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| 1 | Glycogenic hepatopathy:A narrative review显示文摘Glycogenic hepatopathy(GH) is a rare complication of the poorly controlled diabetes mellitus characterized by the transient liver dysfunction with elevated liver enzymes and associated hepatomegaly caused by the reversible accumulation of excess glycogen in the hepatocytes. It is predominantly seen in patients with longstanding type 1 diabetes mellitus and rarely reported in association with type 2 diabetes mellitus. Although it was first observed in the pediatric population, since then, it has been reported in adolescents and adults with or without ketoacidosis. The association of GH with hyperglycemia in diabetes has not been well established. One of the essential elements in the pathophysiology of development of GH is the wide fluctuation in both glucose and insulin levels. GH and non-alcoholic fatty liver disease(NAFLD) are clinically indistinguishable, and latter is more prevalent in diabetic patients and can progress to advanced liver disease and cirrhosis. Gradient dual-echo MRI can distinguish GH from NAFLD; however, GH can reliably be diagnosed only by liver biopsy. Adequate glycemic control can result in complete remission of clinical, laboratory and histological abnormalities. There has been a recent report of varying degree of liver fibrosis identified in patients with GH. Future studies are required to understand the biochemical defects underlying GH, noninvasive, rapid diagnostic tests for GH, and to assess the consequence of the fibrosis identified as severe fibrosis may progress to cirrhosis. Awareness of this entity in the medical community including specialists is low. Here we briefly reviewed the English literature on pathogenesis involved, recent progress in the evaluation, differential diagnosis, and management. | Jagannath M Sherigar Joline De Castro Yong Mei Yin Debra Guss Smruti R Mohanty | 2018 | World Journal of Hepatology2018，10，2： | 7 |
| 2 | Exporting the software engineering component in MIS research 显示文摘 | JOLINE M JOEY F | 1995 | Comm of the ACM1995，38，7： | 1 |
| 3 | Use of set accelerating admixtures in dry-mix shotcrete 显示文摘 | Jolin M Beaupre D Pigeon M | 1997 | Journal of Materials In Civil Engineer1997，9，4： | 1 |
| 4 | Effect of equipment on spray ve- locity distribution in shotcrete applications 显示文摘 | Ginouse N Jolin M Bissonnette B | 2014 | Construction and Building Materials2014，70，： | 1 |
| 5 | EGR - 1 enhances tumor growth and modulates the effect of the Wilms tumorl gene products on tumorigenicity显示文摘 | Volkher S Aswin L M Jolin A | 2000 | Oncogene2000，19，： | 1 |
| 6 | Understanding the pumpability of concrete显示文摘 | JOLIN M BURNS D BISSONNETTE B | 2009 | Proceedings of Shotcrete for Un- derground Support XI2009，，： | 1 |
| 7 | Exporing the Software Engineering Component in MIS Research显示文摘 | JOLINE M JOEY F G | 2000 | Communication of the ACM2000，38，7： | 1 |
| 8 | Pumping con- crete :A aundamental and practical approach显示文摘 | JOLIN M CHAPDELAINE F GAGNON F | 2006 | Shotcrete2006，，： | 1 |
| 9 | Understanding wet - mix shotcrete : mixdesign, specifications, and placement显示文摘 | JOLIN M BEAUPRI D | 2003 | Shotcrete2003，，9： | 1 |
| 10 | Group 2 innate lymphoid cells expressfunctional NKp30 receptor inducing type 2 cytokine produc- tion显示文摘 | Salimi M Xue L Jolin H | 2016 | J Immunol2016，196，1： | 1 |
| 11 | Antigen load and viral se- quence diversification determine the functional profile of HIV-l-specific CD8+ T cells 显示文摘 | Streeck H Brumme ZL Anastario M Cohen KW Jolin JS Meier A Brumme CJ Rosenberg ES Alter G Allen TM Walker BD Altfeld M | 2008 | PLoS Med2008，5，5： | 1 |
| 12 | Understanding Wet-mix Shotcrete:Mix De- sign, Specifications, and Placement 显示文摘 | JOLIN M BEAUPRE D | 2003 | Shotcrete2003，，： | 1 |
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