-
1
-
-
0001747399
-
Hereditary jaundice and disorders of bilirubin metabolism
-
Sriver CR, Beaudet AL, Sly WS, Valle D, editores. Nueva York: McGraw-Hill
-
Chowdhury JR, Wolkoff AW, Chowdhury NR, Arias IM. Hereditary jaundice and disorders of bilirubin metabolism. En: Sriver CR, Beaudet AL, Sly WS, Valle D, editores. The metabolic and molecular basis of inherited diseases. Nueva York: McGraw-Hill, 1995; 2161-2208
-
(1995)
The Metabolic and Molecular Basis of Inherited Diseases
, pp. 2161-2208
-
-
Chowdhury, J.R.1
Wolkoff, A.W.2
Chowdhury, N.R.3
Arias, I.M.4
-
2
-
-
0028276410
-
Bilirubin UDP-glucuronosyltransferase 1 is the only relevant bilirubin glucuronidating isoform in man
-
Bosma PJ, Seppen J, Goldhoorn B. Bilirubin UDP-glucuronosyltransferase 1 is the only relevant bilirubin glucuronidating isoform in man. J Biol Chem 1994; 269: 17960-17964.
-
(1994)
J Biol Chem
, vol.269
, pp. 17960-17964
-
-
Bosma, P.J.1
Seppen, J.2
Goldhoorn, B.3
-
3
-
-
0028867826
-
The genetic basis of the reduced expression of bilirubin UDP-glucuronosyltransferase 1 in Gilbert's syndrome
-
Bosma PJ, Chowdhury JR, Bakker C, Gantla S, de Boer A, Oostra B et al. The genetic basis of the reduced expression of bilirubin UDP-glucuronosyltransferase 1 in Gilbert's syndrome. N Engl J Med 1995; 333: 1171-1175.
-
(1995)
N Engl J Med
, vol.333
, pp. 1171-1175
-
-
Bosma, P.J.1
Chowdhury, J.R.2
Bakker, C.3
Gantla, S.4
De Boer, A.5
Oostra, B.6
-
4
-
-
0030030762
-
Genetic variation in bilirubin UDP-glucoronosyltransferase gen promoter and Gilbert's syndrome
-
Monaghan G, Ryan M, Seddon R, Hume R, Burchell B. Genetic variation in bilirubin UDP-glucoronosyltransferase gen promoter and Gilbert's syndrome. Lancet 1996; 347: 578-581.
-
(1996)
Lancet
, vol.347
, pp. 578-581
-
-
Monaghan, G.1
Ryan, M.2
Seddon, R.3
Hume, R.4
Burchell, B.5
-
5
-
-
0032860652
-
Molecular pathology of Crigler-Najjar type I and II and Gilbert's syndrome
-
Sampietro M, Iolascon A. Molecular pathology of Crigler-Najjar type I and II and Gilbert's Syndrome. Haematologica 1999; 84: 150-157.
-
(1999)
Haematologica
, vol.84
, pp. 150-157
-
-
Sampietro, M.1
Iolascon, A.2
-
6
-
-
0032852420
-
Co-inherited Gilbert's syndrome: A factor determining hyperbilirubinemia in homozygous beta-thalassaemia
-
Galanello R, Cipollina MD, Dessi C, Giagu N, Lai E, Cao A. Co-inherited Gilbert's syndrome: a factor determining hyperbilirubinemia in homozygous beta-thalassaemia. Haematologica 1999; 84: 103-105.
-
(1999)
Haematologica
, vol.84
, pp. 103-105
-
-
Galanello, R.1
Cipollina, M.D.2
Dessi, C.3
Giagu, N.4
Lai, E.5
Cao, A.6
-
7
-
-
0030663191
-
The expression of uridine diphosphate glucoronosyltransferase gene is a major determinant of bilirrubin level in heterozygous β-thalassaemia and in glucose-6-phosphate dehydrogenese deficiency
-
Sampietro M, Lupica L, Perrero L, Comino A, Martínez F, Cappellini D et al. The expression of uridine diphosphate glucoronosyltransferase gene is a major determinant of bilirrubin level in heterozygous β-thalassaemia and in glucose-6-phosphate dehydrogenese deficiency. Br J Haematol 1997; 99: 437-439.
-
(1997)
Br J Haematol
, vol.99
, pp. 437-439
-
-
Sampietro, M.1
Lupica, L.2
Perrero, L.3
Comino, A.4
Martínez, F.5
Cappellini, D.6
-
8
-
-
0008435402
-
Coinheritance of Gilbert syndrome increases the risk for developing gallstones in patients with hereditary spherocytosis
-
Miraglia del Giudice E, Perrotta S, Nobili B, Specchia C, d'Urzo G, Iolascon A. Coinheritance of Gilbert Syndrome increases the risk for developing gallstones in patients with hereditary spherocytosis. Blood 1999; 94: 2259-2262.
-
(1999)
Blood
, vol.94
, pp. 2259-2262
-
-
Miraglia Del Giudice, E.1
Perrotta, S.2
Nobili, B.3
Specchia, C.4
D'Urzo, G.5
Iolascon, A.6
-
9
-
-
0033510908
-
Gilbert's syndrome is a contributory factor in prolonged uncongugated hyperbilirubinemia of the newborn
-
Monaghan G, McLellan A, McGeehan A, Li Volti S, Mollica F, Salemi I et al. Gilbert's syndrome is a contributory factor in prolonged uncongugated hyperbilirubinemia of the newborn. J Pediatr 1999; 134: 441-446.
-
(1999)
J Pediatr
, vol.134
, pp. 441-446
-
-
Monaghan, G.1
McLellan, A.2
McGeehan, A.3
Li Volti, S.4
Mollica, F.5
Salemi, I.6
-
10
-
-
0032493441
-
Racial variability in the UDP-glucuronosyltransferase 1 (UGT-1A1) promoter: A balanced polymorphism for regulation of bilirubin metabolism?
-
Beutler E, Gelbart T, Demina A. Racial variability in the UDP-glucuronosyltransferase 1 (UGT-1A1) promoter: a balanced polymorphism for regulation of bilirubin metabolism? Proc Natl Acad Sci USA 1998; 95: 8170-8174.
-
(1998)
Proc Natl Acad Sci USA
, vol.95
, pp. 8170-8174
-
-
Beutler, E.1
Gelbart, T.2
Demina, A.3
|