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BMC Neurology|August 19, 2018
Phenotypic variability of Niemann-Pick disease type C including a case with clinically pure schizophrenia: a case reportTomoya Kawazoe, Toshiyuki Yamamoto, Aya Narita, et al.Journal of the Neurological Sciences|October 3, 2012
Progressive supranuclear palsy presenting as primary lateral sclerosis but lacking parkinsonism, gaze palsy, aphasia, or dementiaShigeto Nagao, Osamu Yokota, Reiko Nanba, et al.Journal of the Endocrine Society|December 22, 2017
Increased IRS2 mRNA Expression in SGA Neonates: PCR Analysis of Insulin/IGF Signaling in Cord BloodMasanobu Fujimoto, Yuki Kawashima Sonoyama, Kenji Fukushima, et al.CJC Open|March 29, 2021
Impact of Oral Health Status on Postoperative Complications and Functional Recovery After Cardiovascular SurgeryMasato Ogawa, Seimi Satomi-Kobayashi, Naofumi Yoshida, et al.Journal of the American Chemical Society|October 26, 2023
Molybdenum-Ruthenium-Carbon Solid-Solution Alloy Nanoparticles: Can They Be Pseudo-Technetium Carbide?Shinya Okazoe, Kohei Kusada, Yukihiro Yoshida, et al.Psychiatric Genetics|May 23, 2008
Association study of the commonly recognized breakpoints in chromosome 15q11-q13 in Japanese autistic patientsChieko Kato, Mamoru Tochigi, Shinko Koishi, et al.Hinyokika Kiyo. Acta Urologica Japonica|July 10, 1998
[Histopathological findings and clinical effects for acute rejections]S Takahara, K Toki, N Ichimaru, et al.The Journal of Clinical Endocrinology and Metabolism|August 27, 2020
Prevalence of Somatic Mutations in Aldosterone-Producing Adenomas in Japanese PatientsKazutaka Nanba, Yuto Yamazaki, Nolan Bick, et al.Journal of Human Genetics|October 25, 2007
No evidence for significant association between GABA receptor genes in chromosome 15q11-q13 and autism in a Japanese populationMamoru Tochigi, Chieko Kato, Shinko Koishi, et al.International Journal of Hematology|October 7, 2005
Phase II clinical study of cladribine in the treatment of hairy cell leukemiaTakashi Machii, Takaaki Chou, Muneou Suzuki, et al.Pageof 91