(Q39396054)

11 September 2017

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

1 reference

11 September 2017

J J Martin

1

1 reference

PubMed ID

60470

11 September 2017

T de Barsy

series ordinal

2

1 reference

PubMed ID

60470

11 September 2017

W R den Tandt

series ordinal

3

1 reference

11 September 2017

1 August 1976

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11 September 2017

1 reference

11 September 2017

213

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11 September 2017

105-118

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11 September 2017

2

1 reference

https://scigraph.springernature.com/pub.10.1007/bf00313272

11 September 2017

0 references

cites work

Acid maltase deficiency (type II glycogenosis). Morphological and biochemical study of a childhood phenotype

1 reference

12 December 2020

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

1 reference

12 December 2020

Rodent and human acid -glucosidase. Purification, properties and inhibition by antibodies. Investigation in type II glycogenosis

1 reference

12 December 2020

Biochemical and ultrastructural study of leucocytes in type II glycogenosis

1 reference

12 December 2020

Histochemical and quantitative analysis of muscle biopsies.

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

Late Infantile Acid Maltase Deficiency

1 reference

12 December 2020

A method for the colorimetric estimation of glycogen with lodine

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Mutant enzymatic and cytological phenotypes in cultured human fibroblasts

1 reference

12 December 2020

The estimation of glycogen with the anthrone reagent

1 reference

12 December 2020

Infantile metachromatic leukodystrophy. Confirmation of a prenatal diagnosis.

1 reference

12 December 2020

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

1 reference

12 December 2020

Adult acid maltase deficiency. Abnormalities in fibroblasts cultured from patients

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

Acid hydrolases in uncultured amniotic fluid cells

1 reference

12 December 2020

The spectrum and diagnosis of acid maltase deficiency.

1 reference

12 December 2020

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

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)

1 reference

12 December 2020

Muscular glycogenosis of myopathic form caused by acid maltase deficiency

1 reference

12 December 2020

Adult myopathy from glycogen storage disease due to acid maltase deficiency

1 reference

12 December 2020

Late familial pseudo-myopathic muscular glycogenosis with alpha 1,4 glucosidase deficiency. Morphological, histoenzymological and biochemical approach

1 reference

12 December 2020

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

1 reference

12 December 2020

Type II Glycogenosis in Adults

1 reference

12 December 2020

Muscular form of glycogenosis, type II (Pompe)

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00313272

1 reference

11 September 2017

1 reference

PubMed ID

60470