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108篇 您的检索式:作者名="LAURENS C"
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1Nutritional and health benefits of semi-elemental diets: A comprehensive summary of the literature显示文摘AIM:To critically review and summarize the literature on nutritional and health outcomes of semi-elemental formulations on various nutritionally vulnerable patient populations who are unable to achieve adequate nutrition from standard oral diets.METHODS:We conducted a comprehensive literature search of Pubmed and Embase databases.We manually screened articles that examined nutritional and health outcomes(e.g.,growth,disease activity,gastrointestinal impairment,mortality,and economic impact)among various patient groups receiving semi-elemental diets.This review focused on full-text articles of randomized controlled clinical trials and other intervention studies,but pertinent abstracts and case studies were also included.Results pertaining primarily to tolerance,digestion,and absorption were summarized for each patient population in this systematic review.RESULTS:Results pertaining primarily to tolerance,digestion,and absorption were summarized for each patient population.The efficacy of semi-elemental whey hydrolyzed protein(WHP)diet have been reported in various nutritionally high risk patient populations including-Crohn’s disease,short bowel syndrome,acute and chronic pancreatitis,cerebral palsy,cystic fibrosis,cerebrovascular accidents,human immunodeficiency virus,critically ill,and geriatrics.Collectively,the evidence from the medical literature indicates that feeding with a semi-elemental diet performs as well or better than parenteral or amino acid based diets in terms of toler-ance,digestion,and nutrient assimilation measures across various disease conditions.CONCLUSION:Based on this comprehensive review of the literature,patient populations who have difficulty digesting or absorbing standard diets may be able to achieve improved health and nutritional outcomes through the use of semi-elemental WHP diets.Dominik D Alexander Lauren C Bylsma Laura Elkayam Douglas L Nguyen 2016World Journal of Gastrointestinal Pharmacology and Therapeutics2016,7,2:3
2Gangrenous cholecystitis: A silent but potential fatal disease in patients with diabetic neuropathy. A case report显示文摘Gangrenous cholecystitis(GC) is a severe and potentially deadly complication of acute cholecystitis. We present a 83-year-old gentleman with a past medical history of type 2 diabetes mellitus with significant associated neuropathy, presenting to a community hospital in a major metropolitan area with 10 days nausea and vomiting and a benign abdominal exam. While the patient was admitted for hyperglycemia, he was subsequently found to have severe GC requiring urgent surgical intervention.Melorin Mehrzad Charles C Jehle Lauren O Roussel Raman Mehrzad 2018World Journal of Clinical Cases2018,6,15:3
3Chromodomain-helicase-DNA binding protein 5, 7 and pronecrotic mixed lineage kinase domain-like protein serve as potential prognostic biomarkers in patients with resected pancreatic adenocarcinomas显示文摘Pancreatic cancer is one of the deadliest cancers with a very poor prognosis. Recently, there has been a significant increase in research directed towards identifying potential biomarkers that can be used to diagnose and provide prognostic information for pancreatic cancer. These markers can be used clinically to optimize and personalize therapy for individual patients. In this review, we focused on 3 biomarkers involved in the DNA damage response pathway and the necroptosis pathway: Chromodomainhelicase-DNA binding protein 5, chromodomain-helicaseDNA binding protein 7, and mixed lineage kinase domain-like protein. The aim of this article is to review present literature provided for these biomarkers and current studies in which their effectiveness as prognostic biomarkers are analyzed in order to determine their future use as biomarkers in clinical medicine. Based on the data presented, these biomarkers warrant further investigation,and should be validated in future studies.Crystal S Seldon Lauren E Colbert William A Hall Sarah B Fisher David S Yu Jerome C Landry 2016World Journal of Gastrointestinal Oncology2016,8,4:2
4Aberrant p53 protein expression is associated with an increased risk of neoplastic progression in patients with Barrett’s oesophagus显示文摘Florine Kastelein Katharina Biermann Ewout W Steyerberg Joanne Verheij Marit Kalisvaart Leendert H J Looijenga Hans A Stoop Laurens Walter Ernst J Kuipers Manon C W Spaander Marco J Bruno 2013Gut2013,,12:2
5Hydrogen peroxide fluxes and compartmentalization inside growing Escherichia coli 显示文摘Lauren C S James A I 2001J Bacteriol2001,183,24:1
