| scholarly article | Q13442814 |
| P356 | DOI | 10.1007/BF00312870 |
| P953 | full work available at URL | http://link.springer.com/article/10.1007/BF00312870/fulltext.html |
| http://link.springer.com/content/pdf/10.1007/BF00312870 | ||
| http://link.springer.com/content/pdf/10.1007/BF00312870.pdf | ||
| P698 | PubMed publication ID | 61260 |
| P2093 | author name string | H. Mattern | |
| F. Gullotta | |||
| H. Stefan | |||
| P2860 | cites work | Mayo Clin Proc | Q6538184 |
| alpha-Glucosidase deficiency in generalized glycogenstorage disease (Pompe's disease). | Q41854457 | ||
| Electromyography in Type II Glycogenosis | Q44325279 | ||
| Adult myopathy from glycogen storage disease due to acid maltase deficiency | Q44357482 | ||
| Pompe's disease: an inborn lysosomal disorder with storage of glycogen. A study of brain and striated muscle | Q48681355 | ||
| Acid maltase deficiency in adults: studies in four cases of a syndrome which may mimic muscular dystrophy or other myopathies | Q48954051 | ||
| [Sudanophilic (mitochondria) myopathy (author's transl)]. | Q53711169 | ||
| Skeletal muscle glycogenosis type II: biochemical and electron microscopic investigations of one case. | Q54194855 | ||
| The spectrum and diagnosis of acid maltase deficiency. | Q54261710 | ||
| A mild form of muscular glycogenosis in two brothers with alpha-1, 4-glucosidase deficiency | Q64945694 | ||
| Late familial pseudo-myopathic muscular glycogenosis with alpha 1,4 glucosidase deficiency. Morphological, histoenzymological and biochemical approach | Q66845992 | ||
| [Benign course of generalized glycogenosis (Pompe's disease)] | Q68508402 | ||
| [Muscular glycogenosis. A biochemical study] | Q68663511 | ||
| Comparative study of acid maltase deficiency. Biochemical differences between infantile, childhood, and adult types | Q68992811 | ||
| Myopathy due to acid maltase deficiency. Pompe's disease in adolescence and adult (author's transl) | Q69042678 | ||
| Autophagic glycogenosis of late onset with mitochondrial abnormalities: light and electron microscopic observations | Q69869570 | ||
| Muscular glycogenosis caused by alpha-1,4-glucosidase deficiency simulating progressive muscular dystrophy. (Clinical and enzyme study. Optic and electron microscopy) | Q70871669 | ||
| Muscular glycogenosis of myopathic form caused by acid maltase deficiency | Q70874917 | ||
| Muscular form of glycogenosis, type II (Pompe) | Q70908110 | ||
| Late Infantile Acid Maltase Deficiency | Q70936126 | ||
| [A vacuolar myopathy: autophagic glycogenosis of late onset. Ultrastructural study] | Q71059713 | ||
| P433 | issue | 3 | |
| P407 | language of work or name | German | Q188 |
| P921 | main subject | neurology | Q83042 |
| P304 | page(s) | 199-216 | |
| P577 | publication date | 1976-01-01 | |
| P1433 | published in | Journal of Neurology | Q6295649 |
| P1476 | title | Pseudodystrophic muscle glycogenosis in adults. (Acid maltase deficiency syndrome) (author's transl) | |
| P478 | volume | 213 |
| Q48561602 | Comparative pathology of the canine model of glycogen storage disease type II (Pompe's disease). |
| Q40207697 | Glycogen storage diseases in animals and their potential value as models of human disease |
| Q71979814 | High frequency discharges as a non-specific EMG activity in adult acid maltase deficiency (author's transl) |
| Q69844059 | Metabolic myopathies |
| Q44743857 | Severe course of glycogen storage disease type II (Pompe's disease) without development of cardiomegalia |
| Q36245480 | The natural course of non-classic Pompe's disease; a review of 225 published cases |
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