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| 1 | Transjugular intrahepatic portosystemic shunt in cirrhosis: An exhaustive critical update显示文摘More than five decades after it was originally conceptualized as rescue therapy for patients with intractable variceal bleeding,the transjugular intrahepatic portosystemic shunt(TIPS)procedure continues to remain a focus of intense clinical and biomedical research.By the impressive reduction in portal pressure achieved by this intervention,coupled with its minimally invasive nature,TIPS has gained increasing acceptance in the treatment of complications of portal hypertension.The early years of TIPS were plagued by poor long-term patency of the stents and increased incidence of hepatic encephalopathy.Moreover,the diversion of portal flow after placement of TIPS often resulted in derangement of hepatic functions,which was occasionally severe.While the incidence of shunt dysfunction has markedly reduced with the advent of covered stents,hepatic encephalopathy and instances of early liver failure continue to remain a significant issue after TIPS.It has emerged over the years that careful selection of patients and diligent post-procedural care is of paramount importance to optimize the outcome after TIPS.The past twenty years have seen multiple studies redefining the role of TIPS in the management of variceal bleeding and refractory ascites while exploring its application in other complications of cirrhosis like hepatic hydrothorax,portal hypertensive gastropathy,ectopic varices,hepatorenal and hepatopulmonary syndromes,non-tumoral portal vein thrombosis and chylous ascites.It has also been utilized to good effect before extrahepatic abdominal surgery to reduce perioperative morbidity and mortality.The current article aims to review the updated literature on the status of TIPS in the management of patients with liver cirrhosis. | Sasidharan Rajesh Tom George Cyriac Abby Philips Rizwan Ahamed Sandeep Kumbar Narain Mohan Meera Mohanan Philip Augustine | 2020 | World Journal of Gastroenterology2020，26，37： | 26 |
| 2 | Nanocomposites and bone regeneration显示文摘这张手稿用设计策略的织物集中于骨头修理 / 新生,并且加亮导致新奇 nanocomposite 系统的 nanobiotechnology 开发。大约 650 万破裂在美国每年发生,并且大约 550,000 个这些单个盒子要求了骨头接枝的申请。自然发生并且 allogenous 骨头最广泛地为骨头接枝被使用了基于的治疗;然而,象施主缺乏和感染的风险那样有重要问题。用合成、自然的 biomaterials 的选择被开发了,并且一些为要求骨头接枝的临床的应用程序是商业地可得到的。然而,设计很仔细模仿骨头织物在结构上,和罐头的理想的合成接枝仍然是大挑战在造骨细胞和祖先房间人口调制需要的功能。Nanobiomaterials,明确地, nanocomposites hydroxyapatite 创作了(哈) 或骨胶原极其正在答应接枝代用品。biocomposites 能被制作模仿本国的骨头织物的材料作文,并且另外,当使用 nano 时 -- 哈(减少的谷物尺寸) ,一个人模仿本国的骨头的结构的安排。骨头生物学和结构的好理解对骨头 mimicking 接枝代用品的开发批评。哈并且能进一步调制 regenerative/healing 的优秀 osteoconductive 性质处理跟随破裂损害的骨胶原展览。与另外的聚合 biomaterials 结合将增强因此做新奇 nano 的机械性质 -- 哈比得上人的骨头的基于的 composites。我们用 nanocomposites 在最近的研究上报导为部分骨头缺点的新生作为粒子和 nanofibers 被制作了。在 nanocomposites 的研究,在理想的未来发展加亮一个枢轴的角色整形外科植入设备,然而进一步的重要前进是必要的完成临床的使用。 | Roshan JAMES Meng DENG Cato T. LAURENCIN Sangamesh G. KUMBAR | 2011 | Frontiers of Materials Science2011，5，4： | 5 |
| 3 | 查看详情显示文摘 | S G Kumbar S P Nukavarapu R James L S Nair C T Laurencin | | 0，，： | 1 |
