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Fortschritte Der Neurologie-Psychiatrie|August 30, 2013
[Impulsive-compulsive behaviours in a German Parkinson's disease outpatient sample]K Rohde, O Riedel, U Lueken, et al.AJNR. American Journal of Neuroradiology|March 24, 2000
Contrast-enhanced transcranial color-coded duplexsonography in stroke patients with limited bone windowsG Gahn, J Gerber, S Hallmeyer, et al.Bone Marrow Transplantation|January 26, 2010
CD49d blockade by natalizumab in patients with multiple sclerosis affects steady-state hematopoiesis and mobilizes progenitors with a distinct phenotype and functionD Jing, U Oelschlaegel, R Ordemann, et al.Biofactors (Oxford, England)|December 30, 2003
Coenzyme Q10 reduces the toxicity of rotenone in neuronal cultures by preserving the mitochondrial membrane potentialT Menke, G Gille, F Reber, et al.Journal of Medical Genetics|May 4, 2004
Variable penetrance of a familial progressive necrotising encephalopathy due to a novel tRNA(Ile) homoplasmic mutation in the mitochondrial genomeA Limongelli, J Schaefer, S Jackson, et al.Journal of Neural Transmission (Vienna, Austria : 1996)|February 16, 2005
Olfactory bulb volumes in patients with idiopathic Parkinson's disease a pilot studyA Mueller, N D Abolmaali, A R Hakimi, et al.Neurology|May 29, 2001
Cricopharyngeal achalasia is a common cause of dysphagia in patients with mtDNA deletionsC Kornblum, R Broicher, E Walther, et al.American Journal of Medical Genetics|February 11, 1997
Autosomal recessive lateralization and midline defects: blastogenesis recessive 1S Debrus, U Sauer, S Gilgenkrantz, et al.Dementia and Geriatric Cognitive Disorders Extra|January 2, 2013
Alzheimer's Disease: Differences of Transdermal versus Oral Treatment on Caregiving TimeO Riedel, A Emmrich, J Klotsche, et al.European Neurology|February 26, 1998
Follow-up in carriers of the 'MELAS' mutation without strokesM S Damian, A Hertel, P Seibel, et al.Pageof 26