Showing results (11-20 of 56) with videos related to
Sort By:
Pageof 6
Molecular Genetics and Metabolism Reports|November 30, 2016
Risk factors for osteoporosis, falls and fractures in hereditary myopathies and sporadic inclusion body myositis - A cross sectional surveyF Danckworth, N Karabul, A Posa, et al.Der Nervenarzt|October 12, 2002
[Hauptmann-Thannhauser muscular dystrophy and differential diagnosis of myopathies associated with contractures]F Hanisch, S Neudecker, M Wehnert, et al.Clinical Neurology and Neurosurgery|February 7, 2012
Unusual manifestations in two cases of necrotizing myopathy associated with SRP-antibodiesF Hanisch, T Müller, G Stoltenburg, et al.Neuroreport|June 27, 1994
In vivo phosphorylation in the rat basal nucleus induces PHF-like and APP immunoreactivityT Arendt, F Hanisch, M Holzer, et al.Physical Review Letters|January 22, 2002
Large deuterium isotope effect in the optical nonlinearity of dye-doped liquid crystalsM Kreuzer, F Hanisch, R Eidenschink, et al.Cancer Chemotherapy and Pharmacology|June 15, 1999
Local disposition kinetics of floxuridine after intratumoral and subcutaneous injection as monitored by [19F]-nuclear magnetic resonance spectroscopy in vivoR Port, F Hanisch, M Becker, et al.Acta Neurologica Scandinavica|February 4, 2015
Characterization of monoclonal gammopathy in patients with amyotrophic lateral sclerosisH-H Wolf, A Posa, S Panitz, et al.JIMD Reports|January 24, 2015
Morphology and function of cerebral arteries in adults with pompe diseaseOle Hensel, F Hanisch, K Stock, 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.Der Nervenarzt|July 10, 2013
[Treatability of sporadic late onset nemaline myopathy]F Hanisch, I Schneider, T Müller, et al.Pageof 6