(Q72078323)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7683169%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

title

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

1 reference

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23 October 2019

author name string

J M Schröder

1

1 reference

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23 October 2019

R May

2

1 reference

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23 October 2019

Y S Shin

3

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23 October 2019

M Sigmund

4

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23 October 2019

S Nase-Hüppmeier

5

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23 October 2019

publication date

1 January 1993

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23 October 2019

published in

Acta Neuropathologica

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23 October 2019

volume

85

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23 October 2019

issue

4

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23 October 2019

page(s)

419-430

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https://scigraph.springernature.com/pub.10.1007/bf00334454

23 October 2019

exact match

0 references

cites work

Immunological homogeneity of Lafora body, corpora amylacea, basophilic degeneration in heart, and intracytoplasmic inclusions of liver and heart in type IV glycogenosis.

1 reference

12 December 2020

Type IV glycogenosis. Report of a case proven by characterization of glycogen and studied at necropsy

1 reference

12 December 2020

A MYOPATHY PRESENTING IN ADULT LIFE WITH FEATURES SUGGESTIVE OF GLYCOGEN STORAGE DISEASE.

1 reference

12 December 2020

Myopathy with tremor and dementia: a metabolic disorder? Case report with postmortem study

1 reference

12 December 2020

The fine structure of glycogen from type IV glycogen-storage disease

1 reference

12 December 2020

Glycogen metabolism and glycogen-storage diseases

1 reference

12 December 2020

Glycogenosis with amylopectinoid deposits in a 13-year-old girl

1 reference

12 December 2020

Glycogenosis IV: A new cause of infantile hypotonia

1 reference

12 December 2020

Branching enzyme in erythrocytes. Detection of type IV glycogenosis homozygotes and heterozygotes

1 reference

12 December 2020

Type IV glycogen storage disease: branching enzyme deficiency in skin fibroblasts and possible heterozygote detection

1 reference

12 December 2020

A distinct form of adult polyglucosan body disease with massive involvement of central and peripheral neuronal processes and astrocytes: a report of four cases and a review of the occurrence of polyglucosan bodies in other conditions such as Lafora'

1 reference

12 December 2020

Lack of an alpha-1,4-glucan: alpha-1,4-glucan 6-glycosyl transferase in a case of type IV glycogenosis

1 reference

12 December 2020

Nervous system involvement in type IV glycogenosis

1 reference

12 December 2020

Adult polyglucosan body disease: The diagnostic value of axilla skin biopsy

1 reference

12 December 2020

Type IV glycogenosis (amylopectinosis). Light and electron microscopic observations

1 reference

12 December 2020

A new variant of type IV glycogenosis: deficiency of branching enzyme activity without apparent progressive liver disease

1 reference

12 December 2020

Presenile dementia with "Lafora-like" intraneuronal inclusions.

1 reference

12 December 2020

Adult polyglucosan body disease (APBD).

1 reference

12 December 2020

Adult polysaccharidosis. Clinicopathological, ultrastructural, and biochemical features

1 reference

12 December 2020

A mild juvenile variant of type IV glycogenosis

1 reference

12 December 2020

Adult polyglucosan body myopathy with subclinical peripheral neuropathy: case report and review of diseases associated with polyglucosan body accumulation

1 reference

12 December 2020

Polysaccharide (amylopectin-like) storage myopathy histochemical ultrastructural and biochemical studies

1 reference

12 December 2020

A juvenile variant of glycogenosis IV (Andersen disease)

1 reference

12 December 2020

Adult polyglucosan body disease: Clinical and nerve biopsy findings in two cases

1 reference

12 December 2020

Polysaccharide storage myopathy

1 reference

12 December 2020

Disorders of glycogen and lipid metabolism

1 reference

12 December 2020

Basophilic (mucoid) degeneration of myocardium: a disorder of glycogen metabolism

1 reference

12 December 2020

Lafora's disease: peroxisomal storage in skeletal muscle.

1 reference

12 December 2020

Light and electron microscopy of skeletal muscle in type IV glycogenosis

1 reference

12 December 2020

Hereditary branching enzyme dysfunction in adult polyglucosan body disease: A possible metabolic cause in two patients

1 reference

12 December 2020

Adult Polyglucosan Body Myopathy

1 reference

12 December 2020

Type IV glycogenosis. Patient with absence of a branching enzyme alpha-1,4-glucan:alpha-1,4-glucan 6-glycosyl transferase

1 reference

12 December 2020

A peculiar polysaccharide accumulation in muscle in a case of cardioskeletal myopathy

1 reference

12 December 2020

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

1 reference

12 December 2020

Diagnosis of glycogen storage disease

1 reference

12 December 2020

Comparative study of the intracytoplasmic inclusions in Lafora disease and type IV glycogenosis by electron microscopy.

1 reference

12 December 2020

ULTRASTRUCTURE OF CORPORA AMYLACEA

1 reference

12 December 2020

Severe cardiopathy in branching enzyme deficiency

1 reference

12 December 2020

Juvenile polysaccharidosis with cardioskeletal myopathy

1 reference

12 December 2020

An adult case of Andersen's disease--Type IV glycogenosis. A clinical, histochemical, ultrastructural and biochemical study.

1 reference

12 December 2020

Cardiomyopathy, cirrhosis of the liver and deposits of a fibrillar polysaccharide. Report of a case with histochemical and electron microscopic studies

1 reference

12 December 2020

Polyglucosan body disease

1 reference

12 December 2020

A type of adult polyglucosan body disease.

1 reference

12 December 2020

Myopathies due to enzyme deficiencies

1 reference

12 December 2020

A familial metabolic disorder with storage of an unusual polysaccharide complex

1 reference

12 December 2020

Glycogen storage disease, types I to X: criteria for morphologic diagnosis

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00334454

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7683169%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

1 reference