-
1
-
-
0001747399
-
Hereditary jaundice and disorders of bilirubin metabolism
-
Scriver CR, Beaudet AI, Sly WS, Valle D, editors. New York: McGraw-Hill
-
1. Roy Chowdhury J, Wolkoff A, Roy Chowdhury N, Arias IM. Hereditary jaundice and disorders of bilirubin metabolism. In: Scriver CR, Beaudet AI, Sly WS, Valle D, editors. The metabolic basis of inherited disease. 7th ed. New York: McGraw-Hill; 1995. p. 2161-208.
-
(1995)
The Metabolic Basis of Inherited Disease. 7th Ed.
, pp. 2161-2208
-
-
Roy Chowdhury, J.1
Wolkoff, A.2
Roy Chowdhury, N.3
Arias, I.M.4
-
2
-
-
0018574014
-
Postnatal development or uridine diphosphate glucuronosyltransferase activity towards bilirubin and 2-aminophenol in human liver
-
2. Onishi S, Kawade N, Itoh S, Isobe K, Sugiama S. Postnatal development or uridine diphosphate glucuronosyltransferase activity towards bilirubin and 2-aminophenol in human liver. Biochem J 1979;184:705-7.
-
(1979)
Biochem J
, vol.184
, pp. 705-707
-
-
Onishi, S.1
Kawade, N.2
Itoh, S.3
Isobe, K.4
Sugiama, S.5
-
3
-
-
0000621679
-
Prolonged neonatal unconjugated hyperbilirubinaemia associated with breast-feeding and a steroid, pregnane-3α 20β-diol, in maternal milk that inhibits glucuronide formation in vitro
-
3. Arias IM, Gartner L, Seifter S, Furman M. Prolonged neonatal unconjugated hyperbilirubinaemia associated with breast-feeding and a steroid, pregnane-3α 20β-diol, in maternal milk that inhibits glucuronide formation in vitro. J Clin Invest 1964;43: 2037-47.
-
(1964)
J Clin Invest
, vol.43
, pp. 2037-2047
-
-
Arias, I.M.1
Gartner, L.2
Seifter, S.3
Furman, M.4
-
4
-
-
0017861029
-
Clinical study of prolonged jaundice in breast-and bottle-fed babies
-
4. Winfield CR, MacFaul R. Clinical study of prolonged jaundice in breast-and bottle-fed babies. Arch Dis Child 1978;53:506-7.
-
(1978)
Arch Dis Child
, vol.53
, pp. 506-507
-
-
Winfield, C.R.1
MacFaul, R.2
-
6
-
-
0023936363
-
Jaundice in the healthy newborn infant: A new approach to an old problem
-
6. Maisels MJ, Gifford K, Antle CE, Leib GR. Jaundice in the healthy newborn infant: a new approach to an old problem. Pediatrics 1988;81:505-11.
-
(1988)
Pediatrics
, vol.81
, pp. 505-511
-
-
Maisels, M.J.1
Gifford, K.2
Antle, C.E.3
Leib, G.R.4
-
7
-
-
0020639259
-
Neonatal jaundice in full-term infants: Role of breast-feeding and other causes
-
7. Maisels MJ, Gifford K. Neonatal jaundice in full-term infants: role of breast-feeding and other causes. Am J Dis Child 1983;137:561-2.
-
(1983)
Am J Dis Child
, vol.137
, pp. 561-562
-
-
Maisels, M.J.1
Gifford, K.2
-
8
-
-
0028867826
-
The genetic basis of reduced expression of bilirubin UDP-glucuronosyltransferase in Gilbert's syndrome
-
8. Bosma PJ, Roy Chowdhury J, Bakker C, Gantla S, de Boer A, Oostra BA, et al. The genetic basis of reduced expression of bilirubin UDP-glucuronosyltransferase 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
Gantla, S.4
De Boer, A.5
Oostra, B.A.6
-
9
-
-
0030030762
-
Genetic variation in bilirubin UDP-glucuronosyltransferase gene promoter and Gilbert's syndrome
-
9. Monaghan G, Ryan M, Seddon R, Hume R, Burchell B. Genetic variation in bilirubin UDP-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
Hume, R.4
Burchell, B.5
-
11
-
-
0030053274
-
The genetic basis of Gilbert's syndrome
-
11. 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
-
12
-
-
0018611018
-
Improved method for accurate quantitation of total and conjugated bilirubin in serum
-
12. Novros JS, Koch TR, Knoblock EC. Improved method for accurate quantitation of total and conjugated bilirubin in serum. Clin Chem 1979;25:1891-9.