6Cross-cultural differences in test perceptions: Women in Kuwait and the United States Journal of Cross-Cultural Psychology 显示文摘Jerrell C Cassady Ayoub Mohammed Lauren Mathieu 2004Thousand oaks:2004,35,6:1
7Differential Diagnosis of infantile hemangiomas显示文摘Lauren C Garzon MC 0,,08:1
8Management of radial head fractures:current concepts显示文摘Laurens Kaas Jesse B Jupiter C 0,,01:1
9Management of radial head fractures: current concepts 显示文摘Laurens Kaas Jesse B Jupiter C 2011Shoulder & Elbow2011,3,:1
10Establishment of a bioenergy-focused microalgal culture collection显示文摘ELLIOTT L G FEEHAN C LAURENS L M L 2012Algal Research2012,1,2:1
11Human mesenchymal stem cell subpopulations express a variety of neuro-regulatory molecules and promote neuronal cell survival and neuritogenesis显示文摘Lauren C Robey D Amy A 2006Exp Neurol2006,198,2:1
12Evidence of suboptimal management of cardiovascular risk in patients with type 2 diabetes mellitus and symp- tomatic atherosclerosis显示文摘Lauren C Jeffrey A Sumit R 2004CMAJ2004,171,10:1
13Assessment of functional recovery and axonal sprouting in oligodendrocyte myelin glycoprotein(OMgp) null mice after spinal cord injury显示文摘Benxiu J Lauren C 2008Mol Cell Neurosci2008,39,2:1
14Optimizing bioavailability in the treatment of Parkinson's disease显示文摘Lauren C Seeberger Robert A 2007Neuropharmacdogy2007,53,7:1
15Gas chromatographic-mass spectrometric confirmation of atractyloside in a patient poisoned with Callilepis laureola显示文摘Laurens J B Bekker L C Steenkamp V 2001J Chromatogr B2001,765,2:1
16Sensory Properties of Ginseng Solutions Modified by Masking Agents 显示文摘Lauren C Tamamoto Shelly J Schmidt Soo-Yeun Lee 2010Journal of Food Science2010,75,7:1
17Nitriding of titanium under CW CO2 laser radiation显示文摘Laurens P L'enfant H Sainte Catherine M C 1997Thin Solid Films1997,293,:1
18Improving hilt report fo CUS and consistency with the situation, background, assess- ment, recommendation protocol 显示文摘Paul C Mary T G Lauren Y J 2013Journal of Nursing Ad- ministration2013,43,78:1
19Anterior versus posterior spinal instrumentation for the treatment of thoracolumbar curves in adolescent idiopathic scoliosis显示文摘David L Lauren F Kasey C 2003Spine2003,28,5:1
20Tranexamic acid for intracerebral haemorrhage within 2 hours of onset: protocol of a phase Ⅱ randomised placebo-controlled double-blind multicentre trial显示文摘Rationale Haematoma growth is common early after intracerebral haemorrhage(ICH),and is a key determinant of outcome.Tranexamic acid,a widely available antifibrinolytic agent with an excellent safety profile,may reduce haematoma growth.Methods and design Stopping intracerebral haemorrhage with tranexamic acid for hyperacute onset presentation including mobile stroke units(STOP-MSU)is a phase Ⅱ double-blind,randomised,placebo-controlled,multicentre,international investigator-led clinical trial,conducted within the estimand statistical framework.Hypothesis In patients with spontaneous ICH,treatment with tranexamic acid within 2 hours of onset will reduce haematoma expansion compared with placebo.Sample size estimates A sample size of 180 patients(90 in each arm)would be required to detect an absolute difference in the primary outcome of 20%(placebo 39%vs treatment 19%)under a two-tailed significance level of 0.05.An adaptive sample size re-estimation based on the outcomes of 144 patients will allow a possible increase to a prespecified maximum of 326 patients.Intervention Participants will receive 1 g intravenous tranexamic acid over 10 min,followed by 1 g intravenous tranexamic acid over 8 hours;or matching placebo.Primary efficacy measure The primary efficacy measure is the proportion of patients with haematoma growth by 24±6 hours,defined as either≥33%relative increase or≥6 mL absolute increase in haematoma volume between baseline and follow-up CT scan.Discussion We describe the rationale and protocol of STOP-MSU,a phase Ⅱ trial of tranexamic acid in patients with ICH within 2 hours from onset,based in participating mobile stroke units and emergency departments.Nawaf Yassi Henry Zhao Leonid Churilov Bruce C V Campbell Teddy Wu Henry Ma Andrew Cheung Timothy Kleinig Helen Brown Philip Choi Jiann-Shing Jeng Annemarei Ranta Hao-Kuang Wang Geoffrey C Cloud Rohan Grimley Darshan Shah Neil Spratt Der-Yang Cho Karim Mahawish Lauren Sanders John Worthington Ben Clissold Atte Meretoja Vignan Yogendrakumar Mai Duy Ton Duc Phuc Dang Nguyen Thai My Phuong Huy-Thang Nguyen Chung Y Hsu Gagan Sharma Peter J Mitchell Bernard Yan Mark W Parsons Christopher Levi Geoffrey A Donnan Stephen M Davis 2022Stroke & Vascular Neurology2022,7,2:1
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