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Human Pathology|July 17, 2012
Association of Merkel cell polyomavirus infection with clinicopathological differences in Merkel cell carcinomaHiromi Higaki-Mori, Satoshi Kuwamoto, Takeshi Iwasaki, et al.
Brain & Development|September 18, 2007
Mental retardation, spasticity, basal ganglia calcification, cerebral white matter lesions, multiple endocrine defects, telangiectasia and atrophic skin: a new syndrome?Yoshiaki Saito, Mitsuo Toyoshima, Akira Oka, et al.
Gene|February 14, 2012
Genotype/phenotype of 6 Chinese cases with Niemann-Pick disease type CHui Xiong, Katsumi Higaki, Cui-Jie Wei, et al.
Brain & Development|March 23, 2007
Tachykinin 1 (TAC1) gene SNPs and haplotypes with autism: a case-control studyTetsuya Marui, Ikuko Funatogawa, Shinko Koishi, et al.
Medicine|July 7, 2018
A novel mutation causing type 1 Gaucher disease found in a Japanese patient with gastric cancer: A case reportSakura Hosoba, Katsuyuki Kito, Yukako Teramoto, et al.
Molecules (Basel, Switzerland)|April 21, 2018
Probing the Inhibitor versus Chaperone Properties of sp²-Iminosugars towards Human β-Glucocerebrosidase: A Picomolar Chaperone for Gaucher DiseaseTeresa Mena-Barragán, M Isabel García-Moreno, Alen Sevšek, et al.
Chembiochem : a European Journal of Chemical Biology|November 11, 2010
A Fluorescent sp2-iminosugar with pharmacological chaperone activity for gaucher disease: synthesis and intracellular distribution studiesZhuo Luan, Katsumi Higaki, Matilde Aguilar-Moncayo, et al.
The International Journal of Neuropsychopharmacology|July 31, 2008
Association of the neuronal cell adhesion molecule (NRCAM) gene variants with autismTetsuya Marui, Ikuko Funatogawa, Shinko Koishi, et al.
Psychiatry and Clinical Neurosciences|July 1, 2008
No association between the ryanodine receptor 3 gene and autism in a Japanese populationMamoru Tochigi, Chieko Kato, Jun Ohashi, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|January 11, 2008
Association study of the 15q11-q13 maternal expression domain in Japanese autistic patientsChieko Kato, Mamoru Tochigi, Jun Ohashi, et al.
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