Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 1 to 50 of 52

1.

Corrosion and Oxidation Behavior of a Fe-Al-Mn-C Duplex Alloy.

Barella S, Ciuffini AF, Gruttadauria A, Mapelli C, Mombelli D, Longaretti E.

Materials (Basel). 2019 Aug 12;12(16). pii: E2572. doi: 10.3390/ma12162572.

2.

Characterization of Two Cases of Congenital Dyserythropoietic Anemia Type I Shed Light on the Uncharacterized C15orf41 Protein.

Russo R, Marra R, Andolfo I, De Rosa G, Rosato BE, Manna F, Gambale A, Raia M, Unal S, Barella S, Iolascon A.

Front Physiol. 2019 May 22;10:621. doi: 10.3389/fphys.2019.00621. eCollection 2019.

3.

Influence of Microstructure and Shot Peening Treatment on Corrosion Resistance of AISI F55-UNS S32760 Super Duplex Stainless Steel.

Ciuffini AF, Barella S, Peral Martínez LB, Mapelli C, Fernández Pariente I.

Materials (Basel). 2018 Jun 19;11(6). pii: E1038. doi: 10.3390/ma11061038.

4.

Hematological phenotypes in children according to the α-globin genotypes.

Origa R, Barella S, Paglietti ME, Anni F, Danjou F, Denotti AR, Desogus MF, Loi D, Orecchia V, Sollaino MC, Moi P.

Blood Cells Mol Dis. 2018 Mar;69:102-106. doi: 10.1016/j.bcmd.2017.10.003. Epub 2017 Nov 3.

PMID:
29162392
5.

Earlier initiation of transfusional and iron chelation therapies in recently born children with transfusion-dependent thalassemia.

Origa R, Tatti F, Zappu A, Leoni GB, Dessì C, Moi P, Morittu M, Orecchia V, Denotti AR, Pilia MP, Anni F, Perra M, Casini MR, Barella S.

Am J Hematol. 2017 Nov;92(11):E627-E628. doi: 10.1002/ajh.24869. Epub 2017 Sep 25. No abstract available.

6.

Changes in HbA2 and HbF in alpha thalassemia carriers with KLF1 mutation.

Satta S, Paglietti ME, Sollaino MC, Barella S, Moi P, Desogus MF, Demartis FR, Manunza L, Origa R.

Blood Cells Mol Dis. 2017 May;64:30-32. doi: 10.1016/j.bcmd.2017.03.007. Epub 2017 Mar 18.

PMID:
28342932
7.

The Problem of Borderline Hemoglobin A2 Levels in the Screening for β-Thalassemia Carriers in Sardinia.

Paglietti ME, Satta S, Sollaino MC, Barella S, Ventrella A, Desogus MF, Demartis FR, Manunza L, Origa R.

Acta Haematol. 2016;135(4):193-9. doi: 10.1159/000442194. Epub 2016 Jan 22.

PMID:
26794457
8.

The V736A TMPRSS6 polymorphism influences liver iron concentration in nontransfusion-dependent thalassemias.

Cau M, Danjou F, Chessa R, Serrenti M, Addis M, Barella S, Origa R.

Am J Hematol. 2015 Dec;90(12):E225-6. doi: 10.1002/ajh.24197. Epub 2015 Nov 17. No abstract available.

9.

Genome-wide association analyses based on whole-genome sequencing in Sardinia provide insights into regulation of hemoglobin levels.

Danjou F, Zoledziewska M, Sidore C, Steri M, Busonero F, Maschio A, Mulas A, Perseu L, Barella S, Porcu E, Pistis G, Pitzalis M, Pala M, Menzel S, Metrustry S, Spector TD, Leoni L, Angius A, Uda M, Moi P, Thein SL, Galanello R, Abecasis GR, Schlessinger D, Sanna S, Cucca F.

Nat Genet. 2015 Nov;47(11):1264-71. doi: 10.1038/ng.3307. Epub 2015 Sep 14.

10.

Lethal sepsis and malignant transformation in severe congenital neutropenia: report from the Italian Neutropenia Registry.

Fioredda F, Calvillo M, Lanciotti M, Cefalo MG, Tucci F, Farruggia P, Casazza G, Martire B, Bonanomi S, Notarangelo L, Barone A, Palazzi G, Davitto M, Barella S, Cardinale F, Mastrodicasa E, Cugno C, Russo G, Caviglia I, Caruso S, Castagnola E, Dufour C.

