Cao A - Search Results

1

Relationship between genotype and phenotype. Thalassemia intermedia.

Galanello R, Cao A. Galanello R, et al. Among authors: cao a. Ann N Y Acad Sci. 1998 Jun 30;850:325-33. doi: 10.1111/j.1749-6632.1998.tb10489.x. Ann N Y Acad Sci. 1998. PMID: 9668554 Review.

2

Homozygosity for nondeletion delta-beta(0) thalassemia resulting in a silent clinical phenotype.

Galanello R, Barella S, Satta S, Maccioni L, Pintor C, Cao A. Galanello R, et al. Among authors: cao a. Blood. 2002 Sep 1;100(5):1913-4. Blood. 2002. PMID: 12176917 Free article.

3

Somatic deletion of the normal beta-globin gene leading to thalassaemia intermedia in heterozygous beta-thalassaemic patients.

Galanello R, Perseu L, Perra C, Maccioni L, Barella S, Longinotti M, Cao A, Cazzola M. Galanello R, et al. Among authors: cao a. Br J Haematol. 2004 Dec;127(5):604-6. doi: 10.1111/j.1365-2141.2004.05237.x. Br J Haematol. 2004. PMID: 15566365 Free article.

4

Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia.

Uda M, Galanello R, Sanna S, Lettre G, Sankaran VG, Chen W, Usala G, Busonero F, Maschio A, Albai G, Piras MG, Sestu N, Lai S, Dei M, Mulas A, Crisponi L, Naitza S, Asunis I, Deiana M, Nagaraja R, Perseu L, Satta S, Cipollina MD, Sollaino C, Moi P, Hirschhorn JN, Orkin SH, Abecasis GR, Schlessinger D, Cao A. Uda M, et al. Among authors: cao a. 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.

5

Beta-thalassemia.

Cao A, Galanello R. Cao A, et al. Genet Med. 2010 Feb;12(2):61-76. doi: 10.1097/GIM.0b013e3181cd68ed. Genet Med. 2010. PMID: 20098328 Free article. Review.

6

H63D mutation in the HFE gene increases iron overload in beta-thalassemia carriers.

Melis MA, Cau M, Deidda F, Barella S, Cao A, Galanello R. Melis MA, et al. Among authors: cao a. Haematologica. 2002 Mar;87(3):242-5. Haematologica. 2002. PMID: 11869934

7

Normal delta-globin gene sequences in Sardinian nondeletional delta beta-thalassemia.

Loudianos G, Moi P, Lavinha J, Galanello R, Cao A, Pirastu M. Loudianos G, et al. Among authors: cao a. Hemoglobin. 1992;16(6):503-9. doi: 10.3109/03630269208993118. Hemoglobin. 1992. PMID: 1487421

8

Heterozygous beta-thalassemia: relationship between the hematological phenotype and the type of beta-thalassemia mutation.

Rosatelli C, Leoni GB, Tuveri T, Scalas MT, Mosca A, Galanello R, Gasperini D, Cao A. Rosatelli C, et al. Among authors: cao a. Am J Hematol. 1992 Jan;39(1):1-4. doi: 10.1002/ajh.2830390102. Am J Hematol. 1992. PMID: 1536137

9

Hemoglobin Cagliari (beta 60 [E4] Val----Glu): a novel unstable thalassemic hemoglobinopathy.

Podda A, Galanello R, Maccioni L, Melis MA, Rosatelli C, Perseu L, Cao A. Podda A, et al. Among authors: cao a. Blood. 1991 Jan 15;77(2):371-5. Blood. 1991. PMID: 1985702 Free article.

10

Thalassemias in Sardinia: molecular pathology, phenotype-genotype correlation, and prevention.

Cao A, Rosatelli C, Pirastu M, Galanello R. Cao A, et al. Am J Pediatr Hematol Oncol. 1991 Summer;13(2):179-88. Am J Pediatr Hematol Oncol. 1991. PMID: 2069229

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