-
(1979)
Clin Chem
, vol.25
, pp. 1891-1899
-
-
Novros, J.S.1
Koch, T.R.2
Knoblock, E.C.3
-
13
-
-
0030728222
-
Genetic defects of the UDP-glucuronosyltransferase-1 (UGT1) gene that cause familial non-haemolytic unconjugated hyperbilirubinaemias
-
13. Clarke DJ, Moghrabi N, Monaghan G, Cassidy A, Boxer B, Hume R, et al. Genetic defects of the UDP-glucuronosyltransferase-1 (UGT1) gene that cause familial non-haemolytic unconjugated hyperbilirubinaemias. Clin Chim Acta 1998;266:63-74.
-
(1998)
Clin Chim Acta
, vol.266
, pp. 63-74
-
-
Clarke, D.J.1
Moghrabi, N.2
Monaghan, G.3
Cassidy, A.4
Boxer, B.5
Hume, R.6
-
14
-
-
0028904620
-
Analysis of genes for bilirubin UDP-glucuronosyltransferase in Gilbert's syndrome
-
14. Aono S, Adachi Y, Uyama E, Yamada Y, Keino H, Nanno T, et al. Analysis of genes for bilirubin UDP-glucuronosyltransferase in Gilbert's syndrome. Lancet 1995;345:958-9.
-
(1995)
Lancet
, vol.345
, pp. 958-959
-
-
Aono, S.1
Adachi, Y.2
Uyama, E.3
Yamada, Y.4
Keino, H.5
Nanno, T.6
-
15
-
-
0003902055
-
Infant feeding 1995
-
Foster K, Lader D, Cheesbrough S, editors. (Office for National Statistics). London: Government Statistical Service, The Stationery Office
-
15. Foster K, Lader D, Cheesbrough S. Infant feeding 1995. In: Foster K, Lader D, Cheesbrough S, editors. (Office for National Statistics). Infant feeding 1995. London: Government Statistical Service, The Stationery Office; 1997. p. 1-8.
-
(1997)
Infant Feeding 1995
, pp. 1-8
-
-
Foster, K.1
Lader, D.2
Cheesbrough, S.3
-
16
-
-
0024602667
-
The effect of saccharolactone on rat intestinal absorption of bilirubin in the presence of human breast milk
-
16. Gourley GR, Gourley MF, Arend R, Palta M. The effect of saccharolactone on rat intestinal absorption of bilirubin in the presence of human breast milk. Pediatr Res 1989;25:234-8.
-
(1989)
Pediatr Res
, vol.25
, pp. 234-238
-
-
Gourley, G.R.1
Gourley, M.F.2
Arend, R.3
Palta, M.4
-
17
-
-
0030691028
-
Gilbert syndrome and glucose-6-phosphate dehydrogenase deficiency. A dose-dependent genetic interaction crucial to neonatal hyperbilirubinemia
-
17. Kaplan M, Renbaum P, Levy-Lahad E, Hammerman C, Lahad A, Beutler E. Gilbert syndrome and glucose-6-phosphate dehydrogenase deficiency. A dose-dependent genetic interaction crucial to neonatal hyperbilirubinemia. Proc Natl Acad Sci USA 1997;94: 12128-32.
-
(1997)
Proc Natl Acad Sci USA
, vol.94
, pp. 12128-12132
-
-
Kaplan, M.1
Renbaum, P.2
Levy-Lahad, E.3
Hammerman, C.4
Lahad, A.5
Beutler, E.6
-
18
-
-
0032005254
-
UGT promoter polymorphism accounts for increased neonatal appearance of hereditary spherocytosis
-
18. Iolascon A, Faienza MF, Moretti A, Perotta S, Miraglia del Giudice E. UGT promoter polymorphism accounts for increased neonatal appearance of hereditary spherocytosis. Blood 1998;91:1093.
