Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Rong-Tai Cui"'
Autor:
Jia-tang Zhang, Chuanqiang Pu, Rong-Tai Cui, Li-Ping Dou, Chenglin Tian, Shengyuan Yu, Xusheng Huang
Publikováno v:
Hematological Oncology. 33:80-84
Information regarding the characteristics of pleural effusions in patients with POEMS syndrome is limited. The aim of this study was to describe the incidence and risk factors of pleural effusions in patients with POEMS syndrome and characterize the
Publikováno v:
Journal of Clinical Neurophysiology. 29:345-348
OBJECTIVE The purpose of this study was to evaluate the electrophysiological characteristics of polyneuropathy in POEMS syndrome. METHODS A total 46 patients with POEMS syndrome and 46 patients with chronic inflammatory demyelinating polyneuropathy (
Publikováno v:
Internal Medicine Journal. 41:481-485
Background/Aim: The clinical characteristics of POEMS (polyneuropathy, organomegaly, endocrinopathy, M-protein and skin changes) syndrome in China are largely unknown. This work thus studied the clinical manifestations of POEMS syndrome in China. Met
Autor:
Rong-Tai, Cui, Sheng-Yuan, Yu, Xu-Sheng, Huang, Jia-Tang, Zhang, Cheng-Lin, Tian, Li-Ping, Dou, Chuan-Qiang, Pu
Publikováno v:
Hematological oncology. 33(2)
Information regarding the characteristics of pleural effusions in patients with POEMS syndrome is limited. The aim of this study was to describe the incidence and risk factors of pleural effusions in patients with POEMS syndrome and characterize the
Publikováno v:
Journal of neurology. 261(1)
POEMS syndrome is a potentially fatal disease, and prediction of prognostic factors for POEMS syndrome is important for clinicians. Papilloedema is an early sign of the syndrome. The present study was carried out to evaluate whether papilloedema is a
Publikováno v:
Annals of hematology. 92(12)
The characteristics of ascites in patients with POEMS syndrome, which comprise polyneuropathy, organomegaly, endocrinopathy, M protein, and skin changes, are unknown. We described the frequency of ascites at presentation of POEMS syndrome and further
Publikováno v:
Neurology India. 62:257
Background: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) has been reported in many geographical regions. However, relatively few reports about CADASIL in Chinese were reported. Materials and Met
Publikováno v:
Neurology India; May/Jun2014, Vol. 62 Issue 3, p257-261, 5p