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| 1 | Chikungunya, an epidemic arbovirosis显示文摘 | Gilles Pialoux Bernard-Alex Gaüzère Stéphane Jauréguiberry Michel Strobel | 2007 | The Lancet Infectious Diseases2007，，5： | 2 |
| 2 | Methane yield from switchgrass harvested at different stages of development in Eastern Canada显示文摘 | Daniel Massé Yan Gilbert Philippe Savoie Gilles Bélanger Gaétan Parent Daniel Babineau | 2010 | Bioresource Technology2010，，24： | 1 |
| 3 | Comparison of CT findings in symptomatic and incidentally discovered pheochromocytomas显示文摘 | Motta-Ramirez GA Remer EM Herts BR Gill IS Hamrahian AH | | 0，，03： | 1 |
| 4 | Cell biology of laryngeal epithelial defenses in health and disease:further studies显示文摘 | Johnston N Bulmer D Gill GA | 2003 | Ann Otol Rhinol Laryngol2003，112，6： | 1 |
| 5 | Perceived Versus Actual Sedation Practices in Adult Intensive Care Unit Patients Receiving Mechanical Ventilation显示文摘 | Gill KV Voils SA Chenault GA | 2012 | The Annals of Pharmacotherapy2012，46，10： | 1 |
| 6 | Chikungunya, an epidemic arbovirosis显示文摘 | Gilles Pialoux Bernard-Alex Gaüzère Stéphane Jauréguiberry Michel Strobel | 2007 | The Lancet Infectious Diseases2007，，5： | 1 |
| 7 | Fit3 ligand-receptor interaction is important for maintenance of early thymic pro- genitor numbers in steady-state thymopoiesis显示文摘 | Kenins L Gill JW Hollinder GA | 2010 | Eur J Immu nol2010，40，1： | 1 |
| 8 | Plasma citrulline kinetics and prognostic value in critically ill patients显示文摘 | Ga?l Piton Cyril Manzon Elisabeth Monnet Benoit Cypriani Olivier Barbot Jean-Christophe Navellou Franck Carbonnel Gilles Capellier | 2010 | Intensive Care Medicine2010，，4： | 1 |
| 9 | Blocking brain-derived neurotrophic factor inhibits injury-in- duced hyperexcitability of hippocampal CA3 neu- rons显示文摘 | Gill R Chang PK Prenosil GA | 2013 | Eur J Neurosci2013，38，11： | 1 |
| 10 | Cell biology of laryngeal epithelial defenses in health and disease: further studies显示文摘 | Johnston N Bulmer D Gill GA | 2003 | Ann Otol Rhinol Laryngol2003，112，： | 1 |
| 11 | Nitrous oxide emissions from secondary activated sludge in nitrifying conditions of urban wastewater treatment plants: Effect of oxygenation level显示文摘 | Ga?lle Tallec Josette Garnier Gilles Billen Michel Gousailles | 2006 | Water Research2006，，15： | 1 |
| 12 | Cell biology of laryngeal epithelial defences in health and disease: further studies显示文摘 | Johnston N Bulmer D Gill GA | 2003 | Ann Otol Rhinol Laryngol2003，112，6： | 1 |
| 13 | Laryngeal epithelial defences against laryngopharyngeal reflux: investigations of e-cadherin, carbonic anhydrase isoenzyme III, and pepsin 显示文摘 | Gill GA Johnston N Buda A | 2005 | Ann Otol Rhinol La~cngol2005，114，12： | 1 |
| 14 | Laryngeal epithelial defenses against laryngopharyngeal reflux : investigations of E-cadherin, carbonic anhydrase isoenzyme III, and pepsin 显示文摘 | Gill GA Johnston N Buda A | 2005 | Ann Otol Rhinol Laryngo12005，114，： | 1 |
| 15 | Low phospholipid-associated cholelithiasis syndrome:A rare cause of acute pancreatitis that should not be neglected显示文摘BACKGROUND Low phospholipid-associated cholelithiasis(LPAC)syndrome is a very particular form of biliary lithiasis with no excess of cholesterol secretion into bile,but a decrease in phosphatidylcholine secretion,which is responsible for stones forming not only in the gallbladder,but also in the liver.LPAC syndrome may be underreported due to a lack of testing resulting from insufficient awareness among clinicians.AIM To describe the clinical and radiological characteristics of patients with LPAC syndrome to better identify and diagnose the disease.METHODS We prospectively evaluated all patients aged over 18 years old who were consulted or hospitalized in two hospitals in Paris,France(Bichat University Hospital and Croix-Saint-Simon