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Stephan Zierz

Showing results (21-30 of 123) with videos related to

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Biochimica Et Biophysica Acta|February 12, 2004
Different sensitivities of CPT I and CPT II for inhibition by l-aminocarnitine in human skeletal muscleKathrin Traufeller, Frank Norbert Gellerich, Stephan Zierz
Journal of the Neurological Sciences|January 9, 2014
Carnitine palmitoyltransferase II (CPT II) deficiency: genotype-phenotype analysis of 50 patientsPushpa Raj Joshi, Marcus Deschauer, Stephan Zierz
Journal of Neurology|August 21, 2003
Babinski-Nageotte's syndrome and Hemimedullary (Reinhold's) syndrome are clinically and morphologically distinct conditionsMichael Krasnianski, Stephan Neudecker, Andreas Schluter, et al.
Acta Neuropathologica|June 29, 2004
Rimmed vacuoles in facioscapulohumeral muscular dystrophy: a unique ultrastructural featureStephan Neudecker, Michael Krasnianski, Erik Bahn, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|May 21, 2005
Cyclic vertical deviation after ocular myositis and treatment by recession of the inferior rectus muscleViktoria Bau, Maike Sievert, Peter Roggenkämper, et al.
Muscle & Nerve|April 23, 2013
Diagnostic impact of myotonic discharges in myofibrillar myopathiesFrank Hanisch, Torsten Kraya, Malte Kornhuber, et al.
Journal of Neurology|June 16, 2006
Between Wallenberg syndrome and hemimedullary lesion: Cestan-Chenais and Babinski-Nageotte syndromes in medullary infarctionsMichael Krasnianski, Tobias Müller, Karsten Stock, et al.
Biochimica Et Biophysica Acta|October 20, 2015
Malony-CoA inhibits the S113L variant of carnitine-palmitoyltransferase IILeila Motlagh, Ralph Golbik, Wolfgang Sippl, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|November 8, 2014
Frequencies of myohistological mitochondrial changes in patients with mitochondrial DNA deletions and the common m.3243A>G point mutationCharlotte Maria Zierz, Pushpa Raj Joshi, Stephan Zierz
International Journal of Molecular Sciences|January 6, 2017
Muscle Carnitine Palmitoyltransferase II Deficiency: A Review of Enzymatic Controversy and Clinical FeaturesDiana Lehmann, Leila Motlagh, Dina Robaa, et al.
Pageof 13

Showing results (21-30 of 123) with videos related to

Sort By:
Pageof 13
Biochimica Et Biophysica Acta|February 12, 2004
Different sensitivities of CPT I and CPT II for inhibition by l-aminocarnitine in human skeletal muscleKathrin Traufeller, Frank Norbert Gellerich, Stephan Zierz
Journal of the Neurological Sciences|January 9, 2014
Carnitine palmitoyltransferase II (CPT II) deficiency: genotype-phenotype analysis of 50 patientsPushpa Raj Joshi, Marcus Deschauer, Stephan Zierz
Journal of Neurology|August 21, 2003
Babinski-Nageotte's syndrome and Hemimedullary (Reinhold's) syndrome are clinically and morphologically distinct conditionsMichael Krasnianski, Stephan Neudecker, Andreas Schluter, et al.
Acta Neuropathologica|June 29, 2004
Rimmed vacuoles in facioscapulohumeral muscular dystrophy: a unique ultrastructural featureStephan Neudecker, Michael Krasnianski, Erik Bahn, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|May 21, 2005
Cyclic vertical deviation after ocular myositis and treatment by recession of the inferior rectus muscleViktoria Bau, Maike Sievert, Peter Roggenkämper, et al.
Muscle & Nerve|April 23, 2013
Diagnostic impact of myotonic discharges in myofibrillar myopathiesFrank Hanisch, Torsten Kraya, Malte Kornhuber, et al.
Journal of Neurology|June 16, 2006
Between Wallenberg syndrome and hemimedullary lesion: Cestan-Chenais and Babinski-Nageotte syndromes in medullary infarctionsMichael Krasnianski, Tobias Müller, Karsten Stock, et al.
Biochimica Et Biophysica Acta|October 20, 2015
Malony-CoA inhibits the S113L variant of carnitine-palmitoyltransferase IILeila Motlagh, Ralph Golbik, Wolfgang Sippl, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|November 8, 2014
Frequencies of myohistological mitochondrial changes in patients with mitochondrial DNA deletions and the common m.3243A>G point mutationCharlotte Maria Zierz, Pushpa Raj Joshi, Stephan Zierz
International Journal of Molecular Sciences|January 6, 2017
Muscle Carnitine Palmitoyltransferase II Deficiency: A Review of Enzymatic Controversy and Clinical FeaturesDiana Lehmann, Leila Motlagh, Dina Robaa, et al.
Pageof 13