AAAAAA
Results:
1-7
|
Results: 7
Authors:
Taivassalo, T
Shoubridge, EA
Chen, J
Kennaway, NG
DiMauro, S
Arnold, DL
Haller, RG
Citation: T. Taivassalo et al., Aerobic conditioning in patients with mitochondrial myopathies: Physiological, biochemical, and genetic effects, ANN NEUROL, 50(2), 2001, pp. 133-141
Authors:
Vissing, J
MacLean, DA
Vissing, SF
Sander, M
Saltin, B
Haller, RG
Citation: J. Vissing et al., The exercise metaboreflex is maintained in the absence of muscle acidosis:insights from muscle microdialysis in humans with McArdle's disease, J PHYSL LON, 537(2), 2001, pp. 641-649
Authors:
Wariar, R
Gaffke, JN
Haller, RG
Bertocci, LA
Citation: R. Wariar et al., A modular NIRS system for clinical measurement of impaired skeletal muscleoxygenation, J APP PHYSL, 88(1), 2000, pp. 315-325
Authors:
Wolfe, GI
Baker, NS
Haller, RG
Burns, DK
Barohn, RJ
Citation: Gi. Wolfe et al., McArdle's disease presenting with asymmetric, late-onset arm weakness, MUSCLE NERV, 23(4), 2000, pp. 641-645
Authors:
Karadimas, CL
Greenstein, P
Sue, CM
Joseph, JT
Tanji, K
Haller, RG
Taivassalo, T
Davidson, MM
Shanske, S
Bonilla, E
DiMauro, S
Citation: Cl. Karadimas et al., Recurrent myoglobinuria due to a nonsense mutation in the COX I gene of mitochondrial DNA, NEUROLOGY, 55(5), 2000, pp. 644-649
Authors:
Haller, RG
Citation: Rg. Haller, Treatment of McArdle disease, ARCH NEUROL, 57(7), 2000, pp. 923-924
Authors:
Vissing, J
Schmalbruch, H
Haller, RG
Clausen, T
Citation: J. Vissing et al., Muscle phosphoglycerate mutase deficiency with tubular aggregates: Effect of dantrolene, ANN NEUROL, 46(2), 1999, pp. 274-277
Risultati:
1-7
|