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- Carbone, Marco2
- Alisi, Anna1
- Alvaro, Domenico1
- Balsano, Clara1
- Braga, Marco1
- Brunetto, Maurizia R1
- Bruno, Savino1
- Burra, Patrizia1
- Canonico, Pier Luigi1
- Cavalcoli, Federica1
- Craxi, Antonio1
- Floreani, Annarosa1
- Gardini, Ivan1
- Gasbarrini, Antonio1
- Kruger, Paola1
- Lanati, Elena1
- Marzioni, Marco1
- Massironi, Sara1
- Mells, George F1
- Mennini, Francesco Saverio1
- Muratori, Luigi1
- Piscaglia, Fabio1
- Rausa, Emanuele1
- Ronca, Vincenzo1
Keyword
- Alkaline phosphatase1
- Artificial intelligence1
- Big data1
- Budesonide1
- Deep learning1
- Fibrates1
- Hepatology1
- Home-based parenteral nutrition (HPN)1
- Intestinal failure1
- Intestinal transplantation1
- liver diseases1
- Machine learning1
- Malabsorption1
- Obeticholic acid1
- Precision medicine1
- Primary biliary cholangitis1
- Risk-stratification1
- Short bowel syndrome (SBS)1
- Teduglutide1
- Ursodeoxycholic acid1
Reviews
4 Results
- Review
The application of artificial intelligence in hepatology: A systematic review
Digestive and Liver DiseaseVol. 54Issue 3p299–308Published online: July 12, 2021- Clara Balsano
- Anna Alisi
- Maurizia R. Brunetto
- Pietro Invernizzi
- Patrizia Burra
- Fabio Piscaglia
- and others
Cited in Scopus: 4The integration of human and artificial intelligence (AI) in medicine has only recently begun but it has already become obvious that intelligent systems can dramatically improve the management of liver diseases. Big data made it possible to envisage transformative developments of the use of AI for diagnosing, predicting prognosis and treating liver diseases, but there is still a lot of work to do. If we want to achieve the 21st century digital revolution, there is an urgent need for specific national and international rules, and to adhere to bioethical parameters when collecting data. - Review Article
Understanding short bowel syndrome: Current status and future perspectives
Digestive and Liver DiseaseVol. 52Issue 3p253–261Published online: December 28, 2019- Sara Massironi
- Federica Cavalcoli
- Emanuele Rausa
- Pietro Invernizzi
- Marco Braga
- Maurizio Vecchi
Cited in Scopus: 49Short bowel syndrome (SBS) is a rare malabsorptive disorder as a result of the loss of bowel mass mostly secondary to surgical resection of the small intestine. Other causes are vascular diseases, neoplasms or inflammatory bowel disease. The spectrum of the disease is widely variable from single micronutrient malabsorption to complete intestinal failure, depending on the remaining length of the small intestine, the anatomical portion of intestine and the function of the remnant bowel. Over the last years, the management of affected patients has remarkably improved with the increase in patients’ quality of life and survival, mainly thanks to advances in home-based parenteral nutrition (PN). - Special ArticleOpen Access
Primary Biliary Cholangitis: advances in management and treatment of the disease
Digestive and Liver DiseaseVol. 49Issue 8p841–846Published online: May 8, 2017- Pietro Invernizzi
- Annarosa Floreani
- Marco Carbone
- Marco Marzioni
- Antonio Craxi
- Luigi Muratori
- and others
Cited in Scopus: 20Primary Biliary Cholangitis, previously known as Primary Biliary Cirrhosis, is a rare disease, which mainly affects women in their fifth to seventh decades of life. It is a chronic autoimmune disease characterized by a progressive damage of interlobular bile ducts leading to ductopenia, chronic cholestasis and bile acids retention. Even if the disease usually presents a long asymptomatic phase and a slow progression, in many patients it may progress faster toward cirrhosis and its complications. - Review Article
Toward precision medicine in primary biliary cholangitis
Digestive and Liver DiseaseVol. 48Issue 8p843–850Published online: June 17, 2016- Marco Carbone
- Vincenzo Ronca
- Savino Bruno
- Pietro Invernizzi
- George F. Mells
Cited in Scopus: 9Primary biliary cholangitis is a chronic, cholestatic liver disease characterized by a heterogeneous presentation, symptomatology, disease progression and response to therapy. In contrast, clinical management and treatment of PBC is homogeneous with a ‘one size fits all’ approach. The evolving research landscape, with the emergence of the -omics field and the availability of large patient cohorts are creating a unique opportunity of translational epidemiology. Furthermore, several novel disease and symptom-modifying agents for PBC are currently in development.