Detalles de la búsqueda
1.
[Roles of axonal transport affected by K141N mutant HSP22 in the pathogenesis of CMT2L].
Zhonghua Yi Xue Za Zhi
; 92(7): 496-8, 2012 Feb 21.
Artículo
en Zh
| MEDLINE | ID: mdl-22490975
2.
[Mutation analysis of MFN2 gene in Chinese patients with Charcot-Marie-Tooth disease].
Zhonghua Yi Xue Za Zhi
; 89(47): 3324-7, 2009 Dec 22.
Artículo
en Zh
| MEDLINE | ID: mdl-20193559
3.
[Study on aggregate formation mechanism of HSPB8 gene mutation resulting in CMT2L].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 23(6): 601-4, 2006 Dec.
Artículo
en Zh
| MEDLINE | ID: mdl-17160934
4.
[Mutation analysis of small heat shock protein 27 gene in Chinese patients with Charcot-Marie-Tooth disease].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 22(5): 510-3, 2005 Oct.
Artículo
en Zh
| MEDLINE | ID: mdl-16215937
5.
[Detection of duplications or deletions of the PMP22 gene using real-time quantitative PCR].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 22(5): 537-40, 2005 Oct.
Artículo
en Zh
| MEDLINE | ID: mdl-16215943
6.
Mutation analysis of small heat-shock protein 22 gene in Chinese patients with Charcot-Marie-Tooth disease.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 22(4): 361-3, 2005 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-16086267
7.
Mutation screening of Cx32 in Han Chinese patients with Charcot-Marie-Tooth disease.
Beijing Da Xue Xue Bao Yi Xue Ban
; 37(1): 68-71, 2005 Feb 18.
Artículo
en Inglés
| MEDLINE | ID: mdl-15719046
8.
[Analysis of the pathological features and gene mutations of Chinese patients with Charcot-Marie-Tooth disease].
Zhonghua Yi Xue Za Zhi
; 85(34): 2382-5, 2005 Sep 07.
Artículo
en Zh
| MEDLINE | ID: mdl-16321242
9.
[The characteristics of gene mutations in Chinese patients with Charcot-Marie-Tooth disease].
Zhonghua Yi Xue Za Zhi
; 85(26): 1809-12, 2005 Jul 13.
Artículo
en Zh
| MEDLINE | ID: mdl-16253183
10.
[Clinical, pathological and genetic studies in a Chinese Charcot-Marie-Tooth disease type 2 family].
Zhejiang Da Xue Xue Bao Yi Xue Ban
; 34(6): 529-33, 2005 11.
Artículo
en Zh
| MEDLINE | ID: mdl-16331815
11.
C9orf72 mutation is rare in Alzheimer's disease, Parkinson's disease, and essential tremor in China.
Front Cell Neurosci
; 7: 164, 2013.
Artículo
en Inglés
| MEDLINE | ID: mdl-24068985
12.
Small heat-shock protein 22 mutated in autosomal dominant Charcot-Marie-Tooth disease type 2L.
Hum Genet
; 116(3): 222-4, 2005 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-15565283
Resultados
1 -
12
de 12
1
Próxima >
>>