» Articles » PMID: 4181630

A Peculiar Polysaccharide Accumulation in Muscle in a Case of Cardioskeletal Myopathy

Overview
Journal Neurology
Specialty Neurology
Date 1969 Jun 1
PMID 4181630
Citations 5
Authors
Affiliations
Soon will be listed here.
Citing Articles

Juvenile hereditary polyglucosan body disease with complete branching enzyme deficiency (type IV glycogenosis).

Schroder J, May R, Shin Y, Sigmund M Acta Neuropathol. 1993; 85(4):419-30.

PMID: 7683169 DOI: 10.1007/BF00334454.


Exercise-induced pain, stiffness, and tubular aggregation in skeletal muscle.

Brumback R, Staton R, Susag M J Neurol Neurosurg Psychiatry. 1981; 44(3):250-4.

PMID: 7229649 PMC: 490903. DOI: 10.1136/jnnp.44.3.250.


Light and electron microscopy of skeletal muscle in type IV glycogenosis.

SCHOCHET Jr S, MCCORMICK W, Kovarsky J Acta Neuropathol. 1971; 19(2):137-44.

PMID: 5288587 DOI: 10.1007/BF00688492.


Intra-axonal polysaccharide deposits in the peripheral nerve seen in adult polysaccharide storage myopathy.

Komure O, Ichikawa K, Tsutsumi A, Hiyama K, Fujioka A Acta Neuropathol. 1985; 65(3-4):300-4.

PMID: 3976365 DOI: 10.1007/BF00687012.


Primary lipid cardiomyopathy.

Zimmermann A, Wyss P, Stocker F Virchows Arch A Pathol Anat Histopathol. 1990; 416(5):453-9.

PMID: 2107634 DOI: 10.1007/BF01605153.