Dominant encephalopathy mimicking mitochondrial disease

Neurology. 2011 Jan 4;76(1):101-3. doi: 10.1212/WNL.0b013e318203e908.

Authors

T Lönnqvist¹, P Isohanni, L Valanne, T Olli-Lähdesmäki, A Suomalainen, H Pihko

Affiliation

¹ Division of Child Neurology, Department of Neurology, Helsinki University Central Hospital, Helsinki Medical Imaging Center, University of Helsinki, PO Box 280, FIN-00029 HUCH, Finland. tuula.lonnqvist@hus.fi

PMID: 21205700
DOI: 10.1212/WNL.0b013e318203e908

No abstract available

Publication types

Research Support, Non-U.S. Gov't

MeSH terms

Adult
Aged
Child
Child, Preschool
DNA Mutational Analysis / methods
Exons / genetics
Family Health*
Female
Finland
Genes, Dominant*
Humans
Infant
Leukoencephalitis, Acute Hemorrhagic / diagnosis
Leukoencephalitis, Acute Hemorrhagic / genetics*
Leukoencephalitis, Acute Hemorrhagic / physiopathology*
Magnetic Resonance Imaging
Male
Mitochondrial Diseases / physiopathology*
Molecular Chaperones / genetics*
Mutation / genetics
Nuclear Pore Complex Proteins / genetics*

Substances

Molecular Chaperones
Nuclear Pore Complex Proteins
ran-binding protein 2