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Werner Stenzel

Showing results (131-140 of 271) with videos related to

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Brain Pathology (Zurich, Switzerland)|June 30, 2007
A 30-year-old patient with tuberous sclerosisWerner Stenzel, Marek Franitza, Albert J Becker, et al.
Journal of Neuropathology and Experimental Neurology|December 2, 2005
Regulation of the inflammatory response to Staphylococcus aureus-induced brain abscess by interleukin-10Werner Stenzel, Julia Dahm, Monica Sanchez-Ruiz, et al.
The Journal of Experimental Medicine|November 10, 2004
T cell-specific inactivation of the interleukin 10 gene in mice results in enhanced T cell responses but normal innate responses to lipopolysaccharide or skin irritationAxel Roers, Lisa Siewe, Elke Strittmatter, et al.
Neuromuscular Disorders : NMD|December 10, 2013
Inflammatory myopathy with abundant macrophages (IMAM): the immunology revisitedJan Leo Rinnenthal, Hans-Hilmar Goebel, Corinna Preuße, et al.
Journal of Medical Genetics|February 22, 2014
POMK mutation in a family with congenital muscular dystrophy with merosin deficiency, hypomyelination, mild hearing deficit and intellectual disabilityAnja von Renesse, Mina V Petkova, Susanne Lützkendorf, et al.
Brain Pathology (Zurich, Switzerland)|January 17, 2014
Enlarging the nosological spectrum of hereditary diffuse leukoencephalopathy with axonal spheroids (HDLS)Sarah Hoffmann, Jill Murrell, Lutz Harms, et al.
Neurology. Genetics|April 12, 2016
Recessive REEP1 mutation is associated with congenital axonal neuropathy and diaphragmatic palsyGudrun Schottmann, Dominik Seelow, Franziska Seifert, et al.
Mitochondrion|July 9, 2017
Recessive mutation in EXOSC3 associates with mitochondrial dysfunction and pontocerebellar hypoplasiaGudrun Schottmann, Sylvie Picker-Minh, Jana Marie Schwarz, et al.
Muscle & Nerve|August 10, 2013
Novel γ-sarcoglycan-mutation affects cardiac function and N-terminal dystrophin expressionNicolas W J Schröder, Ulrike Grieben, Stefan Prokop, et al.
Annals of Clinical and Translational Neurology|November 28, 2018
Autophagic vacuolar myopathy is a common feature of CLN3 diseaseJosefine Radke, Randi Koll, Esther Gill, et al.
Pageof 28

Showing results (131-140 of 271) with videos related to

Sort By:
Pageof 28
Brain Pathology (Zurich, Switzerland)|June 30, 2007
A 30-year-old patient with tuberous sclerosisWerner Stenzel, Marek Franitza, Albert J Becker, et al.
Journal of Neuropathology and Experimental Neurology|December 2, 2005
Regulation of the inflammatory response to Staphylococcus aureus-induced brain abscess by interleukin-10Werner Stenzel, Julia Dahm, Monica Sanchez-Ruiz, et al.
The Journal of Experimental Medicine|November 10, 2004
T cell-specific inactivation of the interleukin 10 gene in mice results in enhanced T cell responses but normal innate responses to lipopolysaccharide or skin irritationAxel Roers, Lisa Siewe, Elke Strittmatter, et al.
Neuromuscular Disorders : NMD|December 10, 2013
Inflammatory myopathy with abundant macrophages (IMAM): the immunology revisitedJan Leo Rinnenthal, Hans-Hilmar Goebel, Corinna Preuße, et al.
Journal of Medical Genetics|February 22, 2014
POMK mutation in a family with congenital muscular dystrophy with merosin deficiency, hypomyelination, mild hearing deficit and intellectual disabilityAnja von Renesse, Mina V Petkova, Susanne Lützkendorf, et al.
Brain Pathology (Zurich, Switzerland)|January 17, 2014
Enlarging the nosological spectrum of hereditary diffuse leukoencephalopathy with axonal spheroids (HDLS)Sarah Hoffmann, Jill Murrell, Lutz Harms, et al.
Neurology. Genetics|April 12, 2016
Recessive REEP1 mutation is associated with congenital axonal neuropathy and diaphragmatic palsyGudrun Schottmann, Dominik Seelow, Franziska Seifert, et al.
Mitochondrion|July 9, 2017
Recessive mutation in EXOSC3 associates with mitochondrial dysfunction and pontocerebellar hypoplasiaGudrun Schottmann, Sylvie Picker-Minh, Jana Marie Schwarz, et al.
Muscle & Nerve|August 10, 2013
Novel γ-sarcoglycan-mutation affects cardiac function and N-terminal dystrophin expressionNicolas W J Schröder, Ulrike Grieben, Stefan Prokop, et al.
Annals of Clinical and Translational Neurology|November 28, 2018
Autophagic vacuolar myopathy is a common feature of CLN3 diseaseJosefine Radke, Randi Koll, Esther Gill, et al.
Pageof 28