Faculty Profiles - NAKAMURA Masayuki

Papers - NAKAMURA Masayuki

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37. Urata Y, Nakamura M, Sasaki N, Shiokawa N, Nishida Y, Arai K, Hiwatashi H, Izumi Yokoyama I, Narumi S, Terayama Y, Murakami T, Ugawa Y, Sakamoto H, Kaneko S, Nakazawa Y, Yamasaki R, Sadashima S, Sakai T, Arai H, Sano A . Novel pathogenic XK mutations in McLeod syndrome and interaction between XK protein and chorein. . Neurol. Genet.5 2019Novel pathogenic XK mutations in McLeod syndrome and interaction between XK protein and chorein.Reviewed

6. Murakami T, Abe D, Matsumoto H, Tokimura R, Abe M, Tiksnadi A, Kobayashi S, Kaneko C, Urata Y, Nakamura M, Sano A, Ugawa Y . A patient with McLeod syndrome showing involvement of the central sensorimotor tracts for the legs. . BMC Neurol.19 2019A patient with McLeod syndrome showing involvement of the central sensorimotor tracts for the legs.Reviewed

Kawaike Y, Nagata J, Furuya T, Koriyama C, Nakamura M, Sano A . Working memory-related prefrontal hemodynamic responses in university students: A correlation study of aubjective well-being and lifestyle habits. . Front. Behav. Neurosci.13 2019Working memory-related prefrontal hemodynamic responses in university students: A correlation study of aubjective well-being and lifestyle habits.Reviewed

ishida Y, Nakamura M, Urata Y, Kasamo K, Hiwatashi H, Yokoyama I, Mizobuchi M, Sakurai K, Osaki Y, Morita Y, Watanabe M, Yoshida K, Yamane K, Miyakoshi N, Ryouichi Okiyama R, Ueda T, Wakasugi N, Saitoh Y, Sakamoto T, Takahashi Y, Shibano K, Tokuoka H, Hara A, Monma K, Ogata K, Kakuda K, Mochizuki H, Arai T, Araki M, Fujii T, Tsukita K, Sakamaki-Tsukita H, Sano A . Novel pathogenic VPS13A gene mutations in Japanese patients with chorea-acanthocytosis. . Neurol. Genet.5 2019Novel pathogenic VPS13A gene mutations in Japanese patients with chorea-acanthocytosis.Reviewed

Nagata O. . Mouse model of chorea-acanthocytosis exhibits male infertility caused by impaired sperm motility as a result of ultrastructural morphological abnormalities in the mitochondrial sheath in the sperm midpiece . Biochemical and Biophysical Research Communications503 ( 2 ) 915 - 920 2018.9

Ishiura H. . Expansions of intronic TTTCA and TTTTA repeats in benign adult familial myoclonic epilepsy . Nature Genetics50 ( 4 ) 581 - 590 2018.4

Ishiura H, Doi K, Mitsui J, Yoshimura J, ........Nakamura M et al . Expansions of intronic TTTCA and TTTTA repeats in benign adult familial myoclonic epilepsy . Nat. Genet.50 581 - 590 2018Expansions of intronic TTTCA and TTTTA repeats in benign adult familial myoclonic epilepsyReviewed

36. Nagata O, Nakamura M, Sakimoto H, Urata Y, Sasaki N, Shiokawa N, Sano A . Mouse model of chorea-acanthocytosis exhibits male infertility caused by impaired sperm motility as a result of ultrastructural morphological abnormalities in the mitochondrial sheath in the sperm midpiece. . Biochem. Biophys. Res. Commun.503 915 - 920 2018Mouse model of chorea-acanthocytosis exhibits male infertility caused by impaired sperm motility as a result of ultrastructural morphological abnormalities in the mitochondrial sheath in the sperm midpiece.Reviewed

石島洋輔, 新井薫, 肝付洋, 中村雅之, 佐野輝 . 発熱・白血球増多を伴うカタトニアを呈した急速交代型双極性障害の1例 . 精神医学59 ( 10 ) 943 - 948 2017.10発熱・白血球増多を伴うカタトニアを呈した急速交代型双極性障害の1例

