日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Coexisting rathke cleft cyst and pituitary adenoma presenting with pituitary apoplexy: report of two cases

两例同时存在的拉特克囊肿合并垂体腺瘤并发垂体卒中:报告

Gessler, Florian; Coon, Valerie C; Chin, Steven S; Couldwell, William T

Clinical, histological and genetic characterization of reducing body myopathy caused by mutations in FHL1.

FHL1基因突变引起的还原体肌病的临床、组织学和遗传学特征

Schessl Joachim, Taratuto Ana L, Sewry Caroline, Battini Roberta, Chin Steven S, Maiti Baijayanta, Dubrovsky Alberto L, Erro Marcela G, Espada Graciela, Robertella Monica, Saccoliti Maria, Olmos Patricia, Bridges Leslie R, Standring Peter, Hu Ying, Zou Yaqun, Swoboda Kathryn J, Scavina Mena, Goebel Hans-Hilmar, Mitchell Christina A, Flanigan Kevin M, Muntoni Francesco, Bönnemann Carsten G

Creutzfeldt-Jakob disease (CJD) with a mutation at codon 148 of prion protein gene: relationship with sporadic CJD

克雅氏病(CJD)伴有朊病毒蛋白基因148密码子突变:与散发性克雅氏病的关系

Pastore, Manuela; Chin, Steven S; Bell, Karen L; Dong, Zhiqian; Yang, Qiwei; Yang, Lizhu; Yuan, Jue; Chen, Shu G; Gambetti, Pierluigi; Zou, Wen-Quan

A pathogenic peripherin gene mutation in a patient with amyotrophic lateral sclerosis

肌萎缩侧索硬化症患者的致病性外周蛋白基因突变

Leung, Conrad L; He, Cui Zhen; Kaufmann, Petra; Chin, Steven S; Naini, Ali; Liem, Ronald K H; Mitsumoto, Hiroshi; Hays, Arthur P

Signature tau neuropathology in gray and white matter of corticobasal degeneration

皮质基底节变性灰质和白质中的特征性tau蛋白神经病理学

Forman, Mark S; Zhukareva, Victoria; Bergeron, Catherine; Chin, Steven S-M; Grossman, Murray; Clark, Chris; Lee, Virginia M-Y; Trojanowski, John Q