Faculty Profiles - NAKAMURA Masayuki

Papers - NAKAMURA Masayuki

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Sainohira Kazutaka, Ishizuka Takanori, Tabata Kentaro, Yokotsuka Saeko, Arai Kaoru, Shiokawa Nari, Kasugai Motofumi, Nakamura Masayuki, Sano Akira . A Case of Hyperostosis Frontalis Interna with Frontal Lobe Dysfunction . Kyushu Neuropsychiatry63 ( 2 ) 88 - 93 2017

Publisher：The Association of Kyushu Neuropsychiatry

<p>Hyperostosis frontalis interna (HFI) is characterized by the bilateral thickening of the frontal bone of the skull. Although most patients with HFI show no clinical symptoms, a few have been reported to show diverse and non-specific symptoms, including－but not limited to－cognitive decline, epileptic seizure, and endocrine disorder. We experienced the case of an 80-year-old woman with cognitive decline, in whom HFI was discovered on MRI and CT. Neurophychiatric examinations revealed frontal lobe dysfunction. HFI was therefore suggested to be one of the causes of frontal lobe dysfunction.</p>

DOI： 10.11642/kyushuneurop.63.2_88

CiNii Research

34. Yoshimuta H, Nakamura M, Kanda E, Fujita S, Takeuchi K, Fujimoto T, Nakabeppu Y, Akasaki Y, Sano A . The effects of olanzapine treatment on brain regional glucose metabolism in neuroleptic-naive first-episode schizophrenic patients. . Hum. Psychopharmacol. 2016.11Reviewed

asaki N, Nakamura M, Kodama A, Urata Y, Shiokawa N, Hayashi T, Sano A . horein interacts with α-tubulin and HDAC6, and overexpression preserves cell viability during nutrient deprivation in HEK293 cells. . FASEB J 2016Reviewed

arumi S, Natori T, Miyazawa H, Kato T, Yonezawa H, Nishino I, Nakamura M, Sano A, Terayama Y . A patient with McLeod syndrome showing involvement of the central sensorimotor tracts for the legs. . Neurol. Clin. Neurosci.4 115 - 117 2016Reviewed

33. Wakamatsu M, Nakamura M, Kasugai M, Kimotsuki H, Oki T, Orita Y, Togami S, Kobayashi H, Sano A, Douchi T . Predictive validity of the Japanese version of Postpartum Depression Predictors Inventory-Revised (PDPI-R) during pregnancy and the postpartum period. . Medical Journal of Kagoshima University 2016Reviewed

Shiokawa N, Nakamura M, Sameshima M, Deguchi A, Hayashi T, Sasaki N, Sano A . Chorein, the protein responsible for chorea-acanthocytosis, interacts with β-adducin and β-actin. . Biochem Biophys Res Commun441 96 - 101 2013.11Reviewed

*Sangatsuda Y, *Nakamura M, Tomiyasu A, Deguchi A, Toyota Y, Goto Y, Nishino I, Ueno S, Sano A . Heteroplasmic m.1624C>T mutation of the mitochondrial tRNAVal gene in a proband and his mother with repeated consciousness disturbances . Mitochondrion12 ( 6 ) 617 - 622 2012.11Reviewed

*Ishizuka T, *Nakamura M, Ichiba M, Sano A . Different Clinical Phenotypes in Siblings with a Presenilin-1 P264L Mutation . Dement. Geriatr. Cogn. Disord.33 ( 42038 ) 132 - 140 2012.5Reviewed

Mori S, Nakamura M, Yasuda T, Ueno S, Kaneko S, Sano A . Remapping and mutation analysis of benign adult familial myoclonic epilepsy in a Japanese pedigree. . Journal of Human Genetics2011 ( 56 ) 742 - 747 2011.10Reviewed

Ishizuka T, Nakamura M, Ichiba M, Sano A . Familial Semantic Dementia with P301L Mutation in the Tau Gene. . Dementia and geriatric cognitive disorders31 ( 5 ) 334 - 340 2011.5Reviewed

Tomiyasu A, Nakamura M, Ichiba M, Ueno S, Saiki S, Morimoto M, Kobal J, Kageyama Y, Inui T, Wakabayashi K, Yamada T, Kanemori Y, Jung HH, Tanaka H, Orimo S, Afawi Z, Blatt I, Aasly J, Ujike H, Babovic-Vuksanovic D, Josephs KA, Tohge R, Rodrigues GR, Dupre N, Yamada H, Yokochi F, Kotschet K, Takei T, Rudzinska M, Szczudlik A, Penco S, Fujiwara M, Tojo K, Sano A . Novel pathogenic mutations and copy number variations in the VPS13A Gene in patients with chorea-acanthocytosis. . American journal of medical genetics. Part B, Neuropsychiatric genetics156 620 - 631 2011.5Reviewed

Kato M, Nakamura M, Ichiba M, Tomiyasu A, Shimo H, Higuchi I, Ueno S, Sano A. . Mitochondrial DNA deletion mutations in patients with neuropsychiatric symptoms. . Neuroscience Research69 331 - 336 2011.4Reviewed

Shimo H, Nakamura M, Tomiyasu A, Ichiba M, Ueno SI, Sano A . Comprehensive analysis of the genes responsible for neuroacanthocytosis in mood disorder and schizophrenia. . Neuroscience Research69 ( 3 ) 196 - 202 2011.3Reviewed

Hayashi T, Nakamura M, Ichiba M et al. . Adult-type metachromatic leukodystrophy with compound heterozygous ARSA mutations: A case report and phenotypic comparison with a previously reported case. . Psychiatry Clin Neurosci65 105 - 108 2011.1Reviewed

Ratovitski T, Nakamura M, D'Ambola J et al. . N-terminal proteolysis of full-length mutant huntingtin in an inducible PC12 cell model of Huntington's disease. . Cell Cycle6 2970 - 2981 2007.1Reviewed

E Mizuno, M Nakamura, A Agemura, A Kusumoto, M Ichiba, Y Kurano, S Muroya, A Sano, . Brain-specific transcript variants of 5' and 3' ends of mouse VPS13A and VPS13C: . Biochem Biophys Res Commun.353 902 - 907 2007Reviewed

Y Kurano, M Nakamura, M Ichiba, M Matsuda, E Mizuno, M Kato, A Agemura, S.Izumo, A Sano, . In vivo distribution and localization of chorein: . Biochem Biophys Res Commun.353 41 - 435 2007Reviewed

中村雅之　佐野　輝　 . 精神疾患の遺伝子研究． . 精神医学　47 348 - 358 2005

中村雅之　佐野　輝　 . セロトニントランスポーター． . 分子精神医学　5 72 - 74 2005

中村雅之　 . ハンチントン病の発現誘導マウスモデル及びPC12細胞モデルにおける全長変異ハンチンチンのタンパク質分解 . 神経化学43 39 - 46 2004

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Papers - NAKAMURA Masayuki