(Q39400466)

11 September 2017

title

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

1 reference

reason for deprecated rank

11 September 2017

Pseudodystrophische Muskelglykogenose im Erwachsenenalter (Saure-Maltase-Mangel-Syndrom) (German)

marking inconsistent with the registered/official identifier/name

1 reference

reason for deprecated rank

11 April 2022

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

marking inconsistent with the registered/official identifier/name

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A61260

11 April 2022

1 reference

11 April 2022

author name string

F. Gullotta

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A61260

11 April 2022

H. Stefan

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A61260

11 April 2022

H. Mattern

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A61260

11 April 2022

language of work or name

German

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=61260

11 April 2022

publication date

1 January 1976

1 reference

full work available at URL

11 September 2017

http://link.springer.com/content/pdf/10.1007/BF00312870.pdf

file format

Portable Document Format

1 reference

http://link.springer.com/article/10.1007/BF00312870/fulltext.html

11 April 2022

1 reference

http://link.springer.com/content/pdf/10.1007/BF00312870

11 April 2022

1 reference

11 April 2022

1 reference

11 September 2017

volume

213

1 reference

11 September 2017

issue

3

1 reference

11 September 2017

page(s)

199-216

1 reference

https://scigraph.springernature.com/pub.10.1007/bf00312870

11 September 2017

exact match

0 references

cites work

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

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

Electromyography in Type II Glycogenosis

1 reference

12 December 2020

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

1 reference

12 December 2020

Late Infantile Acid Maltase Deficiency

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

[Benign course of generalized glycogenosis (Pompe's disease)]

1 reference

12 December 2020

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

1 reference

12 December 2020

[Muscular glycogenosis. A 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

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

[Sudanophilic (mitochondria) myopathy (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

Muscular form of glycogenosis, type II (Pompe)

1 reference

12 December 2020

10

43

233

A. G. Engel

1968

1 reference

11 April 2022

Identifiers

DOI

10.1007/BF00312870

1 reference

11 September 2017

1 reference