-
1
-
-
0036516338
-
Obstetric cholestasis, outcome with active management: A series of 70 cases
-
Kenyon AP, Nelson-Piercy C, Girling J, et al. Obstetric cholestasis, outcome with active management: a series of 70 cases. BJOG 2002;109:282-8.
-
(2002)
BJOG
, vol.109
, pp. 282-288
-
-
Kenyon, A.P.1
Nelson-Piercy, C.2
Girling, J.3
-
2
-
-
0036893826
-
Prospective study of liver dysfunction in pregnancy in Southwest Wales
-
Ch'ng CL, Morgan M, Hainsworth I, et al. Prospective study of liver dysfunction in pregnancy in Southwest Wales. Gut 2002;51:876-80.
-
(2002)
Gut
, vol.51
, pp. 876-880
-
-
Ch'ng, C.L.1
Morgan, M.2
Hainsworth, I.3
-
3
-
-
0017707182
-
Serum bile acids in cholestasis of pregnancy
-
Laotikainen T, Ikonen E. Serum bile acids in cholestasis of pregnancy. Obstet Gynecol 1977;50:313-18.
-
(1977)
Obstet Gynecol
, vol.50
, pp. 313-318
-
-
Laotikainen, T.1
Ikonen, E.2
-
4
-
-
0017249902
-
Fetal complications of obstetric cholestasis
-
Reid R, Ivey KJ, Rencoret RH, et al. Fetal complications of obstetric cholestasis. Br Med J 1976;1:870-2.
-
(1976)
Br Med J
, vol.1
, pp. 870-872
-
-
Reid, R.1
Ivey, K.J.2
Rencoret, R.H.3
-
5
-
-
0023823177
-
Fetal outcome in obstetric cholestasis
-
Fisk NM, Storey GN. Fetal outcome in obstetric cholestasis. Br J Obstet Gynaecol 1988;95:1137-43.
-
(1988)
Br J Obstet Gynaecol
, vol.95
, pp. 1137-1143
-
-
Fisk, N.M.1
Storey, G.N.2
-
6
-
-
0034912259
-
Risk of obstetric cholestasis in sisters of index patients
-
Eloranta ML, Heinonen S, Mononen T, et al. Risk of obstetric cholestasis in sisters of index patients. Clin Genet 2001;60:42-5.
-
(2001)
Clin Genet
, vol.60
, pp. 42-45
-
-
Eloranta, M.L.1
Heinonen, S.2
Mononen, T.3
-
7
-
-
0031907132
-
A gene encoding a P-type ATPase mutated in two forms of hereditary cholestasis
-
Bull LN, van Eijk MJ, Pawlikowska L, et al. A gene encoding a P-type ATPase mutated in two forms of hereditary cholestasis. Nat Genet 1998;18:219-24.
-
(1998)
Nat Genet
, vol.18
, pp. 219-224
-
-
Bull, L.N.1
Van Eijk, M.J.2
Pawlikowska, L.3
-
8
-
-
17344366172
-
A gene encoding a liver-specific ABC transporter is mutated in progressive familial intrahepatic cholestasis
-
Strautnieks SS, Bull LN, Knisely AS, et al. A gene encoding a liver-specific ABC transporter is mutated in progressive familial intrahepatic cholestasis. Nat Genet 1998;20:233-8.
-
(1998)
Nat Genet
, vol.20
, pp. 233-238
-
-
Strautnieks, S.S.1
Bull, L.N.2
Knisely, A.S.3
-
9
-
-
0040284751
-
Mutations in the MDR3 gene cause progressive familial intrahepatic cholestasis
-
de Vree JM, Jacquemin E, Sturm E, et al. Mutations in the MDR3 gene cause progressive familial intrahepatic cholestasis. Proc Natl Acad Sci U S A 1998;95:282-7.
-
(1998)
Proc Natl Acad Sci U S A
, vol.95
, pp. 282-287
-
-
De Vree, J.M.1
Jacquemin, E.2
Sturm, E.3
-
10
-
-
0026621245
-
ABC transporters: From microorganisms to man
-
Higgins CF. ABC transporters: from microorganisms to man. Annu Rev Cell Biol 1992;8:67-113.
-
(1992)
Annu Rev Cell Biol
, vol.8
, pp. 67-113
-
-
Higgins, C.F.1
-
11
-
-
17644443114
-
Heterozygous MDR3 missense mutation associated with intrahepatic cholestasis of pregnancy: Evidence for a defect in protein trafficking
-
Dixon PH, Weerasekera N, Linton KJ, et al. Heterozygous MDR3 missense mutation associated with intrahepatic cholestasis of pregnancy: evidence for a defect in protein trafficking. Hum Mol Genet 2000;9:1209-17.
-
(2000)
Hum Mol Genet
, vol.9
, pp. 1209-1217
-
-
Dixon, P.H.1
Weerasekera, N.2
Linton, K.J.3
-
12
-
-
0033023251
-
Heterozygous non-sense mutation of the MDR3 gene in familial intrahepatic cholestasis of pregnancy
-
Jacquemin E, Cresteil D, Manouvrier S, et al. Heterozygous non-sense mutation of the MDR3 gene in familial intrahepatic cholestasis of pregnancy. Lancet 1999;353:210-11.
-
(1999)
Lancet
, vol.353
, pp. 210-211
-
-
Jacquemin, E.1
Cresteil, D.2
Manouvrier, S.3
-
13
-
-
0035053975
-
MDR3 gene defect in adults with symptomatic intrahepatic and gallbladder cholesterol cholelithiasis
-
Rosmorduc O, Hermelin B, Poupon R. MDR3 gene defect in adults with symptomatic intrahepatic and gallbladder cholesterol cholelithiasis. Gastroenterology 2001;120:1459-67.
-
(2001)
Gastroenterology
, vol.120
, pp. 1459-1467
-
-
Rosmorduc, O.1
Hermelin, B.2
Poupon, R.3
-
14
-
-
0037362523
-
A second heterozygous MDR3 nonsense mutation associated with intrahepatic cholestasis of pregnancy
-
Gendrot C, Bacq Y, Brechot MC, et al. A second heterozygous MDR3 nonsense mutation associated with intrahepatic cholestasis of pregnancy. J Med Genet 2003;40:e32.
-
(2003)
J Med Genet
, vol.40
-
-
Gendrot, C.1
Bacq, Y.2
Brechot, M.C.3
-
15
-
-
0037379732
-
A multidrug resistance 3 gene mutation causing cholelithiasis, cholestasis of pregnancy, and adulthood biliary cirrhosis
-
Lucena JF, Herrero JI, Quiroga J, et al. A multidrug resistance 3 gene mutation causing cholelithiasis, cholestasis of pregnancy, and adulthood biliary cirrhosis. Gastroenterology 2003;124:1037-42.
-
(2003)
Gastroenterology
, vol.124
, pp. 1037-1042
-
-
Lucena, J.F.1
Herrero, J.I.2
Quiroga, J.3
-
16
-
-
0042278551
-
ABCB4 gene sequence variation in women with intrahepatic cholestasis of pregnancy
-
Mullenbach R, Linton KJ, Wiltshire S, et al. ABCB4 gene sequence variation in women with intrahepatic cholestasis of pregnancy. J Med Genet 2003;40:E70.
-
(2003)
J Med Genet
, vol.40
-
-
Mullenbach, R.1
Linton, K.J.2
Wiltshire, S.3
-
17
-
-
10744220281
-
Sequence analysis of bile salt export pump (ABCB11) and multidrug resistance p-glycoprotein 3 (ABCB4, MDR3) in patients with intrahepatic cholestasis of pregnancy
-
Pauli-Magnus C, Lang T, Meier Y, et al. Sequence analysis of bile salt export pump (ABCB11) and multidrug resistance p-glycoprotein 3 (ABCB4, MDR3) in patients with intrahepatic cholestasis of pregnancy. Pharmacogenetics 2004;14:91-102.
-
(2004)
Pharmacogenetics
, vol.14
, pp. 91-102
-
-
Pauli-Magnus, C.1
Lang, T.2
Meier, Y.3
-
18
-
-
0035045719
-
The wide spectrum of multidrug resistance 3 deficiency: From neonatal cholestasis to cirrhosis of adulthood
-
Jacquemin E, De Vree JM, Cresteil D, et al. The wide spectrum of multidrug resistance 3 deficiency: from neonatal cholestasis to cirrhosis of adulthood. Gastroenterology 2001;120:1448-58.
-
(2001)
Gastroenterology
, vol.120
, pp. 1448-1458
-
-
Jacquemin, E.1
De Vree, J.M.2
Cresteil, D.3
-
19
-
-
3042782537
-
Characterization of mutations in ATP8B1 associated with hereditary cholestasis
-
Klomp LW, Vargas JC, van Mil SW, et al. Characterization of mutations in ATP8B1 associated with hereditary cholestasis. Hepatology 2004;40:27-38.
-
(2004)
Hepatology
, vol.40
, pp. 27-38
-
-
Klomp, L.W.1
Vargas, J.C.2
Van Mil, S.W.3
-
20
-
-
0014442684
-
Byler disease. Fatal familial intrahepatic cholestasis in an Amish kindred
-
Clayton RJ, Iber FL, Ruebner BH, et al. Byler disease. Fatal familial intrahepatic cholestasis in an Amish kindred. Am J Dis Child 1969;117:112-24.
-
(1969)
Am J Dis Child
, vol.117
, pp. 112-124
-
-
Clayton, R.J.1
Iber, F.L.2
Ruebner, B.H.3
-
21
-
-
0017195958
-
Familial benign recurrent intrahepatic cholestasis. Interrelation with intrahepatic cholestasis of pregnancy and from oral contraceptives?
-
de Pagter AG, van Berge Henegouwen GP, ten Bokkel Huinink JA, et al. Familial benign recurrent intrahepatic cholestasis. Interrelation with intrahepatic cholestasis of pregnancy and from oral contraceptives? Gastroenterology 1976;71:202-7.
-
(1976)
Gastroenterology
, vol.71
, pp. 202-207
-
-
De Pagter, A.G.1
Van Berge Henegouwen, G.P.2
Ten Bokkel Huinink, J.A.3
-
22
-
-
0028107618
-
Clinical and biochemical findings in progressive familial intrahepatic cholestasis
-
Whitington PF, Freese DK, Alonso EM, et al. Clinical and biochemical findings in progressive familial intrahepatic cholestasis. J Pediatr Gastroenterol Nutr 1994;18:134-41.
-
(1994)
J Pediatr Gastroenterol Nutr
, vol.18
, pp. 134-141
-
-
Whitington, P.F.1
Freese, D.K.2
Alonso, E.M.3
-
23
-
-
0038121763
-
Genetic evidence of heterogeneity in intrahepatic cholestasis of pregnancy
-
Savander M, Ropponen A, Avela K, et al. Genetic evidence of heterogeneity in intrahepatic cholestasis of pregnancy. Gut 2003;52:1025-9.
-
(2003)
Gut
, vol.52
, pp. 1025-1029
-
-
Savander, M.1
Ropponen, A.2
Avela, K.3
-
24
-
-
0030440081
-
Development and applications of in vivo clinical magnetic resonance spectroscopy
-
Cox U. Development and applications of in vivo clinical magnetic resonance spectroscopy. Prog Biophys Mol Biol 1996;65:45-81.
-
(1996)
Prog Biophys Mol Biol
, vol.65
, pp. 45-81
-
-
Cox, U.1
-
25
-
-
0031043589
-
Liver function tests in pre-eclampsia: Importance of comparison with a reference range derived for normal pregnancy
-
Girling JC, Dow E, Smith JH. Liver function tests in pre-eclampsia: importance of comparison with a reference range derived for normal pregnancy. Br J Obstet Gynaecol 1997;104:246-50.
-
(1997)
Br J Obstet Gynaecol
, vol.104
, pp. 246-250
-
-
Girling, J.C.1
Dow, E.2
Smith, J.H.3
-
26
-
-
0033652101
-
A missense mutation in FIC1 is associated with greenland familial cholestasis
-
Klomp LW, Bull LN, Knisely AS, et al. A missense mutation in FIC1 is associated with greenland familial cholestasis. Hepatology 2000;32:1337-41.
