Neonatal intrahepatic cholestasis caused by citrin deficiency in Korean infants. - Wikidata - awgldk - TriplyDB

Neonatal intrahepatic cholestasis caused by citrin deficiency in Korean infants.

Neonatal intrahepatic cholestasis caused by citrin deficiency in Korean infants.

http://www.wikidata.org/entity/Q37223088

about

Neonatal intrahepatic cholestasis caused by citrin deficiency: prevalence and SLC25A13 mutations among Thai infants.Biochemical characteristics of neonatal cholestasis induced by citrin deficiency Clinical and ABCB11 profiles in Korean infants with progressive familial intrahepatic cholestasis Hypermethioninemias of genetic and non-genetic origin: A review.Blood glucose and insulin and correlation of SLC25A13 mutations with biochemical changes in NICCD patients.Analysis of islet beta cell functions and their correlations with liver dysfunction in patients with neonatal intrahepatic cholestasis caused by citrin deficiency (NICCD).

P2860

Q34445980-08D9FD73-E5DD-4FC6-A753-634D7558BB0A Q36351930-1CF3D06C-28CD-44FB-81C8-FC44EE4F2BEB Q36919455-6F97BCDE-52E2-43AB-850D-4A0BA4C80B60 Q37838882-4108A434-B1E1-495A-A8E5-1828B2207913 Q44730334-F301146C-87ED-45C7-82A8-C976A941F226 Q46834245-9C85C283-AAF5-41A8-9626-C1FB33B12DCD

P2860

Neonatal intrahepatic cholestasis caused by citrin deficiency in Korean infants.

http://www.wikidata.org/entity/Q37223088

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

@tr

scientific article published on December 2007

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Neonatal intrahepatic cholestasis caused by citrin deficiency in Korean infants.

@en

Neonatal intrahepatic cholestasis caused by citrin deficiency in Korean infants.

@nl

type

label

Neonatal intrahepatic cholestasis caused by citrin deficiency in Korean infants.

@en

Neonatal intrahepatic cholestasis caused by citrin deficiency in Korean infants.

@nl

prefLabel

Neonatal intrahepatic cholestasis caused by citrin deficiency in Korean infants.

@en

Neonatal intrahepatic cholestasis caused by citrin deficiency in Korean infants.

@nl

P1433

Q37223088-E8D7B673-A7ED-4A22-91DD-1B06076B6179

P1476

Q37223088-DDFF215A-574E-414E-8E59-7FD8F7B8A577

P2093

Q37223088-4433D5F3-E347-4522-B4A1-66C2F7A3EE56

Q37223088-761507F9-BD06-4361-8D88-22AA4112D0C8

Q37223088-7CF854FD-9BA3-4367-B78A-0A7ECC8784DC

Q37223088-CFC49BB2-57F7-421A-B1F6-796CFFD27BB5

P2860

Q37223088-0D0FE158-5164-4BE7-9997-305886E7DB46

Q37223088-41B8FD79-C06E-42AB-87D8-0BA185B03684

Q37223088-4A95A390-C75B-4AE1-B250-551AE55C5ABE

Q37223088-5B597CFA-A7AB-402E-90E7-A71C00BF8A20

Q37223088-73291CE8-EBBF-4DFE-824F-9D75DA07B65E

Q37223088-774D416E-537C-48E1-8497-36439175974D

Q37223088-7BF938BD-8C83-471F-8934-3BFCAA5D422B

Q37223088-94D5EC8E-D85A-4F11-8EC3-D391D1C36F03

Q37223088-98ED2CDB-E52D-4EB9-9F53-EF3F1EE32C8D

Q37223088-9C96BF27-8D48-4506-886F-326D8EF119DA

P304

Q37223088-88EE77DD-EBBA-4A40-803B-D048A902F997

P31

Q37223088-8AF726CA-0911-4615-850C-C381ABDC5080

P356

Q37223088-38E2FF44-ABF5-4A3C-BDFE-D084FAD068E5

P433

Q37223088-098AEB1E-6EC4-4805-8F1C-6FCAFBD9AF07

P478

Q37223088-4F21AB77-4EE4-4E2C-9E5F-B2F6385C0718

P577

Q37223088-9C71AC0A-2C29-4E48-928E-B2A5821E2884

P698

Q37223088-F1EA6E14-0E09-4884-B4BA-2926B34E2FF6

P932

Q37223088-88A9BB1F-799F-4C94-B2B0-A34F3743E01A

P356

JKMS.2007.22.6.952

P1433

Journal of Korean Medical Science

P1476

Neonatal intrahepatic cholestasis caused by citrin deficiency in Korean infants.

@en

P2093

Jae Sung Ko

http://www.w3.org/2001/XMLSchema#string

Jeong Kee Seo

http://www.w3.org/2001/XMLSchema#string

Jung Han Song

http://www.w3.org/2001/XMLSchema#string

Sung Sup Park

http://www.w3.org/2001/XMLSchema#string

P2860

The gene mutated in adult-onset type II citrullinaemia encodes a putative mitochondrial carrier protein

Mitochondrial aspartate glutamate carrier (citrin) deficiency as the cause of adult-onset type II citrullinemia (CTLN2) and idiopathic neonatal hepatitis (NICCD)

Adult-onset type II citrullinemia and idiopathic neonatal hepatitis caused by citrin deficiency: involvement of the aspartate glutamate carrier for urea synthesis and maintenance of the urea cycle

Living-related liver transplantation for type II citrullinemia using a graft from heterozygote donor.

Frequency and distribution in East Asia of 12 mutations identified in the SLC25A13 gene of Japanese patients with citrin deficiency.

Clinical heterogeneity of neonatal intrahepatic cholestasis caused by citrin deficiency: case reports from 16 patients.

Infantile citrullinemia caused by citrin deficiency with increased dibasic amino acids.

Neonatal intrahepatic cholestasis caused by citrin deficiency: severe hepatic dysfunction in an infant requiring liver transplantation.

Effects of citrin deficiency in the perinatal period: feasibility of newborn mass screening for citrin deficiency.

Genomic structure of the adult-onset type II citrullinemia gene, SLC25A13, and cloning and expression of its mouse homologue.

P304

952-956

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.3346/JKMS.2007.22.6.952

http://www.w3.org/2001/XMLSchema#string

P433

6

http://www.w3.org/2001/XMLSchema#string

P478

22

http://www.w3.org/2001/XMLSchema#string

P577

2007-12-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

18162705

http://www.w3.org/2001/XMLSchema#string

P932

2694627

http://www.w3.org/2001/XMLSchema#string