[Histochemical Studies on Myoclonus Bodies in Progressive Myoclonus Epilepsy (Unverricht Type)]

Overview

Journal Acta Neuropathol

Specialty Neurology

Date 1969 Sep 9

PMID 4186140

Citations 11

Authors

R Schnabel

F SEITELBERGER

Affiliations

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Citing Articles

The retina in Lafora disease: light and electron microscopy.

BERARD-BADIER M, Pellissier J, Gambarelli D, de Barsy T, Roger J, TOGA M Albrecht Von Graefes Arch Klin Exp Ophthalmol. 1980; 212(3-4):285-94.

PMID: 6779655 DOI: 10.1007/BF00410522.

[Cytophotometric studies on the staining dichroism of Lafora bodies (Lafora bodies)].

ROMHANYI G, Schnabel R Acta Neuropathol. 1971; 19(1):33-8.

PMID: 5117995 DOI: 10.1007/BF00690952.

Pompe's disease: an inborn lysosomal disorder with storage of glycogen. A study of brain and striated muscle.

Martin J, de Barsy T, Van Hoof F, Palladini G Acta Neuropathol. 1973; 23(3):229-44.

PMID: 4511788 DOI: 10.1007/BF00687878.

Lafora's disease. An ultrastructural and histochemical study.

Ramon Y Cajal S, Blanes A, Martinez A, Saenz E, Gutierrez M Acta Neuropathol. 1974; 30(3):189-96.

PMID: 4446965 DOI: 10.1007/BF00688920.

Histochemistry and ultrastructure of atypical myoclonus body (type II).

Ota T, Hisatomi Y, Kashiwamura K, Otsu K, Nakamura Y Acta Neuropathol. 1974; 28(1):45-54.

PMID: 4368775 DOI: 10.1007/BF00687517.

References

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YANOFF M, SCHWARZ G . THE RETINAL PATHOLOGY OF LAFORA'S DISEASE: A FORM OF GLYCOPROTEIN-ACID MUCOPOLYSACCHARIDE DYSTROPHY. Trans Am Acad Ophthalmol Otolaryngol. 1965; 69:701-8. View

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