Results 111 to 120 of about 376,481 (188)

Fahr Syndrome, Hypoparathyroidism and Mitochondrial Encephalomyopathy With Lactic Acidosis and Stroke-Like Episodes (MELAS) Syndrome. [PDF]

AACE Endocrinol Diabetes
Li J, Wang X, Guo Y, Wang W, Wu S, Sun J.   +5 more
europepmc   +1 more source

General anesthesia with remimazolam in a patient with mitochondrial encephalomyopathy: a case report. [PDF]

JA Clin Rep, 2021
Suzuki Y, Doi M, Nakajima Y.
europepmc   +1 more source

Dynamic functional connectivity changes in the triple networks in patients with mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes. [PDF]

Quant Imaging Med Surg
Yu Q, Wang R, Sun C, Hu B, Liu X, Yang L, Lin J, Li Y, Geng D.   +8 more
europepmc   +1 more source

Late-onset mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes syndrome with mitochondrial DNA 3243A>G mutation masquerading as autoimmune encephalitis: A case report. [PDF]

World J Clin Cases, 2023
Wang JW, Yuan XB, Chen HF.
europepmc   +1 more source

Leber´s hereditary optic neuroretinopathy [PDF]

, 1993
Toyka, K., Schneider, C., Klopstock, Thomas, Janetzky, B., Seibel, P., Lindner, A., Trappe, J., Reichmann, Heinz   +7 more
core   +1 more source

Commentary: Mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes with an MT-TL1 m.3243A>G point mutation: neuroradiological features and their implications for underlying pathogenesis. [PDF]

Front Neurosci, 2023
Finsterer J, Mehri S.
europepmc   +1 more source

A case of delayed acute intestinal pseudo-obstruction after MELAS crisis in mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes. [PDF]

Front Med (Lausanne)
Liu Q, Yang L, Liu P, Wang X, Peng K, Liu Q, Zhang K.   +6 more
europepmc   +1 more source

Determination of coenzyme Q(10) status in blood mononuclear cells, skeletal muscle, and plasma by HPLC with Di-propoxy-coenzyme Q(10) as an internal standard [PDF]

, 2005
Land, JM, Hargreaves, IP, Heales, SJR, Eaton, S, Duncan, AJ, Mills, K   +5 more
core  

Clinical features, disease burden and impact on quality of life in participants with mitochondrial encephalomyopathy. [PDF]

Front Neurol
Dumbuya JS, Tian C, Deng L, Ahmad B, Chen X, Lu J.   +5 more
europepmc   +1 more source

Infantile TK2 Deficiency Causing Mitochondrial Encephalomyopathy With Migrating Focal Seizures. [PDF]

Neurology
Bergonzini L, Carli S, Pelle S, Pettenuzzo I, Bonetti S, Santi E, Visconti C, Maffei M, Sheremet M, Lamantea E, Marsala A, Klub O, Gentile V, Cordelli DM, Garone C.   +14 more
europepmc   +1 more source