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1. カルチノイド症候群の臨床的特徴 clinical features of the carcinoid syndrome
2. 同名半盲 homonymous hemianopia
3. 脳血管性認知症の病因、臨床症状、および診断 etiology clinical manifestations and diagnosis of vascular dementia
4. 口腔病変 oral lesions
5. シェーグレン症候群の臨床症状：外分泌腺障害 clinical manifestations of sjogrens syndrome exocrine gland disease

Regional cerebral blood flow and abnormal eating behavior in Prader-Willi syndrome.

Ogura K, Fujii T, Abe N, Hosokai Y, Shinohara M, Fukuda H, Mori E.SourceDepartment of Behavioral Neurology and Cognitive Neuroscience, Tohoku University Graduate School of Medicine, Sendai, Japan; Developmental Disability Section, Department of Rehabilitation for Brain Functions, Research Institute of National Rehabilitation Center for Persons with Disabilities, Tokorozawa, Japan. Electronic address: ogura-kaeko@umin.ac.jp.
Brain & development.Brain Dev.2013 May;35(5):427-34. doi: 10.1016/j.braindev.2012.07.013. Epub 2012 Aug 23.
Background: Prader-Willi syndrome (PWS) is a genetically determined neurodevelopmental disorder and is generally regarded as a genetic model of obesity. Individuals with PWS exhibit behavioral symptoms including temper tantrums, rigid thinking, and compulsive behavior. The most striking feature of P
PMID 22921862

Molecular dynamics studies on 3D structures of the hydrophobic region PrP(109-136).

Zhang J, Zhang Y.SourceGraduate School of Sciences, Information Technology and Engineering, CIAO, The University of Ballarat, MT Helen Campus, Victoria 3353, Australia.
Acta biochimica et biophysica Sinica.Acta Biochim Biophys Sin (Shanghai).2013 Apr 5. [Epub ahead of print]
Prion diseases, traditionally referred to as transmissible spongiform encephalopathies, are invariably fatal and highly infectious neurodegenerative diseases that affect a wide variety of mammalian species, manifesting as scrapie in sheep, bovine spongiform encephalopathy (or 'mad-cow' disease) in c
PMID 23563221

Skora L, Fonseca-Ornelas L, Hofele RV, Riedel D, Giller K, Watzlawik J, Schulz-Schaeffer WJ, Urlaub H, Becker S, Zweckstetter M.SourceMax Planck Institute for Biophysical Chemistry, 37077 Göttingen, Germany.
The Journal of biological chemistry.J Biol Chem.2013 Feb 1;288(5):2994-3002. doi: 10.1074/jbc.M112.423715. Epub 2012 Dec 3.
Misfolding of the natively α-helical prion protein into a β-sheet rich isoform is related to various human diseases such as Creutzfeldt-Jakob disease and Gerstmann-Sträussler-Scheinker syndrome. In humans, the disease phenotype is modified by a methionine/valine polymorphism at codon 129 of the p
PMID 23209282

福永典子,徳田佳生
The Japanese Journal of Rehabilitation Medicine 48(9), 628-634, 2011
… Paragraphia due to cerebellar cognitive affective syndrome (CCAS) has not been reported previously. … Although MRI did not detect any abnormality in the cerebral hemispheres, SPECT demonstrated decreased cerebral blood flow in the left angular gyrus, frontal lobe and parieto-occipital lobe, predominantly on the left side. …
NAID 130001142478