(Q48681355)

14 February 2018

title

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

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14 February 2018

author name string

J J Martin

1

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14 February 2018

T de Barsy

2

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14 February 2018

F van Hoof

3

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14 February 2018

G Palladini

4

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14 February 2018

publication date

1 February 1973

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14 February 2018

published in

Acta Neuropathologica

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14 February 2018

volume

23

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14 February 2018

issue

3

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14 February 2018

page(s)

229-244

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14 February 2018

https://scigraph.springernature.com/pub.10.1007/bf00687878

exact match

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cites work

Studies in myoclonus epilepsy (Lafora body form). II. Polyglucosans in the systemic deposits of myoclonus epilepsy and in corpora amylacea

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https://api.crossref.org/works/10.1007%2FBF00687878

Improvements in epoxy resin embedding methods

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CARDIO-MUSCULAR GLYCOGENOSIS. STUDY OF 2 CASES

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Interaction of proteins in staining with Alcian dyes

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12 December 2020

A histochemical and electron microscopic study of skeletal muscle in a case of Pompe's disease (glycogenosis II)

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Ultrastructural study of a muscle biopsy in a type II glycogenosis

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INBORN LYSOSOMAL DISEASES.

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Glycogen disease resembling mongolism, cretinism, and amytonia congenita; case report and review of literature

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STUDY OF 2 CASES OF GENERALIZED GLYCOGENOSIS WITH CARDIOMEGALY (POMPE'S DISEASE)

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AN ELECTRON MICROSCOPIC AND BIOCHEMICAL STUDY OF TYPE II GLYCOGENOSIS

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OCULAR HISTOPATHOLOGY IN GENERALIZED GLYCOGENOSIS (POMEPE'S DISEASE)

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Glycogen storage diseases

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Enzyme patterns in glycogen storage disease type II (Pompe's disease)

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ON STOICHIOMETRY OF GALLOCYANINE CHROME ALUM WITH DESOXYRIBONUCLEIC ACID

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Application of standard micro-anatomical staining methods to epoxy resin-embedded sections

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Glycogenosis type II.

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NEUROPATHOLOGICAL AND NEUROCHEMICAL ASPECTS OF GENERALIZED GLYCOGEN STORAGE DISEASE

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Nonglycogen polysaccharide storage in glycogenosis type 2 (Pompe's disease)

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POMPE'S DISEASE (DIFFUSE GLYCOGENOSIS) WITH NEURONAL STORAGE

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The histochemistry of mucopolysaccharides

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Glycogenosis of the central nervous system in the cat

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Histochemistry of complex lipids. I. Demonstration of vic-glycol groups

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Glycogen-storage disease. Report of a case with generalized glycogenosis and review of the literature

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Muscular form of glycogenosis, type II (Pompe)

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12 December 2020

Identifiers

DOI

10.1007/BF00687878

1 reference

14 February 2018

1 reference

14 February 2018