Research ArticlePediatric Neuroimaging
Open Access
Imaging Patterns Characterizing Mitochondrial Leukodystrophies
S.D. Roosendaal, T. van de Brug, C.A.P.F. Alves, S. Blaser, A. Vanderver, N.I. Wolf and M.S. van der Knaap
American Journal of Neuroradiology July 2021, 42 (7) 1334-1340; DOI: https://doi.org/10.3174/ajnr.A7097
S.D. Roosendaal
aFrom the Departments of Radiology (S.D.R.)
T. van de Brug
bEpidemiology and Biostatistics (T.v.d.B.), Amsterdam UMC, Amsterdam, the Netherlands
C.A.P.F. Alves
cDivision of Neuroradiology (C.A.P.F.A.)
S. Blaser
eDivision of Neuroradiology (S.B.), Department of Diagnostic Imaging, Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada
A. Vanderver
dDepartment of Radiology and Division of Neurology (A.V.), The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania
N.I. Wolf
fDepartment of Pediatric Neurology (M.S.v.d.K, N.I.W.), Emma Children’s Hospital, Amsterdam UMC, Vrije Universiteit and Amsterdam Neuroscience, Amsterdam, the Netherlands
M.S. van der Knaap
fDepartment of Pediatric Neurology (M.S.v.d.K, N.I.W.), Emma Children’s Hospital, Amsterdam UMC, Vrije Universiteit and Amsterdam Neuroscience, Amsterdam, the Netherlands
gDepartment of Functional Genomics (M.S.v.d.K.), Center for Neurogenomics and Cognitive Research, VU University, Amsterdam, the Netherlands.

Submit a Response to This Article
Jump to comment:
No eLetters have been published for this article.
In this issue
American Journal of Neuroradiology
Vol. 42, Issue 7
1 Jul 2021
Advertisement
S.D. Roosendaal, T. van de Brug, C.A.P.F. Alves, S. Blaser, A. Vanderver, N.I. Wolf, M.S. van der Knaap
Imaging Patterns Characterizing Mitochondrial Leukodystrophies
American Journal of Neuroradiology Jul 2021, 42 (7) 1334-1340; DOI: 10.3174/ajnr.A7097
Jump to section
Related Articles
Cited By...
- Glial Origins of Inherited White Matter Disorders
- Biallelic mutation of SUPV3L1 causes an inherited leukodystrophy-associated neurodevelopmental disorder due to aberrant mitochondrial double stranded RNA processing
- Teaching NeuroImage: IBA57 Mutation-Associated Infantile Cavitating Leukoencephalopathy
- Pattern Recognition in Mitochondrial Leukodystrophies is Hampered by the Peculiarities of Mitochondrial Genetics
This article has not yet been cited by articles in journals that are participating in Crossref Cited-by Linking.
More in this TOC Section
Similar Articles
Advertisement