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European Journal of Medical Research|July 28, 1997
Identification of Doppler microembolic signals with a bigate probe in patients with prosthetic heart valvesA Lindner, D Georgiadis, G Fischer, et al.
Stroke|January 28, 1998
Automated intraoperative detection of Doppler microembolic signals using the bigate approachD Georgiadis, A Wenzel, H R Zerkowski, et al.
Neurological Research|May 16, 1998
Influence of transducer frequency on Doppler microemboli signals in an in vivo modelD Georgiadis, A Wenzel, H R Zerkowski, et al.
Der Nervenarzt|February 22, 2003
[Facioscapulohumeral muscular dystrophy. The spectrum of clinical manifestations and molecular genetic changes]M Krasnianski, S Neudecker, K Eger, et al.
Archives of Neurology|April 1, 1978
The syndrome of 'continuous muscle fiber activity.'J Lütschg, F Jerusalem, H P Ludin, et al.
Annals of Neurology|May 1, 1988
Motor neuron syndrome and monoclonal IgM with antibody activity against gangliosides GM1 and GD1bE Nardelli, A J Steck, T Barkas, et al.
Acta Neuropathologica|January 1, 1982
Evidence for a chronic axonal atrophy in oculopharyngeal "muscular dystrophy"A Probst, W Tackmann, H R Stoeckli, et al.
Der Nervenarzt|June 29, 2004
[Attitudes towards patient care at the end of life. A survey of directors of neurological departments]G D Borasio, B Weltermann, R Voltz, et al.
Neuromuscular Disorders : NMD|March 14, 2000
A family with PROMM not linked to the recently mapped PROMM locus DM2T Wieser, D Bönsch, K Eger, et al.
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