(Q36578707)

15 August 2017

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

212

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15 August 2017

3

1 reference

15 August 2017

237-252

1 reference

https://scigraph.springernature.com/pub.10.1007/bf00314526

15 August 2017

0 references

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

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Muscle fiber types: how many and what kind?

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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

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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

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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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12 December 2020

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

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[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

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

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12 December 2020

Late Infantile Acid Maltase Deficiency

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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)

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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

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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]

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12 December 2020

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

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12 December 2020

Type II glycogenosis. Biochemical and electron microscopic study.

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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.

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

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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

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12 December 2020

POMPE'S DISEASE (DIFFUSE GLYCOGENOSIS) WITH NEURONAL STORAGE

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12 December 2020

Glycogenosis. Diagnosis by skin biopsy

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12 December 2020

The floppy infant syndrome in muscular glycogenosis

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12 December 2020

Ultrastructural reactions in muscle disease

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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).

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12 December 2020

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

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12 December 2020

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

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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

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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

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B. I. Brown

1966

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10 April 2022

28

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A. G. Engel

1968

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10 April 2022

Identifiers

DOI

10.1007/BF00314526

1 reference

15 August 2017

1 reference