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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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1995 | 1 |
1997 | 3 |
1998 | 1 |
2024 | 0 |
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Page 1
Gilbert syndrome and glucose-6-phosphate dehydrogenase deficiency: a dose-dependent genetic interaction crucial to neonatal hyperbilirubinemia.
Proc Natl Acad Sci U S A. 1997 Oct 28;94(22):12128-32. doi: 10.1073/pnas.94.22.12128.
Proc Natl Acad Sci U S A. 1997.
PMID: 9342374
Free PMC article.
Hyperbilirubinaemia in heterozygous beta-thalassaemia is related to co-inherited Gilbert's syndrome.
Galanello R, Perseu L, Melis MA, Cipollina L, Barella S, Giagu N, Turco MP, Maccioni O, Cao A.
Galanello R, et al.
Br J Haematol. 1997 Nov;99(2):433-6. doi: 10.1046/j.1365-2141.1997.3703182.x.
Br J Haematol. 1997.
PMID: 9375768
Free article.
Item in Clipboard
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 BA, Lindhout D, Tytgat GN, Jansen PL, Oude Elferink RP, et al.
Bosma PJ, et al.
N Engl J Med. 1995 Nov 2;333(18):1171-5. doi: 10.1056/NEJM199511023331802.
N Engl J Med. 1995.
PMID: 7565971
Free article.
Item in Clipboard
The expression of uridine diphosphate glucuronosyltransferase gene is a major determinant of bilirubin level in heterozygous beta-thalassaemia and in glucose-6-phosphate dehydrogenase deficiency.
Sampietro M, Lupica L, Perrero L, Comino A, Martinez di Montemuros F, Cappellini MD, Fiorelli G.
Sampietro M, et al.
Br J Haematol. 1997 Nov;99(2):437-9. doi: 10.1046/j.1365-2141.1997.4113228.x.
Br J Haematol. 1997.
PMID: 9375769
Free article.
Item in Clipboard
UGT1 promoter polymorphism accounts for increased neonatal appearance of hereditary spherocytosis.
Iolascon A, Faienza MF, Moretti A, Perrotta S, Miraglia del Giudice E.
Iolascon A, et al.
Blood. 1998 Feb 1;91(3):1093.
Blood. 1998.
PMID: 9446675
Free article.
No abstract available.
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