HarrarDBDarrasBTGhoshPS. Acute neuromuscular disorders in the pediatric intensive care unit. J Child Neurol. 2020;35:17–24.
2.
ArslanŞYorulmazASertAAkinF. Management of acute mitochondriopathy and encephalopathy syndrome in pediatric intensive care unite: a new clinical entity. Acta Neurol Belg. https://www.ncbi.nlm.nih.gov/pubmed/30887303. Published 2019.
3.
KogaYPovalkoNKatayamaK, et al.Beneficial effect of pyruvate therapy on Leigh syndrome due to a novel mutation in PDH E1α gene. Brain Dev. 2012;34:87–91.
4.
ZhouYYiJLiuLWangXDongLDuA. Acute mitochondrial myopathy with respiratory insufficiency and motor axonal polyneuropathy. Int J Neurosci. 2018;128:231–236.
5.
JonesHRJrDarrasBT. Acute care pediatric electromyography. Muscle Nerve Suppl. 2000;9:S53–S62.
6.
DaoudHLucoSMLiR, et al.Next-generation sequencing for diagnosis of rare diseases in the neonatal intensive care unit. CMAJ. 2016;188:E254–E260.
7.
PapaioannouVDragoumanisCTheodorouVPneumatikosI. The propofol infusion “syndrome” in intensive care unit: from pathophysiology to prophylaxis and treatment. Acta Anaesthesiol Belg. 2008;59:79–86.
8.
TsuruiSSugieHItoMIgarashiY. Clinical and biochemical analysis of 27 patients with myoglobinuria of unknown causes. Rinsho Shinkeigaku. 1995;35:24–28.
