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Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia.
Proc Natl Acad Sci U S A. 2008 Feb 5;105(5):1620-5. doi: 10.1073/pnas.0711566105. Epub 2008 Feb 1.
Proc Natl Acad Sci U S A. 2008.
PMID: 18245381
Free PMC article.
Co-inherited Gilbert's syndrome: a factor determining hyperbilirubinemia in homozygous beta-thalassemia.
Galanello R, Cipollina MD, Dessì C, Giagu N, Lai E, Cao A.
Galanello R, et al. Among authors: cipollina md.
Haematologica. 1999 Feb;84(2):103-5.
Haematologica. 1999.
PMID: 10091405
Clinical Trial.
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Cholelithiasis and Gilbert's syndrome in homozygous beta-thalassaemia.
Galanello R, Piras S, Barella S, Leoni GB, Cipollina MD, Perseu L, Cao A.
Galanello R, et al. Among authors: cipollina md.
Br J Haematol. 2001 Dec;115(4):926-8. doi: 10.1046/j.1365-2141.2001.03200.x.
Br J Haematol. 2001.
PMID: 11843828
Free article.
Item in Clipboard
Hyperbilirubinemia, glucose-6-phosphate-dehydrogenase deficiency and Gilbert's syndrome.
Galanello R, Cipollina MD, Carboni G, Perseu L, Barella S, Corrias A, Cao A.
Galanello R, et al. Among authors: cipollina md.
Eur J Pediatr. 1999 Nov;158(11):914-6. doi: 10.1007/s004310051241.
Eur J Pediatr. 1999.
PMID: 10541948
Clinical Trial.
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