-
(2000)
Hepatology
, vol.32
, pp. 1337-1341
-
-
Klomp, L.W.1
Bull, L.N.2
Knisely, A.S.3
-
27
-
-
0036161690
-
FIC1 and BSEP defects in Taiwanese patients with chronic intrahepatic cholestasis with low (gamma)-glutamyltranspeptidase levels
-
Chen HL, Chang PS, Hsu HC, et al. FIC1 and BSEP defects in Taiwanese patients with chronic intrahepatic cholestasis with low (gamma)- glutamyltranspeptidase levels. J Pediatr 2002;140:119-24.
-
(2002)
J Pediatr
, vol.140
, pp. 119-124
-
-
Chen, H.L.1
Chang, P.S.2
Hsu, H.C.3
-
28
-
-
0036023931
-
Intractable diarrhea after liver transplantation for Byler's disease: Successful treatment with bile adsorptive resin
-
Egawa H, Yorifuji T, Sumazaki R, et al. Intractable diarrhea after liver transplantation for Byler's disease: successful treatment with bile adsorptive resin. Liver Transpl 2002;8714-16.
-
(2002)
Liver Transpl
, vol.8
, pp. 714-716
-
-
Egawa, H.1
Yorifuji, T.2
Sumazaki, R.3
-
29
-
-
0028962679
-
Effect of functional grade and etiology on in vivo hepatic phosphorus-31 magnetic resonance spectroscopy in cirrhosis: Biochemical basis of spectral appearances
-
Menon DK, Sargentoni J, Taylor-Robinson SD, et al. Effect of functional grade and etiology on in vivo hepatic phosphorus-31 magnetic resonance spectroscopy in cirrhosis: biochemical basis of spectral appearances. Hepatology 1995;21:417-27.
-
(1995)
Hepatology
, vol.21
, pp. 417-427
-
-
Menon, D.K.1
Sargentoni, J.2
Taylor-Robinson, S.D.3
-
30
-
-
0030006936
-
Hepatic phosphorus-31 magnetic resonance spectroscopy in primary biliary cirrhosis and its relation to prognostic models
-
Jalan R, Sargentoni J, Coutts GA, et al. Hepatic phosphorus-31 magnetic resonance spectroscopy in primary biliary cirrhosis and its relation to prognostic models. Gut 1996;39:141-6.
-
(1996)
Gut
, vol.39
, pp. 141-146
-
-
Jalan, R.1
Sargentoni, J.2
Coutts, G.A.3
-
31
-
-
9844259466
-
In vivo and in vitro hepatic 31P magnetic resonance spectroscopy and electron microscopy of the cirrhotic liver
-
Taylor-Robinson SD, Sargentoni J, Bell JD, et al. In vivo and in vitro hepatic 31P magnetic resonance spectroscopy and electron microscopy of the cirrhotic liver. Liver 1997;17:198-209.
-
(1997)
Liver
, vol.17
, pp. 198-209
-
-
Taylor-Robinson, S.D.1
Sargentoni, J.2
Bell, J.D.3
-
32
-
-
7144261057
-
In vivo and in vitro hepatic phosphorus-31 magnetic resonance spectroscopy and electron microscopy in chronic ductopenic rejection of human liver allografts
-
Taylor-Robinson SD, Sargentoni J, Bell JD, et al. In vivo and in vitro hepatic phosphorus-31 magnetic resonance spectroscopy and electron microscopy in chronic ductopenic rejection of human liver allografts. Gut 1998;42:735-43.
-
(1998)
Gut
, vol.42
, pp. 735-743
-
-
Taylor-Robinson, S.D.1
Sargentoni, J.2
Bell, J.D.3
-
33
-
-
0023696866
-
A general approach to selection of multiple cubic volume elements using the ISIS technique
-
Ordidge RJ, Bowley RM, McHale G. A general approach to selection of multiple cubic volume elements using the ISIS technique. Magn Reson Med 1988;8:323-31.
