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
Main Authors: | , |
---|---|
Format: | Article |
Language: | English |
Published: |
Frontiers Media S.A.
2023-04-01
|
Series: | Frontiers in Neuroscience |
Subjects: | |
Online Access: | https://www.frontiersin.org/articles/10.3389/fnins.2023.1173654/full |
_version_ | 1797845570425978880 |
---|---|
author | Josef Finsterer Sounira Mehri |
author_facet | Josef Finsterer Sounira Mehri |
author_sort | Josef Finsterer |
collection | DOAJ |
first_indexed | 2024-04-09T17:42:14Z |
format | Article |
id | doaj.art-e4076e0b697d4006a872d2e5678dd2ae |
institution | Directory Open Access Journal |
issn | 1662-453X |
language | English |
last_indexed | 2024-04-09T17:42:14Z |
publishDate | 2023-04-01 |
publisher | Frontiers Media S.A. |
record_format | Article |
series | Frontiers in Neuroscience |
spelling | doaj.art-e4076e0b697d4006a872d2e5678dd2ae2023-04-17T05:14:45ZengFrontiers Media S.A.Frontiers in Neuroscience1662-453X2023-04-011710.3389/fnins.2023.11736541173654Commentary: 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 pathogenesisJosef Finsterer0Sounira Mehri1Neurology and Neurophysiology Center, Vienna, AustriaBiochemistry Laboratory, LR12ES05 “Nutrition-Functional Foods and Vascular Health”, Faculty of Medicine, Monastir, Tunisiahttps://www.frontiersin.org/articles/10.3389/fnins.2023.1173654/fullMELASmtDNAheteroplasmyrespiratory chainstroke-like episode |
spellingShingle | Josef Finsterer Sounira Mehri 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 Frontiers in Neuroscience MELAS mtDNA heteroplasmy respiratory chain stroke-like episode |
title | 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 |
title_full | 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 |
title_fullStr | 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 |
title_full_unstemmed | 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 |
title_short | 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 |
title_sort | 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 |
topic | MELAS mtDNA heteroplasmy respiratory chain stroke-like episode |
url | https://www.frontiersin.org/articles/10.3389/fnins.2023.1173654/full |
work_keys_str_mv | AT joseffinsterer commentarymitochondrialencephalomyopathywithlacticacidosisandstrokelikeepisodeswithanmttl1m3243agpointmutationneuroradiologicalfeaturesandtheirimplicationsforunderlyingpathogenesis AT souniramehri commentarymitochondrialencephalomyopathywithlacticacidosisandstrokelikeepisodeswithanmttl1m3243agpointmutationneuroradiologicalfeaturesandtheirimplicationsforunderlyingpathogenesis |