Literature DB >> 16443431

Rhabdomyolysis caused by an inherited metabolic disease: very long-chain acyl-CoA dehydrogenase deficiency.

Nicol C Voermans1, Baziel G van Engelen, Leo A Kluijtmans, Nike M Stikkelbroeck, Ad R Hermus.   

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Year:  2006        PMID： 16443431     DOI： 10.1016/j.amjmed.2005.07.064

Source DB:  PubMed          Journal:  Am J Med        ISSN： 0002-9343            Impact factor:   4.965


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  13 in total

1.  Adult-onset very-long-chain acyl-CoA dehydrogenase deficiency (VLCADD).

Authors:  F Fatehi; A A Okhovat; Y Nilipour; M Mroczek; V Straub; A Töpf; A Palibrk; S Peric; V Rakocevic Stojanovic; H Najmabadi; S Nafissi
Journal:  Eur J Neurol       Date:  2020-07-24       Impact factor: 6.089

Review 2.  Rhabdomyolysis: pathogenesis of renal injury and management.

Authors:  Zubaida Al-Ismaili; Melissa Piccioni; Michael Zappitelli
Journal:  Pediatr Nephrol       Date:  2011-01-20       Impact factor: 3.714

3.  Rhabdomyolysis as a manifestation of a metabolic disease: a case report.

Authors:  Marta Sousa Moniz; Maria Inês Mascarenhas; Carlos Escobar; Pedro Nunes; Clara Abadesso; Helena Loureiro; Helena Almeida
Journal:  Rev Bras Ter Intensiva       Date:  2017 Jan-Mar

4.  Expression and characterization of mutations in human very long-chain acyl-CoA dehydrogenase using a prokaryotic system.

Authors:  Eric S Goetzman; Yudong Wang; Miao He; Al-Walid Mohsen; Brittani K Ninness; Jerry Vockley
Journal:  Mol Genet Metab       Date:  2007-03-19       Impact factor: 4.797

Review 5.  Inborn errors of energy metabolism associated with myopathies.

Authors:  Anibh M Das; Ulrike Steuerwald; Sabine Illsinger
Journal:  J Biomed Biotechnol       Date:  2010-05-26

Review 6.  Rhabdomyolysis: a review, with emphasis on the pediatric population.

Authors:  Essam F Elsayed; Robert F Reilly
Journal:  Pediatr Nephrol       Date:  2010-01       Impact factor: 3.714

7.  Rhabdomyolysis with different etiologies in childhood.

Authors:  Demet Alaygut; Meral Torun Bayram; Belde Kasap; Alper Soylu; Mehmet Türkmen; Salih Kavukcu
Journal:  World J Clin Pediatr       Date:  2017-11-08

8.  A novel tandem mass spectrometry method for rapid confirmation of medium- and very long-chain acyl-CoA dehydrogenase deficiency in newborns.

Authors:  Frank ter Veld; Martina Mueller; Simone Kramer; Ulrike Haussmann; Diran Herebian; Ertan Mayatepek; Maurice D Laryea; Sonja Primassin; Ute Spiekerkoetter
Journal:  PLoS One       Date:  2009-07-30       Impact factor: 3.240

9.  Pervasive inflammatory activation in patients with deficiency in very-long-chain acyl-coA dehydrogenase (VLCADD).

Authors:  Abbe N Vallejo; Henry J Mroczkowski; Joshua J Michel; Michael Woolford; Harry C Blair; Patricia Griffin; Elizabeth McCracken; Stephanie J Mihalik; Miguel Reyes-Mugica; Jerry Vockley
Journal:  Clin Transl Immunology       Date:  2021-06-27

10.  Rhabdomyolysis in a neonate due to very long chain acyl CoA dehydrogenase deficiency.

Authors:  Jessica Scott Schwoerer; Gena Cooper; Sandra van Calcar
Journal:  Mol Genet Metab Rep       Date:  2015-03-30
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