Literature DB >> 4522267

Alpha-1,4-glucosidase activity in leucocytes and lymphocytes of 2 adult patients with glycogen-storage disease type II, (Pompe's disease).

D Seiler, R Kelleter, H W Kölmel, R Heene.   

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Year:  1973        PMID： 4522267     DOI： 10.1007/bf01930409

Source DB:  PubMed          Journal:  Experientia        ISSN： 0014-4754


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  12 in total

1.  Acid maltase deficiency in adults: studies in four cases of a syndrome which may mimic muscular dystrophy or other myopathies.

Authors:  A G Engel
Journal:  Brain       Date:  1970       Impact factor: 13.501

2.  Glycogen breakdown in human lymphocytes: activities of phosphorylase and -I,4-glucosidases.

Authors:  R Kelleter; D Seiler
Journal:  Clin Chim Acta       Date:  1972-11       Impact factor: 3.786

3.  Adult myopathy from glycogen storage disease due to acid maltase deficiency.

Authors:  P Hudgson; D Gardner-Medwin; M Worsfold; R J Pennington; J N Walton
Journal:  Brain       Date:  1968-09       Impact factor: 13.501

4.  Late infantile acid maltase deficiency.

Authors:  K F Swaiman; W R Kennedy; H S Sauls
Journal:  Arch Neurol       Date:  1968-06

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

Authors:  H Zellweger; B I Brown; W F McCormick; J B Tu
Journal:  Ann Paediatr       Date:  1965

6.  [Muscular glycogenosis caused by alpha-1,4-glucosidase deficiency simulating progressive muscular dystrophy. (Clinical and enzyme study. Optic and electron microscopy)].

Authors:  V Courtecuissf; P Royer; R Habib; C Monnier; J Demos
Journal:  Arch Fr Pediatr       Date:  1965-12

7.  [Muscular glycogenosis of myopathic form caused by acid maltase deficiency].

Authors:  F Isch; J G Juif; R Sacrez; F Thiebaut
Journal:  Pediatrie       Date:  1966 Jan-Feb

8.  Alpha-1,4-glucosidase activity in leucocytes from the family of two brothers who lack this enzyme in muscle.

Authors:  B I Brown; H Zellweger
Journal:  Biochem J       Date:  1966-10       Impact factor: 3.857

9.  Acid maltase levels in muscle in heterozygous acid maltase deficiency and in non-weak and neuromuscular disease controls.

Authors:  A G Engel; M R Gomez
Journal:  J Neurol Neurosurg Psychiatry       Date:  1970-12       Impact factor: 10.154

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

Authors:  H G HERS
Journal:  Biochem J       Date:  1963-01       Impact factor: 3.857
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  4 in total

1.  Characterization of the molecular defect in infantile and adult acid alpha-glucosidase deficiency fibroblasts.

Authors:  N G Beratis; G U LaBadie; K Hirschhorn
Journal:  J Clin Invest       Date:  1978-12       Impact factor: 14.808

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

Authors:  H W Kölmel; H Assmus; D Seiler
Journal:  Arch Psychiatr Nervenkr (1970)       Date:  1974

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

Authors:  G K Schlenska; R Heene; G Spalke; D Seiler
Journal:  J Neurol       Date:  1976-06-14       Impact factor: 4.849

4.  Clinical diversity in glycogenosis type II. Biosynthesis and in situ localization of acid alpha-glucosidase in mutant fibroblasts.

Authors:  A J Reuser; M Kroos; R Willemsen; D Swallow; J M Tager; H Galjaard
Journal:  J Clin Invest       Date:  1987-06       Impact factor: 14.808
  4 in total

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