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Werner Stenzel

Showing results (141-150 of 271) with videos related to

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Neuromuscular Disorders : NMD|May 19, 2019
1st ENMC European meeting: The EURO-NMD pathology working group Recommended Standards for Muscle Pathology Amsterdam, The Netherlands, 7 December 2018Bjarne Udd, Werner Stenzel, Anders Oldfors, et al.
Skeletal Muscle|July 7, 2016
Characterization of a Dmd (EGFP) reporter mouse as a tool to investigate dystrophin expressionMina V Petkova, Susanne Morales-Gonzales, Karima Relizani, et al.
Neuromuscular Disorders : NMD|August 29, 2018
New variant of necklace fibres display peculiar lysosomal structures and mitophagyJan Leo Rinnenthal, Carsten Dittmayer, Kerstin Irlbacher, et al.
Neurology(R) Neuroimmunology & Neuroinflammation|October 24, 2014
The lymphoid follicle variant of dermatomyositisJosefine Radke, Debora Pehl, Eleonora Aronica, et al.
Journal of Medical Genetics|November 30, 2018
De novo mutation in <i>ELOVL1</i> causes ichthyosis, <i>acanthosis nigricans</i>, hypomyelination, spastic paraplegia, high frequency deafness and optic atrophyNoomi Mueller, Takayuki Sassa, Susanne Morales-Gonzalez, et al.
Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism|December 20, 2012
Early loss of pericytes and perivascular stromal cell-induced scar formation after strokeFrancisco Fernández-Klett, Jason R Potas, Diana Hilpert, et al.
Journal of Neurosurgery. Spine|July 21, 2006
The effect of mitomycin C in reducing epidural fibrosis after lumbar laminectomy in ratsJin-Yul Lee, Werner Stenzel, Peter Impekoven, et al.
Rheumatology (Oxford, England)|October 15, 2024
Inflammation of the temporalis muscle and adjacent nerve tissue in giant cell arteritis: expanding the spectrum of inflammatory lesionsNikolas Ruffer, Marie-Therese Holzer, Leona Kawelke, et al.
Genes|May 28, 2022
New Insights into the Neuromyogenic Spectrum of a Gain of Function Mutation in SPTLC1Heike Kölbel, Florian Kraft, Andreas Hentschel, et al.
Neurology|October 4, 2022
Morphologic and Molecular Patterns of Polymyositis With Mitochondrial Pathology and Inclusion Body MyositisFelix Kleefeld, Akinori Uruha, Anne Schänzer, et al.
Pageof 28

Showing results (141-150 of 271) with videos related to

Sort By:
Pageof 28
Neuromuscular Disorders : NMD|May 19, 2019
1st ENMC European meeting: The EURO-NMD pathology working group Recommended Standards for Muscle Pathology Amsterdam, The Netherlands, 7 December 2018Bjarne Udd, Werner Stenzel, Anders Oldfors, et al.
Skeletal Muscle|July 7, 2016
Characterization of a Dmd (EGFP) reporter mouse as a tool to investigate dystrophin expressionMina V Petkova, Susanne Morales-Gonzales, Karima Relizani, et al.
Neuromuscular Disorders : NMD|August 29, 2018
New variant of necklace fibres display peculiar lysosomal structures and mitophagyJan Leo Rinnenthal, Carsten Dittmayer, Kerstin Irlbacher, et al.
Neurology(R) Neuroimmunology & Neuroinflammation|October 24, 2014
The lymphoid follicle variant of dermatomyositisJosefine Radke, Debora Pehl, Eleonora Aronica, et al.
Journal of Medical Genetics|November 30, 2018
De novo mutation in <i>ELOVL1</i> causes ichthyosis, <i>acanthosis nigricans</i>, hypomyelination, spastic paraplegia, high frequency deafness and optic atrophyNoomi Mueller, Takayuki Sassa, Susanne Morales-Gonzalez, et al.
Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism|December 20, 2012
Early loss of pericytes and perivascular stromal cell-induced scar formation after strokeFrancisco Fernández-Klett, Jason R Potas, Diana Hilpert, et al.
Journal of Neurosurgery. Spine|July 21, 2006
The effect of mitomycin C in reducing epidural fibrosis after lumbar laminectomy in ratsJin-Yul Lee, Werner Stenzel, Peter Impekoven, et al.
Rheumatology (Oxford, England)|October 15, 2024
Inflammation of the temporalis muscle and adjacent nerve tissue in giant cell arteritis: expanding the spectrum of inflammatory lesionsNikolas Ruffer, Marie-Therese Holzer, Leona Kawelke, et al.
Genes|May 28, 2022
New Insights into the Neuromyogenic Spectrum of a Gain of Function Mutation in SPTLC1Heike Kölbel, Florian Kraft, Andreas Hentschel, et al.
Neurology|October 4, 2022
Morphologic and Molecular Patterns of Polymyositis With Mitochondrial Pathology and Inclusion Body MyositisFelix Kleefeld, Akinori Uruha, Anne Schänzer, et al.
Pageof 28