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内部出版物
Wiley电子期刊(4)
SpringerLink电子期刊(192)
Elsevier电子期刊(515)
在“
Elsevier电子期刊
”中,
命中:
515
条,耗时:小于0.01 秒
在所有数据库中总计命中:
711
条
1.
A 10.43 Mb duplication of chromosome region 5q31.2-q32 associated with a general delay in
psychomotor
development
作者:
Eduardo Santoro
a
;
eduu_sl@hotmail.com
;
Henrique Pandolfo
b
;
hen.celta@hotmail.com
;
Jill Rosenfeld
c
;
1
;
Jill.Mokry@bcm.edu
;
Salmo Raskin
b
;
d
;
e
;
genetika@genetika.com.br
关键词:
CGH
;
Delay
;
Development
;
Psychomotor
;
Retardation
;
Mental
;
Duplication
;
Chromosome 5
;
5q31.2-q32
刊名:Meta Gene
出版年:2017
2.
Quinidine therapy for West syndrome with KCNTI mutation: A case report
作者:
Masataka Fukuoka
a
;
Ichiro Kuki
a
;
i-kuki@med.osakacity-hp.or.jp
;
Hisashi Kawawaki
a
;
Shin Okazaki
a
;
Kiyohiro Kim
a
;
Yuka Hattori
a
;
Hitomi Tsuji
a
;
Megumi Nukui
a
;
Takeshi Inoue
a
;
Yoko Yoshida
b
;
Takehiro Uda
c
;
Sadami Kimura
d
;
Yukiko Mogami
d
;
Yasuhiro Suzuki
d
;
Nobuhiko Okamoto
e
;
Hirotomo Saitsu
f
;
g
;
Naomichi Matsumoto
f
关键词:
EOEE
;
early onset epileptic encephalopathy
;
MPSI
;
migrating partial seizures of infancy
;
LTG
;
lamotrigine
;
VPA
;
valproate
刊名:Brain and Development
出版年:2017
3.
Posture-cognitive dual-tasking: A relevant marker of depression-related
psychomotor
retardation
. An illustration of the positive impact of repetitive transcranial magnetic stimulation in patients with major depressive disorder
作者:
Thibault Deschamps
a
;
thibault.deschamps@univ-nantes.fr" class="auth_mail" title="E-mail the corresponding author
;
Anne Sauvaget
b
;
c
;
Anne Pichot
b
;
Pierre Valriviè
;
re
b
;
Maxime Maroulidè
;
s
a
;
Aurore Bois
a
;
Samuel Bulteau
b
;
Vé
;
ronique Thomas-Ollivier
a
关键词:
Depression
;
rTMS
;
Psychomotor
retardation
;
Posture
刊名:Journal of Psychiatric Research
出版年:2016
4.
Opitz C syndrome: Trigonocephaly, mental
retardation
and craniofacial dysmorphism
作者:
J.A. Avina Fierro
a
;
avinafie@megared.net.mx" class="auth_mail" title="E-mail the corresponding author
;
D.A. Hernandez Avina
b
关键词:
Trigonocephaly
;
Facial dysmorphism
;
Balanced translocation
刊名:Egyptian Journal of Medical Human Genetics
出版年:2016
5.
Cognitive and
psychomotor
effects of three months of escitalopram treatment in elderly patients with major depressive disorder
作者:
Lieve Lia Beheydt
a
;
b
;
lieve.beheydt@uantwerpen.be" class="auth_mail" title="E-mail the corresponding author
Author Vitae
;
Didier Schrijvers
a
;
b
Author Vitae
;
Lise Docx
a
;
c
Author Vitae
;
Filip Bouckaert
d
Author Vitae
;
Wouter Hulstijn
a
Author Vitae
;
Bernard Sabbe
a
;
b
Author Vitae
关键词:
Major depression
;
Elderly
;
Psychomotor
retardation
;
Cognitive
;
Escitalopram
;
Functional burden
刊名:Journal of Affective Disorders
出版年:2015
6.
