Gilbert's syndrome--a legitimate genetic anomaly?
- PMID: 7565981
- DOI: 10.1056/NEJM199511023331812
Gilbert's syndrome--a legitimate genetic anomaly?
Comment on
-
The genetic basis of the reduced expression of bilirubin UDP-glucuronosyltransferase 1 in Gilbert's syndrome.N Engl J Med. 1995 Nov 2;333(18):1171-5. doi: 10.1056/NEJM199511023331802. N Engl J Med. 1995. PMID: 7565971
Similar articles
-
The genetic basis of the reduced expression of bilirubin UDP-glucuronosyltransferase 1 in Gilbert's syndrome.N Engl J Med. 1995 Nov 2;333(18):1171-5. doi: 10.1056/NEJM199511023331802. N Engl J Med. 1995. PMID: 7565971
-
[From gene to disease; unconjugated hyperbilirubinemia: Gilbert's syndrome and Crigler-Najjar types I and II].Ned Tijdschr Geneeskd. 2002 Aug 10;146(32):1488-90. Ned Tijdschr Geneeskd. 2002. PMID: 12198827 Review. Dutch.
-
The genetic basis of Gilbert's syndrome.Lancet. 1996 Mar 2;347(9001):557-8. doi: 10.1016/s0140-6736(96)91266-0. Lancet. 1996. PMID: 8596313 No abstract available.
-
Co-occurrence of three different mutations in the bilirubin UDP-glucuronosyltransferase gene in a Chinese family with Crigler-Najjar syndrome type I and Gilbert's syndrome.Clin Genet. 2003 Nov;64(5):420-3. doi: 10.1034/j.1399-0004.2003.00136.x. Clin Genet. 2003. PMID: 14616765
-
Molecular pathology of Crigler-Najjar type I and II and Gilbert's syndromes.Haematologica. 1999 Feb;84(2):150-7. Haematologica. 1999. PMID: 10091414 Review.
Cited by
-
[Unilateral conjunctival chemosis with edematous facial involvement].Ophthalmologe. 2017 Feb;114(2):167-169. doi: 10.1007/s00347-016-0284-y. Ophthalmologe. 2017. PMID: 27251332 German. No abstract available.
-
DNA dynamics is likely to be a factor in the genomic nucleotide repeats expansions related to diseases.PLoS One. 2011;6(5):e19800. doi: 10.1371/journal.pone.0019800. Epub 2011 May 20. PLoS One. 2011. PMID: 21625483 Free PMC article.
-
Exploring the link between Gilbert's syndrome and atherosclerotic cardiovascular disease: insights from a subpopulation-based analysis of over one million individuals.Eur Heart J Open. 2023 Jun 9;3(3):oead059. doi: 10.1093/ehjopen/oead059. eCollection 2023 May. Eur Heart J Open. 2023. PMID: 37377635 Free PMC article. No abstract available.
-
Mixed Dubin-Gilbert Syndrome: A Compound Heterozygous Phenotype of Two Novel Variants in ABCC2 Gene.Chin Med J (Engl). 2017 Apr 20;130(8):1003-1005. doi: 10.4103/0366-6999.204108. Chin Med J (Engl). 2017. PMID: 28397734 Free PMC article. No abstract available.
-
Primary myelofibrosis with thrombophilia as first symptom combined with thalassemia and Gilbert syndrome: A case report.World J Clin Cases. 2022 May 6;10(13):4161-4170. doi: 10.12998/wjcc.v10.i13.4161. World J Clin Cases. 2022. PMID: 35665102 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources