Neonatal hypotonia and cardiomyopathy secondary to type IV glycogenosis

Author:

Tang Thomas T.,Segura Annette D.,Chen Yuan-Tsong,Ricci Lucia M.,Franciosi Ralph A.,Splaingard Mark L.,Lubinsky Mark S.

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Clinical Neurology,Pathology and Forensic Medicine

Reference22 articles.

1. Andersen DH (1952) Studies of glycogen disease with report of a case in which the glycogen was abnormal. In: Najjar VA (ed) Carbohydrate Metabolism. Johns Hopkins, Baltimore, pp 28?42

2. Andersen DH (1956) Familial cirrhosis of the liver with storage of abnormal glycogen. Lab Invest 5: 11?20

3. Bannayan GA, Dean WJ, Howell PR (1976) Type IV glycogen-storage disease, light microscopic, electron microscopic and enzymatic study. Am J Clin Pathol 66: 702?709

4. Brown BI (1985) Diagnosis of glycogen storage disease. In: Wapnir PA (ed) Cogenital metabolic diseases. Dekker, New York, pp 227?250

5. Brown BI, Brown DH (1966) Lack of an ?-1,4-glucan:?-1,4-glucan 6-glycosyl transferase in a case of type IV glycogenosis. Proc Natl Acad Sci USA 56: 725?729

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