Pistidda P - Search Results

1

Application of a new method for GWAS in a related case/control sample with known pedigree structure: identification of new loci for nephrolithiasis.

Tore S, Casula S, Casu G, Concas MP, Pistidda P, Persico I, Sassu A, Maestrale GB, Mele C, Caruso MR, Bonerba B, Usai P, Deiana I, Thornton T, Pirastu M, Forabosco P. Tore S, et al. Among authors: pistidda p. PLoS Genet. 2011 Jan 20;7(1):e1001281. doi: 10.1371/journal.pgen.1001281. PLoS Genet. 2011. PMID: 21283782 Free PMC article.

2

Homozygous beta zero-39 mutation with thalassemia intermedia in northern Sardinia: clinical, hematological and molecular analysis.

Oggiano L, Dore F, Pistidda P, Guiso L, Manca L, Masala B, Pirastu M, Rosatelli C, Cao A, Longinotti M. Oggiano L, et al. Among authors: pistidda p. Hemoglobin. 1988;12(5-6):673-80. doi: 10.3109/03630268808991660. Hemoglobin. 1988. PMID: 2905346

3

A novel Mediterranean "delta beta-thalassemia" determinant containing the delta (+) 27 and beta (0) 39 point mutations in cis.

Oggiano L, Guiso L, Frogheri L, Loudianos G, Pistidda P, Rimini E, Pirastu M, Cao A, Longinotti M. Oggiano L, et al. Among authors: pistidda p. Am J Hematol. 1994 Jan;45(1):81-4. doi: 10.1002/ajh.2830450113. Am J Hematol. 1994. PMID: 7504402

4

A 12-year preventive program for beta-thalassemia in Northern Sardinia.

Longinotti M, Pistidda P, Oggiano L, Guiso L, Frogheri L, Dore F, Pardini S, Bonfigli S, Rimini E, Angioni S, et al. Longinotti M, et al. Among authors: pistidda p. Clin Genet. 1994 Sep;46(3):238-43. doi: 10.1111/j.1399-0004.1994.tb04233.x. Clin Genet. 1994. PMID: 7820938

5

[Differential diagnosis of thalassemia syndromes].

Dore F, Pardini S, Bonfigli S, Oggiano L, Murineddu M, Pistidda P, Guiso L, Frogheri L, Gaviano E, Longinotti M. Dore F, et al. Among authors: pistidda p. Ann Ital Med Int. 1992 Jan-Mar;7(1):34-41. Ann Ital Med Int. 1992. PMID: 1381931 Review. Italian.

6

[Current views of thalassemia intermedia].

Longinotti M, Dore F, Oggiano L, Pardini S, Pistidda P, Guiso L, Frogheri L, Bonfigli S, Murineddu M, Rimini E. Longinotti M, et al. Among authors: pistidda p. Recenti Prog Med. 1992 Apr;83(4):233-40. Recenti Prog Med. 1992. PMID: 1626119 Review. Italian.

7

Haematological phenotypes in a family with triplicated alpha-globin gene, beta zero 39 and delta+27 thalassaemia mutations.

Oggiano L, Rimini E, Frogheri L, Guiso L, Pistidda P, Longinotti M. Oggiano L, et al. Among authors: pistidda p. Clin Lab Haematol. 1992;14(4):289-92. Clin Lab Haematol. 1992. PMID: 1478008

8

Fetal hemoglobin expression in compound heterozygotes for -117 (G-->A)A gamma HPFH and beta zero 39 nonsense thalassemia.

Pistidda P, Frogheri L, Oggiano L, Guiso L, Manca L, Dore F, Masala B, Gilman JG, Longinotti M. Pistidda P, et al. Am J Hematol. 1995 Aug;49(4):267-70. doi: 10.1002/ajh.2830490402. Am J Hematol. 1995. PMID: 7543730

9

Hb Tigraye [beta79(EF3)Asp --> His] in a Caucasian family from Sardinia.

Pistidda P, Cherchi L, Corda M, Guiso L, Pardini S, Pirastru M, Manca L, Longinotti M, Masala B. Pistidda P, et al. Hemoglobin. 2001 Aug;25(3):341-5. doi: 10.1081/hem-100105229. Hemoglobin. 2001. PMID: 11570729 No abstract available.

10

Thalassemia intermedia resulting from a mild beta-thalassemia mutation.

Rosatelli MC, Oggiano L, Battista Leoni G, Tuveri T, Di Tucci A, Scalas MT, Dore F, Pistidda P, Massa A, Longinotti M, et al. Rosatelli MC, et al. Among authors: pistidda p. Blood. 1989 Feb;73(2):601-5. Blood. 1989. PMID: 2917193 Free article.

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