Barella S - Search Results

1

Delta-globin gene expression improves sickle cell disease in a humanised mouse model.

Porcu S, Simbula M, Marongiu MF, Perra A, Poddie D, Perseu L, Kowalik MA, Littera R, Barella S, Caria CA, Demartis FR, Ristaldi MS. Porcu S, et al. Among authors: barella s. Br J Haematol. 2021 Jun;193(6):1228-1237. doi: 10.1111/bjh.17561. Epub 2021 May 28. Br J Haematol. 2021. PMID: 34046885

2

Hb A2-Sant' Antioco [alpha 2 delta (2)93(F9)Cys-->Gly]: a new delta chain variant identified by sequencing of amplified DNA.

Galanello R, Gasperini D, Perseu L, Barella S, Ideo A, Cao A. Galanello R, et al. Among authors: barella s. Hemoglobin. 1994 Nov;18(6):437-9. doi: 10.3109/03630269409045776. Hemoglobin. 1994. PMID: 7713748 No abstract available.

3

Genotype of subjects with borderline hemoglobin A2 levels: implication for beta-thalassemia carrier screening.

Galanello R, Barella S, Ideo A, Gasperini D, Rosatelli C, Paderi L, Paglietti E, Sollaino C, Perseu L, Loi D, et al. Galanello R, et al. Among authors: barella s. Am J Hematol. 1994 Jun;46(2):79-81. doi: 10.1002/ajh.2830460204. Am J Hematol. 1994. PMID: 8172199

4

Normal individuals with high Hb A2 levels.

Gasperini D, Cao A, Paderi L, Barella S, Paglietti E, Perseu L, Loi D, Galanello R. Gasperini D, et al. Among authors: barella s. Br J Haematol. 1993 May;84(1):166-8. doi: 10.1111/j.1365-2141.1993.tb03042.x. Br J Haematol. 1993. PMID: 8338770

5

Hyperbilirubinaemia in heterozygous beta-thalassaemia is related to co-inherited Gilbert's syndrome.

Galanello R, Perseu L, Melis MA, Cipollina L, Barella S, Giagu N, Turco MP, Maccioni O, Cao A. Galanello R, et al. Among authors: barella s. Br J Haematol. 1997 Nov;99(2):433-6. doi: 10.1046/j.1365-2141.1997.3703182.x. Br J Haematol. 1997. PMID: 9375768 Free article.

6

Hyperbilirubinemia, glucose-6-phosphate-dehydrogenase deficiency and Gilbert's syndrome.

Galanello R, Cipollina MD, Carboni G, Perseu L, Barella S, Corrias A, Cao A. Galanello R, et al. Among authors: barella s. Eur J Pediatr. 1999 Nov;158(11):914-6. doi: 10.1007/s004310051241. Eur J Pediatr. 1999. PMID: 10541948 Clinical Trial.

7

Cholelithiasis and Gilbert's syndrome in homozygous beta-thalassaemia.

Galanello R, Piras S, Barella S, Leoni GB, Cipollina MD, Perseu L, Cao A. Galanello R, et al. Among authors: barella s. Br J Haematol. 2001 Dec;115(4):926-8. doi: 10.1046/j.1365-2141.2001.03200.x. Br J Haematol. 2001. PMID: 11843828 Free article.

8

Hb Belfast [beta15(A12)Trp-->Arg]: definition of the clinical and hematological phenotype.

Galanello R, Perseu L, Barella S, Satta S, Fais A, Era B, Corda M. Galanello R, et al. Among authors: barella s. Hemoglobin. 2004 Aug;28(3):217-22. doi: 10.1081/hem-120040219. Hemoglobin. 2004. PMID: 15481889

9

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: barella s. 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.

10

Clinical and molecular analysis of haemoglobin H disease in Sardinia: haematological, obstetric and cardiac aspects in patients with different genotypes.

Origa R, Sollaino MC, Giagu N, Barella S, Campus S, Mandas C, Bina P, Perseu L, Galanello R. Origa R, et al. Among authors: barella s. Br J Haematol. 2007 Jan;136(2):326-32. doi: 10.1111/j.1365-2141.2006.06423.x. Epub 2006 Nov 27. Br J Haematol. 2007. PMID: 17129226 Free article.

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