Pediatr Blood Cancer. 2015 Jun;62(6):1110-2. doi: 10.1002/pbc.25401. Epub 2015 Jan 25. No abstract available.

PMID:
25619745
11.

Differences in the erythropoiesis-hepcidin-iron store axis between hemoglobin H disease and β-thalassemia intermedia.

Origa R, Cazzola M, Mereu E, Danjou F, Barella S, Giagu N, Galanello R, Swinkels DW.

Haematologica. 2015 May;100(5):e169-71. doi: 10.3324/haematol.2014.115733. Epub 2015 Jan 16. No abstract available.

12.

Investigating the alpha1(NcoI) mutation.

Desogus MF, Paglietti ME, Sollaino MC, Barella S, Origa R.

Acta Haematol. 2015;133(2):145-7. doi: 10.1159/000363440. Epub 2014 Sep 20. No abstract available.

PMID:
25247841
13.

The efficiency of quartz addition on electric arc furnace (EAF) carbon steel slag stability.

Mombelli D, Mapelli C, Barella S, Gruttadauria A, Le Saout G, Garcia-Diaz E.

J Hazard Mater. 2014 Aug 30;279:586-96. doi: 10.1016/j.jhazmat.2014.07.045. Epub 2014 Jul 30.

PMID:
25113518
14.

Hepatocellular carcinoma in thalassaemia: an update of the Italian Registry.

Borgna-Pignatti C, Garani MC, Forni GL, Cappellini MD, Cassinerio E, Fidone C, Spadola V, Maggio A, Restivo Pantalone G, Piga A, Longo F, Gamberini MR, Ricchi P, Costantini S, D'Ascola D, Cianciulli P, Lai ME, Carta MP, Ciancio A, Cavalli P, Putti MC, Barella S, Amendola G, Campisi S, Capra M, Caruso V, Colletta G, Volpato S.

Br J Haematol. 2014 Oct;167(1):121-6. doi: 10.1111/bjh.13009. Epub 2014 Jul 3.

PMID:
24992281
15.

Efficacy and safety of deferiprone for the treatment of pantothenate kinase-associated neurodegeneration (PKAN) and neurodegeneration with brain iron accumulation (NBIA): results from a four years follow-up.

Cossu G, Abbruzzese G, Matta G, Murgia D, Melis M, Ricchi V, Galanello R, Barella S, Origa R, Balocco M, Pelosin E, Marchese R, Ruffinengo U, Forni GL.

Parkinsonism Relat Disord. 2014 Jun;20(6):651-4. doi: 10.1016/j.parkreldis.2014.03.002. Epub 2014 Mar 12.

PMID:
24661465
16.

A decisional algorithm to start iron chelation in patients with beta thalassemia.

Danjou F, Cabantchik ZI, Origa R, Moi P, Marcias M, Barella S, Defraia E, Dessì C, Foschini ML, Giagu N, Leoni GB, Morittu M, Galanello R.

Haematologica. 2014 Mar;99(3):e38-40. doi: 10.3324/haematol.2013.098202. No abstract available.

17.

Complexity of the alpha-globin genotypes identified with thalassemia screening in Sardinia.

Origa R, Paglietti ME, Sollaino MC, Desogus MF, Barella S, Loi D, Galanello R.

Blood Cells Mol Dis. 2014 Jan;52(1):46-9. doi: 10.1016/j.bcmd.2013.06.004. Epub 2013 Jul 27.

PMID:
23896219
18.

First detection of Hb Taybe [α38(C3) or α39(C4) Thr→0 (α1)] in an Italian child.

Paglietti ME, Sollaino MC, Loi D, Barella S, Desogus MF, Galanello R.

Hemoglobin. 2012;36(3):299-304. doi: 10.3109/03630269.2012.659780. Epub 2012 Mar 19.

PMID:
22428534
19.

A new β chain hemoglobin variant with increased oxygen affinity: Hb Santa Giusta Sardegna [β93(F9)Cys→Trp; HBB c.282T>G].

Fais A, Sollaino MC, Barella S, Perseu L, Era B, Corda M.

Hemoglobin. 2012;36(2):151-6. doi: 10.3109/03630269.2011.645982. Epub 2012 Jan 4.

