Detalles de la búsqueda
1.
Diagnostic value of nerve conduction study in NOTCH2NLC-related neuronal intranuclear inclusion disease.
J Peripher Nerv Syst
; 28(4): 629-641, 2023 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-37749855
2.
Clinical features of NOTCH2NLC-related neuronal intranuclear inclusion disease.
J Neurol Neurosurg Psychiatry
; 93(12): 1289-1298, 2022 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-36150844
3.
Clinical features and CACNA1A gene mutation in a family with episodic ataxia type 2. / ä¸ä¸ªåä½æ§å ±æµå¤±è°2å家系ç临åºè¡¨ç°åCACNA1Aåºå çªå.
Zhong Nan Da Xue Xue Bao Yi Xue Ban
; 47(6): 801-808, 2022 Jun 28.
Artículo
en Inglés, Zh
| MEDLINE | ID: mdl-35837781
4.
Clinical and imaging features of idiopathic intracranial hypertension. / ç¹åæ§é¢ å åå¢é«ç临åºä¸å½±åå¦ç¹å¾.
Zhong Nan Da Xue Xue Bao Yi Xue Ban
; 46(11): 1241-1250, 2021 Nov 28.
Artículo
en Inglés, Zh
| MEDLINE | ID: mdl-34911859
5.
[Myopathy associated with anti-signal recognition peptide antibodies: Five case reports].
Zhong Nan Da Xue Xue Bao Yi Xue Ban
; 44(12): 1430-1436, 2019 Dec 28.
Artículo
en Zh
| MEDLINE | ID: mdl-31969510
6.
[Clinical and image features for 12 cases of cerebral autosomal dominant arteriopathy with the subcortical infarcts and leukoencephalopathy].
Zhong Nan Da Xue Xue Bao Yi Xue Ban
; 44(5): 549-554, 2019 May 28.
Artículo
en Zh
| MEDLINE | ID: mdl-31303619
7.
Identification of novel SPG11 mutations in a cohort of Chinese families with hereditary spastic paraplegia.
Int J Neurosci
; 128(2): 146-150, 2018 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-28933964
8.
[Etiologies and risk factors for young people with intracerebral hemorrhage].
Zhong Nan Da Xue Xue Bao Yi Xue Ban
; 43(11): 1246-1250, 2018 Nov 28.
Artículo
en Zh
| MEDLINE | ID: mdl-30643071
9.
PSAP variants in Parkinson's disease: a large cohort study in Chinese mainland population.
Brain
; 144(3): e25, 2021 04 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-33793763
10.
[NOTCH3 gene mutations in two Chinese families featuring cerebral autosomal dominant arteriopathy with subcortical infarct and leucoencephalopathy].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 34(6): 816-820, 2017 Dec 10.
Artículo
en Zh
| MEDLINE | ID: mdl-29188607
11.
[Clinical characteristics of hemichorea associated with non-ketotic hyperglycemia in 3 patients: case report and literature review].
Zhong Nan Da Xue Xue Bao Yi Xue Ban
; 42(11): 1341-1347, 2017 Nov 28.
Artículo
en Zh
| MEDLINE | ID: mdl-29187664
12.
Two cases of CLIPPERS with increased number of perivascular CD20-positive B lymphocytes.
Brain
; 141(10): e75, 2018 10 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-30202949
13.
Age of onset correlates with clinical characteristics and prognostic outcomes in neuromyelitis optica spectrum disorder.
Front Immunol
; 13: 1056944, 2022.
Artículo
en Inglés
| MEDLINE | ID: mdl-36569880
14.
Prolonged Hemiplegic Migraine Led to Persistent Hyperperfusion and Cortical Necrosis: Case Report and Literature Review.
Front Neurol
; 12: 748034, 2021.
Artículo
en Inglés
| MEDLINE | ID: mdl-34777219
15.
NOTCH3 Variants and Genotype-Phenotype Features in Chinese CADASIL Patients.
Front Genet
; 12: 705284, 2021.
Artículo
en Inglés
| MEDLINE | ID: mdl-34335700
16.
Olfactory Dysfunction and Its Relationship With Clinical Features of Parkinson's Disease.
Front Neurol
; 11: 526615, 2020.
Artículo
en Inglés
| MEDLINE | ID: mdl-33178098
17.
GCH1 variants contribute to the risk and earlier age-at-onset of Parkinson's disease: a two-cohort case-control study.
Transl Neurodegener
; 9(1): 31, 2020 08 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-32746945
18.
Non-coding RNA in Fragile X Syndrome and Converging Mechanisms Shared by Related Disorders.
Front Genet
; 10: 139, 2019.
Artículo
en Inglés
| MEDLINE | ID: mdl-30881383
19.
Clinical features and genetic characteristics of two Chinese pedigrees with fatal family insomnia.
Prion
; 13(1): 116-123, 2019 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-31122137
20.
Cerebellar Swelling Followed by Atrophy in Anti-Homer-3 Antibody Associated Cerebellitis.
Neurology
; 2022 Jul 20.
Artículo
en Inglés
| MEDLINE | ID: mdl-35858816