Translating research into practice: lessons from trials of thrombolysis in acute stroke [0.03%]
从溶栓治疗急性卒中的试验谈如何把科研成果应用于临床实践
Graham Venables
Graham Venables
There exist individual, institutional and national barriers to change, none more so than when introducing new therapies into medical practice especially those that involve organizational change. This paper, presented as an address to the jo...
Sanjeev V Thomas
Sanjeev V Thomas
Hemi orolingual angioedema [0.03%]
半舌黏膜血管性水肿
Dheeraj Khurana,Mukesh Sharma,Sudesh Prabhakar
Dheeraj Khurana
S Raghavendra,V Vibhin,H K Anand
S Raghavendra
Sanjeev V Thomas
Sanjeev V Thomas
Epilepsia partialis continua in mitochondrial dysfunction: Interesting phenotypic and MRI observations [0.03%]
线粒体功能异常的局灶性运动性癫痫持续状态的临床及MRI表现分析
Kalyani Karkare,Sanjib Sinha,Shivashankar Ravishankar et al.
Kalyani Karkare et al.
An 11-year-old girl manifested with photophobia, ptosis, external ophthalmoplegia, hypotonia, weakness of proximal limb muscles, hyporeflexia, and generalized seizures (six months). Her elder sister had had uncontrolled seizures and photoph...
A Nalini,Arundhati Biswas
A Nalini
We report the case of a 16-year-old boy diagnosed to have Sotos syndrome, with rare association of bilateral primary optic atrophy and epilepsy. He presented with accelerated linear growth, facial gestalt, distinctive facial features, seizu...
Giant cell arteritis (temporal arteritis): A report of four cases from north east India [0.03%]
巨细胞动脉炎（颞动脉炎）：印度东北部四例报告
Judy Laldinpuii,Pratap Sanchetee,Adityendra Lal Borah et al.
Judy Laldinpuii et al.
Giant cell arteritis (GCA) is a common disease of the geriatric age group in the western world, with a prevalence of 0.2% in the fifty plus age group. It is an important cause of morbidity, with irreversible visual loss being the most omino...
N Gayathri,T C Yasha,Makarand Kanjalkar et al.
N Gayathri et al.
Fabry's disease, an X linked recessive disorder caused by the deficiency of alpha-galactosidase A (alpha-gal A), leads to progressive accumulation of glycosphingolipids. We report this rare disease in a 19-year-old boy who presented with an...
Mohan L Noone,V G Pradeep Kumar,K Ummer et al.
Mohan L Noone et al.
Cirrhosis presenting as Parkinsonism is a distinct subset of acquired chronic hepatocerebral degeneration. The entity is not rare, and unless suspected, cirrhosis can easily be overlooked. We report our experience with three such patients. ...