|1.||Hadchouel, Michelle: 2 articles (05/2007 - 09/2002)|
|2.||Crosnier, C: 2 articles (11/2000 - 09/2000)|
|3.||Hadchouel, M: 2 articles (11/2000 - 09/2000)|
|4.||Meunier-Rotival, M: 2 articles (11/2000 - 09/2000)|
|5.||Yachha, Surender Kumar: 1 article (01/2014)|
|6.||Srivastava, Anshu: 1 article (01/2014)|
|7.||Bolia, Rishi: 1 article (01/2014)|
|8.||Poddar, Ujjal: 1 article (01/2014)|
|9.||Goel, Deepak: 1 article (01/2014)|
|10.||Sutcuoglu, Sumer: 1 article (10/2013)|
02/01/2013 - "Paucity of interlobular bile ducts (PIBD), defined as absence or marked decrease in the number of interlobular bile ducts, is one of the causes of neonatal cholestasis. "
09/01/2009 - "Cholestasis was due to paucity of interlobular bile ducts (PILBD). "
09/01/2009 - "Concurrent course of transient neonatal diabetes with cholestasis and paucity of interlobular bile ducts: a case report."
11/01/2001 - "Chronic cholestasis secondary to paucity of interlobular bile ducts is traditionally both a clinical and a pathologic hallmark of this disease at diagnosis. "
05/01/1996 - "Sixteen Chinese children with cholestasis since early infancy were diagnosed to have paucity of interlobular bile ducts (PILBD) or its equivalent. "
06/01/1981 - "Syndromatic hepatic ductular hypoplasia (arteriohepatic dysplasia): a clinical and hepatic histologic study of three patients."
09/01/2000 - "The strong JAGGED1 expression during human embryo- and feto-genesis both in the vascular system and in other mesenchymal and epithelial tissues implicates abnormal angiogenesis in the pathogenesis of Alagille syndrome and particularly the paucity of interlobular bile ducts. "
01/01/1995 - "Fatty acid (FA) concentrations were studied in lymphocytes isolated from children with syndromic paucity of interlobular bile ducts (PILBD), Alagille syndrome. "
01/01/1995 - "Fatty acid content in lymphocytes from children with syndromic paucity of interlobular bile ducts, Alagille syndrome."
02/01/1987 - "Syndromic paucity of interlobular bile ducts (Alagille syndrome or arteriohepatic dysplasia): review of 80 cases."
07/01/1996 - "There was no statistically significant difference between Group 6 and Groups 3 and 4, but the MST of Group 5 was significantly shorter than those of Groups 3 and 4. Microscopic studies demonstrated marked portal and lobular infiltration and endothelialitis, as well as necrosis of the parenchyma and paucity of interlobular bile ducts in Groups 1, 2, and 5. While in Groups 3, 4, and 6 these findings were considerably mild. "
10/01/1996 - "Alagille syndrome (arteriohepatic dysplasia, AHD) is a well defined genetic disorder with five major features: distinctive facies, cardiovascular anomalies, paucity of interlobular bile ducts (PILBD), ocular anomalies and minor skeletal malformations. "
05/01/2007 - "Alagille syndrome (AGS; Online Mendelian Inheritance in Man no. 118450) is a multisystem autosomal dominant disorder with highly variable expression characterized by chronic cholestasis caused by a paucity of interlobular bile ducts, skeletal abnormalities, peculiar facies, ocular abnormalities, and cardiovascular disorders. "
03/01/2005 - "Alagille syndrome, a rare genetic disorder with autosomal dominant transmission, manifests 5 major features: paucity of interlobular bile ducts, characteristic facies, posterior embryotoxon, vertebral defects and peripheral pulmonic stenosis. "
04/01/2000 - "Alagille syndrome consists of 5 major features comprising paucity of interlobular bile ducts, characteristic facies, posterior embryotoxon, vertebral defects and peripheral pulmonic stenosis. "
01/01/1998 - "Alagille syndrome is a rare autosomal dominant developmental disorder, characterized by congenital paucity of interlobular bile ducts, peculiar facies, posterior embryotoxon, bone abnormalities, and peripheral pulmonary artery stenosis. "
10/01/2006 - "Three cases of PFIC are described that were diagnosed on the basis of family history, pruritus, cirrhosis and / or paucity of interlobular bile ducts on liver biopsy and presence of extrahepatic biliary tree on imaging. "
10/01/2001 - "A liver biopsy showed caseating granulomatous hepatitis with secondary portal fibrosis and paucity of interlobular bile ducts. "
01/01/1997 - "In addition to a paucity of interlobular bile ducts, histology revealed intracellular cholestasis in all, portal fibrosis in four, and regenerative nodules in two patients. "
01/01/1988 - "Morphologic findings of the liver in syndromatic paucity of intrahepatic bile ducts (SPIHBD) during infancy include paucity of interlobular bile ducts, features of "giant cell hepatitis," dilated lymphatics and veins in the portal tract, perisinusoidal fibrosis, and bile duct epithelial changes with a concentric layering of mesenchymal cells around bile ducts reminiscent of renal dysplasia. "
11/01/1984 - "From birth to four months of age, the pathology consistent of cholestasis, paucity of interlobular bile ducts and portal fibrosis. "
|1.||Linoleic Acid (Linoleate)
|7.||Fatty Acids (Saturated Fatty Acids)
|8.||Deoxyglucose (2 Deoxy D glucose)
|1.||Transplantation (Transplant Recipients)