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Karin Jurkat-Rott

Showing results (71-80 of 82) with videos related to

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Neuroscience Letters|August 7, 2003
Quantification of brain atrophy in patients with myotonic dystrophy and proximal myotonic myopathy: a controlled 3-dimensional magnetic resonance imaging studyJan Kassubek, Freimut D Juengling, Stefanie Hoffmann, et al.
Radiology|April 16, 2016
7-T (35)Cl and (23)Na MR Imaging for Detection of Mutation-dependent Alterations in Muscular Edema and Fat Fraction with Sodium and Chloride Concentrations in Muscular Periodic ParalysesMarc-André Weber, Armin M Nagel, Anja M Marschar, et al.
Radiology|June 16, 2006
Evaluation of patients with paramyotonia at 23Na MR imaging during cold-induced weaknessMarc-André Weber, Sonia Nielles-Vallespin, Hagen B Huttner, et al.
Radiology|September 20, 2016
7-T (35)Cl and (23)Na MR Imaging for Detection of Mutation-dependent Alterations in Muscular Edema and Fat Fraction with Sodium and Chloride Concentrations in Muscular Periodic ParalysesMarc-André Weber, Armin M Nagel, Anja M Marschar, et al.
Orphanet Journal of Rare Diseases|January 18, 2014
Functional and genetic characterization of clinical malignant hyperthermia crises: a multi-centre studyWerner Klingler, Sebastian Heiderich, Thierry Girard, et al.
Human Molecular Genetics|October 3, 2015
SCN4A pore mutation pathogenetically contributes to autosomal dominant essential tremor and may increase susceptibility to epilepsyAlberto Bergareche, Marcin Bednarz, Elena Sánchez, et al.
British Journal of Sports Medicine|August 4, 2018
Fascial tissue research in sports medicine: from molecules to tissue adaptation, injury and diagnostics: consensus statementMartina Zügel, Constantinos N Maganaris, Jan Wilke, et al.
Epilepsia|May 18, 2004
Benign familial infantile convulsions: linkage to chromosome 16p12-q12 in 14 familiesYvonne G Weber, Andrea Berger, Nerses Bebek, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|October 18, 2011
Altered stress stimulation of inward rectifier potassium channels in Andersen-Tawil syndromeGuiscard Seebohm, Nathalie Strutz-Seebohm, Oana N Ursu, et al.
American Journal of Human Genetics|September 13, 2003
Confirmation of the type 2 myotonic dystrophy (CCTG)n expansion mutation in patients with proximal myotonic myopathy/proximal myotonic dystrophy of different European origins: a single shared haplotype indicates an ancestral founder effectLinda L Bachinski, Bjarne Udd, Giovanni Meola, et al.
Pageof 9

Showing results (71-80 of 82) with videos related to

Sort By:
Pageof 9
Neuroscience Letters|August 7, 2003
Quantification of brain atrophy in patients with myotonic dystrophy and proximal myotonic myopathy: a controlled 3-dimensional magnetic resonance imaging studyJan Kassubek, Freimut D Juengling, Stefanie Hoffmann, et al.
Radiology|April 16, 2016
7-T (35)Cl and (23)Na MR Imaging for Detection of Mutation-dependent Alterations in Muscular Edema and Fat Fraction with Sodium and Chloride Concentrations in Muscular Periodic ParalysesMarc-André Weber, Armin M Nagel, Anja M Marschar, et al.
Radiology|June 16, 2006
Evaluation of patients with paramyotonia at 23Na MR imaging during cold-induced weaknessMarc-André Weber, Sonia Nielles-Vallespin, Hagen B Huttner, et al.
Radiology|September 20, 2016
7-T (35)Cl and (23)Na MR Imaging for Detection of Mutation-dependent Alterations in Muscular Edema and Fat Fraction with Sodium and Chloride Concentrations in Muscular Periodic ParalysesMarc-André Weber, Armin M Nagel, Anja M Marschar, et al.
Orphanet Journal of Rare Diseases|January 18, 2014
Functional and genetic characterization of clinical malignant hyperthermia crises: a multi-centre studyWerner Klingler, Sebastian Heiderich, Thierry Girard, et al.
Human Molecular Genetics|October 3, 2015
SCN4A pore mutation pathogenetically contributes to autosomal dominant essential tremor and may increase susceptibility to epilepsyAlberto Bergareche, Marcin Bednarz, Elena Sánchez, et al.
British Journal of Sports Medicine|August 4, 2018
Fascial tissue research in sports medicine: from molecules to tissue adaptation, injury and diagnostics: consensus statementMartina Zügel, Constantinos N Maganaris, Jan Wilke, et al.
Epilepsia|May 18, 2004
Benign familial infantile convulsions: linkage to chromosome 16p12-q12 in 14 familiesYvonne G Weber, Andrea Berger, Nerses Bebek, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|October 18, 2011
Altered stress stimulation of inward rectifier potassium channels in Andersen-Tawil syndromeGuiscard Seebohm, Nathalie Strutz-Seebohm, Oana N Ursu, et al.
American Journal of Human Genetics|September 13, 2003
Confirmation of the type 2 myotonic dystrophy (CCTG)n expansion mutation in patients with proximal myotonic myopathy/proximal myotonic dystrophy of different European origins: a single shared haplotype indicates an ancestral founder effectLinda L Bachinski, Bjarne Udd, Giovanni Meola, et al.
Pageof 9