A case of 3p deletion syndrome associated with cerebellar hemangioblastoma
作者:
Sato Suzuki-Muromoto
a
;
Naomi Hino-Fukuyo
a
;
b
;
naomi-h@zc4.so-net.ne.jp" class="auth_mail" title="E-mail the corresponding author
;
Kazuhiro Haginoya
a
;
c
;
Atsuo Kikuchi
a
;
Hiroki Sato
a
;
Yuko Sato
a
;
Tojo Nakayama
a
;
Yuki Kubota
a
;
Yosuke Kakisaka
a
;
Mitsugu Uematsu
a
;
Toshihiro Kumabe
d
;
Shigeo Kure MD
a
关键词:
3p deletion syndrome
;
von Hippel&ndash
;
Lindau disease
;
Hemangioblastoma
;
Cerebellar hemangioblastoma
刊名:Brain and Development
出版年:2016
7.
The first Mongolian cases of phenylketonuria in selective screening of inborn errors of metabolism
作者:
Jamiyan Purevsuren
a
;
p_jamiyand@yahoo.com
;
Baasandai Bolormaa
a
;
Chogdon Narantsetseg
a
;
Renchindorj Batsolongo
a
;
Ochirbat Enkhchimeg
a
;
Munkhuu Bayalag
a
;
Yuki Hasegawa
b
;
Haruo Shintaku
c
;
SeijiYamaguchi
b
关键词:
Phenylketonuria
;
Inborn errors of metabolism
;
Mongolia
;
Screening
刊名:Molecular Genetics and Metabolism Reports
出版年:2016
8.
Psychomotor
retardation
is linked to frontal alpha asymmetry in major depression
作者:
Andrea Cantisani
a
;
b
;
andrea.cantisani@puk.unibe.ch" class="auth_mail" title="E-mail the corresponding author
;
andrea.cantisani@unifi.it" class="auth_mail" title="E-mail the corresponding author
;
Thomas Koenig
a
;
Helge Horn
a
;
Thomas Mü
;
ller
a
;
Werner Strik
a
;
Sebastian Walther
a
关键词:
Major depression
;
Psychomotor
disturbances
;
Actigraphy
;
EEG
;
Frontal alpha asymmetry
;
Alpha oscillations
刊名:Journal of Affective Disorders
出版年:2015
9.
Novel mutation in STXBP1 gene in a patient with non-lesional Ohtahara syndrome
作者:
L. Ortega-Moreno
a
;
b
;
B.G. Girá
;
ldez
a
;
b
;
A. Verdú
;
c
;
O. Garcí
;
a-Campos
c
;
G. Sá
;
nchez-Martí
;
n
a
;
b
;
J.M. Serratosa
a
;
b
;
joseserratosa@me.com" class="auth_mail" title="E-mail the corresponding author
;
R. Guerrero-Ló
;
pez
a
;
b
关键词:
Clinical genetics
;
Early-onset epileptic encephalopathy
;
Epilepsy
;
Ohtahara syndrome
;
STXBP1
刊名:Neurología (English Edition)
出版年:2016
10.
Five novel SUCLG1 mutations in three Chinese patients with succinate-CoA ligase deficiency noticed by mild methylmalonic aciduria
作者:
Yupeng Liu
;
Xiyuan Li
;
Qiao Wang
;
Yuan Ding
;
Jinqing Song
;
Yanling Yang
;
organic.acid@126.com" class="auth_mail" title="E-mail the corresponding author
;
yanlingy@vip.sina.com" class="auth_mail" title="E-mail the corresponding author
关键词:
Methylmalonic aciduria
;
Succinate-CoA ligase deficiency
;
Encephalomyopathy
;
Mitochondrial DNA depletion
;
SUCLG1
刊名:Brain and Development
出版年:2016
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