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Rinsho Shinkeigaku = Clinical Neurology|May 22, 2004
[Development of therapeutics for spinal and bulbar muscular atrophy (SBMA)]Gen SobueRinsho Shinkeigaku = Clinical Neurology|September 17, 2011
[Molecular-targeted therapy for spinal and bulbar muscular atrophy (SBMA)]Gen SobueRinsho Shinkeigaku = Clinical Neurology|January 27, 2012
[Development of disease-modifying therapy for neurodegenerative diseases]Gen SobueRinsho Shinkeigaku = Clinical Neurology|February 2, 2006
[Pathogenesis and treatment of CIDP]Gen SobueRinsho Shinkeigaku = Clinical Neurology|May 22, 2004
[Clinical phenotype of Charcot-Marie-Tooth disease (CMT) and familial amyloid polyneuropathy (FAP)]Gen SobueJournal of Neurology|September 30, 2008
Electrophysiological features of late-onset transthyretin Met30 familial amyloid polyneuropathy unrelated to endemic fociHaruki Koike, Yuichi Kawagashira, Masahiro Iijima, et al.Neurology|October 30, 2016
Schwann cell and endothelial cell damage in transthyretin familial amyloid polyneuropathyHaruki Koike, Shohei Ikeda, Mie Takahashi, et al.Neurology and Therapy|January 19, 2022
ANCA-Associated Vasculitic Neuropathies: A ReviewHaruki Koike, Ryoji Nishi, Ken Ohyama, et al.Journal of Neuropathology and Experimental Neurology|November 7, 2007
Nonmyelinating Schwann cell involvement with well-preserved unmyelinated axons in Charcot-Marie-Tooth disease type 1AHaruki Koike, Masahiro Iijima, Keiko Mori, et al.Internal Medicine (Tokyo, Japan)|September 16, 2016
Gene Expression Profile of Inflammatory Myopathy with Malignancy is Similar to that of Dermatomyositis rather than PolymyositisTomoko Noda, Masahiro Iijima, Seiya Noda, et al.Pageof 67