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1.
Neurology Asia ; : 373-376, 2017.
Article in English | WPRIM | ID: wpr-732052

ABSTRACT

Clinical mild encephalitis/encephalopathy with a reversible splenial lesion (MERS) is a clinicradiologicalsyndrome, which has been reported to be associated with many conditions and the mostcommon pathogens are virus. However, bacteria are rare pathogens for MERS. We report a 20-year-oldman diagnosed with definite infective endocarditis, who presented with transient encephalopathy withreversible lesions in the entire corpus callosum and bilateral white matter on magnetic resonance imaging(MRI). The blood culture indicated a Staphylococcus aureus infection. His neurological manifestationimproved and imaging abnormalities faded after receiving a combination of intravenous immunoglobulin,methylprednisolone, and antibiotics. Clinicians should be aware of transient encephalopathy withreversible callosal lesions as a potential unusual presentation of infective endocarditis.

2.
Neurology Asia ; : 203-206, 2014.
Article in English | WPRIM | ID: wpr-628468

ABSTRACT

A 23-year-old man in remission from acute myeloblastic leukemia after allogeneic peripheral blood stem cell transplantation developed peripheral neuropathy presenting as sciatic and peroneal nerve deficits. Electrophysiological tests localized the lesions to the left sciatic and common peroneal nerve. Magnetic resonance imaging revealed nerve thickening and enhancement, while a positron emission tomography-computed tomography scan demonstrated increased fluorodeoxyglucose uptake tracking along the nerve, suggesting peripheral nerve infiltration. This report demonstrates an unusual presentation of acute leukemia relapse presenting as focal neuropathy

3.
Journal of Huazhong University of Science and Technology (Medical Sciences) ; (6): 309-314, 2013.
Article in English | WPRIM | ID: wpr-343099

ABSTRACT

Physician payment system (PPS) is a principal incentive system to motivate doctors to provide excellent care for patients. During the past decade, physician remuneration in China has not been in proportional to physician's average work load and massive responsibilities. This paper reviewed the constitution of the PPS in China, and further discussed the problems and issues to be addressed with respect to pay for performance. Our study indicated that the lower basic salary and bonus distribution tied to "profits" was the major contributor to the physician's profit-driven incentive and the potential cause for the speedy growth of health expenditures. We recommend that government funding to hospitals should be increased to fully cover physicians' basic salary, a flexible human resource and talent management mechanism needs to be established that severs personal interest between physicians and hospitals, and modern performance assessment and multiplexed payment systems should be piloted to encourage physicians to get the more legitimate compensation.


Subject(s)
China , Models, Economic , National Health Programs , Economics , Physician Incentive Plans , Economics , Physicians , Economics , Salaries and Fringe Benefits , Economics
4.
Journal of Huazhong University of Science and Technology (Medical Sciences) ; (6): 309-14, 2013.
Article in English | WPRIM | ID: wpr-636428

ABSTRACT

Physician payment system (PPS) is a principal incentive system to motivate doctors to provide excellent care for patients. During the past decade, physician remuneration in China has not been in proportional to physician's average work load and massive responsibilities. This paper reviewed the constitution of the PPS in China, and further discussed the problems and issues to be addressed with respect to pay for performance. Our study indicated that the lower basic salary and bonus distribution tied to "profits" was the major contributor to the physician's profit-driven incentive and the potential cause for the speedy growth of health expenditures. We recommend that government funding to hospitals should be increased to fully cover physicians' basic salary, a flexible human resource and talent management mechanism needs to be established that severs personal interest between physicians and hospitals, and modern performance assessment and multiplexed payment systems should be piloted to encourage physicians to get the more legitimate compensation.

5.
Acta Physiologica Sinica ; (6): 351-358, 2006.
Article in Chinese | WPRIM | ID: wpr-265444

ABSTRACT

In the experiment, we designed and synthesized two siRNAs based on the sequence of nuclear receptor-related factor 1 (Nurr1) mRNA. They were separately subcloned into the plasmid of pSilenCircle (pSC) containing U6 promoter. The pSC-Nurr1 vectors (pSC-N1 and pSC-N2) specific to Nurr1 gene and the negative control vector of short-hairpin RNA (shRNA) eukaryotic expression vector were constructed. We cultured the dopaminergic cell line MN9D and the verified vectors were transfected with LipofectamineTM 2000 in vitro. The positive cell clones transfected with pSC were obtained after being screened with 500 mug/ml G418. After that, the silencing effects of Nurr1 and TH mRNA or protein were detected by real time RT-PCR and Western blot. The neurite extension of MN9D cells was observed and photographed by inverted microscope. The results showed that Nurr1 mRNA expression in MN9D cells was specifically down-regulated by the vectors of pSC-N1 and pSC-N2, and the silencing effects were 62.3% and 45.6%, respectively. The dopaminergic phenotype of TH mRNA was also suppressed significantly and the silencing effects were 76.3% and 62.6%, respectively. Meanwhile, the expressions of Nurr1 and TH proteins were also significantly suppressed, and the silencing effects of Nurr1 and TH protein were 57.4%, 72.0% and 79.1%, 70.1% respectively. The negative control and liposome groups had no effect on the two genes. In conclusion, Nurr1 shRNA expressing vectors can inhibit the expressions of Nurr1 and TH mRNA or protein in MN9D cells, and Nurr1 might play a role in neurite extension of MN9D cells. Nurr1 shRNA expressing vector may provide a novel applicable strategy for the study on the function of the genes associated with Parkinson disease and the development of dopaminergic neuron.


Subject(s)
Humans , Cell Line , Dopaminergic Neurons , Cell Biology , Metabolism , Down-Regulation , Fetus , Mesencephalon , Cell Biology , Neurites , Physiology , Nuclear Receptor Subfamily 4, Group A, Member 2 , Genetics , Metabolism , RNA, Messenger , Genetics , Metabolism , RNA, Small Interfering , Genetics , Transfection , Tyrosine 3-Monooxygenase , Genetics , Metabolism
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