-
1
-
-
0028013251
-
Acute fatty liver of pregnancy and long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
-
WR Treem P Rinaldo DE Hale Acute fatty liver of pregnancy and long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Hepatology 19 1994 339 345
-
(1994)
Hepatology
, vol.19
, pp. 339-345
-
-
Treem, WR1
Rinaldo, P2
Hale, DE3
-
2
-
-
0027409820
-
Pregnancy and fetal long-chain 3-hydroxyacyl coenzyme A dehydrogenase deficiency
-
B Wilcken K-C Leung J Hammond R Kamath JV Leonard Pregnancy and fetal long-chain 3-hydroxyacyl coenzyme A dehydrogenase deficiency Lancet 341 1993 407 408
-
(1993)
Lancet
, vol.341
, pp. 407-408
-
-
Wilcken, B1
Leung, K-C2
Hammond, J3
Kamath, R4
Leonard, JV5
-
3
-
-
0026515859
-
Novel fatty acid β-oxidation enzymes in rat liver mitochondria, II: purification and properties of enoyl-coenzyme A (CoA) hydratase/3-hydroxyacyl-CoA dehydrogenase/3-ketoacyl-CoA thiolase trifunctional protein
-
Y Uchida K Izai T Orii T. Hashimoto Novel fatty acid β-oxidation enzymes in rat liver mitochondria, II: purification and properties of enoyl-coenzyme A (CoA) hydratase/3-hydroxyacyl-CoA dehydrogenase/3-ketoacyl-CoA thiolase trifunctional protein J Biol Chem 267 1992 1034 1041
-
(1992)
J Biol Chem
, vol.267
, pp. 1034-1041
-
-
Uchida, Y1
Izai, K2
Orii, T3
Hashimoto, T.4
-
4
-
-
0026558042
-
Human liver long-chain 3-hydroxyacyl-coenzyme A dehydrogenase is a multifunctional membrane-bound beta-oxidation enzyme of mitochondria
-
K Carpenter RJ Pollitt B Middleton Human liver long-chain 3-hydroxyacyl-coenzyme A dehydrogenase is a multifunctional membrane-bound beta-oxidation enzyme of mitochondria Biochem Biophys Res Commun 183 1992 443 448
-
(1992)
Biochem Biophys Res Commun
, vol.183
, pp. 443-448
-
-
Carpenter, K1
Pollitt, RJ2
Middleton, B3
-
5
-
-
0029020112
-
Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: high frequency of the G1528C mutation with no apparent correlation with the clinical phenotype
-
L IJlst S Ushikubo T Kamijo Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: high frequency of the G1528C mutation with no apparent correlation with the clinical phenotype J Inher Metab Dis 18 1995 241 244
-
(1995)
J Inher Metab Dis
, vol.18
, pp. 241-244
-
-
IJlst, L1
Ushikubo, S2
Kamijo, T3
-
6
-
-
0028597508
-
Molecular basis of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: identification of the major disease-causing mutation in the alpha-subunit of the mitochondrial trifunctional protein
-
L IJlst RJA Wanders S Ushikubo T Kamijo T Hashimoto Molecular basis of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: identification of the major disease-causing mutation in the alpha-subunit of the mitochondrial trifunctional protein Biochim Biophys Acta 1215 1994 347 350
-
(1994)
Biochim Biophys Acta
, vol.1215
, pp. 347-350
-
-
IJlst, L1
Wanders, RJA2
Ushikubo, S3
Kamijo, T4
Hashimoto, T5
-
7
-
-
0029835610
-
Common missense mutation G1528C in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency—characterization and expression of the mutant protein, mutation analysis on genomic DNA and chromosomal localization of the mitochondrial trifunctional protein alpha subunit gene
-
L IJlst JPN Ruiter JMN Hoovers ME Jakobs RJA. Wanders Common missense mutation G1528C in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency—characterization and expression of the mutant protein, mutation analysis on genomic DNA and chromosomal localization of the mitochondrial trifunctional protein alpha subunit gene J Clin Invest 98 1996 1028 1033
-
(1996)
J Clin Invest
, vol.98
, pp. 1028-1033
-
-
IJlst, L1
Ruiter, JPN2
Hoovers, JMN3
Jakobs, ME4
Wanders, RJA.5
-
8
-
-
0030271551
-
The genes for the α and β subunits of the mitochondrial trifunctional protein are both located in the same region of human chromosome 2p23
-
B-H Yang H Heng J-H Ding C. Roe The genes for the α and β subunits of the mitochondrial trifunctional protein are both located in the same region of human chromosome 2p23 Genomics 37 1996 141 143
-
(1996)
Genomics
, vol.37
, pp. 141-143
-
-
Yang, B-H1
Heng, H2
Ding, J-H3
Roe, C.4
-
9
-
-
0029933864
-
The clinical spectrum of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency
-
R Pons M Roig E Riudor The clinical spectrum of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency Pediatr Neurol 14 1996 236 243
-
(1996)
Pediatr Neurol
, vol.14
, pp. 236-243
