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Journal of the Peripheral Nervous System : JPNS|June 30, 2021
Charcot-Marie-Tooth disease: Genetic profile of patients from a large Brazilian neuromuscular reference centerEduardo Boiteux Uchôa Cavalcanti, Savana Camilla de Lima Santos, Carlos Eduardo Speck Martins, et al.Journal of the Peripheral Nervous System : JPNS|January 11, 2021
Cutaneous and muscular afferents from the foot and sensory fusion processing: Physiology and pathology in neuropathiesGuido Felicetti, Philippe Thoumie, Manh-Cuong Do, et al.Journal of the Peripheral Nervous System : JPNS|January 12, 2021
Electrophysiological investigation of motor axonal excitability in a mouse model of nerve constriction injuryPreet G S Makker, Brooke A Keating, Justin G Lees, et al.Journal of the Peripheral Nervous System : JPNS|June 25, 2022
Associations of Guillain-Barré syndrome with coronavirus disease 2019 vaccination: Disproportionality analysis using the World Health Organization pharmacovigilance databaseJee-Eun Kim, Jin Park, Young Gi Min, et al.Journal of the Peripheral Nervous System : JPNS|July 13, 2021
Antecedent infections in Guillain-Barré syndrome patients from south IndiaDebprasad Dutta, Monojit Debnath, Madhu Nagappa, et al.Journal of the Peripheral Nervous System : JPNS|January 19, 2021
Platinum accumulation in oxaliplatin-induced peripheral neuropathyGuoli Wei, Zhancheng Gu, Jialin Gu, et al.Journal of the Peripheral Nervous System : JPNS|February 8, 2021
Clinical and serological prognostic factors in childhood Guillain-Barré syndrome: A prospective cohort study in BangladeshImran Hasan, Nowshin Papri, Shoma Hayat, et al.Journal of the Peripheral Nervous System : JPNS|December 6, 2016
Handwriting difficulties of children with Charcot-Marie-Tooth disease type 1ADaniel Kunovsky, Reinie Cordier, Paula Bray, et al.Journal of the Peripheral Nervous System : JPNS|December 17, 2016
A novel NDRG1 mutation in a non-Romani patient with CMT4D/HMSN-LomGiuseppe Piscosquito, Stefania Magri, Paola Saveri, et al.Journal of the Peripheral Nervous System : JPNS|April 23, 2014
A novel INF2 mutation in a Korean family with autosomal dominant intermediate Charcot-Marie-Tooth disease and focal segmental glomerulosclerosisHyung J Park, Hye J Kim, Young B Hong, et al.Pageof 115