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  Altered cerebral glucose metabolism in a family with clinical features resembling mitochondrial neurogastrointestinal encephalomyopathy syndrome in association with multiple mitochondrial DNA deletions

Lehnhardt, F.-G., Horvath, R., Ullrich, R., Kracht, L., Sobesky, J., Möller-Hartmann, W., et al. (2008). Altered cerebral glucose metabolism in a family with clinical features resembling mitochondrial neurogastrointestinal encephalomyopathy syndrome in association with multiple mitochondrial DNA deletions. Archives of Neurology, 65(3), 407-411.

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 Creators:
Lehnhardt, Fritz-Georg, Author
Horvath, Rita, Author
Ullrich, Roland1, Author           
Kracht, Lutz1, Author           
Sobesky, Jan1, Author           
Möller-Hartmann, Walter, Author
Jacobs, Andreas H.2, Author           
Haupt, Walter F., Author
Affiliations:
1Klinisches PET, Neurologische Abteilung, Max-Planck-Institut für neurologische Forschung, Managing Director: D. Yves von Cramon, Max Planck Institute for Metabolism Research, Managing Director: Jens Brüning, Max Planck Society, ou_2149663              
2Gentherapie und Molekulare Bildgebung, Neurologische Abteilung, Max-Planck-Institut für neurologische Forschung, Managing Director: D. Yves von Cramon, Max Planck Institute for Metabolism Research, Managing Director: Jens Brüning, Max Planck Society, ou_2149662              

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Language(s): eng - English
 Dates: 2008
 Publication Status: Published in print
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: eDoc: 376141
 Degree: -

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Title: Archives of Neurology
Source Genre: Journal
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Pages: - Volume / Issue: 65 (3) Sequence Number: - Start / End Page: 407 - 411 Identifier: -