|1.||Kobayashi, Keiko: 27 articles (11/2012 - 01/2002)|
|2.||Saheki, Takeyori: 21 articles (11/2012 - 01/2002)|
|3.||Ushikai, Miharu: 7 articles (11/2012 - 01/2005)|
|4.||Iijima, Mikio: 7 articles (01/2008 - 02/2002)|
|5.||Song, Yuan-Zong: 6 articles (07/2011 - 04/2006)|
|6.||Ohura, Toshihiro: 5 articles (05/2009 - 10/2004)|
|7.||Hwu, Wuh-Liang: 4 articles (10/2012 - 11/2003)|
|8.||Kobayashi, K: 4 articles (01/2010 - 06/2008)|
|9.||Okano, Yoshiyuki: 4 articles (05/2009 - 11/2003)|
|10.||Tabata, Ayako: 4 articles (01/2008 - 11/2004)|
10/01/2012 - "A scoring system may help to differentiate patients with NICCD from those with biliary atresia."
11/01/2013 - "[A case of neonatal intrahepatic cholestasis caused by citrin deficiency complicated with congenital biliary atresia]."
10/21/2012 - "Thirty-two NICCD patients, 250 INC patients, and 39 infants with cholangiography-confirmed biliary atresia (BA) were enrolled. "
10/01/2012 - "The patients with NICCD tended to score ≥ 4 points, whereas biliary atresia and other infantile cholestasis tended to score <4 points (P < .0001). "
10/01/2012 - "To establish a scoring system, clinical features of 20 patients with NICCD diagnosed in Taiwan between the years 2000 and 2008 were compared with those of 47 patients with biliary atresia and 35 with infantile cholestasis. "
01/01/2010 - "Mutation study of the SLC25A13 gene showed the compound heterozygotes, 851del4 and IVS16ins3kb, which confirmed the diagnosis of NICCD in the patient and her three-year-old female sibling, who also had unexplained neonatal cholestasis. "
07/01/2012 - "NICCD should be suspected in the presence of cholestasis during infancy. "
01/01/2012 - "NICCD should be considered in infants with idiopathic cholestasis. "
12/01/2011 - "The presence of AGC2 deficiency in other ethnic groups besides Asian population suggests further consideration for NICCD diagnosis of any neonate with an unexplained cholestasis; a prompt diagnosis is crucial to resolve the metabolic decompensation with an appropriate dietary treatment."
12/01/2011 - "NICCD arises within the first few weeks of life resulting in prolonged cholestasis and metabolic abnormalities including aminoacidemia and galactosuria. "
05/01/2006 - "Metabolic and genetic studies for NICCD should be performed in Asian infants with idiopathic intrahepatic cholestasis and hepatic steatosis. "
01/01/2012 - "Mutations of the SLC25A13 gene are responsible for neonatal intrahepatic cholestasis (NICCD) and adult-onset type II citrullinemia (CTLN2). "
12/01/2011 - "AGC2 deficiency is an autosomal recessive disorder with two age related phenotypes: neonatal intrahepatic cholestasis (NICCD, OMIM#605814) and adult-onset type II citrullinemia (CTLN2, OMIM#603471). "
04/01/2010 - "Twenty-six patients with NICCD were collected because of idiopathic intrahepatic cholestasis and jaundice. "
06/01/2015 - "Citrin deficiency causes neonatal intrahepatic cholestasis (NICCD), which usually resolves within the first year of life. "
12/01/2011 - "In this study we report a new Caucasian case of NICCD, a seven week old Romanian boy with prolonged jaundice. "
01/01/2012 - "Jaundice resolved in all NICCD and in 87.5% of non-NICCD infants at the median age of 9.5 and 4.0 months, respectively. "
04/01/2010 - "The NICCD patients showed low birth weight and the average onset of jaundice was 29 days. "
01/01/2010 - "The diagnosis of NICCD should be considered in infants with unexplained prolonged jaundice. "
06/01/2008 - "Clinically, CTLN2 is characterized by hyperammonaemia and citrullinaemia, whereas NICCD has a much more varied and transient presentation that can include multiple aminoacidaemias, hypoproteinaemia, galactosaemia, hypoglycaemia, and jaundice. "
|5.||Obstructive Jaundice (Cholestatic Jaundice)
01/01/2012 - "To study the prevalence of NICCD and SLC25A13 mutations in Thai infants, and to compare manifestations of NICCD and non-NICCD, infants with idiopathic cholestatic jaundice or INH were enrolled. "
06/01/2010 - "NICCD should be considered in the differential diagnosis of cholestatic jaundice in Malaysian infants regardless of ethnic origin."
12/01/2007 - "NICCD should be considered in the differential diagnosis of cholestatic jaundice in Korean infants."
|1.||Neonatal-onset citrullinemia type 2
|1.||Transplantation (Transplant Recipients)
|2.||Total Parenteral Nutrition