| 4 | Pulmonary hypertension in peritoneal dialysis patients 显示文摘 | Kumbar L Fein PA Rafiq MA | 2007 | Adv Perit Dial2007，23，： | 1 |
| 5 | The receptor tyrosine kinase EphB4 is overexpressed in ovarian cancer, provides survival signals and predicts poor outcome 显示文摘 | Kumbar S R Masood R Spannuth W A | 2007 | Br J Cancer2007，96，7： | 1 |
| 6 | Electrospun poly(lacticacid-co-glycolic acid)scaffolds for skin tissue engineering显示文摘 | Kumbar S G Nukavarapu S P James R | 2008 | Biomaterials2008，29，： | 1 |
| 7 | Biological y active chitosan systems for tissue engineering and regenerative medicine显示文摘 | Jiang T Kumbar SG Nair LS | | 0，，04： | 1 |
| 8 | Biodegradable polyphosphazene - nanohydroxyapatite composite nanofibers : scaffolds for bone tissue engineering 显示文摘 | Bhattacharyya S Kumbar SG Khan YM | 2009 | J Biota Nanotechnol2009，5，： | 1 |
| 9 | Biologically active chitosan systems for tissue engineering and regenerative medicine显示文摘 | Jiang T Kumbar SG Nair LS | | 0，，04： | 1 |
| 10 | Tendon tissue engineering:adipose-derived stem cell and GDF-5 mediated regeneration using electrospun matrix systems显示文摘 | James R Kumbar SG Laurencin CT | | 0，，02： | 1 |
| 11 | Miscibility and in vitro osteocompatibility of biodegradable blends of poly[(ethyl alanato) ( p -phenyl phenoxy) phosphazene] and poly(lactic acid-glycolic acid)显示文摘 | Meng Deng Lakshmi S. Nair Syam P. Nukavarapu Sangamesh G. Kumbar Tao Jiang Nicholas R. Krogman Anurima Singh Harry R. Allcock Cato T. Laurencin | 2007 | Biomaterials2007，，3： | 1 |
| 12 | Pulmonary hypertension in perito- neal dialysis patients显示文摘 | Kumbar L Fein PA Rafiq MA | 2007 | Adv Petit Dial2007，23，： | 1 |
| 13 | Surveillance and moni- toring of dialysis access 显示文摘 | Kumbar L Karim J Besarab A | 2011 | International Journal of Nephrology2011，10，11： | 1 |
| 14 | A preliminary report on a novel electrospray tech- nique for nanoparticle based biomedical implants coating:Precision electrospraying显示文摘 | KUMBAR S G BHATTACHARYYA S SETHURAMAN S | 2007 | Journal of Biomedical Materials Research Part B Applied Biomaterials2007，81，1： | 1 |
| 15 | Electrospun poly (lactic acid-co-glycolic acid) scaffolds for skin tissue engineering显示文摘 | Kumbar S G Nukavarapu S P James R | 2008 | Biomaterials2008，29，30： | 1 |
| 16 | Adapter molecule DOC-2 is differentially expressed in pressure and volume overload hypertrophy and inhibits collagen synthesis in cardiac fibroblasts 显示文摘 | Kumbar D H VanBergen A Ocampo C | 2007 | J Appl Physiol2007，102，5： | 1 |
| 17 | Pervaporation separation of water and dioxane mixtures with sodium alginate-g-polyacrylamide copolymeric membranes显示文摘 | Kurkuri M D Kumbar S G Aminabhavi T M | 2003 | J Appl Polym Sci2003，89，： | 1 |
| 18 | Complications of arteriovenous fistulae: be- yond venous stenosis显示文摘 | Kumbar L | 2012 | Adv Chronic Kidney Dis2012，19，3： | 1 |
| 19 | Novel mechanically competent polysaccharide scaffolds for bone tissue engi- neering显示文摘 | Kumbar SG Toti US Deng M | 2011 | Biomed Mater2011，6，6： | 1 |
| 20 | Electrospun nanofiber scaffolds: engineering soft tissues 显示文摘 | Kumbar SG James R Nukavarapu SP | 2008 | Biomed Ma- ter2008，3，3： | 1 |
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