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Quoted phrase not found in phrase index: "Jaundice, familial obstructive, of infancy"
Page 1
Synopsis report from the pilot USA Kernicterus Registry.
Bhutani VK, Johnson L. Bhutani VK, et al. J Perinatol. 2009 Feb;29 Suppl 1:S4-7. doi: 10.1038/jp.2008.210. J Perinatol. 2009. PMID: 19177058
Innovative investigative strategies are needed to seek more sensitive surrogates for kernicterus (often diagnosed late in infancy) and to overcome the limitations of retrospective continuity of adverse neonatal experiences because of severe hyperbilirubinemia. ...Clinician …
Innovative investigative strategies are needed to seek more sensitive surrogates for kernicterus (often diagnosed late in infancy) an …
Cholelithiasis in infancy: a study of 40 cases.
Debray D, Pariente D, Gauthier F, Myara A, Bernard O. Debray D, et al. J Pediatr. 1993 Mar;122(3):385-91. doi: 10.1016/s0022-3476(05)83421-3. J Pediatr. 1993. PMID: 8441092
In the remaining 34 infants with lithiasis of the common duct or cystic duct or both, the initial symptoms were cholestatic jaundice in 21, acholic stools in 8, sepsis in 4, and abdominal pain in 1. ...These results suggest that common bile duct lithiasis should be conside …
In the remaining 34 infants with lithiasis of the common duct or cystic duct or both, the initial symptoms were cholestatic jaundice …
Progressive intrahepatic cholestasis of infancy and childhood. A clinicopathological study of patient surviving to the age of 18 years.
Jones EA, Rabin L, Buckley CH, Webster GK, Owens D. Jones EA, et al. Gastroenterology. 1976 Oct;71(4):675-82. Gastroenterology. 1976. PMID: 955355
A patient who developed chronic cholestatic jaundice during the 1st year of life and eventually died of liver cell failure at the age of 18 years is described. ...At autopsy, a mixed macronodular and micronodular cirrhosis was found and cholangiography and dissection of bi …
A patient who developed chronic cholestatic jaundice during the 1st year of life and eventually died of liver cell failure at the age …
PFIC type III in infant presenting as acute liver cell failure.
Zaki SA, Shanbag P, Amarapurkar A. Zaki SA, et al. Indian J Pathol Microbiol. 2010 Apr-Jun;53(2):334-6. doi: 10.4103/0377-4929.64326. Indian J Pathol Microbiol. 2010. PMID: 20551550
An eight-month-old female, delivered to consanguineous parents, presented with acute liver cell failure. Her investigations showed progressive cholestatic jaundice, high liver enzymes and high gamma-glutamyl transferase. Hepatitis and inborn errors of metabolism were exclu …
An eight-month-old female, delivered to consanguineous parents, presented with acute liver cell failure. Her investigations showed progressi …