山野恒一 (Tsunekazu Yamano) - マイポータル - researchmap

基本情報

所属: 大阪市立大学大学院医学研究科臨床医科学専攻（生殖発達医学大講座）医学研究科教授

J-GLOBAL ID: 200901061481756674
researchmap会員ID: 1000049653

研究キーワード

1

Pediatrics

研究分野

1

ライフサイエンス / 胎児医学、小児成育学 /

経歴

1

1999年

大阪市立大学教授

委員歴

4

MISC

37

Brain magnetic resonance imaging in 23 patients with mucopolysaccharidoses and the effect of bone marrow transplantation

T Seto, K Kono, K Morimoto, Y Inoue, H Shintaku, H Hattori, O Matsuoka, T Yamano, A Tanaka

ANNALS OF NEUROLOGY 50(1) 79-92 2001年7月
Hemadsorption expressed by cloned H genes from subacute sclerosing panencephalitis (SSPE) viruses and their possible progenitor measles viruses isolated in Osaka, Japan

K Furukawa, M Ayata, M Kimura, T Seto, Matsunaga, I, R Murata, T Yamano, H Ogura

MICROBIOLOGY AND IMMUNOLOGY 45(1) 59-68 2001年
Heterotopia in microcephaly induced by cytosine arabinoside: hippocampus in the neocortex

K Ono-Yagi, M Ohno, M Iwami, T Takano, T Yamano, M Shimada

ACTA NEUROPATHOLOGICA 100(4) 403-408 2000年10月
Disappearance of hypointernse multiple sclerotic lesions on FLAIR MAI, (共著)

Pediatric Neurology 21(1) 500-502 1999年
A case of anorexia nervosa with hyperbilirubinaemia in a patient homozygous for a mutation in the bilirubin UDP-gurucuronosyltransferase gene(共著)

Europian Jourmal of Pediatrics 158(7) 545-549 1999年
Hypertension in leigh syndrome - A case report

T Narita, T Yamano, M Ohno, T Takano, R Ito, M Shimada

NEUROPEDIATRICS 29(5) 265-267 1998年10月
Enhanced expression of full-length TrkB receptors in young rat brain with hypoxic/ischemic injyury(共著)

Brain Research 797(2) 278-286 1998年
Gilbert syndrome caused by a homozygous missens mutation(Tyr486Asp)of bilirubin UDP-gurucuronosyltransferase gene(共著)

Journal of Pediatrics. 132(6) 1045-1047 1998年
Multiple abnormal magnetic resonance imaging signals in a patient with minimal Neurological symptomes. (共著)

European Journal of Pediatric Neurology 1(1) 39-40 1997年
Age-dependent susceptibility in mumps-associated hydrocephalus : neuropathologic features and brain barriers. (共著)

Acta Neuropathologica 94(2) 207-215 1997年
Efficacy of pyridoxal physphate in treating and adult with intractalble status epilepticus. (共著)

Neurology. 48 1468-1469 1997年
Novel missense and frameshift mutations in the adrenoleukodystrophy gene

H Ueyama, T Yamano, M Shimada, Ohkubo, I

JAPANESE JOURNAL OF HUMAN GENETICS 41(4) 407-411 1996年12月
Development of corticospinal tract fibers and their plasticity. II : Neonatal unilateral cortical damage and subsequent development of the corticospinal tract in mice. (共著)

Brain and Development. 18(3) 173-178 1996年
Development of corticospinal tract fibers and their plasticity. I: Quantitative analysis of the developing corticospinal tract in mice.(共著)

Brain and Development 18(1) 29-34 1996年
Congenital hydrocephalus : Role of placental myxovirous infection.(共著)

Congenital Anomaly 35 15-24 1995年
COPPER DISTRIBUTION IN FETUS AND PLACENTA OF THE MACULAR MUTANT MOUSE AS A MODEL OF MENKES KINKY HAIR DISEASE

GQ XU, T YAMANO, M SHIMADA

BIOLOGY OF THE NEONATE 66(5) 302-310 1994年11月
HISTOCHEMICAL-STUDY OF MITOCHONDRIAL-ENZYMES IN CEREBELLAR CORTEX OF MACULAR MUTANT MOUSE, A MODEL OF MENKES KINKY HAIR DISEASE

M KUMODE, T YAMANO, M SHIMADA

ACTA NEUROPATHOLOGICA 87(3) 313-316 1994年3月
PATHOGENESIS OF CEREBELLAR DEFORMITY IN EXPERIMENTAL CHIARI TYPE-I MALFORMATION CAUSED BY MUMPS-VIRUS

T TAKANO, M UNO, T YAMANO, M SHIMADA

ACTA NEUROPATHOLOGICA 87(2) 168-173 1994年2月
Axonal ramification following unilateral cortical ablation in neonatal rats.(共著)

Brain and Development 16(3) 264-266 1994年
Neuropathological study on cerebellum of macular mutant mouse heterozygote. (共著)

Acta Neuropathologica 86(4) 411-417 1993年

もっとみる

書籍等出版物

1

Menkes Kinky hair disease. (共著)

Mineral and Metal Neurotoxicology, CRC Press. 1996年

所属学協会

4

共同研究・競争的資金等の研究課題

5