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Clinical and Experimental Nephrology|November 13, 2019
Optimal bacterial colony counts for the diagnosis of upper urinary tract infections in infantsYuko Akagawa, Takahisa Kimata, Shohei Akagawa, et al.Archives of Neurology|November 16, 2002
Dementia and delirium in 4 patients with Machado-Joseph diseaseAtsushi Ishikawa, Mitsunori Yamada, Kunihiko Makino, et al.Journal of Human Genetics|November 19, 2002
Epidemiology of X-linked adrenoleukodystrophy in JapanYasuhiko Takemoto, Yasuyuki Suzuki, Akiko Tamakoshi, et al.Annals of Neurology|February 3, 2004
SCA17 homozygote showing Huntington's disease-like phenotypeYasuko Toyoshima, Mitsunori Yamada, Osamu Onodera, et al.Journal of Human Genetics|April 20, 2018
No novel, high penetrant gene might remain to be found in Japanese patients with unknown MODYYukio Horikawa, Kazuyoshi Hosomichi, Mayumi Enya, et al.Plos One|December 30, 2014
Top-down but not bottom-up visual scanning is affected in hereditary pure cerebellar ataxiaShunichi Matsuda, Hideyuki Matsumoto, Toshiaki Furubayashi, et al.Neurology|September 21, 2022
APOE Alleles With Tau and Aβ Pathology in Patients With Amyotrophic Lateral Sclerosis and Parkinsonism-Dementia Complex in the Kii PeninsulaRyogen Sasaki, Satoru Morimoto, Fumiko Ozawa, et al.Bioscience of Microbiota, Food and Health|July 2, 2026
Urinary indoxyl sulfate in children: age-related decline and its association with Bacteroidota in the gut microbiotaYuko Akagawa, Shohei Akagawa, Shoji Tsuji, et al.Human Genome Variation|June 15, 2017
A novel UBE2A mutation causes X-linked intellectual disability type NascimentoYoshinori Tsurusaki, Ikuko Ohashi, Yumi Enomoto, et al.Journal of the Neurological Sciences|January 10, 2025
A subgroup of multiple system atrophy with rapid decline in vital capacitySo Okubo, Kenta Orimo, Takashi Matsukawa, et al.Pageof 53