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Burkhard Gess

Showing results (31-40 of 45) with videos related to

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Brain Sciences|February 10, 2021
Semi-Automatic MRI Muscle Volumetry to Diagnose and Monitor Hereditary and Acquired PolyneuropathiesFriederike S Bähr, Burkhard Gess, Madlaine Müller, et al.
Therapeutic Advances in Neurological Disorders|August 11, 2021
Progressive multifocal leukoencephalopathy and immune reconstitution inflammatory syndrome in seven patients with sarcoidosis: a critical discussion of treatment and prognosisMaike F Dohrn, Gisa Ellrichmann, Rastislav Pjontek, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|November 25, 2011
Sodium-dependent vitamin C transporter 2 deficiency causes hypomyelination and extracellular matrix defects in the peripheral nervous systemBurkhard Gess, Dominik Röhr, Robert Fledrich, et al.
Neurology|October 3, 2014
HSJ1-related hereditary neuropathies: novel mutations and extended clinical spectrumBurkhard Gess, Michaela Auer-Grumbach, Anja Schirmacher, et al.
Journal of Proteome Research|July 26, 2018
Characterization of Naïve and Vitamin C-Treated Mouse Schwann Cell Line MSC80: Induction of the Antioxidative Thioredoxin Related Transmembrane Protein 1Vietxuan Phan, Jens Schmidt, Vitali Matyash, et al.
Pain|March 3, 2022
Deoxy-sphingolipids, oxidative stress, and vitamin C correlate with qualitative and quantitative patterns of small fiber dysfunction and degenerationMaike F Dohrn, Christina Dumke, Thorsten Hornemann, et al.
The American Journal of Pathology|October 22, 2016
Molecular Analysis of Hybrid Neurofibroma/Schwannoma Identifies Common Monosomy 22 and α-T-Catenin/CTNNA3 as a Novel Candidate Tumor SuppressorVerena Stahn, Inga Nagel, Susan Fischer-Huchzermeyer, et al.
Neurological Research and Practice|February 1, 2022
Heterozygous POLG variant Ser1181Asn co-segregating in a family with autosomal dominant axonal neuropathy, proximal muscle fatigability, ptosis, and ragged red fibersMaike F Dohrn, Corina Heller, Diana Zengeler, et al.
Science Signaling|March 30, 2017
Caveolin-1-mediated internalization of the vitamin C transporter SVCT2 in microglia triggers an inflammatory phenotypeCamila C Portugal, Renato Socodato, Teresa Canedo, et al.
Brain : a Journal of Neurology|February 11, 2022
NCAM1 and GDF15 are biomarkers of Charcot-Marie-Tooth disease in patients and miceMatthew J Jennings, Alexia Kagiava, Leen Vendredy, et al.
Pageof 5

Showing results (31-40 of 45) with videos related to

Sort By:
Pageof 5
Brain Sciences|February 10, 2021
Semi-Automatic MRI Muscle Volumetry to Diagnose and Monitor Hereditary and Acquired PolyneuropathiesFriederike S Bähr, Burkhard Gess, Madlaine Müller, et al.
Therapeutic Advances in Neurological Disorders|August 11, 2021
Progressive multifocal leukoencephalopathy and immune reconstitution inflammatory syndrome in seven patients with sarcoidosis: a critical discussion of treatment and prognosisMaike F Dohrn, Gisa Ellrichmann, Rastislav Pjontek, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|November 25, 2011
Sodium-dependent vitamin C transporter 2 deficiency causes hypomyelination and extracellular matrix defects in the peripheral nervous systemBurkhard Gess, Dominik Röhr, Robert Fledrich, et al.
Neurology|October 3, 2014
HSJ1-related hereditary neuropathies: novel mutations and extended clinical spectrumBurkhard Gess, Michaela Auer-Grumbach, Anja Schirmacher, et al.
Journal of Proteome Research|July 26, 2018
Characterization of Naïve and Vitamin C-Treated Mouse Schwann Cell Line MSC80: Induction of the Antioxidative Thioredoxin Related Transmembrane Protein 1Vietxuan Phan, Jens Schmidt, Vitali Matyash, et al.
Pain|March 3, 2022
Deoxy-sphingolipids, oxidative stress, and vitamin C correlate with qualitative and quantitative patterns of small fiber dysfunction and degenerationMaike F Dohrn, Christina Dumke, Thorsten Hornemann, et al.
The American Journal of Pathology|October 22, 2016
Molecular Analysis of Hybrid Neurofibroma/Schwannoma Identifies Common Monosomy 22 and α-T-Catenin/CTNNA3 as a Novel Candidate Tumor SuppressorVerena Stahn, Inga Nagel, Susan Fischer-Huchzermeyer, et al.
Neurological Research and Practice|February 1, 2022
Heterozygous POLG variant Ser1181Asn co-segregating in a family with autosomal dominant axonal neuropathy, proximal muscle fatigability, ptosis, and ragged red fibersMaike F Dohrn, Corina Heller, Diana Zengeler, et al.
Science Signaling|March 30, 2017
Caveolin-1-mediated internalization of the vitamin C transporter SVCT2 in microglia triggers an inflammatory phenotypeCamila C Portugal, Renato Socodato, Teresa Canedo, et al.
Brain : a Journal of Neurology|February 11, 2022
NCAM1 and GDF15 are biomarkers of Charcot-Marie-Tooth disease in patients and miceMatthew J Jennings, Alexia Kagiava, Leen Vendredy, et al.
Pageof 5