Recurrent brain hematomas in MELAS associated with an ND5 gene mitochondrial mutation
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Neurology (clinical)
Reference7 articles.
1. A mutation in the tRNALeu(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies
2. Identification of a Novel Mutation in the mtDNA ND5 Gene Associated with MELAS
3. The mitochondrial DNA G13513A transition in ND5 is associated with a LHON/MELAS overlap syndrome and may be a frequent cause of MELAS
4. Cytopathie mitochondriale en réanimation À propos d'un cas
5. Mitochondrial Encephalomyopathies: CT and MRI Findings and Correlations with Clinical Features
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1. Phenotypic Heterogeneity of the Mitochondrial DNA Variant m.13513 G > A;Journal of Pediatric Genetics;2023-04-27
2. Microhemorrhages in MELAS Lesions: A Case Report;Journal of the Belgian Society of Radiology;2022
3. Mitochondrial Nuclear Retrograde Regulator 1 (MNRR1) rescues the cellular phenotype of MELAS by inducing homeostatic mechanisms;Proceedings of the National Academy of Sciences;2020-11-30
4. Primary Mitochondrial Disorders of the Pediatric Central Nervous System: Neuroimaging Findings;RadioGraphics;2020-11
5. Haemorrhagic Transformation of a MELAS Stroke-Like Lesion;Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques;2019-11-18
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