Literature DB >> 4112649

Skeletal muscle glycogenosis type II: biochemical and electron microscopic investigations of one case.

N Canal, L Frattola, G Pellegrini.   

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Year:  1972        PMID: 4112649     DOI: 10.1007/bf00316197

Source DB:  PubMed          Journal:  Z Neurol        ISSN: 0012-1037


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  20 in total

1.  PHOSPHOFRUCTOKINASE DEFICIENCY IN SKELETAL MUSCLE. A NEW TYPE OF GLYCOGENOSIS.

Authors:  S TARUI; G OKUNO; Y IKURA; T TANAKA; M SUDA; M NISHIKAWA
Journal:  Biochem Biophys Res Commun       Date:  1965-05-03       Impact factor: 3.575

2.  Glycogen disease of skeletal muscle; report of two cases and review of literature.

Authors:  H ZELLWEGER; A DARK; G A ABU-HAIDAR
Journal:  Pediatrics       Date:  1955-06       Impact factor: 7.124

3.  Glycogen storage disease of the muscles. Report of a case with unusual features.

Authors:  P A DI SANT'AGNESE; D H ANDERSEN; K M METCALF
Journal:  J Pediatr       Date:  1962-09       Impact factor: 4.406

4.  Phosphorylase and glycogen levels in skeletal muscle and liver of hibernating and non-hibernating bats.

Authors:  S L LEONARD; W A WIMSATT
Journal:  Am J Physiol       Date:  1959-11

5.  A MYOPATHY PRESENTING IN ADULT LIFE WITH FEATURES SUGGESTIVE OF GLYCOGEN STORAGE DISEASE.

Authors:  J M Holmes; C R Houghton; A L Woolf
Journal:  J Neurol Neurosurg Psychiatry       Date:  1960-11       Impact factor: 10.154

6.  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

7.  Late infantile acid maltase deficiency.

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

8.  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

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

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

10.  A histochemical and electron microscopic study of skeletal muscle in a case of Pompe's disease (glycogenosis II).

Authors:  R D Cardiff
Journal:  Pediatrics       Date:  1966-02       Impact factor: 7.124

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  7 in total

1.  [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

2.  Pompe's disease: an inborn lysosomal disorder with storage of glycogen. A study of brain and striated muscle.

Authors:  J J Martin; T de Barsy; F van Hoof; G Palladini
Journal:  Acta Neuropathol       Date:  1973-02-19       Impact factor: 17.088

Review 3.  The natural course of non-classic Pompe's disease; a review of 225 published cases.

Authors:  Léon P F Winkel; Marloes L C Hagemans; Pieter A van Doorn; M Christa B Loonen; Wim J C Hop; Arnold J J Reuser; Ans T van der Ploeg
Journal:  J Neurol       Date:  2005-08       Impact factor: 4.849

4.  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

Review 5.  The glycogen storage diseases.

Authors:  B E Ryman
Journal:  J Clin Pathol Suppl (R Coll Pathol)       Date:  1974

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

Authors:  F Gullotta; H Stefan; H Mattern
Journal:  J Neurol       Date:  1976       Impact factor: 4.849

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

Authors:  J J Martin; T de Barsy; W R den Tandt
Journal:  J Neurol       Date:  1976-08-06       Impact factor: 4.849

  7 in total

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