Maccioni L - Search Results

1

Experiences in the measurement of RBC-bound IgG as markers of cell age.

Paleari R, Ceriotti F, Azzario F, Maccioni L, Galanello R, Mosca A. Paleari R, et al. Among authors: maccioni l. Bioelectrochemistry. 2004 May;62(2):175-9. doi: 10.1016/j.bioelechem.2003.07.006. Bioelectrochemistry. 2004. PMID: 15039023

2

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. Galanello R, et al. Among authors: maccioni l. Blood. 2002 Sep 1;100(5):1913-4. Blood. 2002. PMID: 12176917 Free article.

3

Liver iron concentrations and urinary hepcidin in beta-thalassemia.

Origa R, Galanello R, Ganz T, Giagu N, Maccioni L, Faa G, Nemeth E. Origa R, et al. Among authors: maccioni l. Haematologica. 2007 May;92(5):583-8. doi: 10.3324/haematol.10842. Haematologica. 2007. PMID: 17488680 Free article.

4

Globin chain synthesis analysis by high performance liquid chromatography in the screening of thalassemia syndromes.

Galanello R, Satta S, Pirroni MG, Travi M, Maccioni L. Galanello R, et al. Among authors: maccioni l. Hemoglobin. 1998 Sep-Nov;22(5-6):501-8. doi: 10.3109/03630269809071547. Hemoglobin. 1998. PMID: 9859933

5

Posttranslational deamidation of proteins: the case of hemoglobin J Sardegna [alpha50(CD8)His-->Asn-->Asp].

Paleari R, Paglietti E, Mosca A, Mortarino M, Maccioni L, Satta S, Cao A, Galanello R. Paleari R, et al. Among authors: maccioni l. Clin Chem. 1999 Jan;45(1):21-8. Clin Chem. 1999. PMID: 9895333

6

An evaluation of the Diamat HPLC analyser for simultaneous determination of haemoglobins A(2) and F.

Mosca A, Carpinelli A, Majavacca R, Cantu'-Rajnoldi A, Garatti M, Paleari R, Ferrari M, Agape V, Maccioni L, Pisano S, Galanello R. Mosca A, et al. Among authors: maccioni l. J Automat Chem. 1989;11(6):273-9. doi: 10.1155/S1463924689000520. J Automat Chem. 1989. PMID: 18925255 Free PMC article.

7

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: maccioni l. 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.

8

Delayed fetal hemoglobin switching in subjects with KLF1 gene mutation.

Satta S, Perseu L, Maccioni L, Giagu N, Galanello R. Satta S, et al. Among authors: maccioni l. Blood Cells Mol Dis. 2012 Jan 15;48(1):22-4. doi: 10.1016/j.bcmd.2011.10.003. Epub 2011 Nov 16. Blood Cells Mol Dis. 2012. PMID: 22093801

9

Heterozygous beta-thalassemia with thalassemia intermedia phenotype.

Gasperini D, Perseu L, Melis MA, Maccioni L, Sollaino MC, Paglietti E, Cao A, Galanello R. Gasperini D, et al. Among authors: maccioni l. Am J Hematol. 1998 Jan;57(1):43-7. doi: 10.1002/(sici)1096-8652(199801)57:1<43::aid-ajh7>3.0.co;2-1. Am J Hematol. 1998. PMID: 9423815 Free article.

10

Compound heterozygosity for KLF1 mutations associated with remarkable increase of fetal hemoglobin and red cell protoporphyrin.

Satta S, Perseu L, Moi P, Asunis I, Cabriolu A, Maccioni L, Demartis FR, Manunza L, Cao A, Galanello R. Satta S, et al. Among authors: maccioni l. Haematologica. 2011 May;96(5):767-70. doi: 10.3324/haematol.2010.037333. Epub 2011 Jan 27. Haematologica. 2011. PMID: 21273267 Free PMC article.

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