Detalles de la búsqueda
1.
[Efficacy and safety of cyclophosphamide as a sequential immunotherapy drug for anti-N-methyl-D-aspartate receptor encephalitis in children].
Zhongguo Dang Dai Er Ke Za Zhi
; 19(6): 668-671, 2017 Jun.
Artículo
en Zh
| MEDLINE | ID: mdl-28606234
2.
IgLON5 autoimmunity in a patient with Creutzfeldt-Jakob disease: case report and review of literature.
Front Neurol
; 15: 1367361, 2024.
Artículo
en Inglés
| MEDLINE | ID: mdl-38572492
3.
DNA hypermethylation of NOTCH2NLC in neuronal intranuclear inclusion disease: a case-control study.
J Neurol
; 269(11): 6049-6057, 2022 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-35857137
4.
Novel PANK2 Mutations in Patients With Pantothenate Kinase-Associated Neurodegeneration and the Genotype-Phenotype Correlation.
Front Aging Neurosci
; 14: 848919, 2022.
Artículo
en Inglés
| MEDLINE | ID: mdl-35462688
5.
ADGRV1 Variants in Febrile Seizures/Epilepsy With Antecedent Febrile Seizures and Their Associations With Audio-Visual Abnormalities.
Front Mol Neurosci
; 15: 864074, 2022.
Artículo
en Inglés
| MEDLINE | ID: mdl-35813073
6.
CHD4 variants are associated with childhood idiopathic epilepsy with sinus arrhythmia.
CNS Neurosci Ther
; 27(10): 1146-1156, 2021 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-34109749
7.
Is elevated SUA associated with a worse outcome in young Chinese patients with acute cerebral ischemic stroke?
BMC Neurol
; 10: 82, 2010 Sep 18.
Artículo
en Inglés
| MEDLINE | ID: mdl-20849639
8.
The clinical study of POEMS syndrome in China.
Neuro Endocrinol Lett
; 31(2): 229-37, 2010.
Artículo
en Inglés
| MEDLINE | ID: mdl-20424579
9.
Analysis of SCA2 and SCA3/MJD repeats in Parkinson's disease in mainland China: genetic, clinical, and positron emission tomography findings.
Mov Disord
; 24(13): 2007-11, 2009 Oct 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-19672991
10.
[Clinical manifestations and detection of pantothenate kinase 2 gene mutation in a patient with Hallervorden-Spatz syndrome].
Zhonghua Yi Xue Za Zhi
; 89(47): 3320-3, 2009 Dec 22.
Artículo
en Zh
| MEDLINE | ID: mdl-20193558
11.
Ataxia with novel compound heterozygous PEX10 mutations and a literature review of PEX10-related peroxisome biogenesis disorders.
Clin Neurol Neurosurg
; 177: 92-96, 2019 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-30640048
12.
[Study on the single-nucleotide substitution (c.-16C to T) of the PURATROPHIN-1 gene in Chinese patients with spinocerebellar ataxia].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 25(6): 646-8, 2008 Dec.
Artículo
en Zh
| MEDLINE | ID: mdl-19065522
13.
[Studies on the CTA/CTG trinucleotide repeats of ATXN8OS gene in Chinese Hans].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 25(5): 511-4, 2008 Oct.
Artículo
en Zh
| MEDLINE | ID: mdl-18841561
14.
A novel CLN2/TPP1 mutation in a Chinese patient with late infantile neuronal ceroid lipofuscinosis.
Neurogenetics
; 12(1): 93-5, 2011 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-20820830
15.
[Clinical characteristics and molecular biology of hereditary spinocerebellar ataxia type 7: study of 3 Chinese families].
Zhonghua Yi Xue Za Zhi
; 86(25): 1755-8, 2006 Jul 04.
Artículo
en Zh
| MEDLINE | ID: mdl-17054842
16.
[Frequency of different subtypes of spinocerebellar ataxia in the Han nationality of Hunan province in China].
Zhong Nan Da Xue Xue Bao Yi Xue Ban
; 31(5): 702-5, 2006 Oct.
Artículo
en Zh
| MEDLINE | ID: mdl-17062934
17.
Acute dystonia induced by lamivudine.
Clin Neuropharmacol
; 28(4): 193-4, 2005.
Artículo
en Inglés
| MEDLINE | ID: mdl-16062101
18.
[Clinical features and treatment of giant cell arteritis in Chinese, a prospective study].
Zhonghua Yi Xue Za Zhi
; 82(7): 453-5, 2002 Apr 10.
Artículo
en Zh
| MEDLINE | ID: mdl-12133513
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