Rosatelli MC - 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. 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 silent beta-thalassemia mutation in the distal CACCC box affects the binding and responsiveness to EKLF.

Moi P, Faà V, Marini MG, Asunis I, Ibba G, Cao A, Rosatelli MC. Moi P, et al. Among authors: rosatelli mc. Br J Haematol. 2004 Sep;126(6):881-4. doi: 10.1111/j.1365-2141.2004.05146.x. Br J Haematol. 2004. PMID: 15352994 Free article.

3

Thalassaemia-like carriers not linked to the beta-globin gene cluster.

Faà V, Meloni A, Moi L, Ibba G, Travi M, Vitucci A, Cao A, Rosatelli MC. Faà V, et al. Among authors: rosatelli mc. Br J Haematol. 2006 Mar;132(5):640-50. doi: 10.1111/j.1365-2141.2005.05915.x. Br J Haematol. 2006. PMID: 16445840 Free article.

4

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: rosatelli mc. Prenat Diagn. 1992 Nov;12(11):903-8. doi: 10.1002/pd.1970121109. Prenat Diagn. 1992. PMID: 1494543

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. Among authors: rosatelli mc. 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

Erythropoiesis following bone marrow transplantation from donors heterozygous for beta-thalassaemia.

Galanello R, Barella S, Maccioni L, Paglietti E, Melis MA, Rosatelli MC, Argiolu F, Cao A. Galanello R, et al. Among authors: rosatelli mc. Br J Haematol. 1989 Aug;72(4):561-6. doi: 10.1111/j.1365-2141.1989.tb04324.x. Br J Haematol. 1989. PMID: 2476170

7

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. Br J Haematol. 1994 Nov;88(3):562-5. doi: 10.1111/j.1365-2141.1994.tb05074.x. Br J Haematol. 1994. PMID: 7819068

8

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. Among authors: rosatelli mc. Hum Mutat. 1994;3(3):309-11. doi: 10.1002/humu.1380030322. Hum Mutat. 1994. PMID: 8019567 No abstract available.

9

Genotype-phenotype correlations in beta-thalassemias.

Cao A, Galanello R, Rosatelli MC. Cao A, et al. Among authors: rosatelli mc. Blood Rev. 1994 Mar;8(1):1-12. doi: 10.1016/0268-960x(94)90002-7. Blood Rev. 1994. PMID: 8205005 Review.

10

Screening and prenatal diagnosis of the haemoglobinopathies.

Cao A, Rosatelli MC. Cao A, et al. Among authors: rosatelli mc. Baillieres Clin Haematol. 1993 Mar;6(1):263-86. doi: 10.1016/s0950-3536(05)80072-1. Baillieres Clin Haematol. 1993. PMID: 8394756 Review.

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