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Journal of the Neurological Sciences|September 15, 1996
Muscle phosphofructokinase deficiency in two generationsM Vorgerd, J Karitzky, M Ristow, et al.Journal of Neurology|January 12, 2011
Phenotype variability and histopathological findings in centronuclear myopathy due to DNM2 mutationsF Hanisch, T Müller, A Dietz, et al.Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|October 1, 1988
[Concordance of Kearns-Sayre syndrome and Klinefelter syndrome]A S Everding, G Kurlemann, H Gerding, et al.Neurology|February 16, 2006
Pure myopathy associated with a novel mitochondrial tRNA gene mutationH Swalwell, M Deschauer, H Hartl, et al.Neurology|July 26, 2006
Subtle cognitive dysfunction in adult onset myotonic dystrophy type 1 (DM1) and type 2 (DM2)C Gaul, T Schmidt, G Windisch, et al.Virchows Archiv. A, Pathological Anatomy and Histopathology|January 1, 1991
Ultrastructural abnormalities of mitochondria and deficiency of myocardial cytochrome c oxidase in a patient with ventricular tachycardiaB Schwartzkopff, S Zierz, H Frenzel, et al.Der Nervenarzt|July 10, 2013
[Treatability of sporadic late onset nemaline myopathy]F Hanisch, I Schneider, T Müller, et al.Stroke|November 22, 1997
Influence of oxygen ventilation on Doppler microemboli signals in patients with artificial heart valvesD Georgiadis, A Wenzel, D Lehmann, et al.Biochemical Society Transactions|May 18, 2000
Function of the mitochondrial outer membrane as a diffusion barrier in health and diseasesF N Gellerich, S Trumbeckaite, J R Opalka, et al.Clinical Neuropathology|August 19, 2007
Frequency of calpain-3 c.550delA mutation in limb girdle muscular dystrophy type 2 and isolated hyperCKemia in German patientsF Hanisch, C R Müller, D Grimm, et al.Pageof 19