Nutrition rehabilitation-related complications in primary mitochondrial disorders.
暂无分享,去创建一个
[1] G. Sacks,et al. ASPEN Consensus Recommendations for Refeeding Syndrome. , 2020, Nutrition in clinical practice : official publication of the American Society for Parenteral and Enteral Nutrition.
[2] Marni J. Falk,et al. Mitochondrial disease patient motivations and barriers to participate in clinical trials , 2018, PloS one.
[3] Young-Mock Lee,et al. Enteral Tube Feeding in Paediatric Mitochondrial Diseases , 2017, Scientific Reports.
[4] Marni J. Falk,et al. Patient care standards for primary mitochondrial disease: a consensus statement from the Mitochondrial Medicine Society , 2017, Genetics in Medicine.
[5] Robert W. Taylor,et al. Prevalence of nuclear and mitochondrial DNA mutations related to adult mitochondrial disease , 2015, Annals of neurology.
[6] Marni J. Falk,et al. Diagnosis and management of mitochondrial disease: a consensus statement from the Mitochondrial Medicine Society , 2014, Genetics in Medicine.
[7] A. Amiot,et al. Frequency of mitochondrial defects in patients with chronic intestinal pseudo-obstruction. , 2009, Gastroenterology.
[8] M. Morimoto,et al. Intestinal pseudo-obstruction in a patient with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) associated with phenytoin therapy , 2008, Brain and Development.
[9] D. Thorburn,et al. Minimum birth prevalence of mitochondrial respiratory chain disorders in children. , 2003, Brain : a journal of neurology.
[10] A. Schapira,et al. Mitochondrial disorders: an overview. , 1997, Journal of bioenergetics and biomembranes.
[11] S. Travis,et al. Unexplained gastrointestinal symptoms: think mitochondrial disease. , 2014, Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver.