Sabbadini G - Search Results

1

Genetic fitness in Huntington's Disease and Spinocerebellar Ataxia 1: a population genetics model for CAG repeat expansions.

Frontali M, Sabbadini G, Novelletto A, Jodice C, Naso F, Spadaro M, Giunti P, Jacopini AG, Veneziano L, Mantuano E, Malaspina P, Ulizzi L, Brice A, Durr A, Terrenato L. Frontali M, et al. Among authors: sabbadini g. Ann Hum Genet. 1996 Sep;60(5):423-35. doi: 10.1111/j.1469-1809.1996.tb00440.x. Ann Hum Genet. 1996. PMID: 8912795 Free article.

2

Episodic ataxia type 2 (EA2) and spinocerebellar ataxia type 6 (SCA6) due to CAG repeat expansion in the CACNA1A gene on chromosome 19p.

Jodice C, Mantuano E, Veneziano L, Trettel F, Sabbadini G, Calandriello L, Francia A, Spadaro M, Pierelli F, Salvi F, Ophoff RA, Frants RR, Frontali M. Jodice C, et al. Among authors: sabbadini g. Hum Mol Genet. 1997 Oct;6(11):1973-8. doi: 10.1093/hmg/6.11.1973. Hum Mol Genet. 1997. PMID: 9302278

3

Acetazolamide-responsive episodic ataxia in an Italian family refines gene mapping on chromosome 19p13.

Calandriello L, Veneziano L, Francia A, Sabbadini G, Colonnese C, Mantuano E, Jodice C, Trettel F, Viviani P, Manfredi M, Frontali M. Calandriello L, et al. Among authors: sabbadini g. Brain. 1997 May;120 ( Pt 5):805-12. doi: 10.1093/brain/120.5.805. Brain. 1997. PMID: 9183251 Free article.

4

Analysis of (CAG)n size heterogeneity in somatic and sperm cell DNA from intermediate and expanded Huntington disease gene carriers.

Giovannone B, Sabbadini G, Di Maio L, Calabrese O, Castaldo I, Frontali M, Novelleto A, Squitieri F. Giovannone B, et al. Among authors: sabbadini g. Hum Mutat. 1997;10(6):458-64. doi: 10.1002/(SICI)1098-1004(1997)10:6<458::AID-HUMU7>3.0.CO;2-9. Hum Mutat. 1997. PMID: 9401009

5

The role of the SCA2 trinucleotide repeat expansion in 89 autosomal dominant cerebellar ataxia families. Frequency, clinical and genetic correlates.

Giunti P, Sabbadini G, Sweeney MG, Davis MB, Veneziano L, Mantuano E, Federico A, Plasmati R, Frontali M, Wood NW. Giunti P, et al. Among authors: sabbadini g. Brain. 1998 Mar;121 ( Pt 3):459-67. doi: 10.1093/brain/121.3.459. Brain. 1998. PMID: 9549522

6

Family and molecular data for a fine analysis of age at onset in Huntington disease.

Squitieri F, Sabbadini G, Mandich P, Gellera C, Di Maria E, Bellone E, Castellotti B, Nargi E, de Grazia U, Frontali M, Novelletto A. Squitieri F, et al. Among authors: sabbadini g. Am J Med Genet. 2000 Dec 11;95(4):366-73. doi: 10.1002/1096-8628(20001211)95:4<366::aid-ajmg13>3.0.co;2-2. Am J Med Genet. 2000. PMID: 11186892

7

Polymorphism analysis of the huntingtin gene in Italian families affected with Huntington disease.

Novelletto A, Persichetti F, Sabbadini G, Mandich P, Bellone E, Ajmar F, Squitieri F, Campanella G, Bozza A, MacDonald ME, et al. Novelletto A, et al. Among authors: sabbadini g. Hum Mol Genet. 1994 Jul;3(7):1129-32. doi: 10.1093/hmg/3.7.1129. Hum Mol Genet. 1994. PMID: 7981682

8

Analysis of the trinucleotide repeat expansion in Italian families affected with Huntington disease.

Novelletto A, Persichetti F, Sabbadini G, Mandich P, Bellone E, Ajmar F, Pergola M, Del Senno L, MacDonald ME, Gusella JF, et al. Novelletto A, et al. Among authors: sabbadini g. Hum Mol Genet. 1994 Jan;3(1):93-8. doi: 10.1093/hmg/3.1.93. Hum Mol Genet. 1994. PMID: 8162059

9

Ordering of 44 genetic markers in the 6p22 cytogenetic band.

Trettel F, Malaspina P, Blasi P, Jodice C, Novelletto A, Sabbadini G, Veneziano L, Frontali M, Terrenato L. Trettel F, et al. Among authors: sabbadini g. DNA Seq. 1996;7(1):51-2. doi: 10.3109/10425179609015648. DNA Seq. 1996. PMID: 9063639 No abstract available.

10

Predictive testing for Huntington's disease: ten years' experience in two Italian centres.

Mandich P, Jacopini G, Di Maria E, Sabbadini G, Abbruzzese G, Chimirri F, Bellone E, Novelletto A, Ajmar F, Frontali M. Mandich P, et al. Among authors: sabbadini g. Ital J Neurol Sci. 1998 Apr;19(2):68-74. doi: 10.1007/BF02427559. Ital J Neurol Sci. 1998. PMID: 10935839

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