-
(1988)
Magn Reson Med
, vol.8
, pp. 323-331
-
-
Ordidge, R.J.1
Bowley, R.M.2
McHale, G.3
-
34
-
-
0346308381
-
Improved method for accurate and efficient quantification of MRS data with use of prior knowledge
-
Vanhamme L, van den Boogaart A, Van Huffel S. Improved method for accurate and efficient quantification of MRS data with use of prior knowledge. J Magn Reson 1997;129:35-43.
-
(1997)
J Magn Reson
, vol.129
, pp. 35-43
-
-
Vanhamme, L.1
Van Den Boogaart, A.2
Van Huffel, S.3
-
35
-
-
0000549759
-
-
Proceedings of the ESMRMB 13th Annual Meeting, Prague
-
van den Boogaart A, Van Hecke P, Van Huffel S, et al. MRUI: a graphical user interface for accurate routine MRS data analysis, Proceedings of the ESMRMB 13th Annual Meeting, Prague, 1996:318.
-
(1996)
MRUI: A Graphical User Interface for Accurate Routine MRS Data Analysis
, pp. 318
-
-
Van Den Boogaart, A.1
Van Hecke, P.2
Van Huffel, S.3
-
36
-
-
0042129985
-
Prior knowledge for time domain quantification of in vivo brain or liver 31P MR spectra
-
Hamilton G, Patel N, Forton DM, et al. Prior knowledge for time domain quantification of in vivo brain or liver 31P MR spectra. NMR Biomed 2003;16:168-76.
-
(2003)
NMR Biomed
, vol.16
, pp. 168-176
-
-
Hamilton, G.1
Patel, N.2
Forton, D.M.3
-
37
-
-
0034812920
-
Familial intrahepatic cholestasis 1: Studies of localization and function
-
Ujhazy P, Ortiz D, Misra S, et al. Familial intrahepatic cholestasis 1: studies of localization and function. Hepatology 2001;34(4 Pt 1):768-75.
-
(2001)
Hepatology
, vol.34
, Issue.4 PART 1
, pp. 768-775
-
-
Ujhazy, P.1
Ortiz, D.2
Misra, S.3
-
38
-
-
0037117313
-
Genetic defects in hepatobiliary transport
-
Elferink RO, Groen AK. Genetic defects in hepatobiliary transport. Biochim Biophys Acta 2002;1586:129-45.
-
(2002)
Biochim Biophys Acta
, vol.1586
, pp. 129-145
-
-
Elferink, R.O.1
Groen, A.K.2
-
39
-
-
10744227867
-
Progressive familial intrahepatic cholestasis, type 1, is associated with decreased rarnesoid X receptor activity
-
Chen F, Ananthanarayanan M, Emre S, et al. Progressive familial intrahepatic cholestasis, type 1, is associated with decreased rarnesoid X receptor activity. Gastroenterology 2004;126:756-64.
-
(2004)
Gastroenterology
, vol.126
, pp. 756-764
-
-
Chen, F.1
Ananthanarayanan, M.2
Emre, S.3
-
40
-
-
0033547277
-
Differential expression of putative transbilayer amphipath transporters
-
Halleck MS, Lawler JJ, Blackshaw S, et al. Differential expression of putative transbilayer amphipath transporters. Physiol Genomics 1999;1:139-50.
-
(1999)
Physiol Genomics
, vol.1
, pp. 139-150
-
-
Halleck, M.S.1
Lawler, J.J.2
Blackshaw, S.3
-
41
-
-
0031953722
-
Multiple members of a third subfamily of P-type ATPases identified by genomic sequences and ESTs
-
Halleek MS, Pradhan D, Blackman C, et al. Multiple members of a third subfamily of P-type ATPases identified by genomic sequences and ESTs. Genome Res 1998;8:354-61.