Publisher：(株)医学書院

カタトニア(緊張病)は,さまざまな精神疾患や身体疾患を背景に生じ,精神運動の失調を来す症候群である。DSM-5ではカタトニアが特定用語となり,統合失調症以外の疾患にも適応が広がった。また,発熱や自律神経失調を呈するカタトニアは悪性カタトニアと呼ばれ,抗精神病薬による悪性症候群との関連性が議論されている。我々は双極性障害の症例において,発熱と白血球増多がカタトニアに先行し,カタトニアの改善とともに消退した現象を観察した。本症例は悪性カタトニアの症候を部分的に呈しており,非悪性と悪性カタトニアの連続性が示唆された。また,発熱・白血球増多に着目することは,カタトニアの早期診断に寄与すると考えられた。(著者抄録)

齊之平一隆, 石塚貴周, 田畑健太郎, 横塚紗永子, 新井薫, 塩川奈理, 春日井基文, 中村雅之, 佐野輝 . 前頭葉機能障害を呈した前頭骨内板過骨症の1例 . 九州神経精神医学63 ( 2 ) 88 - 93 2017.8前頭葉機能障害を呈した前頭骨内板過骨症の1例

Publisher：九州精神神経学会

前頭葉機能障害を中心とした認知症機能低下と前頭骨内板過骨症(HFI)を有する80代の女性の症例を報告した。2年前の夏頃より「お金の管理に自信がない」「運転するのが怖い」と訴えるようになり、物忘れや脱抑制的言動が目立つようになり、認知症の鑑別と治療目的で入院となった。Mini Mental State Examinationは28/30点と保たれていたが、Frontal Assessment Batteryをはじめとする前頭葉機能検査では顕著な障害を認めた。頭部CTやMRIにおいて前頭骨に限局した結節性の過骨性変化と軽度の前頭葉の萎縮や両側側脳室下角の開大を認め、大脳白質にはT2延長領域を認めた。AD index(tau×Aβ40/42)は11697を示し、血管性の病変に加えてアルツハイマー病理の存在も示唆された。脱抑制症状や徘徊等の異常行動に対してquetiapineの内服を開始し、125mgまで漸増したところ、神経心理学的検査においては明らかな改善は見られなかったが、情動は安定し病棟内で落ち着いて生活できるようになった。

新井薫, 肝付洋, 春日井基文, 中村雅之, 佐野輝 . 回避・制限性食物摂取障害にrisperidoneが有効であった1例 . 精神医学59 ( 1 ) 91 - 94 2017.1回避・制限性食物摂取障害にrisperidoneが有効であった1例

Publisher：(株)医学書院

回避・制限性食物摂取障害(avoidant/restrictive food intake disorder;ARFID)はDSM-5において追加されたボディイメージの歪みがない摂食障害である。思春期発症のARFIDの19歳女性の1例を提示する。患者は腹部の手術と腸閉塞の既往を持ち,15歳から食後の腹痛を恐れて食事を制限するようになった。SSRIやbenzodiazepineで治療されたが十分に反応しなかった。19歳時にrisperidone 1mgの投与を契機に腹痛に対する不安が軽減し,食事摂取が可能になった。ARFIDに対して抗精神病薬が治療の選択肢となり得ることが示唆された。(著者抄録)

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

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. 2016.11The effects of olanzapine treatment on brain regional glucose metabolism in neuroleptic-naive first-episode schizophrenic patients.Reviewed

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 2016A patient with McLeod syndrome showing involvement of the central sensorimotor tracts for the legs.Reviewed

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 2016Predictive validity of the Japanese version of Postpartum Depression Predictors Inventory-Revised (PDPI-R) during pregnancy and the postpartum period.Reviewed

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 2016horein interacts with α-tubulin and HDAC6, and overexpression preserves cell viability during nutrient deprivation in HEK293 cells. Reviewed

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 2013.11Chorein, the protein responsible for chorea-acanthocytosis, interacts with β-adducin and β-actin.Reviewed

*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 2012.11Heteroplasmic m.1624C>T mutation of the mitochondrial tRNAVal gene in a proband and his mother with repeated consciousness disturbancesReviewed

*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 2012.5Different Clinical Phenotypes in Siblings with a Presenilin-1 P264L MutationReviewed

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 2011.10Remapping and mutation analysis of benign adult familial myoclonic epilepsy in a Japanese pedigree.Reviewed

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Papers - NAKAMURA Masayuki