. Thiébaut,et al.  [Muscular glycogenosis of myopathic form caused by acid maltase deficiency]. , 1966, Pediatrie.

[13]  T. Lehoczky,et al.  Glycogenic myopathy. A case of skeletal muscle-glycogenosis in twins. , 1965, Journal of the neurological sciences.

[14]  T. Tanaka,et al.  PHOSPHOFRUCTOKINASE DEFICIENCY IN SKELETAL MUSCLE. A NEW TYPE OF GLYCOGENOSIS. , 1965, Biochemical and biophysical research communications.

[15]  J. Demos,et al.  Glycogenose musculaire par deficit d'alpha-1-4-glucosidase simulant une dystrophie musculaire progressive. (Etude clinique et enzymatique. Microscopie optique electronique) , 1965 .

[16]  E. Satoyoshi,et al.  A new myopathy due to glycolytic abnormalities. , 1965, Transactions of the American Neurological Association.

[17]  B. Brown,et al.  A mild form of muscular glycogenosis in two brothers with alpha-1, 4-glucosidase deficiency. , 1965, Annales paediatrici. International review of pediatrics.

[18]  J. Prineas,et al.  Skeletal muscle glycogenosis: an investigation of two dissimilar cases1 , 1963, Journal of neurology, neurosurgery, and psychiatry.

[19]  H. Hers alpha-Glucosidase deficiency in generalized glycogenstorage disease (Pompe's disease). , 1963, The Biochemical journal.

[20]  H. Hers α-Glucosidase deficiency in generalized glycogen-storage disease (Pompe's disease) , 1963 .

[21]  P. A. Sant'agnese,et al.  Glycogen storage disease of the muscles , 1962 .

[22]  L. Leloir,et al.  [14] Glycogen synthetase from rat liver: (Glucose)n+(UDPG)→(Glucose)n+1+UDP , 1962 .

[23]  P. di Sant'Agnese,et al.  Glycogen storage disease of the muscles. Report of a case with unusual features. , 1962, The Journal of pediatrics.

[24]  C. Houghton,et al.  A MYOPATHY PRESENTING IN ADULT LIFE WITH FEATURES SUGGESTIVE OF GLYCOGEN STORAGE DISEASE , 1960, Journal of neurology, neurosurgery, and psychiatry.

[25]  W. A. Wimsatt,et al.  Phosphorylase and glycogen levels in skeletal muscle and liver of hibernating and non-hibernating bats. , 1959, The American journal of physiology.

[26]  R. Montgomery,et al.  Determination glycogen. , 1957, Archives of biochemistry and biophysics.

[27]  H. Zellweger,et al.  Glycogen disease of skeletal muscle; report of two cases and review of literature. , 1955, Pediatrics.

[28]  W. Bonner [121] Succinic dehydrogenase , 1955 .