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Brain : a Journal of Neurology|October 22, 2025
Antisense oligonucleotides reverse SPTLC1-related hereditary sensory neuropathy in a mouse modelJinhong Meng, Shunyi Ma, Museer A Lone, et al.Pain|July 13, 2010
A-995662 [(R)-8-(4-methyl-5-(4-(trifluoromethyl)phenyl)oxazol-2-ylamino)-1,2,3,4-tetrahydronaphthalen-2-ol], a novel, selective TRPV1 receptor antagonist, reduces spinal release of glutamate and CGRP in a rat knee joint pain modelPamela S Puttfarcken, Ping Han, Shailen K Joshi, et al.The Journal of Surgical Research|March 21, 2022
Emotional Regulation in Surgery: Fostering Well-Being, Performance, and LeadershipAnya L Greenberg, Veronica F Sullins, Timothy R Donahue, et al.American Journal of Human Genetics|January 4, 2011
Targeted high-throughput sequencing identifies mutations in atlastin-1 as a cause of hereditary sensory neuropathy type IChristian Guelly, Peng-Peng Zhu, Lea Leonardis, et al.Journal of Neurology, Neurosurgery, and Psychiatry|September 14, 2021
Charcot-Marie-Tooth disease type 2CC due to <i>NEFH</i> variants causes a progressive, non-length-dependent, motor-predominant phenotypeMenelaos Pipis, Andrea Cortese, James M Polke, et al.Cell Reports|June 30, 2021
FGF21 promotes thermogenic gene expression as an autocrine factor in adipocytesMohammad Abu-Odeh, Yuan Zhang, Shannon M Reilly, et al.Proceedings of the National Academy of Sciences of the United States of America|October 8, 2008
Temperature increase of 21st century mitigation scenariosD P Van Vuuren, M Meinshausen, G-K Plattner, et al.Medrxiv : the Preprint Server for Health Sciences|July 15, 2024
Biallelic variants in <i>COX18</i> cause a mitochondrial disorder primarily manifesting as peripheral neuropathyCamila Armirola-Ricaurte, Laura Morant, Isabelle Adant, et al.Journal of Neurology, Neurosurgery, and Psychiatry|July 3, 2023
Intronic <i>FGF14</i> GAA repeat expansions are a common cause of ataxia syndromes with neuropathy and bilateral vestibulopathyDavid Pellerin, Carlo Wilke, Andreas Traschütz, et al.Genes, Brain, and Behavior|October 3, 2012
Genetic variation in DNMT3B and increased global DNA methylation is associated with suicide attempts in psychiatric patientsT M Murphy, N Mullins, M Ryan, et al.Pageof 163