-
1
-
-
8044223564
-
Constitutional hepatic dysfunction (Gilbert’s disease): Its natural history and related syndromes
-
Foulk WT, Butt HR, Owen CA, et al. Constitutional hepatic dysfunction (Gilbert’s disease): Its natural history and related syndromes. Medicine (Baltimore) 1959; 38: 25-46.
-
(1959)
Medicine (Baltimore)
, vol.38
, pp. 25-46
-
-
Foulk, W.T.1
Butt, H.R.2
Owen, C.A.3
-
2
-
-
0028791598
-
Molecular biology of bilirubin metabolism
-
Boyer JL, Ockner RK, eds, Philadelphia: WB Saunders
-
Jansen PLM, Bosma PJ, Roy Chowdhury J. Molecular biology of bilirubin metabolism. In: Boyer JL, Ockner RK, eds. Progress in Liver Disease, Vol 13. Philadelphia: WB Saunders, 1995: 125-50.
-
(1995)
Progress in Liver Disease
, vol.13
, pp. 125-150
-
-
Jansen, P.L.M.1
Bosma, P.J.2
Roy Chowdhury, J.3
-
3
-
-
0033001454
-
Association of neonatal hyperbilirubinemia with bilirubin UDP-glucuronosyltransferase polymorphism
-
Maruo Y, Nishizawa K, Sato H, et al. Association of neonatal hyperbilirubinemia with bilirubin UDP-glucuronosyltransferase polymorphism. Pediatrics 1999; 103: 1224-7.
-
(1999)
Pediatrics
, vol.103
, pp. 1224-1227
-
-
Maruo, Y.1
Nishizawa, K.2
Sato, H.3
-
4
-
-
0031813575
-
Gilbert syndrome caused by a homozygous missense mutation (Try486Asp) of bilirubin UDP-glucuronosyltransferase gene
-
Maruo Y, Sato H, Yamano T, et al. Gilbert syndrome caused by a homozygous missense mutation (Try486Asp) of bilirubin UDP-glucuronosyltransferase gene. J Pediatr 1998; 132: 1045-7.
-
(1998)
J Pediatr
, vol.132
, pp. 1045-1047
-
-
Maruo, Y.1
Sato, H.2
Yamano, T.3
-
5
-
-
0028287482
-
A new type of defect in the gene for bilirubin uridine 5-diphosphate-glucuronosyltransferase in a patient with Crigler-Najjar syndrome type I
-
Aono S, Yamada Y, Keino H, et al. A new type of defect in the gene for bilirubin uridine 5-diphosphate-glucuronosyltransferase in a patient with Crigler-Najjar syndrome type I. Pediatr Res 1994; 35: 629-32.
-
(1994)
Pediatr Res
, vol.35
, pp. 629-632
-
-
Aono, S.1
Yamada, Y.2
Keino, H.3
-
6
-
-
0022498189
-
Analysis of bilirubin conjugates in human bile by column liquid chromatography
-
Yamashita M, Adachi Y, Yamamoto T. Analysis of bilirubin conjugates in human bile by column liquid chromatography. J ChromatogrA 1986; 375: 386-91.
-
(1986)
J ChromatogrA
, vol.375
, pp. 386-391
-
-
Yamashita, M.1
Adachi, Y.2
Yamamoto, T.3
-
7
-
-
0030053274
-
The genetic basis of Gilbert’s syndrome
-
Sato H, Adachi Y, Koiwai O. The genetic basis of Gilbert’s syndrome. Lancet 1996; 347: 557-8.
-
(1996)
Lancet
, vol.347
, pp. 557-558
-
-
Sato, H.1
Adachi, Y.2
Koiwai, O.3
-
8
-
-
0033000014
-
A case of anorexia nervosa with hyperbilirubinemia in a patient homozygous for a mutation in the bilirubin UDP-glucuronosyltransferase gene
-
Maruo Y, Wada S, Yamamoto K, et al. A case of anorexia nervosa with hyperbilirubinemia in a patient homozygous for a mutation in the bilirubin UDP-glucuronosyltransferase gene. Eur J Pediatr 1999; 158: 547-9.
-
(1999)
Eur J Pediatr
, vol.158
, pp. 547-549
-
-
Maruo, Y.1
Wada, S.2
Yamamoto, K.3
-
10
-
-
0028867826
-
The genetic basis of the reduced expression of bilirubin UDP-glucuronosyltransferase 1 in Gilbert’s syndrome
-
Bosma PJ, Roy Chowdhury J, 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
Roy Chowdhury, J.2
Bakker, C.3
-
11
-
-
0031864410
-
Contribution of two missense mutations (G71R and Y486D) of the bilirubin UDP-glycosyltransferase (UGT1A1) gene to phenotypes of Gilbert’s syndrome and Crigler-Najjar syndrome type II
-
Yamamoto K, Sato H, Fujiyama Y, et al. Contribution of two missense mutations (G71R and Y486D) of the bilirubin UDP-glycosyltransferase (UGT1A1) gene to phenotypes of Gilbert’s syndrome and Crigler-Najjar syndrome type II. Biochim Biophys Acta 1998; 1406: 267-73.
-
(1998)
Biochim Biophys Acta
, vol.1406
, pp. 267-273
-
-
Yamamoto, K.1
Sato, H.2
Fujiyama, Y.3
-
12
-
-
0014959720
-
The reciprocal relation between caloric intake and the degree of hyperbilirubinemia in Gilbert’s syndrome
-
Felsher BF, Rickard D, Redeker AG. The reciprocal relation between caloric intake and the degree of hyperbilirubinemia in Gilbert’s syndrome. N Engl J Med 1970; 283: 170-2.
-
(1970)
N Engl J Med
, vol.283
, pp. 170-172
-
-
Felsher, B.F.1
Rickard, D.2
Redeker, A.G.3
-
13
-
-
0015958267
-
Unconjugated hyperbilirubinemia in achalasia
-
Fevery J, Heirwegh KPM, De Groote J. Unconjugated hyperbilirubinemia in achalasia. Gut 1974; 15: 121-4.
-
(1974)
Gut
, vol.15
, pp. 121-124
-
-
Fevery, J.1
Heirwegh, K.P.M.2
De Groote, J.3
-
14
-
-
0021822511
-
Pharmacology of mitoxantrone: Mode of action and pharmacokinetics
-
Alberts DS, Peng YM, Bowden GT, et al. Pharmacology of mitoxantrone: mode of action and pharmacokinetics. Invest New Drugs 1985; 3: 101-7.
-
(1985)
Invest New Drugs
, vol.3
, pp. 101-107
-
-
Alberts, D.S.1
Peng, Y.M.2
Bowden, G.T.3
-
15
-
-
0014353705
-
Effect of the vinca alkaloids on RNA synthesis in human cells in vitro
-
Wagner EK, Roizman B. Effect of the vinca alkaloids on RNA synthesis in human cells in vitro. Science 1968; 162: 569-70.
-
(1968)
Science
, vol.162
, pp. 569-570
-
-
Wagner, E.K.1
Roizman, B.2
-
16
-
-
0020561580
-
Inhibition of human lymphoma DNA-dependent RNA polymerase activity by 6-mercaptopurine ribonucleoside triphosphate
-
Kawahara RT, Chuang LF, Holmberg CA, et al. Inhibition of human lymphoma DNA-dependent RNA polymerase activity by 6-mercaptopurine ribonucleoside triphosphate. Cancer Res 1983; 43: 3655-9.
-
(1983)
Cancer Res
, vol.43
, pp. 3655-3659
-
-
Kawahara, R.T.1
Chuang, L.F.2
Holmberg, C.A.3
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