Literature DB >> 24379101

Child neurology: Recurrent rhabdomyolysis due to a fatty acid oxidation disorder.

Gaetano Terrone1, Margherita Ruoppolo, Nicola Brunetti-Pierri, Carla Cozzolino, Emanuela Scolamiero, Giancarlo Parenti, Alfonso Romano, Generoso Andria, Francesco Salvatore, Giulia Frisso.   

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Year:  2014        PMID： 24379101     DOI： 10.1212/01.wnl.0000438217.31437.72

Source DB:  PubMed          Journal:  Neurology        ISSN： 0028-3878            Impact factor:   9.910


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  3 in total

1.  Noncompaction in mitochondrial trifunctional protein deficiency due to a HADHB mutation.

Authors:  Josef Finsterer; Sinda Zarrouk-Majoub
Journal:  Eur J Pediatr       Date:  2015-07-24       Impact factor: 3.183

Review 2.  Propofol infusion syndrome: a structured review of experimental studies and 153 published case reports.

Authors:  Adéla Krajčová; Petr Waldauf; Michal Anděl; František Duška
Journal:  Crit Care       Date:  2015-11-12       Impact factor: 9.097

3.  Analysis of a family with mitochondrial trifunctional protein deficiency caused by HADHA gene mutations.

Authors:  Jinling Yang; Dejian Yuan; Xiaohui Tan; Yexi Zeng; Ning Tang; Dayu Chen; Jianqiang Tan; Ren Cai; Jun Huang; Tizhen Yan
Journal:  Mol Med Rep       Date:  2021-12-08       Impact factor: 2.952
  3 in total

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