Detalles de la búsqueda
1.
Clinical manifestations and spinal cord magnetic resonance imaging findings in Chinese neuromyelitis optica patients.
Eur Neurol
; 71(1-2): 35-41, 2014.
Artículo
en Inglés
| MEDLINE | ID: mdl-24281652
2.
Changes of c-fos, malondialdehyde and lactate in brain tissue after global cerebral ischemia under different brain temperatures.
J Huazhong Univ Sci Technolog Med Sci
; 34(3): 354-358, 2014 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-24939298
3.
High frequency of Machado-Joseph disease identified in southeastern Chinese kindreds with spinocerebellar ataxia.
BMC Med Genet
; 11: 47, 2010 Mar 25.
Artículo
en Inglés
| MEDLINE | ID: mdl-20334689
4.
A novel mutation in the senataxin gene identified in a Chinese patient with sporadic amyotrophic lateral sclerosis.
Amyotroph Lateral Scler
; 10(2): 118-22, 2009 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-19058054
5.
[Characteristics of gene structure in facioscapulohumeral muscular dystrophy-related 4q35 subtelomere and genotype-phenotype correlation in Chinese Han population].
Zhonghua Yi Xue Za Zhi
; 89(5): 304-9, 2009 Feb 10.
Artículo
en Zh
| MEDLINE | ID: mdl-19563705
6.
Association between Ngb polymorphisms and ischemic stroke in the Southern Chinese Han population.
BMC Med Genet
; 9: 110, 2008 Dec 16.
Artículo
en Inglés
| MEDLINE | ID: mdl-19087291
7.
Novel mutation in the ABCA1 gene identified in a chinese patient with dementia and atherothrombotic cerebral infarction.
Dement Geriatr Cogn Disord
; 26(3): 234-8, 2008.
Artículo
en Inglés
| MEDLINE | ID: mdl-18841006
8.
[Deficient mRNA expression of specific protein 3 gene in peripheral blood mononuclear cells from patients with multiple sclerosis].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 25(2): 187-9, 2008 Apr.
Artículo
en Zh
| MEDLINE | ID: mdl-18393243
9.
Molecular analysis and prenatal prediction of spinal muscular atrophy in Chinese patients by the combination of restriction fragment length polymorphism analysis, denaturing high-performance liquid chromatography, and linkage analysis.
Arch Neurol
; 64(2): 225-31, 2007 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-17296838
10.
Mutation analysis of 218 Chinese patients with Wilson disease revealed no correlation between the canine copper toxicosis gene MURR1 and Wilson disease.
J Mol Med (Berl)
; 84(5): 438-42, 2006 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-16649058
11.
[Analysis of alleles 4qA and 4qB of the chromosome 4q subtelomere in Chinese Han population].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 24(3): 334-7, 2007 Jun.
Artículo
en Zh
| MEDLINE | ID: mdl-17557251
12.
New Insights into Genotype-phenotype Correlations in Chinese Facioscapulohumeral Muscular Dystrophy: A Retrospective Analysis of 178 Patients.
Chin Med J (Engl)
; 128(13): 1707-13, 2015 Jul 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-26112708
13.
Molecular diagnosis and prophylactic therapy for presymptomatic Chinese patients with Wilson disease.
Arch Neurol
; 60(5): 737-41, 2003 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-12756138
14.
[Study on EcoR I fragment polymorphism of the subtelomeric domains within 4q35 and 10q26 with pulsed field gel electrophoresis in the Chinese population].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 21(6): 552-6, 2004 Dec.
Artículo
en Zh
| MEDLINE | ID: mdl-15583980
15.
[The quantitative analysis of protein particles of erythrocyte membrane from Duchenne muscular dystrophy patients and the gene carriers].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 21(1): 68-9, 2004 Feb.
Artículo
en Zh
| MEDLINE | ID: mdl-14767914
16.
[Genotype-phenotype correlation of patients with wilson disease in Chinese population].
Zhonghua Yi Xue Za Zhi
; 83(4): 309-11, 2003 Feb 25.
Artículo
en Zh
| MEDLINE | ID: mdl-12812649
17.
[Mechanism of translocation between chromosomes 4q and 10q in facioscapulohumeral muscular dystrophy].
Zhonghua Yi Xue Za Zhi
; 83(8): 650-3, 2003 Apr 25.
Artículo
en Zh
| MEDLINE | ID: mdl-12887821
18.
Variations of IGHMBP2 gene was not the major cause of Han Chinese patients with non-5q-spinal muscular atrophies.
J Child Neurol
; 29(8): NP35-9, 2014 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-24022109
19.
Noninvasive urine-derived cell lines derived from neurological genetic patients.
Neuroreport
; 24(4): 161-6, 2013 Mar 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-23358449
20.
Molecular analysis of SMN1, SMN2, NAIP, GTF2H2, and H4F5 genes in 157 Chinese patients with spinal muscular atrophy.
Gene
; 518(2): 325-9, 2013 Apr 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-23352792