Acute liver failure in children: The role of defects in fatty acid oxidation

被引：15

作者：

Alonso, EM ^{[1
]}

机构：

[1] Childrens Mem Hosp, Chicago, IL 60614 USA

来源：

HEPATOLOGY | 2005年 / 41卷 / 04期

关键词：

D O I：

10.1002/hep.20680

中图分类号：

R57 [消化系及腹部疾病];

学科分类号：

摘要：

引用

页码：696 / 699

页数：4

共 25 条

[1] A defect in the transport of long-chain fatty acids associated with acute liver failure
Al Odaib, A
Shneider, BL
Bennett, MJ
Pober, BR
Reyes-Mugica, M
Friedman, AL
Suchy, FJ
Rinaldo, P
[J]. NEW ENGLAND JOURNAL OF MEDICINE, 1998, 339 (24) : 1752 - 1757
[2] FULMINANT-HEPATITIS ASSOCIATED WITH CENTRILOBULAR HEPATIC-NECROSIS IN YOUNG-CHILDREN
ALONSO, EM
SOKOL, RJ
HART, J
TYSON, RW
NARKEWICZ, MR
WHITTINGTON, PF
[J]. JOURNAL OF PEDIATRICS, 1995, 127 (06) : 888 - 894
[3] Reye's syndrome in the United States from 1981 through 1997
Belay, ED
Bresee, JS
Holman, RC
Khan, AS
Shahriari, A
Schonberger, LB
[J]. NEW ENGLAND JOURNAL OF MEDICINE, 1999, 340 (18) : 1377 - 1382
[4] Fatal hepatic short-chain L-3-hydroxyacyl-coenzyme A dehydrogenase deficiency:: Clinical, biochemical, and pathological studies on three subjects with this recently identified disorder of mitochondrial β-oxidation
Bennett, MJ
Spotswood, SD
Ross, KF
Comfort, S
Koonce, R
Boriack, RL
IJlst, L
Wanders, RJA
[J]. PEDIATRIC AND DEVELOPMENTAL PATHOLOGY, 1999, 2 (04) : 337 - 345
[5] Retrospective biochemical screening of fatty acid oxidation disorders in postmortem livers of 418 cases of sudden death in the first year of life
Boles, RG
Buck, EA
Blitzer, MG
Platt, MS
Cowan, TM
Martin, SK
Yoon, HR
Madsen, JA
Reyes-Mugica, M
Rinaldo, P
[J]. JOURNAL OF PEDIATRICS, 1998, 132 (06) : 924 - 933
[6] Reye syndrome revisited: a descriptive term covering a group of heterogeneous disorders
Casteels-Van Daele, M
Van Geet, C
Wouters, C
Eggermont, E
[J]. EUROPEAN JOURNAL OF PEDIATRICS, 2000, 159 (09) : 641 - 648
[7] Devictor D, 1993, Crit Care Med, V21, pS348, DOI 10.1097/00003246-199309001-00027
[8] Reye syndrome - insights on causation and prognosis
Glasgow, JFT
Middleton, B
[J]. ARCHIVES OF DISEASE IN CHILDHOOD, 2001, 85 (05) : 351 - 353
[9] CLINICAL AND BIOCHEMICAL PRESENTATION OF LONG-CHAIN 3-HYDROXYACYL-COA DEHYDROGENASE-DEFICIENCY
HAGENFELDT, L
VENIZELOS, N
VONDOBELN, U
[J]. JOURNAL OF INHERITED METABOLIC DISEASE, 1995, 18 (02) : 245 - 248
[10] A fetal fatty-acid oxidation disorder as a cause of liver disease in pregnant women
Ibdah, JA
Bennett, MJ
Rinaldo, P
Zhao, YW
Gibson, B
Sims, HF
Strauss, AW
[J]. NEW ENGLAND JOURNAL OF MEDICINE, 1999, 340 (22) : 1723 - 1731

← 1 2 3 →