Results 101 to 110 of about 3,285 (240)

Anesthetic considerations in mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes syndrome: a case series [PDF]

, 2011
Carmelina Gurrieri, Jonathon E. Kivela, Katarina Bojanić, Ralitza H. Gavrilova, Randall P. Flick, Juraj Šprung, Toby N. Weingarten   +6 more
openalex   +1 more source

Mitochondrial encephalomyopathy: six cases report and review of literature

Chinese Journal of Contemporary Neurology and Neurosurgery, 2014
The clinical characteristics, imaging examinations and muscle biopsies in 6 cases with mitochondrial encephalomyopathy were retrospectively analyzed.
Yuan GUO, Jun TUO, Bo WU
doaj  

Post-transcriptional regulation of the steady-state levels of mitochondrial tRNAs in HeLa cells [PDF]

, 1993
In human mitochondrial DNA (mtDNA), the tRNA genes are located in three different transcription units that are transcribed at three different rates. To analyze the regulation of tRNA formation by the three transcription units, we have examined the steady-
Attardi, Giuseppe, King, Michael P.
core  

Mitochondrial neurogastrointestinal encephalomyopathy syndrome with an unusual pattern of inheritance [PDF]

, 2015
Nastaran Rafiei, Shrikant Mishra, H. Mohammadkhanli, Bhavesh Trikamji   +3 more
openalex   +1 more source

NEURO-IMAGE: MELAS (mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes syndrome)

, 2021
Louise Pichon, Adrian Ivanoiu, Thierry Duprez, Douglas Lacomblez, G. Wilms   +4 more
openalex   +2 more sources

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
Duncan, AJ, Eaton, S, Hargreaves, IP, Heales, SJR, Land, JM, Mills, K   +5 more
core   +1 more source

Liver transplantation for mitochondrial neurogastrointestinal encephalomyopathy [PDF]

, 2016
Roberto De Giorgio, Loris Pironi, Rita Rinaldi, Elisa Boschetti, Leonardo Caporali, Mariantonietta Capristo, Carlo Casali, Giovanna Cenacchi, Manuela Contin, Roberto D’Angelo, Antonietta D’Errico, Laura Ludovica Gramegna, Raffaele Lodi, Alessandra Maresca, Susan Mohamed, Maria Cristina Morelli, Valentina Papa, Caterina Tonon, Vitaliano Tugnoli, Valério Carelli, Roberto D’Alessandro, Antonio Daniele Pinna   +21 more
openalex   +1 more source

Mice with Mitochondrial Complex I Deficiency Develop a Fatal Encephalomyopathy [PDF]

, 2008
Shane E. Kruse, W. C. Watt, David J. Marcinek, Raj P. Kapur, Kenneth A. Schenkman, Richard D. Palmiter   +5 more
openalex   +1 more source

Bioenergetic Consequences of PINK1 Mutations in Parkinson Disease [PDF]

, 2011
Background: Mutations of the gene for PTEN-induced kinase 1 (PINK1) are a cause of familial Parkinson's disease (PD). PINK1 protein has been localised to mitochondria and PINK1 gene knockout models exhibit abnormal mitochondrial function.
Abramov, AY, Gegg, M, Grunewald, A, Klein, C, Schapira, AHV, Wood, NW   +5 more
core  

Mitochondrial encephalomyopathies--fifty years on: the Robert Wartenberg Lecture. [PDF]

Neurology, 2013
DiMauro S.
europepmc   +1 more source