Cao A - Search Results

1

Genetic mapping of autosomal dominant primary open-angle glaucoma (POAG) in Sardinia.

Fossarello M, Zucca I, Galantuomo S, Serra A, Pirastu M, Loi A, Sole G, Cao A. Fossarello M, et al. Among authors: cao a. Int Ophthalmol. 1996-1997;20(1-3):1-5. doi: 10.1007/BF00212936. Int Ophthalmol. 1996. PMID: 9112154

2

Deletion in the peripherin/RDS gene in two unrelated Sardinian families with autosomal dominant butterfly-shaped macular dystrophy.

Fossarello M, Bertini C, Galantuomo MS, Cao A, Serra A, Pirastu M. Fossarello M, et al. Among authors: cao a. Arch Ophthalmol. 1996 Apr;114(4):448-56. doi: 10.1001/archopht.1996.01100130444016. Arch Ophthalmol. 1996. PMID: 8602784

3

A novel mutation in the GLC1A gene causes juvenile open-angle glaucoma in 4 families from the Italian region of Puglia.

Angius A, De Gioia E, Loi A, Fossarello M, Sole G, Orzalesi N, Grignolo F, Cao A, Pirastu M. Angius A, et al. Among authors: cao a. Arch Ophthalmol. 1998 Jun;116(6):793-7. doi: 10.1001/archopht.116.6.793. Arch Ophthalmol. 1998. PMID: 9639450

4

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. Among authors: cao a. Prenat Diagn. 1994 Oct;14(10):999-1002. doi: 10.1002/pd.1970141018. Prenat Diagn. 1994. PMID: 7899276

5

Molecular basis of open-angle glaucoma in Italy.

Angius A, Pisano M, Sanca A, Casu G, Persico I, Pitzalis S, De Gioia E, Grignolo FM, Loi A, Sole G, Cao A, Spinelli P, Ghillotti G, Bonomi L, Fossarello M, Serra A, Gandolfi S, Alberti G, Maraini G, Serru A, Orzalesi N, Pirastu M. Angius A, et al. Among authors: cao a. Acta Ophthalmol Scand Suppl. 1998;(227):16-7. doi: 10.1111/j.1600-0420.1998.tb00865.x. Acta Ophthalmol Scand Suppl. 1998. PMID: 9972327

6

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. Among authors: cao a. Haematologica. 1992 Jul-Aug;77(4):361-2. Haematologica. 1992. PMID: 1427447

7

Thalassemias in Sardinia: molecular pathology, phenotype-genotype correlation, and prevention.

Cao A, Rosatelli C, Pirastu M, Galanello R. Cao A, et al. Am J Pediatr Hematol Oncol. 1991 Summer;13(2):179-88. Am J Pediatr Hematol Oncol. 1991. PMID: 2069229

8

Delineation of specific beta-thalassemia mutations in high-risk areas of Italy: a prerequisite for prenatal diagnosis.

Pirastu M, Saglio G, Camaschella C, Loi A, Serra A, Bertero T, Gabutti W, Cao A. Pirastu M, et al. Among authors: cao a. Blood. 1988 Apr;71(4):983-8. Blood. 1988. PMID: 3355899 Free 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. Among authors: cao a. Hum Genet. 1996 Dec;98(6):640-2. doi: 10.1007/s004390050275. Hum Genet. 1996. PMID: 8931691

10

[Does a genetic predisposition for infarction expansion exist? Evaluation of genetic polymorphisms of the renin-angiotensin system].

Zedda N, Onnis E, Angius A, Balata F, Cherchi PA, Sole G, Olla N, Poddie D, Cao A, Cherchi A, Pirastu M. Zedda N, et al. Among authors: cao a. Cardiologia. 1997 Mar;42(3):281-5. Cardiologia. 1997. PMID: 9172934 Italian.

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