-
-
Pons, R1
Roig, M2
Riudor, E3
-
10
-
-
0030775662
-
Long-chain 3-hydroxyacyl coenzyme A dehydrogenase deficiency with the G1528C mutation: clinical presentation of 13 patients
-
T Tyni A Palotie L Viinikka Long-chain 3-hydroxyacyl coenzyme A dehydrogenase deficiency with the G1528C mutation: clinical presentation of 13 patients J Pediatr 130 1997 67 76
-
(1997)
J Pediatr
, vol.130
, pp. 67-76
-
-
Tyni, T1
Palotie, A2
Viinikka, L3
-
11
-
-
0025828169
-
Progressive neuropathy and recurrent myoglobinuria in a child with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency
-
C Dionisi Vici A Burlina E Bertini Progressive neuropathy and recurrent myoglobinuria in a child with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency J Pediatr 118 1991 744 746
-
(1991)
J Pediatr
, vol.118
, pp. 744-746
-
-
Dionisi Vici, C1
Burlina, A2
Bertini, E3
-
12
-
-
0029811021
-
Maternal acute fatty liver of pregnancy associated with fetal trifunctional protein deficiency: molecular characterization of a novel maternal mutant allele
-
JJ Isaacs H Sims C Powell Maternal acute fatty liver of pregnancy associated with fetal trifunctional protein deficiency: molecular characterization of a novel maternal mutant allele Pediatr Res 40 1996 393 398
-
(1996)
Pediatr Res
, vol.40
, pp. 393-398
-
-
Isaacs, JJ1
Sims, H2
Powell, C3
-
13
-
-
0029803779
-
Acute fatty liver of pregnancy, hemolysis, elevated liver enzymes, and low platelets syndrome, and long chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
-
W Treem M Shoup D Hale Acute fatty liver of pregnancy, hemolysis, elevated liver enzymes, and low platelets syndrome, and long chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Am J Gastroenterol 91 1996 2293 2300
-
(1996)
Am J Gastroenterol
, vol.91
, pp. 2293-2300
-
-
Treem, W1
Shoup, M2
Hale, D3
-
14
-
-
0029850402
-
Assessment of the prevalence of genetic metabolic defects in acute fatty liver of pregnancy
-
A Mansouri B Fromenty F Durand C Degott J Bernuau D Pessayre Assessment of the prevalence of genetic metabolic defects in acute fatty liver of pregnancy J Hepatol 25 1996 781
-
(1996)
J Hepatol
, vol.25
, pp. 781
-
-
Mansouri, A1
Fromenty, B2
Durand, F3
Degott, C4
Bernuau, J5
Pessayre, D6
-
15
-
-
0030001168
-
Potential pathogenic roles of aberrant lipoprotein and fatty acid metabolism in pre-eclampsia
-
N Sattar A Gaw C Packard I Greer Potential pathogenic roles of aberrant lipoprotein and fatty acid metabolism in pre-eclampsia Br J Obstet Gynaecol 103 1996 614 620
-
(1996)
Br J Obstet Gynaecol
, vol.103
, pp. 614-620
-
-
Sattar, N1
Gaw, A2
Packard, C3
Greer, I4
-
17
-
-
0025909958
-
Placental bed spiral arteries in the hypertensive disorders of pregnancy
-
R Pijnenborg J Anthony D Davey Placental bed spiral arteries in the hypertensive disorders of pregnancy Br J Obstet Gynaecol 98 1991 648 655
-
(1991)
Br J Obstet Gynaecol
, vol.98
, pp. 648-655
-
-
Pijnenborg, R1
Anthony, J2
Davey, D3
-
18
-
-
0015999543
-
Maternal lipid metabolism
-
J Biezenski Maternal lipid metabolism Obstet Gynecol Ann 3 1974 203 233
-
(1974)
Obstet Gynecol Ann
, vol.3
, pp. 203-233
-
-
Biezenski, J1
-
19
-
-
0027405002
-
Decreased mitochondrial oxidation of fatty acids in pregnant mice: possible relevance to development of acute fatty liver of pregnancy
-
S Grimbert B Fromenty C Fisch Decreased mitochondrial oxidation of fatty acids in pregnant mice: possible relevance to development of acute fatty liver of pregnancy Hepatology 17 1993 628 637
-
(1993)
Hepatology
, vol.17
, pp. 628-637
-
-
Grimbert, S1
Fromenty, B2
Fisch, C3
-
20
-
-
0025868680
-
Long-chain 3-hydroxyacyl-coA dehydrogenase deficiency
-
S Jackson K Bartlett J Land Long-chain 3-hydroxyacyl-coA dehydrogenase deficiency Pediatr Res 29 1991 406 411
-
(1991)
Pediatr Res
, vol.29
, pp. 406-411
-
-
Jackson, S1
Bartlett, K2
Land, J3
-
21
-
-
0028888960
-
The molecular basis of pediatric long chain 3-hydroxyacyl-coA dehydrogenase deficiency associated with maternal acute fatty liver of pregnancy
-
HF Sims JC Brackett CK Powell The molecular basis of pediatric long chain 3-hydroxyacyl-coA dehydrogenase deficiency associated with maternal acute fatty liver of pregnancy Proc Natl Acad Sci U S A 92 1995 841 845
-
(1995)
Proc Natl Acad Sci U S A
, vol.92
, pp. 841-845
-
-
Sims, HF1
Brackett, JC2
Powell, CK3
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