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内部出版物
CNKI学位论文(14)
知网期刊论文(2)
在“
Elsevier电子期刊
”中,
命中:
9
条,耗时:小于0.01 秒
在所有数据库中总计命中:
16
条
1.
Another promising treatment option for neuroblastoma-associated opsoclonus-myoclonus syndrome by oral high-dose dexamethasone pulse: Lymphocyte markers as disease activity
作者:
Makiko Oguma
;
Akira Morimoto
;
akira@jichi.ac.jp
;
Akiko Takada
;
Yoshifumi Kashii
;
Tokiko Fukuda
;
Masato Mori
;
Takanori Yamagata
;
Hideo
Sugie
;
Mariko Y. Momoi
关键词:
Opsoclonus&ndash
;
myoclonus syndrome
;
Neuroblastoma
;
Dexamethasone
;
CD4/CD8 ratio
刊名:Brain and Development
出版年:2012
2.
Study of HOXD genes in autism particularly regarding the ratio of second to fourth digit length
作者:
Yoko
Sugie
;
Hideo
Sugie
;
Tokiko Fukuda
;
Junko Osawa
关键词:
Autism
;
HOXD
;
2D/4D
;
Endophenotype
;
Genetic polymorphism
刊名:Brain and Development
出版年:2010
3.
Distal lipid storage myopathy due to PNPLA2
作者:
Aya Ohkuma
;
Ikuya Nonaka
;
May Christine V. Malicdan
;
Satoru Noguchi
;
Satoru Ohji
;
Kyoichi Nomura
;
Hideo
Sugie
;
Yukiko K. Hayashi
;
Ichizo Nishino
关键词:
Distal myopathy
;
Lipid storage myopathy
;
Neutral lipid storage disease with myopathy
;
PNPLA2
刊名:Neuromuscular Disorders
出版年:2008
4.
A novel PYGM
作者:
Eun Hee Sohn
;
Hyang-Sook Kim
;
Ae Young Lee
;
Tokiko Fukuda
;
Hideo
Sugie
;
Dae-Seong Kim
关键词:
McArdle disease
;
Mutation
;
Myophosphorylase
;
RNA
刊名:Neuromuscular Disorders
出版年:2008
5.
Identification of Alu-mediated, large deletion-spanning introns 19–26 in PHKA2 in a patient with X-linked liver glycogenosis (hepatic phosphorylase kinase deficiency)
作者:
Toshiyuki Fukao
;
Gaixiu Zhang
;
Yusuke Aoki
;
Takahiro Arai
;
Takahide Teramoto
;
Hideo
Kaneko
;
Hideo
Sugie
;
Naomi Kondo
关键词:
Alu elements
;
Mutation
;
X-linked liver glycogenosis
;
Homologous recombination
刊名:Molecular Genetics and Metabolism
出版年:2007
6.
Frequent mutations in Japanese patients with acid maltase deficiency
作者:
Tsujino
;
Seiichi
;
Huie
;
Maryann
;
Kanazawa
;
Naomi
;
Sugie
;
Hideo
;
Goto
;
Yu-ichi
;
Kawai
;
Mitsuru
;
et. al.
关键词:
Acid maltase deficiency
;
Japanese
;
Mutation
;
Genetic diagnosis
刊名:Neuromuscular Disorders
出版年:2000
7.
Glycogen storage disease type Ib without neutropenia
作者:
Shigeo Kure
;
Dian-Chang Hou
;
Yasuyuki Suzuki
;
Atsushi Yamagishi
;
Masahiro Hiratsuka
;
Tokiko Fukuda
;
Hideo
Sugie
;
Naomi Kondo
;
Yoichi Matsubara
;
Kuniaki Narisawa
刊名:The Journal of Pediatrics
出版年:2000
8.
Bilateral Facial Palsy Caused by Bilateral Masked Mastoiditis
作者:
Fukuda
;
Tokiko
;
Sugie
;
Hideo
;
Ito
;
Masataka
;
Kikawada
;
Toru
刊名:Pediatric Neurology
出版年:1998
9.
Genetic analysis of Japanese patients with myophosphorylase deficiency (McArdle's disease): single-codon deletion in exon 17 is the predominant mutation
作者:
Sugie
;
Hideo
;
Sugie
;
Yoko
;
Ito
;
Masataka
;
Fukuda
;
Tokiko
;
Nonaka
;
Ikuya
;
Igarashi
;
Yoshio
关键词:
Myophosphorylase deficiency
;
McArdle's disease
;
Molecular biology
;
Single-codon deletion
;
Polymerase chain reaction
刊名:Clinica Chimica Acta
出版年:1995
1
按检索点细分(9)
作者(9)
按出版年细分(9)
2012年(1)
2010年(1)
2008年(2)
2007年(1)
2000年(2)
2000年及以前(2)
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