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L H Bennett

Showing results (111-120 of 121) with videos related to

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Journal of Neurology, Neurosurgery, and Psychiatry|April 19, 2019
Development of MRC Centre MRI calf muscle fat fraction protocol as a sensitive outcome measure in Hereditary Sensory Neuropathy Type 1Umaiyal Kugathasan, Matthew R B Evans, Jasper M Morrow, et al.
Pain|June 27, 2023
Long-term tactile hypersensitivity after nerve crush injury in mice is characterized by the persistence of intact sensory axonsHyoung Woo Kim, Sang Wook Shim, Anna Mae Zhao, et al.
Wellcome Open Research|February 16, 2019
DOLORisk: study protocol for a multi-centre observational study to understand the risk factors and determinants of neuropathic painMathilde M V Pascal, Andreas C Themistocleous, Ralf Baron, et al.
Brain Communications|March 10, 2023
Investigating genotype-phenotype relationship of extreme neuropathic pain disorders in a UK national cohortAndreas C Themistocleous, Georgios Baskozos, Iulia Blesneac, et al.
Human Molecular Genetics|December 4, 2014
A novel SOD1-ALS mutation separates central and peripheral effects of mutant SOD1 toxicityPeter I Joyce, Philip Mcgoldrick, Rachele A Saccon, et al.
The Lancet. Neurology|April 19, 2025
Pharmacotherapy and non-invasive neuromodulation for neuropathic pain: a systematic review and meta-analysisNadia Soliman, Xavier Moisset, Michael C Ferraro, et al.
Pain|June 9, 2017
Stratifying patients with peripheral neuropathic pain based on sensory profiles: algorithm and sample size recommendationsJan Vollert, Christoph Maier, Nadine Attal, et al.
American Journal of Human Genetics|September 3, 2016
Rare Variants in MME, Encoding Metalloprotease Neprilysin, Are Linked to Late-Onset Autosomal-Dominant Axonal PolyneuropathiesMichaela Auer-Grumbach, Stefan Toegel, Maria Schabhüttl, et al.
Brain : a Journal of Neurology|December 19, 2017
A novel human pain insensitivity disorder caused by a point mutation in ZFHX2Abdella M Habib, Ayako Matsuyama, Andrei L Okorokov, et al.
Nature Genetics|May 26, 2015
Transcriptional regulator PRDM12 is essential for human pain perceptionYa-Chun Chen, Michaela Auer-Grumbach, Shinya Matsukawa, et al.
Pageof 13

Showing results (111-120 of 121) with videos related to

Sort By:
Pageof 13
Journal of Neurology, Neurosurgery, and Psychiatry|April 19, 2019
Development of MRC Centre MRI calf muscle fat fraction protocol as a sensitive outcome measure in Hereditary Sensory Neuropathy Type 1Umaiyal Kugathasan, Matthew R B Evans, Jasper M Morrow, et al.
Pain|June 27, 2023
Long-term tactile hypersensitivity after nerve crush injury in mice is characterized by the persistence of intact sensory axonsHyoung Woo Kim, Sang Wook Shim, Anna Mae Zhao, et al.
Wellcome Open Research|February 16, 2019
DOLORisk: study protocol for a multi-centre observational study to understand the risk factors and determinants of neuropathic painMathilde M V Pascal, Andreas C Themistocleous, Ralf Baron, et al.
Brain Communications|March 10, 2023
Investigating genotype-phenotype relationship of extreme neuropathic pain disorders in a UK national cohortAndreas C Themistocleous, Georgios Baskozos, Iulia Blesneac, et al.
Human Molecular Genetics|December 4, 2014
A novel SOD1-ALS mutation separates central and peripheral effects of mutant SOD1 toxicityPeter I Joyce, Philip Mcgoldrick, Rachele A Saccon, et al.
The Lancet. Neurology|April 19, 2025
Pharmacotherapy and non-invasive neuromodulation for neuropathic pain: a systematic review and meta-analysisNadia Soliman, Xavier Moisset, Michael C Ferraro, et al.
Pain|June 9, 2017
Stratifying patients with peripheral neuropathic pain based on sensory profiles: algorithm and sample size recommendationsJan Vollert, Christoph Maier, Nadine Attal, et al.
American Journal of Human Genetics|September 3, 2016
Rare Variants in MME, Encoding Metalloprotease Neprilysin, Are Linked to Late-Onset Autosomal-Dominant Axonal PolyneuropathiesMichaela Auer-Grumbach, Stefan Toegel, Maria Schabhüttl, et al.
Brain : a Journal of Neurology|December 19, 2017
A novel human pain insensitivity disorder caused by a point mutation in ZFHX2Abdella M Habib, Ayako Matsuyama, Andrei L Okorokov, et al.
Nature Genetics|May 26, 2015
Transcriptional regulator PRDM12 is essential for human pain perceptionYa-Chun Chen, Michaela Auer-Grumbach, Shinya Matsukawa, et al.
Pageof 13