-
(1998)
Genome Res
, vol.8
, pp. 354-361
-
-
Halleek, M.S.1
Pradhan, D.2
Blackman, C.3
-
42
-
-
0038612980
-
Natural variation in human membrane transporter genes reveals evolutionary and functional constraints
-
Leabman MK, Huang CC, DeYoung J, et al. Natural variation in human membrane transporter genes reveals evolutionary and functional constraints. Proc Natl Acad Sci U S A 2003;100:5896-901.
-
(2003)
Proc Natl Acad Sci U S A
, vol.100
, pp. 5896-5901
-
-
Leabman, M.K.1
Huang, C.C.2
DeYoung, J.3
-
43
-
-
0023940614
-
Ethinylestradiol administration selectively alters liver sinusoidal membrane lipid fluidity and protein composition
-
Rosario J, Sutherland E, Zaccaro L, et al. Ethinylestradiol administration selectively alters liver sinusoidal membrane lipid fluidity and protein composition. Biochemistry 1988;27:3939-46.
-
(1988)
Biochemistry
, vol.27
, pp. 3939-3946
-
-
Rosario, J.1
Sutherland, E.2
Zaccaro, L.3
-
44
-
-
0030470648
-
Ethinyl estradiol cholestasis involves alterations in expression of liver sinusoidal transporters
-
Simon FR, Fortune J, Iwahashi M, et al. Ethinyl estradiol cholestasis involves alterations in expression of liver sinusoidal transporters. Am J Physiol 1996;271(6 Pt 1):G1043-52.
-
(1996)
Am J Physiol
, vol.271
, Issue.6 PART 1
-
-
Simon, F.R.1
Fortune, J.2
Iwahashi, M.3
-
45
-
-
0033991960
-
Molecular cloning and characterization of the murine bile salt export pump
-
Green RM, Hoda F, Ward KL. Molecular cloning and characterization of the murine bile salt export pump. Gene 2000;241:117-23.
-
(2000)
Gene
, vol.241
, pp. 117-123
-
-
Green, R.M.1
Hoda, F.2
Ward, K.L.3
-
46
-
-
0037427956
-
Regulation of basolateral organic anion transporters in ethinylestradiol-induced cnolestasis in the rat
-
Geier A, Dietrich CG, Gerloff T, et al. Regulation of basolateral organic anion transporters in ethinylestradiol-induced cnolestasis in the rat. Biochim Biophys Acta 2003;1609:87-94.
-
(2003)
Biochim Biophys Acta
, vol.1609
, pp. 87-94
-
-
Geier, A.1
Dietrich, C.G.2
Gerloff, T.3
-
47
-
-
0036667784
-
Effect of ursodeoxycholic acid on the expression of the hepatocellular bile acid transporters (Ntcp and bsep) in rats with estrogen-induced cholestasis
-
Micheline D, Emmanuel J, Serge E. Effect of ursodeoxycholic acid on the expression of the hepatocellular bile acid transporters (Ntcp and bsep) in rats with estrogen-induced cholestasis. J Pediatr Gastroenterol Nutr 2002;35:185-91.
-
(2002)
J Pediatr Gastroenterol Nutr
, vol.35
, pp. 185-191
-
-
Micheline, D.1
Emmanuel, J.2
Serge, E.3
-
48
-
-
0032542355
-
Familial gestational hyperthyroidism caused by a mutant thyrotropin receptor hypersensitive to human chorionic gonadotropin
-
Rodien P, Bremont C, Sanson ML, et al. Familial gestational hyperthyroidism caused by a mutant thyrotropin receptor hypersensitive to human chorionic gonadotropin. N Engl J Med 1998;339:1823-6.
-
(1998)
N Engl J Med
, vol.339
, pp. 1823-1826
-
-
Rodien, P.1
Bremont, C.2
Sanson, M.L.3
-
49
-
-
0027924217
-
A 31P and 1H-NMR investigation in vitro of normal and abnormal human liver
-
Bell JD, Cox IJ, Sargentoni J, et al. A 31P and 1H-NMR investigation in vitro of normal and abnormal human liver. Biochim Biophys Acta 1993;1225:71-7.
-
(1993)
Biochim Biophys Acta
, vol.1225
, pp. 71-77
-
-
Bell, J.D.1
Cox, I.J.2
Sargentoni, J.3
|