-
1
-
-
0037230622
-
Inherited disorders of bilirubin metabolism
-
Bosma PJ. Inherited disorders of bilirubin metabolism. J Hepatol 2003;38:107-17.
-
(2003)
J Hepatol
, vol.38
, pp. 107-117
-
-
Bosma, P.J.1
-
2
-
-
0015405377
-
Detection of Gilbert's syndrome in patients with hemolysis: A method using radioactive chromium
-
Berk PD, Blaschke TF. Detection of Gilbert's syndrome in patients with hemolysis: a method using radioactive chromium. Ann Intern Med 1972;77:527-31.
-
(1972)
Ann Intern Med
, vol.77
, pp. 527-531
-
-
Berk, P.D.1
Blaschke, T.F.2
-
3
-
-
0016784220
-
Population studies on Gilbert's syndrome
-
Owens D, Evans J. Population studies on Gilbert's syndrome. J Med Genet 1975;12:152-6.
-
(1975)
J Med Genet
, vol.12
, pp. 152-156
-
-
Owens, D.1
Evans, J.2
-
5
-
-
0023217260
-
Prevalence of Gilbert's syndrome in Germany
-
Sieg A, Arab L, Schlierf G, et al. Prevalence of Gilbert's syndrome in Germany. Dtsch Med Wochenschr 1987;112:1206-8.
-
(1987)
Dtsch Med Wochenschr
, vol.112
, pp. 1206-1208
-
-
Sieg, A.1
Arab, L.2
Schlierf, G.3
-
6
-
-
0008690963
-
Bilirubin metabolism and the pathophysiology of jaundice
-
Schiff ER, Sorrell MF, Maddrey WC, editors, Philadelphia: Lippincott-Raven Publishers;
-
Berg CL, Crawford JM, Gollan JL. Bilirubin metabolism and the pathophysiology of jaundice. In: Schiff ER, Sorrell MF, Maddrey WC, editors. Schiff's Diseases of the Liver. Philadelphia: Lippincott-Raven Publishers; 1999. p. 147-92.
-
(1999)
Schiff's Diseases of the Liver
, pp. 147-192
-
-
Berg, C.L.1
Crawford, J.M.2
Gollan, J.L.3
-
7
-
-
0036551617
-
Understanding neonatal hyperbilirubinemia in the era of genomics
-
Watchko JF, Daood MJ, Biniwale M. Understanding neonatal hyperbilirubinemia in the era of genomics. Semin Neonatol 2002;7:143-52.
-
(2002)
Semin Neonatol
, vol.7
, pp. 143-152
-
-
Watchko, J.F.1
Daood, M.J.2
Biniwale, M.3
-
8
-
-
0036204931
-
Hemolysis and bilirubin conjugation in association with UDP-glucuronosyltransferase 1A1 promoter polymorphism
-
Kaplan M, Hammerman C, Rubaltelli FF, et al. Hemolysis and bilirubin conjugation in association with UDP-glucuronosyltransferase 1A1 promoter polymorphism. Hepatology 2002;35:905-11.
-
(2002)
Hepatology
, vol.35
, pp. 905-911
-
-
Kaplan, M.1
Hammerman, C.2
Rubaltelli, F.F.3
-
9
-
-
0028867826
-
The genetic basis of the reduced expression of bilirubin UDP-glucuronosyltransferase 1 in Gilbert's syndrome
-
Bosma PJ, Chowdhury RJ, Bakker C, et al. The genetic basis of the reduced expression of bilirubin UDP-glucuronosyltransferase 1 in Gilbert's syndrome. N Engl J Med 1995;333:1171-5.
-
(1995)
N Engl J Med
, vol.333
, pp. 1171-1175
-
-
Bosma, P.J.1
Chowdhury, R.J.2
Bakker, C.3
-
10
-
-
0030030762
-
Genetic variation in bilirubin UPD-glucuronosyltransferase gene promoter and Gilbert's syndrome
-
Monaghan G, Ryan M, Seddon R, et al. Genetic variation in bilirubin UPD-glucuronosyltransferase gene promoter and Gilbert's syndrome. Lancet 1996;347:578-81.
-
(1996)
Lancet
, vol.347
, pp. 578-581
-
-
Monaghan, G.1
Ryan, M.2
Seddon, R.3
-
11
-
-
0033802568
-
Molecular diagnosis of a familial nonhemolytic hyperbilirubinemia (Gilbert's syndrome) in healthy subjects
-
Borlak J, Thum T, Landt O, et al. Molecular diagnosis of a familial nonhemolytic hyperbilirubinemia (Gilbert's syndrome) in healthy subjects. Hepatology 2000;32:792-5.
-
(2000)
Hepatology
, vol.32
, pp. 792-795
-
-
Borlak, J.1
Thum, T.2
Landt, O.3
-
12
-
-
0037230427
-
Combined polymorphisms in UDP-glucuronosyltransferases 1A1 and 1A6: Implications for patients with Gilbert's syndrome
-
Peters WH, te Morsche RH, Roelofs HM. Combined polymorphisms in UDP-glucuronosyltransferases 1A1 and 1A6: implications for patients with Gilbert's syndrome. J Hepatol 2003;38:3-8.
-
(2003)
J Hepatol
, vol.38
, pp. 3-8
-
-
Peters, W.H.1
te Morsche, R.H.2
Roelofs, H.M.3
-
13
-
-
0015399576
-
Defective bromosulfophthalein clearance in patients with constitutional hepatic dysfunction (Gilbert's syndrome)
-
Berk PD, Blaschke TF, Waggoner JG. Defective bromosulfophthalein clearance in patients with constitutional hepatic dysfunction (Gilbert's syndrome). Gastroenterology 1972;63:472-81.
-
(1972)
Gastroenterology
, vol.63
, pp. 472-481
-
-
Berk, P.D.1
Blaschke, T.F.2
Waggoner, J.G.3
-
14
-
-
0035127524
-
Hepatic uptake of organic anions affects the plasma bilirubin level in subjects with Gilbert's syndrome mutations in UGT1A1
-
Persico M, Persico E, Bakker CT, et al. Hepatic uptake of organic anions affects the plasma bilirubin level in subjects with Gilbert's syndrome mutations in UGT1A1. Hepatology 2001;33:627-32.
-
(2001)
Hepatology
, vol.33
, pp. 627-632
-
-
Persico, M.1
Persico, E.2
Bakker, C.T.3
-
15
-
-
0031827649
-
Genetic testing for Gilbert's syndrome: How useful is it in determining the cause of jaundice?
-
Rudenski AS, Halsall D. Genetic testing for Gilbert's syndrome: how useful is it in determining the cause of jaundice? Clin Chem 1998;44:1604-9.
-
(1998)
Clin Chem
, vol.44
, pp. 1604-1609
-
-
Rudenski, A.S.1
Halsall, D.2
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