職名 助教
氏名 よねかわ たかひろ
米川 貴博
生年月  
所属 部局 附属病院
学科・専攻 小児科
講座  
教育研究分野  
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学歴 2002年3月三重大学医学部医学科卒業
2011年4月山梨大学大学院医学工学総合教育部博士課程入学
2014年3月山梨大学大学院医学工学総合教育部博士課程卒業
学位 博士(医学)
所属学会 日本小児科学会
日本小児神経学会
社会活動 日本小児神経学会災害対策小委員会委員
職歴 2002年-2009年3月三重県下、和歌山県新宮市の病院で小児科医として勤務
2009年4月国立精神神経医療研究センター病院小児神経科(レジデント)
2012年4月国立精神神経医療研究センター神経研究所疾病研究第一部(流動研究員)
2014年11月Howard Hughes Medical Institute、アイオワ大学(博士後研究員)
2018年7月三重大学大学院医学系研究科臨床医学系講座小児科学分野(助教)
学術(芸術)賞  
専門分野 小児神経疾患、筋病学
現在の研究課題  
担当科目  
主な業績等 Beltrán D, Anderson ME, Bharathy N, Settelmeyer TP, Svalina MN, Bajwa Z, Shern JF, Gultekin SH, Cuellar MA, Yonekawa T, Keller C, Campbell KP. Exogenous expression of the glycosyltransferase LARGE1 restores α-dystroglycan matriglycan and laminin binding in rhabdomyosarcoma. Skelet Muscle 2019; 9: 11.
Tomioka I, Ishibashi H, Minakawa EN, Motohashi HH, Takayama O, Saito Y, Popiel HA, Puentes S, Owari K, Nakatani T, Nogami N, Yamamoto K, Noguchi S, Yonekawa T, Tanaka Y, Fujita N, Suzuki H, Kikuchi H, Aizawa S, Nagano S, Yamada D, Nishino I, Ichinohe N, Wada K, Kohsaka S, Nagai Y, Seki K. Transgenic monkey model of the polyglutamine diseases recapitulating progressive neurological symptoms. eNeuro 2017; 4.
Zhu W, Mitsuhashi S, Yonekawa T, Noguchi S, Huei JC, Nalini A, Preethish-Kumar V, Yamamoto M, Murakata K, Mori-Yoshimura M, Kamada S, Yahikozawa H, Karasawa M, Kimura S, Yamashita F, Nishino I. Missing genetic variations in GNE myopathy: rearrangement hotspots encompassing 5'UTR and founder allele. J Hum Genet. 2017; 62: 159-166.
Uruha A, Noguchi S, Hayashi YK, Tsuburaya RS, Yonekawa T, Nonaka I, Nishino I. Hepatitis C virus infection in inclusion body myositis: A case-control study. Neurology. 2016; 86: 211-7.
Yonekawa T, Nishino I. Ullrich congenital muscular dystrophy: clinicopathological features, natural history and pathomechanism(s). J Neurol Neurosurg Psychiatry 2015, 86: 280-287.
Yonekawa T, Oya Y, Higuchi Y, Hashiguchi A, Takashima H, Sugai K, Sasaki M. A Case of Extremely Severe Complicated Spastic Paraplegia 3A with Neonatal Onset. Pediatr Neurol 2014; 51: 726–729.
Suzuki S, Yonekawa T, Kuwana M, Hayashi KY, Okazaki Y, Kawaguchi Y, Suzuki N, Nishino I. Clinical and histological findings associated with autoantibodies detected by RNA immunoprecipitation in inflammatory myopathies. J Neuroimmunol 2014; 274: 202–208.
Yonekawa T, Malicdan MCV, Cho A, Hayashi KY, Nonaka I, Mine T, Yamamoto T, Nishino I, Noguchi S. Sialyllactose ameliorates myopathic phenotypes in symptomatic GNE myopathy model mice. Brain 2014; 137: 2670–2679.
Iwamoto S, Yonekawa T, Azuma E, Fujisawa T, Nagao M, Shimada E, Nakamura R, Tashima R, Ohichi K, Toyoda H, Komada Y. Pediatr Blood Cancer 2014; 61: 1160–1161.
Yonekawa T, Komaki H, Okada M, Hayashi KY, Nonaka I, Sugai K, Sasaki M, Nishino I. Rapidly progressive scoliosis and respiratory deterioration in Ullrich congenital muscular dystrophy. J Neurol Neurosurg Psychiatry 2013; 84: 982–988.
Yonekawa T, Komaki H, Saito Y, Takashima H, Sasaki M. Congenital hypomyelinating neuropathy attributable to a de novo p.Asp61Asn mutation of the myelin protein zero gene. Pediatr Neurol 2013; 48: 59–62.
Yonekawa T, Komaki H, Saito Y, Sugai K, Sasaki M. Peripheral nerve abnormalities in pediatric patients with spinal muscular atrophy. Brain Dev 2012; 35: 165–171.
Yonekawa T, Nakagawa E, Takeshita E, Inoue Y, Inagaki M, Kaga M, Sugai K, Sasaki M, Kaido T, Takahashi A, Otsuki T. Effect of corpus callosotomy on attention deficit and behavioral problems in pediatric patients with intractable epilepsy. Epilepsy Behav 2011; 22: 697–704.
Tanaka Y, Ohishi K, Yonekawa T, Yodoya N, Iwamoto S, Nishioka Y, Tatara Y, Matsumoto T, Masuya M. Effect of washing solution on platelet counts following transfusion with twice-washed platelets: a single-patient experience. Transfus Med 2010; 20: 358–360.
Yonekawa T, Mitani Y, Ohashi H. Three-dimentional echocardiographic imaging of a giant Eustachian valve in an infant with reversed cyanosis. Pediatr Cardiol 2010; 31: 1114–1115.
Yonekawa T, Saito Y, Sakuma H, Sugai K, Shimizu Y, Inagaki M, Sasaki M. Augmented startle responses in opsoclonus-myoclonus syndrome. Brain Dev 2010; 33: 335–338.