Mitochondrial Genomic Variation in Rare and Metabolic Diseases: From Heteroplasmy to Precision Medicine. [PDF]
Mancio-Cárdenas AA +12 more
europepmc +1 more source
From confusion to diagnosis: a rare case of melas syndrome in a patient with familial consanguinity, recurrent stroke-like episodes, and concurrent FSGS. [PDF]
Mohsen M +5 more
europepmc +1 more source
Outcome of General Anesthesia With Remimazolam in a m.3243A>G Carrier. [PDF]
Finsterer J.
europepmc +1 more source
Severe Diabetic Ketoacidosis as the Initial Presentation of m.3243A>G-Related Mitochondrial Diabetes in a 19-Year-Old Woman. [PDF]
Ly R +11 more
europepmc +1 more source
Cerebral vasodilation and lesion patterns in stroke-like episodes of MELAS: a quantitative angiographic investigation. [PDF]
Song K +6 more
europepmc +1 more source
Primary Mitochondrial-Disorders-Associated Nephropathy in Adulthood. [PDF]
Bakis H +6 more
europepmc +1 more source
Perianesthetic Complications in Genetic Mitochondrial Disease: A Review of Case Reports. [PDF]
Johnson BM, Johnson SC.
europepmc +1 more source
Lamotrigine-induced Stevens-Johnson syndrome in the setting of mitochondrial encephalomyopathy: A case report. [PDF]
Tian Y, Chen T, Liu J, Wang J, Zhang L.
europepmc +1 more source

