松石豊次郎 (Toyojiro Matsuishi) - マイポータル - researchmap

基本情報

所属: 久留米大学医学部医学科小児科学

学位: 医学博士(久留米大学)

J-GLOBAL ID: 200901093002807161
researchmap会員ID: 1000366334

外部リンク: http://www.med.kurume-u.ac.jp/med/ped/

研究キーワード

4

研究分野

2

学歴

2

- 1986年

久留米大学
久留米大学医学部医学科小児科

MISC

29

Zhou G, Miura Y, Shoji H, Yamada S, Matsuishi T: Platelet Monoamine Oxidase B and Plasma β-Phenylethylamine in Parkinson's Disease. J Neural Neurosurg Ps 70: 229-231, 2001."

2002年
Kusaga A, Yamashita Y, Koeda T, Hiratani M, Kaneko M, Yamada M, and Matsuishi T: Increased urine phenylethylamine after methylphenidate treatment in children with ADHD. Am Neurol. 2002; 52: 371-374."

2002年
Koga Y, Ishibashi M, Ueki I, S. Yatsuga, Fukiyama R, Akira Y, and Matsuishi T: Effects of L-arginine on the acute phase of strokes in three patients with MELAS. Neurology 2002; 58: 827-828."

2002年
Shimizu T, Matsuishi T, Iwamoto R, Handa K, Yoshioka H, Kato H, Ueda S, Hara H, Tabira T, Mekada E: Elevated levels of anti-CD9 antibodies in the cerebrospinal fluid of patients with subacute sclerosing panencephalitis. J Infect Dis 2002; 185: 346-50."

2002年
Yamashita Y, Matsuishi T, Kondo I, Iwanaga R, Nagamitsu S, Kusaga A, Obata K, Fukuda T, Kato H: Mutation Type in the Methyl-CpG Binding Protein 2 (MECP2) in Rett Patients with Preserved Speech. Brain Dev-JPN 23 S157-S160, 2001."

2001年
Nagamitsu S, Matsuishi T, Yamashita Y, Shimizu T, Iwanaga R, Murakami Y, Miyazaki M, Hashimoto T, Kato H: Decreased Cerebrospinal Fluid Levels of β-Endorphin and ACTH in Children with Infantile Spasms. J Neural Transm 108: 363-371, 2001."

2001年
Preliminary Evidence of Decveased Substance Pand Enkephalinergic Activity in Rett Syndrome

Brain Dev 23, s122-126 2001年
Neurobiology and Neurochemistry of Rett Syndrome

Brain Dev 23,s 58-61 2001年
Mutation Type in the Methy1-CpG Binding Protein2 (MECP2) in Rett Patients with Preserved Speech

Brain Dev 23, 157-160 2001年
Platelet Monoamine Oxidase B and Plasma B-phenylethylamine in Parkinson's Disease

J Neurol Neurosur Ps 70, 229-231 2001年
Decreased cerebrospinal fluid levels of beta-endorphin and ACTH in children with infantile spasms

S Nagamitsu, T Matsuishi, Y Yamashita, T Shimizu, R Iwanaga, Y Murakami, M Miyazaki, T Hashimoto, H Kato

JOURNAL OF NEURAL TRANSMISSION 108(3) 363-371 2001年
The test of variables of attention (TOVA) is useful in the diagnosis of Japanese male children with attention deficit hyperactivity disorder

N Wada, Y Yamashita, T Matsuishi, Y Ohtani, H Kato

BRAIN & DEVELOPMENT 22(6) 378-382 2000年9月
Decreased cerebrospinal fluid levels of beta-phenylethylamine in patients with Rett syndrome

M Satoi, T Matsuishi, S Yamada, Y Yamashita, E Ohtaki, K Mori, R Riikonen, H Kato, AK Percy

ANNALS OF NEUROLOGY 47(6) 801-803 2000年6月
Single-fiber analysis of mitochondrial A3243G mutation in four different phenotypes

Y Koga, A Koga, R Iwanaga, Y Akita, J Tubone, T Matsuishi, N Takane, Y Sato, H Kato

ACTA NEUROPATHOLOGICA 99(2) 186-190 2000年2月
Koga Y, Koga A, Iwanaga R, Akita Y, Tubone J, Matsuishi T, Takane N, Sato Y, Kato H: Single-Fiber Analysis of Mitochondrial A3243G Mutation in Four Different Phenotypes. Acta Neuropathol 99: 186-190, 2000."

2000年
Satoi M, Matsuishi T, Yamada S, Yamashita Y, Ohtaki E, Mori K, Riikonen R, Kato H, Percy AK: Decreased Cerebrospinal Fluid Levels of β-Phenylethylamine in Patients with Rett Syndrome. Ann Neurol 47: 801-803, 2000."

2000年
Obata K, Matsuishi T, Yamashita Y, Fukuda T, Kuwajima K, Horiuchi I, Nagamitsu S, Iwanaga R, Kimura A, Omori I, Endo S, Mori K, Kondo K: Mutation Analysis of the Methyl-CpG Binding Protein 2 Gene (MECP2) in Patients with Rett Syndrome. J Med Genet 37: ・・・

2000年
Matsuishi T, Yamashita Y: Neurobiology and Neurochemistry of Rett Syndrome. Brain Dev-JPN 23: S58-S61, 2001."

2000年
Mutation analysis of the methyl-CpG binding protein 2 gene(MECP2)in patients with Rett syndrome

Journal of Medical Genetics 37 608-610 2000年
Nezu J, Tamai I, Oku A, Ohashi R, Yabuushi H, Hashimoto N, Nikaido H, Sai Y, Koizumi A, Shoji Y, Takada G, Matsuishi T, Yoshino M, Kato H, Ohura T, Tsujimoto G, Hayakawa J, Shimane M, Tsuji A: Primary Systemic Carnitine Deficiency is Caused by Mutation・・・

1999年

もっとみる

書籍等出版物

1

Multiple sclerosis, acute disseminated encephalomyelitis

Today's therapy in Pediatrics 2000年

所属学協会

14

Works(作品等)

5

共同研究・競争的資金等の研究課題

12

産業財産権

5