Items where Author is "Kornblum, C."

Yes

Ullrich, N. D. and Fischer, D. and Kornblum, C. and Walter, M. C. and Niggli, E. and Zorzato, F. and Treves, S.. (2011) Alterations of excitation-contraction coupling and excitation coupled Ca(2+) entry in human myotubes carrying CAV3 mutations linked to rippling muscle. Human Mutation, 32 (3). pp. 309-317.

Boes, M. and Bauer, J. and Urbach, H. and Elger, C. E. and Frank, S. and Baron, M. and Zsurka, G. and Kunz, W. S. and Kornblum, C.. (2009) Proof of progression over time : finally fulminant brain, muscle, and liver affection in Alpers syndrome associated with the A467T POLG1 mutation. Seizure : European journal of epilepsy, Vol. 18. pp. 232-234.

Kornblum, C. and Schröder, R. and Müller, K. and Vorgerd, M. and Eggers, J. and Bogdanow, M. and Papassotiropoulos, A. and Fabian, K. and Klockgether, T. and Zange, J.. (2005) Creatine has no beneficial effect on skeletal muscle energy metabolism in patients with single mitochondrial DNA deletions : a placebo-controlled, double-blind 31P-MRS crossover study. European journal of neurology, Vol. 12, H. 4. pp. 300-309.

Schröder, R. and Vielhaber, S. and Wiedemann, F. R. and Kornblum, C. and Papassotiropoulos, A. and Broich, P. and Zierz, S. and Elger, C. E. and Reichmann, H. and Seibel, P. and Klockgether, T. and Kunz, W. S.. (2000) New insights into the metabolic consequences of large-scale mtDNA deletions : a quantitative analysis of biochemical, morphological, and genetic findings in human skeletal muscle. Journal of neuropathology and experimental neurology, Vol. 59, H. 5. pp. 353-360.