PMID:
22217259
20.

KLF1 gene mutations cause borderline HbA(2).

Perseu L, Satta S, Moi P, Demartis FR, Manunza L, Sollaino MC, Barella S, Cao A, Galanello R.

Blood. 2011 Oct 20;118(16):4454-8. doi: 10.1182/blood-2011-04-345736. Epub 2011 Aug 5.

21.

A pilot trial of deferiprone for neurodegeneration with brain iron accumulation.

Abbruzzese G, Cossu G, Balocco M, Marchese R, Murgia D, Melis M, Galanello R, Barella S, Matta G, Ruffinengo U, Bonuccelli U, Forni GL.

Haematologica. 2011 Nov;96(11):1708-11. doi: 10.3324/haematol.2011.043018. Epub 2011 Jul 26.

22.

Seroma in lipoabdominoplasty and abdominoplasty: a comparative study using ultrasound.

Di Martino M, Nahas FX, Barbosa MV, Montecinos Ayaviri NA, Kimura AK, Barella SM, Novo NF, Ferreira LM.

Plast Reconstr Surg. 2010 Nov;126(5):1742-51. doi: 10.1097/PRS.0b013e3181efa6c5.

PMID:
20639797
23.

Amelioration of Sardinian beta0 thalassemia by genetic modifiers.

Galanello R, Sanna S, Perseu L, Sollaino MC, Satta S, Lai ME, Barella S, Uda M, Usala G, Abecasis GR, Cao A.

Blood. 2009 Oct 29;114(18):3935-7. doi: 10.1182/blood-2009-04-217901. Epub 2009 Aug 20.

24.

A mutation in the TMPRSS6 gene, encoding a transmembrane serine protease that suppresses hepcidin production, in familial iron deficiency anemia refractory to oral iron.

Melis MA, Cau M, Congiu R, Sole G, Barella S, Cao A, Westerman M, Cazzola M, Galanello R.

Haematologica. 2008 Oct;93(10):1473-9. doi: 10.3324/haematol.13342. Epub 2008 Jul 4.

25.

No evidence of cardiac iron in 20 never- or minimally-transfused patients with thalassemia intermedia.

Origa R, Barella S, Argiolas GM, Bina P, Agus A, Galanello R.

Haematologica. 2008 Jul;93(7):1095-6. doi: 10.3324/haematol.12484. Epub 2008 May 27. No abstract available.

26.

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.

Br J Haematol. 2007 Jan;136(2):326-32. Epub 2006 Nov 27.

PMID:
17129226
27.

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.

Br J Haematol. 2004 Dec;127(5):604-6.

PMID:
15566365
28.

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.

Hemoglobin. 2004 Aug;28(3):217-22.

PMID:
15481889
29.

Identification and functional characterization of a new hemoglobin variant in Sardinia: Hb Muravera [beta47 GAT->GTT, (CD6) Asp->Val].

Corda M, Fais A, Perseu L, Cipollina L, Barella S, Galanello R.

Haematologica. 2002 Oct;87(10):1111-2. No abstract available.

30.

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.

Blood. 2002 Sep 1;100(5):1913-4.

31.

Sterol-regulatory element-binding protein (SREBP)-2 contributes to polygenic hypercholesterolaemia.

Miserez AR, Muller PY, Barella L, Barella S, Staehelin HB, Leitersdorf E, Kark JD, Friedlander Y.

Atherosclerosis. 2002 Sep;164(1):15-26. Erratum in: Atherosclerosis. 2003 Jun;167(2):371.

PMID:
12119189
32.

H63D mutation in the HFE gene increases iron overload in beta-thalassemia carriers.

Melis MA, Cau M, Deidda F, Barella S, Cao A, Galanello R.

Haematologica. 2002 Mar;87(3):242-5.

33.

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

Galanello R, Piras S, Barella S, Leoni GB, Cipollina MD, Perseu L, Cao A.

Br J Haematol. 2001 Dec;115(4):926-8.

PMID:
11843828
34.

Leaf-to-shoot apex movement of symplastic tracer is restricted coincident with flowering in Arabidopsis.

Gisel A, Hempel FD, Barella S, Zambryski P.

Proc Natl Acad Sci U S A. 2002 Feb 5;99(3):1713-7. Epub 2002 Jan 29.

35.

