Cerebellar atrophy is common among mitochondrial disorders
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cellular and Molecular Neuroscience,Neurology (clinical),Biochemistry
Link
http://link.springer.com/article/10.1007/s11011-018-0238-y/fulltext.html
Reference21 articles.
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2. Finsterer J, Scorza FA (2018) Phenotypic spectrum of POLG1 mutations. Neurol Sci 39:571–573
3. Inbar-Feigenberg M, Blaser S, Hawkins C, Shannon P, Hewson S, Chitayat D (2018) Mitochondrial POLG related disorder presenting prenatally with fetal cerebellar growth arrest. Metab Brain Dis. https://doi.org/10.1007/s11011-018-0218-2
4. Mehta AR, Fox SH, Tarnopolsky M, Yoon G (2011) Mitochondrial mimicry of multiple system atrophy of the cerebellar subtype. Mov Disord 26:753–755
5. Tsujikawa K, Senda J, Yasui K, Hasegawa Y, Hoshiyama M, Katsuno M, Sobue G (2016) Distinctive distribution of brain volume reductions in MELAS and mitochondrial DNA A3243G mutation carriers: A voxel-based morphometric study. Mitochondrion 30:229–235
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