Showing results (551-560 of 687) with videos related to

Sort By:
Pageof 69
Revista Espanola De Cardiologia|March 28, 2008
[Sex differences in left ventricular noncompaction in patients with and without neuromuscular disorders]Claudia Stöllberger, Gerhard Blazek, Maria Winkler-Dworak, et al.
Journal of Electromyography and Kinesiology : Official Journal of the International Society of Electrophysiological Kinesiology|July 18, 2002
Influence of disposable, concentric needle electrodes on muscle enzyme and lactate serum levelsJosef Finsterer, Bettina Mittendorfer, Werner Neuhuber, et al.
International Journal of Cardiology|February 8, 2008
Atrial fibrillation in left ventricular noncompaction with and without neuromuscular disorders is associated with a poor prognosisClaudia Stöllberger, Gerhard Blazek, Maria Winkler-Dworak, et al.
International Journal of Cardiology|October 7, 2006
Cardiologic and neurologic findings in left ventricular hypertrabeculation/noncompaction relating to echocardiographic indicationClaudia Stöllberger, Maria Winkler-Dworak, Gerhard Blazek, et al.
International Journal of Cardiology|December 20, 2008
In- and outpatients with noncompaction: differences in cardiac and neuromuscular co-morbidityClaudia Stöllberger, Gerhard Blazek, Maria Winkler-Dworak, et al.
The Journal of Infection|August 6, 2005
Anti-GQ1b-negative Miller-Fisher syndrome with lower cranial nerve involvement from parasinusoidal aspergillomaJosef Finsterer, Anton Niedermayr, Peter G Weigl, et al.
Acta Neurologica Belgica|February 29, 2012
Dopamine-deficiency-enhanced hyperthermia and rhabdomyolysis during a heat wave in a metachromatic leucodystrophy heterozygote with metabolic myopathyJosef Finsterer, Alice Reining-Festa, Claudia Stollbergr, et al.
Folia Neuropathologica|July 29, 2015
Adult, isolated respiratory chain complex IV deficiency with minimal manifestationsJosef Finsterer, Gabor G Kovacs, Helmut Rauschka, et al.
Cardiology|December 16, 2014
Dilated, arrhythmogenic cardiomyopathy in emery-dreifuss muscular dystrophy due to the emerin splice-site mutation c.449 + 1G>AJosef Finsterer, Claudia Stöllberger, Ernst Sehnal, et al.
Pageof 69