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Molecular and Cellular Biochemistry|October 6, 1997
Mitochondrial DNA mutations in multiple symmetric lipomatosisT Klopstock, M Naumann, P Seibel, et al.Acta Neurologica Scandinavica|December 15, 2004
Efficacy of combining levodopa with entacapone on quality of life and activities of daily living in patients experiencing wearing-off type fluctuationsH Reichmann, J Boas, D Macmahon, et al.Journal of Neurology|March 1, 1992
Neurological long-term follow-up in left atrial myxoma: are late complications frequent or rare?H Reichmann, R Romberg-Hahnloser, E Hofmann, et al.Muscle & Nerve|February 1, 1992
Becker muscular dystrophy: detection of unusual disease courses by combined approach to dystrophin analysisR Gold, W Kress, B Meurers, et al.Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|February 1, 1992
[Neurocysticercosis in an 8-year-old girl]W Jost, N Graf, A Quinten, et al.European Journal of Pediatrics|May 1, 1991
Myopathy in Williams-Beuren syndromeT Voit, H Kramer, C Thomas, et al.Fortschritte Der Neurologie-Psychiatrie|February 16, 2013
[The prevalence of Parkinson's disease, associated dementia, and depression in Dresden]O Riedel, C Schneider, J Klotsche, et al.Der Nervenarzt|April 1, 1994
[MELAS syndrome. Clinical aspects, MRI, biochemistry and molecular genetics]M S Damian, H Reichmann, P Seibel, et al.Muscle & Nerve|July 1, 1997
Mitochondrial dysfunction with myoclonus epilepsy and ragged-red fibers point mutation in nerve, muscle, and adipose tissue of a patient with multiple symmetric lipomatosisM Naumann, R Kiefer, K V Toyka, et al.Pageof 26