Detalhe da pesquisa
1.
Intronic pentanucleotide TTTCA repeat insertion in the SAMD12 gene causes familial cortical myoclonic tremor with epilepsy type 1.
Brain
; 141(8): 2280-2288, 2018 08 01.
Artigo
Inglês
| MEDLINE | ID: mdl-29939203
2.
A comparison of six clock-drawing test scoring methods in a nursing home.
Aging Clin Exp Res
; 30(7): 775-781, 2018 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-29022271
3.
Clinical and neurophysiological features of familial cortical myoclonic tremor with epilepsy.
Mov Disord
; 31(11): 1704-1710, 2016 11.
Artigo
Inglês
| MEDLINE | ID: mdl-27613677
4.
pERK1/2 silencing sensitizes pancreatic cancer BXPC-3 cell to gemcitabine-induced apoptosis via regulating Bax and Bcl-2 expression.
World J Surg Oncol
; 13: 66, 2015 Feb 21.
Artigo
Inglês
| MEDLINE | ID: mdl-25880226
5.
[Genetic and clinical analysis in a Parkinson's disease family caused by expansion of SCA2].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 32(6): 776-9, 2015 Dec.
Artigo
Chinês
| MEDLINE | ID: mdl-26663046
6.
Fine mapping and whole-exome sequencing of a familial cortical myoclonic tremor with epilepsy family.
Am J Med Genet B Neuropsychiatr Genet
; 168(7): 595-9, 2015 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-26130016
7.
[A pedigree with dentatorubralpallidolyysian atrophy].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 34(6): 934-935, 2017 Dec 10.
Artigo
Chinês
| MEDLINE | ID: mdl-29188634
8.
[Silver syndrome: report of a family with 5 cases].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 30(4): 500, 2013 Aug.
Artigo
Chinês
| MEDLINE | ID: mdl-23926023
9.
Genetic analysis of the CHCHD2 gene in a cohort of Chinese patients with Parkinson disease.
Neurosci Lett
; 629: 116-118, 2016 08 26.
Artigo
Inglês
| MEDLINE | ID: mdl-27353515
10.
Genetic analysis of the CHCHD2 gene in Chinese patients with familial essential tremor.
Neurosci Lett
; 634: 104-106, 2016 Nov 10.
Artigo
Inglês
| MEDLINE | ID: mdl-27717833
11.
BSCL2 S90L mutation in a Chinese family with Silver syndrome with a review of the literature.
J Clin Neurosci
; 22(2): 429-30, 2015 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-25487175
12.
Genetic analysis of SPG4 and SPG3A genes in a cohort of Chinese patients with hereditary spastic paraplegia.
J Neurol Sci
; 347(1-2): 368-71, 2014 Dec 15.
Artigo
Inglês
| MEDLINE | ID: mdl-25454648
13.
Genetic analysis of the TMEM230 gene in Chinese patients with familial Parkinson disease.
Parkinsonism Relat Disord
; 36: 105-106, 2017 03.
Artigo
Inglês
| MEDLINE | ID: mdl-28038866