(Q71979814)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6930199%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

title

[High frequency discharges as a non-specific EMG activity in adult acid maltase deficiency (author's transl)] (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6930199%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

author name string

F Manz

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6930199%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

publication date

1 January 1980

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6930199%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

volume

228

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6930199%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

issue

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6930199%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

page(s)

45-51

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6930199%20AND%20SRC:MED&resulttype=core&format=json

Electromyography in Type II Glycogenosis

22 October 2019

cites work

1 reference

12 December 2020

Pompe's disease. Electromyographic, electron microscopic, and cardiovascular aspects

1 reference

12 December 2020

Clinical, biochemical, morphological and electrophysiological studies of glycogenosis Type II in childhood with double deficiency of enzymes (author's transl)

1 reference

12 December 2020

Adult myopathy from glycogen storage disease due to acid maltase deficiency

1 reference

12 December 2020

Residual acid maltase activity in late-onset 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

Glycogen storage disease (Pompe's disease) presenting as myopathy in the adult (author's transl)

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

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

The symptomatology, morphology and biochemistry of glycogenosis type II (Pompe) in the adult

1 reference

12 December 2020

EMG-findings in typ-II-glycogenosis (Pompe's disease, acid maltase deficiency) (author's transl)

1 reference

12 December 2020

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

1 reference

12 December 2020

Periods of spontaneous discharges in paretic muscles. Low frequency rhythms of repetitive single, grouped and serial discharges (author's transl)

1 reference

12 December 2020

Muscular glycogenosis of myopathic form caused by acid maltase deficiency

1 reference

12 December 2020

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

1 reference

12 December 2020

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

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

The spectrum and diagnosis of acid maltase deficiency.

1 reference

12 December 2020

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

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00365743

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6930199%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

1 reference