Institution
Leicester General Hospital
Healthcare•Leicester, United Kingdom•
About: Leicester General Hospital is a healthcare organization based out in Leicester, United Kingdom. It is known for research contribution in the topics: Population & Transplantation. The organization has 2481 authors who have published 3034 publications receiving 107437 citations.
Topics: Population, Transplantation, Diabetes mellitus, Kidney, Kidney disease
Papers published on a yearly basis
Papers
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TL;DR: The CCKNOW score provides a valuable index of overall knowledge and is self-administered and psychometric tests show it to be valid, reliable, and readable.
148 citations
Coventry University1, McMaster University2, Kaiser Permanente3, Leicester General Hospital4, Case Western Reserve University5, University of Pennsylvania6, University of Wisconsin-Madison7, University of Warwick8, University of Washington9, Worcestershire Acute Hospitals NHS Trust10, Harvard University11, Johns Hopkins University12, Houston Methodist Hospital13, Queen's University Belfast14, St Mary's Hospital15, Mayo Clinic16, University of East Anglia17, University of Manchester18, University Hospital Southampton NHS Foundation Trust19, University of Adelaide20, Queen Alexandra Hospital21, Katholieke Universiteit Leuven22, Shiraz University of Medical Sciences23, Nottingham University Hospitals NHS Trust24, University of Amsterdam25, Oregon Health & Science University26, University of Pittsburgh27, University of Chicago28, University of Nottingham29, University of Arizona30, Utrecht University31, Fox Chase Cancer Center32, Washington University in St. Louis33, National University of Singapore34, Durham University35, Otto-von-Guericke University Magdeburg36, University of British Columbia37, Gloucestershire Hospitals NHS Foundation Trust38, University Hospitals Coventry and Warwickshire NHS Trust39
TL;DR: An international, multidisciplinary, systematic search and evidence-based review of Barrett’s esophagus and provided consensus recommendations for clinical use in patients with nondysplastic, indefinite, and low-grade dysplasia (LGD).
146 citations
Boston Children's Hospital1, Université de Montréal2, Scott & White Hospital3, University of Toronto4, Imperial College London5, Leicester General Hospital6, John Radcliffe Hospital7, University of Washington8, LSU Health Sciences Center Shreveport9, Leiden University10, Columbia University11, Case Western Reserve University12, Mayo Clinic13, University of Amsterdam14, Vanderbilt University15, Western Infirmary16, German Cancer Research Center17, Johns Hopkins University18, St. Vincent's Health System19, University of Florida20, University of North Carolina at Chapel Hill21, University of Alabama at Birmingham22, Jikei University School of Medicine23, The Chinese University of Hong Kong24, Nanjing University25, Austral University of Chile26, University of Bari27, Juntendo University28, Peking University29, Erasmus University Rotterdam30, Wakayama Medical University31
TL;DR: The cross-sectional correlation between pathology and proteinuria was similar in adults and children and the predictive value of each specific lesion on the rate of decline of renal function or renal survival in IgA nephropathy was not different between children and adults.
146 citations
TL;DR: Pay-for-performance incentives have not addressed disparities in the management and control of diabetes between ethnic groups and quality improvement initiatives must place greater emphasis on minority communities to avoid continued disparities in mortality from cardiovascular disease and the other major complications of diabetes.
Abstract: The Wandsworth Primary Care Research Centre and the
Wandsworth Prospective Diabetes Study are funded by the Department of Health. The Wandsworth Prospective Diabetes Study has also received support from the Medical
Research Council through the Virtual Organisation of Trials and Epidemiological Studies (VOTES) project.
146 citations
TL;DR: A better understanding of this process and the effect of disease may allow better selection of patients for partial hepatectomy and allow an insight into the possible application of clinical stimulation of regeneration.
Abstract: Background:
Partial hepatectomy is the strongest stimulator of hepatic regeneration. The process of initiation and the control of the final size of the regenerated liver have been the subject of research for many years. A better understanding of this process and the effect of disease may allow better selection of patients for partial hepatectomy. It may also allow an insight into the possible application of clinical stimulation of regeneration.
Methods:
Data were reviewed from the published literature using the Medline database.
Results:
Most knowledge comes from in vitro studies and the study of resection in the rat model. A variety of cytokines, hormones and growth factors are involved in regeneration but very few have been found capable of stimulating regeneration in vitro. The exact interactions are not known, but there is probably a cascade involving different factors at differing stages of regeneration.
Conclusion:
Further in vivo research should allow greater understanding of liver regeneration, thereby providing a potential therapeutic tool in patients for whom regeneration has failed, or is likely to fail. Such research is also important in respect of liver support devices, which may inhibit liver regeneration by filtration of many of the factors involved. © 2002 British Journal of Surgery Society Ltd
145 citations
Authors
Showing all 2487 results
| Name | H-index | Papers | Citations |
|---|---|---|---|
| Janet Treasure | 114 | 831 | 44104 |
| John P. Neoptolemos | 112 | 648 | 52928 |
| Paul Moayyedi | 104 | 531 | 36144 |
| Alex J. Sutton | 95 | 307 | 47411 |
| Traolach S. Brugha | 95 | 215 | 81818 |
| Kamlesh Khunti | 91 | 1030 | 37429 |
| Melanie J. Davies | 89 | 814 | 36939 |
| Kenneth J. O'Byrne | 87 | 629 | 39193 |
| Martin Roland | 86 | 410 | 31220 |
| Keith R. Abrams | 86 | 355 | 30980 |
| Charles D. Pusey | 83 | 422 | 30154 |
| Hans W. Hoek | 82 | 263 | 81606 |
| Richard Poulsom | 80 | 242 | 20567 |
| Alex J. Mitchell | 79 | 251 | 24227 |
| David C. Wheeler | 77 | 328 | 25238 |