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

Galanello R, Cipollina MD, Carboni G, Perseu L, Barella S, Corrias A, Cao A.

Eur J Pediatr. 1999 Nov;158(11):914-6.

PMID:
10541948
36.

Soluble transferrin receptor as a potential determinant of iron loading in congenital anaemias due to ineffective erythropoiesis.

Cazzola M, Beguin Y, Bergamaschi G, Guarnone R, Cerani P, Barella S, Cao A, Galanello R.

Br J Haematol. 1999 Sep;106(3):752-5.

37.

Temporal and spatial regulation of symplastic trafficking during development in Arabidopsis thaliana apices.

Gisel A, Barella S, Hempel FD, Zambryski PC.

Development. 1999 May;126(9):1879-89.

38.

Alpha-thalassemia carrier identification by DNA analysis in the screening for thalassemia.

Galanello R, Sollaino C, Paglietti E, Barella S, Perra C, Doneddu I, Pirroni MG, Maccioni L, Cao A.

Am J Hematol. 1998 Dec;59(4):273-8.

39.

Limits to the use of the glucose 6-phosphate dehydrogenase/6-phosphogluconate dehydrogenase index for the detection of glucose 6-phosphate dehydrogenase deficiency.

Mosca A, Paleari R, Sollaino C, Barella S, Galanello R.

Clin Chem Lab Med. 1998 Sep;36(9):737-8. No abstract available.

PMID:
9804400
40.

Hb Sassari [alpha 126(H9)Asp-->His] results from a GAC-->CAC mutation in the alpha 1-globin gene.

Paglietti E, Barella S, Satta S, Perra C, Cao A, Galanello R.

Hemoglobin. 1998 Jan;22(1):65-7. No abstract available.

PMID:
9494049
41.

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.

Br J Haematol. 1997 Nov;99(2):433-6.

PMID:
9375768
42.

Hb Puttelange [beta 140(H19)Ala-->Val] in an Italian man with polycythemia.

Galanello R, Paleari R, Perseu L, Barella S, Maccioni L, Cao A, Mulas G, Cocco E, Mosca A.

Hemoglobin. 1997 Jan;21(1):17-26.

PMID:
9028820
43.

Simultaneous automated determination of glucose 6-phosphate dehydrogenase and 6-phosphogluconate dehydrogenase activities in whole blood.

Mosca A, Paleari R, Rosti E, Luzzana M, Barella S, Sollaino C, Galanello R.

Eur J Clin Chem Clin Biochem. 1996 May;34(5):431-8.

PMID:
8790979
44.

Relationship between transfusion regimen and suppression of erythropoiesis in beta-thalassaemia major.

Cazzola M, De Stefano P, Ponchio L, Locatelli F, Beguin Y, Dessi C, Barella S, Cao A, Galanello R.

Br J Haematol. 1995 Mar;89(3):473-8.

PMID:
7734344
45.

Evaluation of an automatic HPLC analyser for thalassemia and haemoglobin variants screening.

Galanello R, Barella S, Gasperini D, Perseu L, Paglietti E, Sollaino C, Paderi L, Pirroni MG, Maccioni L, Mosca A.

J Automat Chem. 1995;17(2):73-6.

46.

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.

Hemoglobin. 1994 Nov;18(6):437-9. No abstract available.

PMID:
7713748
47.

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.

Am J Hematol. 1994 Jun;46(2):79-81.

PMID:
8172199
48.

Serum erythropoietin and erythropoiesis in high- and low-fetal hemoglobin beta-thalassemia intermedia patients.

Galanello R, Barella S, Turco MP, Giagu N, Cao A, Dore F, Liberato NL, Guarnone R, Barosi G.

Blood. 1994 Jan 15;83(2):561-5.

49.

Normal individuals with high Hb A2 levels.

Gasperini D, Cao A, Paderi L, Barella S, Paglietti E, Perseu L, Loi D, Galanello R.

Br J Haematol. 1993 May;84(1):166-8.

PMID:
8338770
50.

HbH disease in Sardinia: molecular, hematological and clinical aspects.

Galanello R, Aru B, Dessì C, Addis M, Paglietti E, Melis MA, Cocco S, Massa P, Giagu N, Barella S, et al.

Acta Haematol. 1992;88(1):1-6.

PMID:
1414154

Supplemental Content

Loading ...
Support Center