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Biallelic COX10 Mutations and PMP22 Deletion in a Family With Leigh Syndrome and Hereditary Neuropathy With Liability to Pressure Palsy.
Kuroha Y, Ishiguro T, Tada M, Hara N, Murayama K, Kawachi I, Kasuga K, Miyashita A, Hasegawa A, Takahashi T, Matsubara N, Onodera O, Kakita A, Koike R, Ikeuchi T. Kuroha Y, et al. Among authors: matsubara n. Neurol Genet. 2022 Sep 27;8(5):e200030. doi: 10.1212/NXG.0000000000200030. eCollection 2022 Oct. Neurol Genet. 2022. PMID: 36176336 Free PMC article.
Multifocal hits for propagation of prion protein in sporadic Creutzfeldt-Jakob disease.
Kasuga K, Takeuchi R, Takahashi T, Matsubara N, Koike R, Yokoseki A, Nishizawa M. Kasuga K, et al. Among authors: matsubara n. Neurol Neuroimmunol Neuroinflamm. 2014 Dec 23;2(1):e53. doi: 10.1212/NXI.0000000000000053. eCollection 2015 Feb. Neurol Neuroimmunol Neuroinflamm. 2014. PMID: 25566543 Free PMC article. No abstract available.
509 results