(Q54194855)

English

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

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

26 May 2018

http://europepmc.org/abstract/MED/4112649

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

1 reference

Europe PubMed Central

PubMed publication ID

26 May 2018

http://europepmc.org/abstract/MED/4112649

author name string

N Canal

1

1 reference

Europe PubMed Central

PubMed publication ID

26 May 2018

http://europepmc.org/abstract/MED/4112649

L Frattola

2

1 reference

Europe PubMed Central

PubMed publication ID

26 May 2018

http://europepmc.org/abstract/MED/4112649

G Pellegrini

3

1 reference

Europe PubMed Central

PubMed publication ID

26 May 2018

http://europepmc.org/abstract/MED/4112649

publication date

1 January 1972

1 reference

Europe PubMed Central

PubMed publication ID

26 May 2018

http://europepmc.org/abstract/MED/4112649

Zeitschrift fur Neurologie

1 reference

Europe PubMed Central

PubMed publication ID

26 May 2018

http://europepmc.org/abstract/MED/4112649

201

1 reference

Europe PubMed Central

PubMed publication ID

26 May 2018

http://europepmc.org/abstract/MED/4112649

2

1 reference

Europe PubMed Central

PubMed publication ID

26 May 2018

http://europepmc.org/abstract/MED/4112649

98-108

1 reference

Europe PubMed Central

PubMed publication ID

26 May 2018

http://europepmc.org/abstract/MED/4112649

PHOSPHOFRUCTOKINASE DEFICIENCY IN SKELETAL MUSCLE. A NEW TYPE OF GLYCOGENOSIS.

1 reference

https://pubmed.ncbi.nlm.nih.gov/4112649

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/4112649

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/4112649

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Glycogen storage disease of the muscles. Report of a case with unusual features

1 reference

https://pubmed.ncbi.nlm.nih.gov/4112649

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/4112649

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Late Infantile Acid Maltase Deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/4112649

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/4112649

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phosphorylase and glycogen levels in skeletal muscle and liver of hibernating and nonhibernating bats

1 reference

https://pubmed.ncbi.nlm.nih.gov/4112649

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/4112649

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/4112649

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Determination glycogen

1 reference

https://pubmed.ncbi.nlm.nih.gov/4112649

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Skeletal muscle glycogenosis: an investigation of two dissimilar cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/4112649

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/4112649

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Muscular glycogenosis of myopathic form caused by acid maltase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/4112649

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Adult myopathy from glycogen storage disease due to acid maltase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/4112649

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A new myopathy due to glycolytic abnormalities

1 reference

https://pubmed.ncbi.nlm.nih.gov/4112649

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/4112649

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Simultaneous absence of alpha-1,4-glucosidase and alpha-1,6-glucosidase activities (pH 4) in tissues of children with type II glycogen storage disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/4112649

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Glycogenic myopathy. A case of skeletal muscle-glycogenosis in twins

1 reference

https://pubmed.ncbi.nlm.nih.gov/4112649

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Muscular form of glycogenosis, type II (Pompe)

1 reference

https://pubmed.ncbi.nlm.nih.gov/4112649

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

26 May 2018

http://europepmc.org/abstract/MED/4112649

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