Meloni A - Search Results

1

A promoter mutation, C-->T at position -92, leading to silent beta-thalassaemia.

Rosatelli MC, Faà V, Meloni A, Fiorenza F, Galanello R, Gasperini D, Amendola G, Cao A. Rosatelli MC, et al. Among authors: meloni a. Br J Haematol. 1995 Jun;90(2):483-5. doi: 10.1111/j.1365-2141.1995.tb05182.x. Br J Haematol. 1995. PMID: 7794779

2

A novel beta-thalassemia mutation (G-->A) at the initiation codon of the beta-globin gene.

Saba L, Meloni A, Sardu R, Travi M, Primignani P, Rosatelli MC, Cao A. Saba L, et al. Among authors: meloni a. Hum Mutat. 1992;1(5):420-2. doi: 10.1002/humu.1380010512. Hum Mutat. 1992. PMID: 1301952 No abstract available.

3

A simple electrophoretic procedure for fetal diagnosis of beta-thalassaemia due to short deletions.

Faà V, Rosatelli MC, Sardu R, Meloni A, Toffoli C, Cao A. Faà V, et al. Among authors: meloni a. Prenat Diagn. 1992 Nov;12(11):903-8. doi: 10.1002/pd.1970121109. Prenat Diagn. 1992. PMID: 1494543

4

Molecular screening and fetal diagnosis of beta-thalassemia in the Italian population.

Rosatelli MC, Tuveri T, Scalas MT, Leoni GB, Sardu R, Faà V, Meloni A, Pischedda MA, Demurtas M, Monni G, et al. Rosatelli MC, et al. Among authors: meloni a. Hum Genet. 1992 Aug;89(6):585-9. doi: 10.1007/BF00221942. Hum Genet. 1992. PMID: 1511973

5

Promoter mutations producing mild beta-thalassaemia in the Italian population.

Meloni A, Rosatelli MC, Faà V, Sardu R, Saba L, Murru S, Sciarratta GV, Baldi M, Tannoia N, Vitucci A, et al. Meloni A, et al. Br J Haematol. 1992 Feb;80(2):222-6. doi: 10.1111/j.1365-2141.1992.tb08904.x. Br J Haematol. 1992. PMID: 1550780

6

Molecular characterization of beta-thalassemia in the Sardinian population.

Rosatelli MC, Dozy A, Faà V, Meloni A, Sardu R, Saba L, Kan YW, Cao A. Rosatelli MC, et al. Among authors: meloni a. Am J Hum Genet. 1992 Feb;50(2):422-6. Am J Hum Genet. 1992. PMID: 1734721 Free PMC article.

7

Molecular mechanism accounting for milder types of thalassemia major.

Furbetta M, Tuveri T, Rosatelli C, Angius A, Falchi AM, Cossu P, Meloni A, Giagu N, Cao A. Furbetta M, et al. Among authors: meloni a. J Pediatr. 1983 Jul;103(1):35-9. doi: 10.1016/s0022-3476(83)80771-9. J Pediatr. 1983. PMID: 6191017

8

Two novel mutations in the transmembrane domains of the CFTR gene in subjects of Sardinian descent.

Saba L, Leoni GB, Meloni A, Faà V, Cao A, Rosatelli MC. Saba L, et al. Among authors: meloni a. Hum Mol Genet. 1993 Oct;2(10):1739-40. doi: 10.1093/hmg/2.10.1739. Hum Mol Genet. 1993. PMID: 7505693 No abstract available.

9

Homozygous beta-thalassaemia resulting in the beta-thalassaemia carrier state phenotype.

Rosatelli MC, Pischedda A, Meloni A, Saba L, Pomo A, Travi M, Fattore S, Cao A. Rosatelli MC, et al. Among authors: meloni a. Br J Haematol. 1994 Nov;88(3):562-5. doi: 10.1111/j.1365-2141.1994.tb05074.x. Br J Haematol. 1994. PMID: 7819068

10

A novel beta-thalassemia mutation: frameshift at codon 59 detected in an Italian carrier.

Meloni A, Demurtas M, Moi L, Faà V, Cao A, Rosatelli MC. Meloni A, et al. Hum Mutat. 1994;3(3):309-11. doi: 10.1002/humu.1380030322. Hum Mutat. 1994. PMID: 8019567 No abstract available.

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