Literature DB >> 10399098

Recurrent rhabdomyolysis in a child with glutaric aciduria type I.

C J Wilson1, J E Collins, J V Leonard.   

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Year:  1999        PMID： 10399098     DOI： 10.1023/a:1005542400135

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


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  3 in total

Review 1.  Myoglobinuria, malignant hyperthermia, neuroleptic malignant syndrome and serotonin syndrome.

Authors:  T E Bertorini
Journal:  Neurol Clin       Date:  1997-08       Impact factor: 3.806

2.  Early signs and course of disease of glutaryl-CoA dehydrogenase deficiency.

Authors:  G F Hoffmann; H J Böhles; A Burlina; M Duran; J Herwig; W Lehnert; J V Leonard; A Muntau; F K Plecko-Starting; A Superti-Furga
Journal:  J Inherit Metab Dis       Date:  1995       Impact factor: 4.982

Review 3.  Glutaric aciduria type 1 (glutaryl-CoA-dehydrogenase deficiency): advances and unanswered questions. Report from an international meeting.

Authors:  A Superti-Furga; G F Hoffmann
Journal:  Eur J Pediatr       Date:  1997-11       Impact factor: 3.183
  3 in total
  2 in total

Review 1.  Recurrent rhabdomyolysis and glutaric aciduria type I: a case report and literature review.

Authors:  Gu-Ling Qian; Fang Hong; Fan Tong; Hai-Dong Fu; Ai-Min Liu
Journal:  World J Pediatr       Date:  2016-06-29       Impact factor: 2.764

2.  Rhabdomyolysis in glutaric aciduria type I.

Authors:  S L Chow; C Rohan; A A M Morris
Journal:  J Inherit Metab Dis       Date:  2003       Impact factor: 4.982
  2 in total

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