Cao A - Search Results

1

Heterozygous beta-thalassemia with thalassemia intermedia phenotype.

Gasperini D, Perseu L, Melis MA, Maccioni L, Sollaino MC, Paglietti E, Cao A, Galanello R. Gasperini D, et al. Among authors: cao a. Am J Hematol. 1998 Jan;57(1):43-7. doi: 10.1002/(sici)1096-8652(199801)57:1<43::aid-ajh7>3.0.co;2-1. Am J Hematol. 1998. PMID: 9423815 Free article.

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

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.

5

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

6

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.

7

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

8

Fetal hydrops in Sardinia: implications for genetic counselling.

Galanello R, Sanna MA, Maccioni L, Gasperini D, Melis MA, Rosatelli C, Monni G, Cao A. Galanello R, et al. Among authors: cao a. Clin Genet. 1990 Nov;38(5):327-31. doi: 10.1111/j.1399-0004.1990.tb03590.x. Clin Genet. 1990. PMID: 2282712

9

Interaction between deletion delta-thalassemia and beta zero-thalassemia (codon 39 nonsense mutation) in a Sardinian family.

Galanello R, Podda A, Melis MA, Monne M, Cao A. Galanello R, et al. Among authors: cao a. Prog Clin Biol Res. 1989;316B:113-21. Prog Clin Biol Res. 1989. PMID: 2482492

10

Interaction of heterozygous beta zero-thalassemia with single functional alpha-globin gene.

Galanello R, Paglietti E, Melis MA, Crobu MG, Addis M, Moi P, Cao A. Galanello R, et al. Among authors: cao a. Am J Hematol. 1988 Oct;29(2):63-6. doi: 10.1002/ajh.2830290202. Am J Hematol. 1988. PMID: 3189303

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