| scholarly article | Q13442814 |
| P356 | DOI | 10.1007/BF00314526 |
| P953 | full work available at URL | http://link.springer.com/article/10.1007/BF00314526/fulltext.html |
| http://link.springer.com/content/pdf/10.1007/BF00314526 | ||
| http://link.springer.com/content/pdf/10.1007/BF00314526.pdf | ||
| P698 | PubMed publication ID | 58976 |
| P2093 | author name string | G. Spalke | |
| R. Heene | |||
| D. Seiler | |||
| G. K. Schlenska | |||
| P2860 | cites work | Glycogen disease of skeletal muscle; report of two cases and review of literature | Q35531389 |
| Biochemical Journal | Q864221 | ||
| Mayo Clin Proc | Q6538184 | ||
| Autophagic glycogenosis of late onset with mitochondrial abnormalities: light and electron microscopic observations | Q69869570 | ||
| Biochemistry and clinical picture of glycogenoses | Q69878294 | ||
| Reduced muscle alpha-glucosidase (acid-maltase) activity in hypothyroid myopathy | Q70125175 | ||
| 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 | ||
| [Glycogenosis type II (Pompe's disease) associated with alpha-amylase and hyaluronidase deficiency] | Q70974849 | ||
| Pompe's disease | Q70982390 | ||
| Ultrastructural reactions in muscle disease | Q71010711 | ||
| AN ELECTRON MICROSCOPIC AND BIOCHEMICAL STUDY OF TYPE II GLYCOGENOSIS | Q76951870 | ||
| Diseases of glycogen storage with special reference to the cardiac type of generalized glycogenosis | Q78545210 | ||
| Lysosomes in type II glycogenosis. Changes during administration of extract from Aspergillus niger | Q36188497 | ||
| Acid maltase levels in muscle in heterozygous acid maltase deficiency and in non-weak and neuromuscular disease controls | Q37072936 | ||
| Alpha-1,4-glucosidase activity in leucocytes from the family of two brothers who lack this enzyme in muscle | Q39254988 | ||
| alpha-Glucosidase deficiency in generalized glycogenstorage disease (Pompe's disease). | Q41854457 | ||
| Studies on type II glycogenosis. Effects of cortisone derivatives on acid -glucosidase | Q41934267 | ||
| The substrate specificity of acid α-glucosidase from rabbit muscle | Q42922922 | ||
| Control of glycogen metabolism in human muscle. Evidence from glycogen storage diseases | Q43405579 | ||
| Spontaneous electrical activity in muscle. Description of two patients with motor neurone disease | Q44092924 | ||
| 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 | ||
| Type II glycogenosis. Biochemical and electron microscopic study. | Q51191884 | ||
| POMPE'S DISEASE (DIFFUSE GLYCOGENOSIS) WITH NEURONAL STORAGE | Q51260553 | ||
| Glycogen breakdown in human lymphocytes: Activities of phosphorylase and α-1,4-glucosidases | Q51679302 | ||
| The use of leucocytes as an aid in the diagnosis of a variant of glycogen storage disease type II (Pompe's disease). | Q53809604 | ||
| The role of lysosomes in the pathogeny of storage diseases. | Q53827923 | ||
| A method for rapid prenatal diagnosis of glycogenosis II (Pompe's disease). | Q54115158 | ||
| Renal cortical tubular glycogen localization in glycogenosis type II (Pompe's disease). | Q54160911 | ||
| Muscle fiber types: how many and what kind? | Q54171280 | ||
| Skeletal muscle glycogenosis type II: biochemical and electron microscopic investigations of one case. | Q54194855 | ||
| The spectrum and diagnosis of acid maltase deficiency. | Q54261710 | ||
| [On 2 cases of Pompe's disease] | Q54262772 | ||
| Glycogenosis type II: glycogen storage in cell cultures from muscle. | Q54387751 | ||
| Incidence of glycogen storage disease in Sweden | Q54482733 | ||
| A mild form of muscular glycogenosis in two brothers with alpha-1, 4-glucosidase deficiency | Q64945694 | ||
| Glycogen metabolism of human diploid fibroblast cells in culture. I. Studies of cells from patients with glycogenosis types II, 3, and V | Q67259817 | ||
| A histochemical and electron microscopic study of skeletal muscle in a case of Pompe's disease (glycogenosis II) | Q68376293 | ||
| Nonglycogen polysaccharide storage in glycogenosis type 2 (Pompe's disease) | Q68426866 | ||
| Pompe's disease. Electromyographic, electron microscopic, and cardiovascular aspects | Q68457459 | ||
| The experimental production of glycogen storage in cultured human fibroblasts | Q68488395 | ||
| The floppy infant syndrome in muscular glycogenosis | Q68499288 | ||
| The role of lysosomes in the pathogeny of storage diseases | Q68505851 | ||
| Pompe's disease--detection of maternal heterozygote and antenatal exclusion in the fetus | Q68513291 | ||
| [Results of clinical, biochemical, light-microscopical and ultrastructural studies of childhood glycogenosis in two brothers and their sister (author's transl)] | Q68520872 | ||
| Glycogen storage diseases | Q68656660 | ||
| Comparative study of acid maltase deficiency. Biochemical differences between infantile, childhood, and adult types | Q68992811 | ||
| Glycogen storage disease in Norway | Q69002138 | ||
| Adult acid maltase deficiency. Abnormalities in fibroblasts cultured from patients | Q69004663 | ||
| Glycogenosis. Diagnosis by skin biopsy | Q69005067 | ||
| Type II Glycogenosis in Adults | Q69008958 | ||
| α-1,4-Glucosidase activity in leucocytes and lymphocytes of 2 adult patients with glycogen-storage disease type II, (Pompe's disease) | Q69042469 | ||
| Myopathy due to acid maltase deficiency. Pompe's disease in adolescence and adult (author's transl) | Q69042678 | ||
| Glycogenosis | Q69212562 | ||
| Tuberculin Reactions (Cont.) | Q69468313 | ||
| Subcellular distribution of acid and neutral alpha-glucosidases in normal, acid maltase deficient, and myophosphorylase deficient human skeletal muscle | Q69571071 | ||
| [Glycogenoses] | Q69862245 | ||
| P433 | issue | 3 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | neurology | Q83042 |
| P304 | page(s) | 237-252 | |
| P577 | publication date | 1976-06-01 | |
| 1976-06-14 | |||
| P1433 | published in | Journal of Neurology | Q6295649 |
| P1476 | title | The symptomatology, morphology and biochemistry of glycogenosis type II (Pompe) in the adult | |
| P478 | volume | 212 |
| Q71979814 | High frequency discharges as a non-specific EMG activity in adult acid maltase deficiency (author's transl) |
| Q34216280 | Metabolic cardiomyopathies |
| Q38800985 | Pompe Disease: Diagnosis and Management. Evidence-Based Guidelines from a Canadian Expert Panel |
| Q36245480 | The natural course of non-classic Pompe's disease; a review of 225 published cases |
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