Sole G - Search Results

1

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: sole g. Arch Ophthalmol. 1998 Jun;116(6):793-7. doi: 10.1001/archopht.116.6.793. Arch Ophthalmol. 1998. PMID: 9639450

2

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: sole g. Int Ophthalmol. 1996-1997;20(1-3):1-5. doi: 10.1007/BF00212936. Int Ophthalmol. 1996. PMID: 9112154

3

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: sole g. Acta Ophthalmol Scand Suppl. 1998;(227):16-7. doi: 10.1111/j.1600-0420.1998.tb00865.x. Acta Ophthalmol Scand Suppl. 1998. PMID: 9972327

4

Myocilin Gln368stop mutation and advanced age as risk factors for late-onset primary open-angle glaucoma.

Angius A, Spinelli P, Ghilotti G, Casu G, Sole G, Loi A, Totaro A, Zelante L, Gasparini P, Orzalesi N, Pirastu M, Bonomi L. Angius A, et al. Among authors: sole g. Arch Ophthalmol. 2000 May;118(5):674-9. doi: 10.1001/archopht.118.5.674. Arch Ophthalmol. 2000. PMID: 10815160

5

A common beta ig-h3 gene mutation (delta f540) in a large cohort of Sardinian Reis Bücklers corneal dystrophy patients. Mutations in brief no. 180. Online.

Rozzo C, Fossarello M, Galleri G, Sole G, Serru A, Orzalesi N, Serra A, Pirastu M. Rozzo C, et al. Among authors: sole g. Hum Mutat. 1998;12(3):215-6. Hum Mutat. 1998. PMID: 10660331

6

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: sole g. Am J Hum Genet. 1995 Dec;57(6):1318-24. Am J Hum Genet. 1995. PMID: 8533760 Free PMC article.

7

Complete congenital stationary night blindness maps on Xp11.4 in a Sardinian family.

Rozzo C, Fossarello M, Galleri G, Miano MG, Ciccodicola A, Sole G, Pirastu M. Rozzo C, et al. Among authors: sole g. Eur J Hum Genet. 1999 Jul;7(5):574-8. doi: 10.1038/sj.ejhg.5200332. Eur J Hum Genet. 1999. PMID: 10439964

8

[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: sole g. Cardiologia. 1997 Mar;42(3):281-5. Cardiologia. 1997. PMID: 9172934 Italian.

9

Molecular and biochemical data on some glucose-6-phosphate dehydrogenase variants from southern Sardinia.

Frigerio R, Sole G, Lovicu M, Passiu G. Frigerio R, et al. Among authors: sole g. Haematologica. 1994 Jul-Aug;79(4):319-21. Haematologica. 1994. PMID: 7806085

10

Iron overload and lysosomal stability in beta (0)-thalassemia intermedia: N-acetyl-beta-D-glucosaminidase isoenzymatic pattern.

Frigerio R, Sole G, Olla N, Lovicu M, Mela Q, Cacace E, Passiu G, Pitzus F, Carcassi U. Frigerio R, et al. Among authors: sole g. Birth Defects Orig Artic Ser. 1988;23(5B):25-8. Birth Defects Orig Artic Ser. 1988. PMID: 3390549 No abstract available.

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