Loi D - Search Results

1

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: loi d. Br J Haematol. 1993 May;84(1):166-8. doi: 10.1111/j.1365-2141.1993.tb03042.x. Br J Haematol. 1993. PMID: 8338770

2

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: loi d. Am J Hematol. 1994 Jun;46(2):79-81. doi: 10.1002/ajh.2830460204. Am J Hematol. 1994. PMID: 8172199

3

Association of α globin gene quadruplication and heterozygous β thalassemia in patients with thalassemia intermedia.

Sollaino MC, Paglietti ME, Perseu L, Giagu N, Loi D, Galanello R. Sollaino MC, et al. Among authors: loi d. Haematologica. 2009 Oct;94(10):1445-8. doi: 10.3324/haematol.2009.005728. Haematologica. 2009. PMID: 19794088 Free PMC article.

4

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. Paglietti ME, et al. Among authors: loi d. Hemoglobin. 2012;36(3):299-304. doi: 10.3109/03630269.2012.659780. Epub 2012 Mar 19. Hemoglobin. 2012. PMID: 22428534

5

Elevation of serum creatine kinase as the only manifestation of an intragenic deletion of the dystrophin gene in three unrelated families.

Melis MA, Cau M, Muntoni F, Mateddu A, Galanello R, Boccone L, Deidda F, Loi D, Cao A. Melis MA, et al. Among authors: loi d. Eur J Paediatr Neurol. 1998;2(5):255-61. doi: 10.1016/s1090-3798(98)80039-1. Eur J Paediatr Neurol. 1998. PMID: 10726828

6

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. Origa R, et al. Among authors: loi d. Blood Cells Mol Dis. 2014 Jan;52(1):46-9. doi: 10.1016/j.bcmd.2013.06.004. Epub 2013 Jul 27. Blood Cells Mol Dis. 2014. PMID: 23896219

7

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. Origa R, et al. Among authors: loi d. Blood Cells Mol Dis. 2018 Mar;69:102-106. doi: 10.1016/j.bcmd.2017.10.003. Epub 2017 Nov 3. Blood Cells Mol Dis. 2018. PMID: 29162392

8

A new glucose 6 phosphate dehydrogenase variant G6PD Sinnai (34 G-->T). Mutations in brief no. 156. Online.

Galanello R, Loi D, Sollaino C, Dessì S, Cao A, Melis MA. Galanello R, et al. Among authors: loi d. Hum Mutat. 1998;12(1):72-3. doi: 10.1002/(SICI)1098-1004(1998)12:1<72::AID-HUMU19>3.0.CO;2-T. Hum Mutat. 1998. PMID: 10627140

9

Thalassaemia and glucose-6-phosphate dehydrogenase screening in 13- to 14-year-old students of the Sardinian population: preliminary findings.

Cao A, Congiu R, Sollaino MC, Desogus MF, Demartis FR, Loi D, Cau M, Galanello R. Cao A, et al. Among authors: loi d. Community Genet. 2008;11(3):121-8. doi: 10.1159/000113873. Epub 2008 Mar 26. Community Genet. 2008. PMID: 18376107

10

Novel nonsense mutation (C-->A nt 10512) in exon 72 of dystrophin gene leading to exon skipping in a patient with a mild dystrophinopathy.

Melis MA, Muntoni F, Cau M, Loi D, Puddu A, Boccone L, Mateddu A, Cianchetti C, Cao A. Melis MA, et al. Among authors: loi d. Hum Mutat. 1998;Suppl 1:S137-8. doi: 10.1002/humu.1380110146. Hum Mutat. 1998. PMID: 9452067 No abstract available.

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