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Neurocase|July 17, 2020
Selective impairment of On-reading (Chinese-style pronunciation) in alexia with agraphia for kanji due to subcortical hemorrhage in the left posterior middle temporal gyrusMizuho Yoshida, Toshihiro Hayashi, Kurumi Fujii, et al.Arquivos De Neuro-Psiquiatria|January 15, 2025
Neurology pioneers in JapanHélio A Ghizoni Teive, Léo Coutinho, Francisco E C Cardoso, et al.Internal Medicine (Tokyo, Japan)|March 3, 2024
Paraneoplastic Cerebellar Degeneration Leading to an Early Diagnosis of Peritoneal Serous Papillary CarcinomaTsutomu Yasuda, Jun Shimizu, Toji Miyagawa, et al.European Journal of Human Genetics : EJHG|February 12, 2026
Delineating the Genetic Basis of RNF213-related vasculopathies: The association of PKHD1 variants with bilateral cerebral vasculopathyDaiichiro Ishigami, Shinichi Namba, Satoru Miyawaki, et al.Acta Paediatrica (Oslo, Norway : 1992)|April 25, 2013
B-type natriuretic peptide for assessment of haemodynamically significant patent ductus arteriosus in premature infantsKenji Mine, Atsushi Ohashi, Shoji Tsuji, et al.Frontiers in Immunology|November 29, 2023
Dysbiosis of the gut microbiota as a susceptibility factor for Kawasaki diseaseYoshiki Teramoto, Shohei Akagawa, Shin-Ichiro Hori, et al.RNA Biology|December 9, 2014
Comprehensive silencing of target-sharing microRNAs is a mechanism for SIRT1 overexpression in cancerKotaro Kiga, Yoko Fukuda-Yuzawa, Masanobu Tanabe, et al.Journal of Human Genetics|January 14, 2022
Elderly patients with suspected Charcot-Marie-Tooth disease should be tested for the TTR gene for effective treatmentsTakaki Taniguchi, Masahiro Ando, Yuji Okamoto, et al.Neurology|January 28, 2014
Evaluation of SLC20A2 mutations that cause idiopathic basal ganglia calcification in JapanMegumi Yamada, Masaki Tanaka, Mari Takagi, et al.Journal of Human Genetics|January 29, 2022
An NEFH founder mutation causes broad phenotypic spectrum in multiple Japanese familiesMasahiro Ando, Yujiro Higuchi, Yuji Okamoto, et al.Pageof 53