Showing results (141-150 of 185) with videos related to
Sort By:
Pageof 19
Radiology|July 1, 1994
Mitochondrial encephalomyopathy: correlation of P-31 exercise MR spectroscopy with clinical findingsC K Kuhl, G Layer, F Träber, et al.Archives of Neurology|November 16, 2001
Hearing impairment is common in various phenotypes of the mitochondrial DNA A3243G mutationM Deschauer, T Müller, T Wieser, et al.Der Nervenarzt|July 9, 2011
[Muscular dystrophy due to mutations in anoctamin 5: clinical and molecular genetic findings]M Deschauer, P R Joshi, D Gläser, et al.Journal of Neurology|May 16, 2012
C19orf12 mutations in neurodegeneration with brain iron accumulation mimicking juvenile amyotrophic lateral sclerosisM Deschauer, C Gaul, C Behrmann, et al.Neurology|April 23, 2003
Late-onset encephalopathy associated with a C11777A mutation of mitochondrial DNAM Deschauer, C Bamberg, D Claus, et al.Journal of the Neurological Sciences|February 27, 1997
Sporadic adult-onset distal myopathy with rimmed vacuoles, 15-18 nm tubulofilaments and extensive rod formationJ P Sieb, J VonOertzen, K Tolksdorf, et al.European Heart Journal|February 10, 2000
Cerebrovascular reactivity is impaired in patients with cardiac failureD Georgiadis, M Sievert, S Cencetti, et al.Cerebrovascular Diseases (Basel, Switzerland)|July 7, 1999
Venous microemboli in patients with artificial heart valvesD Georgiadis, R W Baumgartner, F Uhlmann, et al.The Journal of Heart Valve Disease|October 23, 1997
Time course of high-intensity transient signals in patients undergoing elective heart valve replacement: a prospective studyA Lindner, D Georgiadis, A Lühmann, et al.Journal of Neurology|February 1, 1990
Mitochondrial myopathies: divergences of genetic deletions, biochemical defects and the clinical syndromesK D Gerbitz, B Obermaier-Kusser, S Zierz, et al.Pageof 19