The symptomatology, morphology and biochemistry of glycogenosis type II (Pompe) in the adult (Q36578707)

15 August 2017

title

The symptomatology, morphology and biochemistry of glycogenosis type II (Pompe) in the adult (English)

2 references

15 August 2017

10 April 2022

1 reference

10 April 2022

author name string

G. K. Schlenska

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A58976

10 April 2022

R. Heene

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A58976

10 April 2022

G. Spalke

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A58976

10 April 2022

D. Seiler

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A58976

10 April 2022

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=58976

10 April 2022

publication date

1 June 1976

1 reference

15 August 2017

14 June 1976

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=58976

10 April 2022

1 reference

15 August 2017

volume

212

1 reference

15 August 2017

issue

3

1 reference

15 August 2017

page(s)

237-252

1 reference

Studies on type II glycogenosis. Effects of cortisone derivatives on acid -glucosidase

15 August 2017

cites work

1 reference

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Muscle fiber types: how many and what kind?

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https://api.crossref.org/works/10.1007%2FBF00314526

Control of glycogen metabolism in human muscle. Evidence from glycogen storage diseases

21 January 2018

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The spectrum and diagnosis of acid maltase deficiency.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF00314526

alpha-Glucosidase deficiency in generalized glycogenstorage disease (Pompe's disease).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF00314526

Lysosomes in type II glycogenosis. Changes during administration of extract from Aspergillus niger

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF00314526

The substrate specificity of acid α-glucosidase from rabbit muscle

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF00314526

Glycogen storage disease in Norway

21 January 2018

1 reference

12 December 2020

Reduced muscle alpha-glucosidase (acid-maltase) activity in hypothyroid myopathy

1 reference

12 December 2020

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

1 reference

12 December 2020

Glycogenosis type II: glycogen storage in cell cultures from muscle.

1 reference

12 December 2020

[Glycogenosis type II (Pompe's disease) associated with alpha-amylase and hyaluronidase deficiency]

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12 December 2020

Comparative study of acid maltase deficiency. Biochemical differences between infantile, childhood, and adult types

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12 December 2020

Pompe's disease. Electromyographic, electron microscopic, and cardiovascular aspects

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12 December 2020

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12 December 2020

Glycogen breakdown in human lymphocytes: Activities of phosphorylase and α-1,4-glucosidases

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12 December 2020

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12 December 2020

Alpha-1,4-glucosidase activity in leucocytes from the family of two brothers who lack this enzyme in muscle

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12 December 2020

Acid maltase deficiency in adults: studies in four cases of a syndrome which may mimic muscular dystrophy or other myopathies

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12 December 2020

AN ELECTRON MICROSCOPIC AND BIOCHEMICAL STUDY OF TYPE II GLYCOGENOSIS

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12 December 2020

Acid maltase levels in muscle in heterozygous acid maltase deficiency and in non-weak and neuromuscular disease controls

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12 December 2020

Glycogen storage diseases

1 reference

12 December 2020

Late Infantile Acid Maltase Deficiency

1 reference

12 December 2020

α-1,4-Glucosidase activity in leucocytes and lymphocytes of 2 adult patients with glycogen-storage disease type II, (Pompe's disease)

1 reference

12 December 2020

Biochemistry and clinical picture of glycogenoses

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12 December 2020

Skeletal muscle glycogenosis type II: biochemical and electron microscopic investigations of one case.

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12 December 2020

A mild form of muscular glycogenosis in two brothers with alpha-1, 4-glucosidase deficiency

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12 December 2020

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12 December 2020

Pompe's disease--detection of maternal heterozygote and antenatal exclusion in the fetus

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12 December 2020

Glycogen metabolism of human diploid fibroblast cells in culture. I. Studies of cells from patients with glycogenosis types II, 3, and V

1 reference

12 December 2020

Glycogen disease of skeletal muscle; report of two cases and review of literature

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12 December 2020

Spontaneous electrical activity in muscle. Description of two patients with motor neurone disease

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12 December 2020

Adult acid maltase deficiency. Abnormalities in fibroblasts cultured from patients

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12 December 2020

[On 2 cases of Pompe's disease]

1 reference

12 December 2020

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

1 reference

12 December 2020

Type II glycogenosis. Biochemical and electron microscopic study.

1 reference

12 December 2020

Myopathy due to acid maltase deficiency. Pompe's disease in adolescence and adult (author's transl)

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12 December 2020

[Results of clinical, biochemical, light-microscopical and ultrastructural studies of childhood glycogenosis in two brothers and their sister (author's transl)]

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12 December 2020

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

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12 December 2020

The role of lysosomes in the pathogeny of storage diseases

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12 December 2020

The experimental production of glycogen storage in cultured human fibroblasts

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12 December 2020

The role of lysosomes in the pathogeny of storage diseases.

1 reference

12 December 2020

Muscular glycogenosis caused by alpha-1,4-glucosidase deficiency simulating progressive muscular dystrophy. (Clinical and enzyme study. Optic and electron microscopy)

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12 December 2020

Diseases of glycogen storage with special reference to the cardiac type of generalized glycogenosis

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12 December 2020

Incidence of glycogen storage disease in Sweden

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12 December 2020

Muscular glycogenosis of myopathic form caused by acid maltase deficiency

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12 December 2020

A method for rapid prenatal diagnosis of glycogenosis II (Pompe's disease).

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12 December 2020

Adult myopathy from glycogen storage disease due to acid maltase deficiency

1 reference

12 December 2020

POMPE'S DISEASE (DIFFUSE GLYCOGENOSIS) WITH NEURONAL STORAGE

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12 December 2020

Glycogenosis. Diagnosis by skin biopsy

1 reference

12 December 2020

The floppy infant syndrome in muscular glycogenosis

1 reference

12 December 2020

Ultrastructural reactions in muscle disease

1 reference

12 December 2020

The use of leucocytes as an aid in the diagnosis of a variant of glycogen storage disease type II (Pompe's disease).

1 reference

12 December 2020

Autophagic glycogenosis of late onset with mitochondrial abnormalities: light and electron microscopic observations

1 reference

12 December 2020

Renal cortical tubular glycogen localization in glycogenosis type II (Pompe's disease).

1 reference

12 December 2020

Subcellular distribution of acid and neutral alpha-glucosidases in normal, acid maltase deficient, and myophosphorylase deficient human skeletal muscle

1 reference

12 December 2020

Type II Glycogenosis in Adults

1 reference

12 December 2020

Muscular form of glycogenosis, type II (Pompe)

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12 December 2020

Tuberculin Reactions (Cont.)

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C. Angelini

1973

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10 April 2022

13

101

160

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1966

1 reference

10 April 2022

28

43

233

A. G. Engel

1968

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10 April 2022

Identifiers

DOI

10.1007/BF00314526

1 reference

15 August 2017

1 reference