Hospital)between January 1,2017 and August 31,2018.All patients whose profiles led to a clinical suspicion of LPAC syndrome underwent a liver ultrasound examination performed by an experienced radiologist to confirm the diagnosis of LPAC syndrome.Twenty-four patients were selected.Data about the patients’general characteristics,their medical history,their symptoms,and their blood tests results were collected during both their initial hospitalization and follow-up.Cytolysis and cholestasis were expressed compared to the normal values(N)of serum aspartate and alanine transaminase activities,and to the normal value of alkaline phosphatase level,respectively.The subjects were systematically reevaluated and asked about their symptoms 6 mo after inclusion in the study through an in-person medical appointment or phone call.Genetic testing was not performed systematically,but according to the decision of each physician.RESULTS Most patients were young(median age of 37 years),male(58%),and not overweight(median body mass index was 24).Many had a personal history of acute pancreatitis(54%)or cholecystectomy(42%),and a family history of gallstones in first-degree relatives(30%).LPAC syndrome was identified primarily in patients with recurring biliary pain(88%)or after a new episode of acute pancreatitis(38%).When present,cytolysis and cholestasis were not severe(2.8N and 1.7N,respectively)and disappeared quickly.Interestingly,four patients from the same family were diagnosed with LPAC syndrome.At ultrasound examination,the most frequent findings in intrahepatic bile ducts were comet-tail artifacts(96%),microlithiasis(83%),and acoustic shadows(71%).Computed tomography scans and magnetic resonance imaging were performed on 15 and three patients,respectively,but microlithiasis was not detected.Complications of LPAC syndrome required hospitalizing 18 patients(75%)in a conventional care unit for a mean duration of 6.8 d.None of them died.Treatment with ursodeoxycholic acid(UDCA)was effective and well-tolerated in almost all patients(94%)with a rapid onset of action(3.4 wk).Twelve patients’(67%)adherence to UDCA treatment was considered“good.”Five patients(36%)underwent cholecystectomy(three of them were treated both by UDCA and cholecystectomy).Despite UDCA efficacy,biliary pain recurred in five patients(28%),three of whom adhered well to treatment guidelines.CONCLUSION LPAC syndrome is easy to diagnose and treat;therefore,it should no longer be overlooked.To increase its detection rate,all patients who experience recurrent biliary symptoms following an episode of acute pancreatitis should undergo an ultrasound examination performed by a radiologist with knowledge of the disease. | Nicolas Gille Pascale Karila-Cohen Gaël Goujon Dimitrios Konstantinou Samia Rekik Hakim Bécheur Anne-Laure Pelletier | 2020 | World Journal of Hepatology2020，12，6： | 1 |
| 16 | Cell biology of laryngeal epithe- lial defenses in health and disease: further studies 显示文摘 | Johnston N Bulmer D Gill GA | 2003 | Ann Otol Rhi- nol Laryngol2003，112，6： | 1 |
| 17 | Cell biology of laryngeal epithelial defenses in health and disease: further studies显示文摘 | Johnston N Bulmer D Gill GA | 2003 | Ann Otol Rhinol Laryngol2003，112，6： | 1 |
| 18 | Benthic ex- change of nutrients in Galveston Bay, Texas显示文摘 | Warnken KW Gill GA Santschi PH | 2000 | Estuaries2000，23，5： | 1 |
| 19 | Laryngeal epithelial de-fenses against laryngopharyngeal reflux: investigations of E-cadherin, carbonic anhydrase isoenzyme III,and pepsin显示文摘 | Gill GA Johnstoti N Buola A | 2005 | Ann Otol Rhinol Laryngol2005，114，： | 1 |
| 20 | Deletion of PKB alpha/Akt1 affects thymic development显示文摘 | Fayard E Gill J Paolino M Hynx D Hollnder GA Hemmings BA | 2007 | PLoS One2007，2，10： | 1 |
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