-
(1998)
Blood
, vol.91
, pp. 1093
-
-
Iolascon, A.1
Faienza, M.F.2
Moretti, A.3
Perotta, S.4
Miraglia Del Giudice, E.5
-
19
-
-
0030663191
-
The expression of UDP-glucuronosyltransferase is a major determinant of bilirubin level in heterozygous β-thalassaemia and in glucose-6-phosphate dehydrogenase deficiency
-
19. Sanpietro M, Lupica L, Perrero L, Comino A, Martinez DI, Mantemuros F, et al. The expression of UDP-glucuronosyltransferase is a major determinant of bilirubin level in heterozygous β-thalassaemia and in glucose-6-phosphate dehydrogenase deficiency. Br J Haematol 1997;99:437-9.
-
(1997)
Br J Haematol
, vol.99
, pp. 437-439
-
-
Sanpietro, M.1
Lupica, L.2
Perrero, L.3
Comino, A.4
Martinez, D.I.5
Mantemuros, F.6
-
21
-
-
0032493441
-
Racial variability in the UDP-glucuronosyltransferase 1 (UGTIAI) promoter: A balanced polymorphism for regulation of bilirubin metabolism
-
21. Beutler E, Gelbert T, Demina A. Racial variability in the UDP-glucuronosyltransferase 1 (UGTIAI) promoter: a balanced polymorphism for regulation of bilirubin metabolism. Proc Natl Acad Sci USA 1998;95: 8170-4.
-
(1998)
Proc Natl Acad Sci USA
, vol.95
, pp. 8170-8174
-
-
Beutler, E.1
Gelbert, T.2
Demina, A.3
-
22
-
-
0031719562
-
Neonatal hyperbilirubinaemia and mutation of bilirubin UDP-glucuronosyltransferase gene: A common missense mutation among Japanese, Koreans and Chinese
-
22. Akaba K, Kimura T, Sasaki A, Tanabe S, Ikogami T, Hashimoto M, et al. Neonatal hyperbilirubinaemia and mutation of bilirubin UDP-glucuronosyltransferase gene: a common missense mutation among Japanese, Koreans and Chinese. Biochem Mol Biol Int 1998;46:21-6.
-
(1998)
Biochem Mol Biol Int
, vol.46
, pp. 21-26
-
-
Akaba, K.1
Kimura, T.2
Sasaki, A.3
Tanabe, S.4
Ikogami, T.5
Hashimoto, M.6
-
23
-
-
0016242097
-
Navajo jaundice: A variant of neonatal hyperbilirubinemia associated with breast-feeding
-
23. Saland J, McNamara H, Cohen MI. Navajo jaundice: a variant of neonatal hyperbilirubinemia associated with breast-feeding. J Pediatr 1974;85:271-5.
-
(1974)
J Pediatr
, vol.85
, pp. 271-275
-
-
Saland, J.1
McNamara, H.2
Cohen, M.I.3
-
24
-
-
0018216093
-
Jaundice and breast-feeding among Alaska Eskimo newborns
-
24. Fisher Q, Cohen MI, Curda L. Jaundice and breast-feeding among Alaska Eskimo newborns. Am J Dis Child 1978;132:859-63.
-
(1978)
Am J Dis Child
, vol.132
, pp. 859-863
-
-
Fisher, Q.1
Cohen, M.I.2
Curda, L.3
-
25
-
-
0027085807
-
Jaundice in Navajo neonates
-
25. Johnson JD. Jaundice in Navajo neonates. Clin Pediatr (Phila) 1992; 12:716-8.
-
(1992)
Clin Pediatr (Phila)
, vol.12
, pp. 716-718
-
-
Johnson, J.D.1
-
26
-
-
0031949264
-
Gilbert syndrome accelerates development of neonatal jaundice
-
26. Bancroft JD, Kreamer B, Gourley GR. Gilbert syndrome accelerates development of neonatal jaundice. J Pediatr 1998;132:656-60.
-
(1998)
J Pediatr
, vol.132
, pp. 656-660
-
-
Bancroft, J.D.1
Kreamer, B.2
Gourley, G.R.3
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