Metabolic and electrophysiologic phenotype in myophosphorylase deficiency (Glycogenosis Type V, McArdle's disease)

Müller, K. and Zange, J. and Vorgerd, M. and Malin, J.P. (2000) Metabolic and electrophysiologic phenotype in myophosphorylase deficiency (Glycogenosis Type V, McArdle's disease). 8. KBF-Symposium "Complexity in Medicine", Cologne, Germany, 13-15 Sept. 2000.

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Item URL in elib:

https://elib.dlr.de/5005/

Document Type:

Conference or Workshop Item (Speech)

Additional Information:

LIDO-Berichtsjahr=2002,

Title:

Metabolic and electrophysiologic phenotype in myophosphorylase deficiency (Glycogenosis Type V, McArdle's disease)

Authors:

Authors	Institution or Email of Authors	Author's ORCID iD	ORCID Put Code
Müller, K.	UNSPECIFIED	UNSPECIFIED	UNSPECIFIED
Zange, J.	UNSPECIFIED	UNSPECIFIED	UNSPECIFIED
Vorgerd, M.	Dept. of Neurology, Ruhr University Bochum, Bochum, Germany	UNSPECIFIED	UNSPECIFIED
Malin, J.P.	Dept. of Neurology, Ruhr University Bochum, Bochum, Germany	UNSPECIFIED	UNSPECIFIED

Date:

2000

Open Access:

Gold Open Access:

In SCOPUS:

In ISI Web of Science:

Page Range:

B44-

Status:

Published

Keywords:

Muscle metabolism, 31P-MRS, McArdle's disease, EMG

Event Title:

8. KBF-Symposium "Complexity in Medicine", Cologne, Germany, 13-15 Sept. 2000

HGF - Research field:

Aeronautics, Space and Transport (old)

HGF - Program:

Space (old)

HGF - Program Themes:

W FR - Forschung unter Weltraumbedingungen (old)

DLR - Research area:

Space

DLR - Program:

W FR - Forschung unter Weltraumbedingungen

DLR - Research theme (Project):

UNSPECIFIED

Location:

Köln-Porz

Institutes and Institutions:

Institute of Aerospace Medicine

Deposited By:

DLR-Beauftragter, elib

Deposited On:

16 Sep 2005

Last Modified:

06 Jan 2010 18:22

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