(Q48561602)

12 February 2018

title

Comparative pathology of the canine model of glycogen storage disease type II (Pompe's disease). (English)

1 reference

12 February 2018

main subject

glycogen storage disease

1 reference

glycogen metabolic process

inferred from title

1 reference

H C Walvoort

1

1 reference

12 February 2018

J A Dormans

series ordinal

2

1 reference

12 February 2018

T S van den Ingh

series ordinal

3

1 reference

12 February 2018

publication date

1 January 1985

1 reference

12 February 2018

Journal of Inherited Metabolic Disease

published in

1 reference

12 February 2018

volume

8

1 reference

12 February 2018

issue

1

1 reference

12 February 2018

page(s)

38-46

1 reference

12 February 2018

The spectrum and diagnosis of acid maltase deficiency.

cites work

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FBF01805484

The influence of lysosomes on glycogen metabolism

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FBF01805484

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

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FBF01805484

Mechanism of glycogenosome formation in axons of cadmium-induced neuropathy--ultrastructural and biochemical studies

21 January 2018

1 reference

12 December 2020

The effect of temperature on the pH stability of myosin ATPase as demonstrated histochemically

1 reference

12 December 2020

ELECTRON MICROSCOPIC STUDIES OF THE PROXIMAL TUBULE OF THE RAT KIDNEY. II. CYTOSEGRESOMES AND CYTOSOMES: THEIR RELATIONSHIP TO EACH OTHER AND TO THE LYSOSOME CONCEPT

1 reference

12 December 2020

Pseudodystrophic muscle glycogenosis in adults. (Acid maltase deficiency syndrome) (author's transl)

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

Generalised glycogenosis in Brahman cattle

1 reference

12 December 2020

Pompe's Disease: Ultrastructural Alterations of Muscle Tissue in Parents

1 reference

12 December 2020

INBORN LYSOSOMAL DISEASES.

1 reference

12 December 2020

Adult-onset acid maltase deficiency: A postmortem study

1 reference

12 December 2020

Myopathy due to glycogen storage disease: pathological and biochemical studies in relation to glycogenosome formation

1 reference

12 December 2020

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

1 reference

12 December 2020

[A vacuolar myopathy: autophagic glycogenosis of late onset. Ultrastructural study]

1 reference

12 December 2020

A case of glycogenic cardiomegaly in a dog

1 reference

12 December 2020

AN ELECTRON MICROSCOPIC AND BIOCHEMICAL STUDY OF TYPE II GLYCOGENOSIS

1 reference

12 December 2020

The fine structure of the normal, neonatal mouse liver

1 reference

12 December 2020

Ultrastructural and biochemical studies of glycogenosome formation in ascites hepatoma AH 13 cells

1 reference

12 December 2020

Autophagic degradation of glycogen in skeletal muscles of the newborn rat

1 reference

12 December 2020

Acid maltase deficiency in non-identical adult twins. A morphological and biochemical study

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

Cytochemical demonstration of phosphatases in the rat liver by a cerium-based method in combination with osmium tetroxide and potassium ferrocyanide postfixation

1 reference

12 December 2020

Glycogen depletion in the newborn rat liver an electron microscopic and electron histochemical study

1 reference

12 December 2020

Type II glycogenosis. Biochemical and electron microscopic study.

1 reference

12 December 2020

The adult form of acid maltase (alpha-1,4-glucosidase) deficiency

1 reference

12 December 2020

The apparent activity in vivo of the lysosomal pathway of glycogen catabolism in cultured human skin fibroblasts from patients with type III glycogen storage disease

1 reference

12 December 2020

[The physiological segregation of glycogen. A precondition of the liver cell changes in glycogenosis type II (Pompe) (author's transl)]

1 reference

12 December 2020

The pathology of type II skeletal muscle glycogenosis. A light and electron-microscopic study

1 reference

12 December 2020

Glycogen storage diseases in animals and their potential value as models of human disease

1 reference

12 December 2020

Infantile acid maltase deficiency. I. Muscle fiber destruction after lysosomal rupture

1 reference

12 December 2020

Glycogen storage disease. Studies related to the mechanism of glycogenosome formation

1 reference

12 December 2020

Glycogen storage disease in skeletal muscle. Morphological, ultrastructural and biochemical aspects in 10 cases

1 reference

12 December 2020

Canine glycogen storage disease type II. A biochemical study of an acid alpha-glucosidase-deficient Lapland dog

1 reference

12 December 2020

Autophagic vacuoles in heart muscle and liver. A comparative morphometric study including circadian variations in meal-fed rats

1 reference

12 December 2020

Subcellular fractionation studies on hepatic tissue from a patient with Pompe's disease (type II glycogen-storage disease)

1 reference

12 December 2020

Biochemical genetics of the Lapland dog model of glycogen storage disease type II (acid alpha-glucosidase deficiency)

1 reference

12 December 2020

Physicochemical and ultrastructural studies on glycogenosomes in newborn rat hepatocytes

1 reference

12 December 2020

Type II Glycogenosis in Adults

1 reference

12 December 2020

Glycogen, its chemistry and morphologic appearance in the electron microscope. I. A modified OsO 4 fixative which selectively contrasts glycogen

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF01805484

1 reference

12 February 2018

1 reference

12 February 2018