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Front Neurosci 516.9763889 2021 PMC8549820 Werth M, Schmidt-Ott KM, Leete T, Qiu A, Hinze C, Viltard M, Paragas N, Shawber CJ, Yu W, Lee P, Chen X, Sarkar A, Mu W, Rittenberg A, Lin CS, Kitajewski J, Al-Awqati Q, Barasch J

reported two cases of new variants of primary creatine deficiency syndrome [37].One of these cases involved CCDS with recurrent seizures and neurological deterioration caused by a genetic variant in the SLC6A8 gene

Furthermore, Rg 1 significantly reduced OS-induced ERS marker levels, suah as CCAAT/enhancer binding protein (C/EBP) homologous protein (CHOP), glucose-regulated protein78 (GRP78) and Caspase-12

242 PKC activation enhances excitatory currents in the dorsal horn and trigeminal neurons, contributing to nociceptive hypersensitivity in DPN