Hyperglycemic Crisis in Patients With Mitochondrial Encephalopathy, Lactic Acidosis, and Stroke-like Episodes (MELAS)
Tài liệu tham khảo
Goto, 1990, A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies, Nature, 348, 651, 10.1038/348651a0
Kadowaki, 1994, A subtype of diabetes mellitus associated with a mutation of mitochondrial DNA, N Engl J Med, 330, 962, 10.1056/NEJM199404073301403
El-Hattab, 2014, Glucose metabolism derangements in adults with the MELAS m.3243A>G mutation, Mitochondrion, 18, 63, 10.1016/j.mito.2014.07.008
Yatsuga, 2012, MELAS: a nationwide prospective cohort study of 96 patients in Japan, Biochim Biophys Acta, 1820, 619, 10.1016/j.bbagen.2011.03.015
Sproule, 2008, Mitochondrial encephalopathy, lactic acidosis, and strokelike episodes: basic concepts, clinical phenotype, and therapeutic management of MELAS syndrome, Ann N Y Acad Sci, 1142, 133, 10.1196/annals.1444.011
Maassen, 2004, Mitochondrial diabetes: molecular mechanisms and clinical presentation, Diabetes, 53, S103, 10.2337/diabetes.53.2007.S103
Dungan, 2009, Stress hyperglycaemia, Lancet, 373, 1798, 10.1016/S0140-6736(09)60553-5
Al-Gadi, 2018, Endocrine disorders in primary mitochondrial disease, J Endocr Soc, 2, 361, 10.1210/js.2017-00434
Schaefer, 2013, Endocrine disorders in mitochondrial disease, Mol Cell Endocrinol, 379, 2, 10.1016/j.mce.2013.06.004
Whittaker, 2007, Prevalence and progression of diabetes in mitochondrial disease, Diabetologia, 50, 2085, 10.1007/s00125-007-0779-9
Guillausseau, 2004, Heterogeneity of diabetes phenotype in patients with 3243 bp mutation of mitochondrial DNA (maternally inherited diabetes and deafness or MIDD), Diabetes Metab, 30, 181, 10.1016/S1262-3636(07)70105-2
Yee, 2018, Mitochondrial disease: an uncommon but important cause of diabetes mellitus, Endocrinol Diabetes Metab Case Rep, 2018
Takamura, 2000, Ketosis-onset diabetes without islet-associated autoantibodies in a patient with MELAS, Diabetes Care, 23, 1018, 10.2337/diacare.23.7.1018