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Page 1
The role of lipids in nephrosclerosis and glomerulosclerosis.
Gröne EF, Walli AK, Gröne HJ, Miller B, Seidel D. Gröne EF, et al. Atherosclerosis. 1994 May;107(1):1-13. doi: 10.1016/0021-9150(94)90136-8. Atherosclerosis. 1994. PMID: 7945552 Review.
Even though the significance of lipid deposition in renal tissue and the role of lipoproteins in the pathogenesis of renal disease in man is unclear, experimental and clinical data indicate a possible damaging effect of a disturbed lipid metabolism on the kidney. In humans, glome …
Even though the significance of lipid deposition in renal tissue and the role of lipoproteins in the pathogenesis of renal disease in man is …
Bile canalicular morphometry in arteriohepatic dysplasia.
Witzleben CL, Finegold M, Piccoli DA, Treem WR. Witzleben CL, et al. Hepatology. 1987 Nov-Dec;7(6):1262-6. doi: 10.1002/hep.1840070614. Hepatology. 1987. PMID: 3679090
The diagnosis of arteriohepatic dysplasia may be difficult, particularly in very young patients with no family history, and the pathogenesis of the disorder remains obscure. ...The results of these morphometric studies corroborated the previous observation th …
The diagnosis of arteriohepatic dysplasia may be difficult, particularly in very young patients with no family history, and th …
Arteriohepatic dysplasia: phenotypic features and family studies.
Mueller RF, Pagon RA, Pepin MG, Haas JE, Kawabori I, Stevenson JG, Stephan MJ, Blumhagen JD, Christie DL. Mueller RF, et al. Clin Genet. 1984 Apr;25(4):323-31. doi: 10.1111/j.1399-0004.1984.tb01998.x. Clin Genet. 1984. PMID: 6424981
Arteriohepatic dysplasia (AHD) is a disorder characterized by intrahepatic cholestasis and peripheral pulmonary artery stenosis. We have reviewed the phenotypic features in the 56 previously reported cases and 7 persons from our institutions with AHD to summarize th …
Arteriohepatic dysplasia (AHD) is a disorder characterized by intrahepatic cholestasis and peripheral pulmonary artery stenosi …
Arteriohepatic dysplasia. II. Hepatobiliary morphology.
Kahn EI, Daum F, Markowitz J, Aiges HW, Schneider KM, So HB, Altman P, Chandra RS, Silverberg M. Kahn EI, et al. Hepatology. 1983 Jan-Feb;3(1):77-84. doi: 10.1002/hep.1840030113. Hepatology. 1983. PMID: 6822378
Five children were noted to have arteriohepatic dysplasia (Alagille's syndrome) between 3 and 7 months of age. ...Hypoplasia of the gallbladder occurred in two patients. Changes were observed in the porta hepatis. Eighty of 208 micrometers bile ducts were ass …
Five children were noted to have arteriohepatic dysplasia (Alagille's syndrome) between 3 and 7 months of age. ...Hypoplasia o …
Glomerular mesangiolipidosis in Alagille syndrome (arteriohepatic dysplasia).
Habib R, Dommergues JP, Gubler MC, Hadchouel M, Gautier M, Odievre M, Alagille D. Habib R, et al. Pediatr Nephrol. 1987 Jul;1(3):455-64. doi: 10.1007/BF00849254. Pediatr Nephrol. 1987. PMID: 3153318
The extent of mesangiolipidosis was not related to age but to the degree of cholestasis, the most severe lesions being observed in patients aged 3, 6, 8, and 14 months. The glomerular lesions observed in Alagille syndrome are strikingly similar to those observed …
The extent of mesangiolipidosis was not related to age but to the degree of cholestasis, the most severe lesions being observed in pa …
Renal histopathology in Alagille's syndrome.
Russo PA, Ellis D, Hashida Y. Russo PA, et al. Pediatr Pathol. 1987;7(5-6):557-68. doi: 10.3109/15513818709161419. Pediatr Pathol. 1987. PMID: 3329721
Various renal abnormalities have been reported in Alagille's syndrome (arteriohepatic dysplasia), usually as single case reports. The renal findings at autopsy of four patients with Alagille's syndrome, ranging in age from 4 1/2 months to 7 years, 2 of whom had evid …
Various renal abnormalities have been reported in Alagille's syndrome (arteriohepatic dysplasia), usually as single case repor …
Anthropometric evaluation of children with chronic liver disease.
Sokol RJ, Stall C. Sokol RJ, et al. Am J Clin Nutr. 1990 Aug;52(2):203-8. doi: 10.1093/ajcn/52.2.203. Am J Clin Nutr. 1990. PMID: 2375285
Patients with arteriohepatic dysplasia showed more severe depression of all three variables. ...Depressions of midarm-circumference and midarm-muscle-area Z scores were intermediate. Mean-head-circumference Z score was depressed in children aged less t …
Patients with arteriohepatic dysplasia showed more severe depression of all three variables. ...Depressions of midarm-circumfe …
Syndromic paucity of interlobular bile ducts (Alagille syndrome or arteriohepatic dysplasia): review of 80 cases.
Alagille D, Estrada A, Hadchouel M, Gautier M, Odièvre M, Dommergues JP. Alagille D, et al. J Pediatr. 1987 Feb;110(2):195-200. doi: 10.1016/s0022-3476(87)80153-1. J Pediatr. 1987. PMID: 3806290
We have observed two types of paucity of interlobular bile ducts (PILBD) in children with chronic cholestasis: the syndromic type, which is more frequent (80 cases), and the nonsyndromic type (31 cases). ...Other less frequent features were observed in patients with …
We have observed two types of paucity of interlobular bile ducts (PILBD) in children with chronic cholestasis: the syndromic type, wh …
del(20p) with manifestations of arteriohepatic dysplasia.
Byrne JL, Harrod MJ, Friedman JM, Howard-Peebles PN. Byrne JL, et al. Am J Med Genet. 1986 Aug;24(4):673-8. doi: 10.1002/ajmg.1320240411. Am J Med Genet. 1986. PMID: 3740100
Mild peripheral pulmonic stenosis, skeletal anomalies, and cholestasis with paucity of intrahepatic bile ducts were observed, and she was diagnosed as having arteriohepatic dysplasia. ...
Mild peripheral pulmonic stenosis, skeletal anomalies, and cholestasis with paucity of intrahepatic bile ducts were observed, and she …
Localization of Alagille syndrome to 20p11.2-p12 by linkage analysis of a three-generation family.
Hol FA, Hamel BC, Geurds MP, Hansmann I, Nabben FA, Daniëls O, Mariman EC. Hol FA, et al. Hum Genet. 1995 Jun;95(6):687-90. doi: 10.1007/BF00209488. Hum Genet. 1995. PMID: 7789956 Free article.
Alagille syndrome (AGS) or arteriohepatic dysplasia is a rare but well-defined clinical entity that is usually inherited as an autosomal dominant trait. ...Linkage analysis was performed with markers from the 20p candidate region. A lod score of Z = 2.96 was …
Alagille syndrome (AGS) or arteriohepatic dysplasia is a rare but well-defined clinical entity that is usually inherited as an …
13 results