Loudianos G - Search Results

1

Detection of a rare Wilson disease mutation associated with arylsulfatase A pseudodeficiency.

Battisti C, Loudianos G, Rufa A, Dotti MT, Sangiorgi S, Dessì V, Lovicu M, Pirastu M, Federico A. Battisti C, et al. Among authors: loudianos g. Am J Med Genet. 1999 Jul 16;85(2):175-8. doi: 10.1002/(sici)1096-8628(19990716)85:2<175::aid-ajmg13>3.0.co;2-5. Am J Med Genet. 1999. PMID: 10406672

2

Delta-thalassemia due to a mutation in an erythroid-specific binding protein sequence 3' to the delta-globin gene.

Moi P, Loudianos G, Lavinha J, Murru S, Cossu P, Casu R, Oggiano L, Longinotti M, Cao A, Pirastu M. Moi P, et al. Among authors: loudianos g. Blood. 1992 Jan 15;79(2):512-6. Blood. 1992. PMID: 1309671 Free article.

3

Feasibility of prenatal diagnosis of beta-thalassemia using two highly polymorphic microsatellites 5' to the beta-globin gene.

Loudianos G, Cao A, Pirastu M. Loudianos G, et al. Haematologica. 1992 Jul-Aug;77(4):361-2. Haematologica. 1992. PMID: 1427447

4

Molecular characterization of beta-thalassemia intermedia in patients of Italian descent and identification of three novel beta-thalassemia mutations.

Murru S, Loudianos G, Deiana M, Camaschella C, Sciarratta GV, Agosti S, Parodi MI, Cerruti P, Cao A, Pirastu M. Murru S, et al. Among authors: loudianos g. Blood. 1991 Mar 15;77(6):1342-7. Blood. 1991. PMID: 2001456 Free article.

5

A new delta chain variant hemoglobin A2-Corfu or alpha 2 delta 2 116 Arg----Cys (G18), detected by delta-globin gene analysis in a Greek family.

Loudianos G, Murru S, Kanavakis E, Metaxotou-Mavromati A, Theodoropoulou D, Kattamis C, Cao A, Pirastu M. Loudianos G, et al. Hum Genet. 1991 Jun;87(2):237-8. doi: 10.1007/BF00204193. Hum Genet. 1991. PMID: 2066116 No abstract available.

6

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: loudianos g. Am J Hematol. 1994 Jan;45(1):81-4. doi: 10.1002/ajh.2830450113. Am J Hematol. 1994. PMID: 7504402

7

Improvement of prenatal diagnosis of Wilson disease using microsatellite markers.

Loudianos G, Figus AL, Loi A, Angius A, Dessì V, Deiana M, De Virgiliis S, Monni G, Cao A, Pirastu M. Loudianos G, et al. Prenat Diagn. 1994 Oct;14(10):999-1002. doi: 10.1002/pd.1970141018. Prenat Diagn. 1994. PMID: 7899276

8

Molecular pathology and haplotype analysis of Wilson disease in Mediterranean populations.

Figus A, Angius A, Loudianos G, Bertini C, Dessi V, Loi A, Deiana M, Lovicu M, Olla N, Sole G, et al. Figus A, et al. Among authors: loudianos g. Am J Hum Genet. 1995 Dec;57(6):1318-24. Am J Hum Genet. 1995. PMID: 8533760 Free PMC article.

9

Wilson disease mutations associated with uncommon haplotypes in Mediterranean patients.

Loudianos G, Dessì V, Angius A, Lovicu M, Loi A, Deiana M, Akar N, Vajro P, Figus A, Cao A, Pirastu M. Loudianos G, et al. Hum Genet. 1996 Dec;98(6):640-2. doi: 10.1007/s004390050275. Hum Genet. 1996. PMID: 8931691

10

The -75A-->C substitution in the 5' UTR of the Wilson disease gene is a sequence polymorphism in the Mediterranean population.

Loudianos G, Dessi V, Lovicu M, Angius A, Cao A, Pirastu M. Loudianos G, et al. Am J Hum Genet. 1998 Feb;62(2):484-5. doi: 10.1086/301724. Am J Hum Genet. 1998. PMID: 9463339 Free PMC article. No abstract available.

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