Literature DB >> 11596653

Early-onset lysosomal glycogen storage disease with normal acid maltase.

R M Dayan1, D L Renaud.   

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Year:  2001        PMID： 11596653     DOI： 10.1023/a:1010585714729

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN： 0141-8955            Impact factor:   4.982


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  6 in total

1.  Lysosomal glycogen storage disease with normal acid maltase.

Authors:  M J Danon; S J Oh; S DiMauro; J R Manaligod; A Eastwood; S Naidu; L H Schliselfeld
Journal:  Neurology       Date:  1981-01       Impact factor: 9.910

2.  Fatal infantile cardiac glycogenosis without acid maltase deficiency presenting as congenital hydrops.

Authors:  J Atkin; J W Snow; H Zellweger; W J Rhead
Journal:  Eur J Pediatr       Date:  1984-06       Impact factor: 3.183

3.  Primary LAMP-2 deficiency causes X-linked vacuolar cardiomyopathy and myopathy (Danon disease).

Authors:  I Nishino; J Fu; K Tanji; T Yamada; S Shimojo; T Koori; M Mora; J E Riggs; S J Oh; Y Koga; C M Sue; A Yamamoto; N Murakami; S Shanske; E Byrne; E Bonilla; I Nonaka; S DiMauro; M Hirano
Journal:  Nature       Date:  2000-08-24       Impact factor: 49.962

4.  Nosology of lysosomal glycogen storage diseases without in vitro acid maltase deficiency. Delineation of a neonatal form.

Authors:  A Verloes; M Massin; J Lombet; B Grattagliano; D Soyeur; J Rigo; L Koulischer; F Van Hoof
Journal:  Am J Med Genet       Date:  1997-10-17

5.  Lysosomal glycogen storage disease with normal acid maltase with early fatal outcome.

Authors:  Y Morisawa; M Fujieda; N Murakami; K Naruse; T Okada; H Morita; K Sawada; J Miyazaki; T Kurashige; I Nonaka
Journal:  J Neurol Sci       Date:  1998-10-08       Impact factor: 3.181

6.  Glycogen storage disease with normal acid maltase: skeletal and cardiac muscles.

Authors:  N Tachi; M Tachi; K Sasaki; H Tomita; S Wakai; S Annaka; R Minami; S Tsurui; H Sugie
Journal:  Pediatr Neurol       Date:  1989 Jan-Feb       Impact factor: 3.372
  6 in total

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