Frontali M - 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. 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

DNA markers in diagnosis of adult dominant polycystic kidney disease.

Veneziano L, D'Angelo AR, Burrai L, Perugia G, Gentile V, Potenza L, Iampieri MP, Novelletto A, Novelli G, Frontali M. Veneziano L, et al. Among authors: frontali m. Eur Urol. 1992;21 Suppl 1:57-9. doi: 10.1159/000474892. Eur Urol. 1992. PMID: 1425839

3

Autosomal dominant pure cerebellar ataxia. Neurological and genetic study.

Frontali M, Spadaro M, Giunti P, Bianco F, Jodice C, Persichetti F, Colazza GB, Lulli P, Terrenato L, Morocutti C. Frontali M, et al. Brain. 1992 Dec;115 ( Pt 6):1647-54. doi: 10.1093/brain/115.6.1647. Brain. 1992. PMID: 1486455

4

HLA-linked spinocerebellar ataxia: a clinical and genetic study of large Italian kindreds.

Spadaro M, Giunti P, Lulli P, Frontali M, Jodice C, Cappellacci S, Morellini M, Persichetti F, Trabace S, Anastasi R, et al. Spadaro M, et al. Among authors: frontali m. Acta Neurol Scand. 1992 Apr;85(4):257-65. doi: 10.1111/j.1600-0404.1992.tb04041.x. Acta Neurol Scand. 1992. PMID: 1585797

5

Spinocerebellar ataxia (SCA1) in two large Italian kindreds: evidence in favour of a locus position distal to GLO1 and the HLA cluster.

Frontali M, Iodice C, Lulli P, Spadaro M, Cappellacci S, Giunti P, Malaspina P, Morellini M, Morocutti C, Novelletto A. Frontali M, et al. Ann Hum Genet. 1991 Jan;55(1):7-15. doi: 10.1111/j.1469-1809.1991.tb00393.x. Ann Hum Genet. 1991. PMID: 1675045

6

Non-random association between DNA markers and Huntington disease locus in the Italian population.

Novelletto A, Mandich P, Bellone E, Malaspina P, Vivona G, Ajmar F, Frontali M. Novelletto A, et al. Among authors: frontali m. Am J Med Genet. 1991 Sep 1;40(3):374-6. doi: 10.1002/ajmg.1320400326. Am J Med Genet. 1991. PMID: 1683157

7

[Clinical study of two families with late-onset autosomal dominant spinal-cerebellar ataxia linked with HLA. Preliminary results].

Giunti P, Spadaro M, Frontali M, Bianco F, Morocutti C. Giunti P, et al. Among authors: frontali m. Riv Neurol. 1990 Sep-Oct;60(5):176-9. Riv Neurol. 1990. PMID: 2100035 Italian.

8

Epidemiological and linkage studies on Huntington's disease in Italy.

Frontali M, Malaspina P, Rossi C, Jacopini AG, Vivona G, Pergola MS, Palena A, Novelletto A. Frontali M, et al. Hum Genet. 1990 Jul;85(2):165-70. doi: 10.1007/BF00193190. Hum Genet. 1990. PMID: 2142473

9

On the estimation of the age at onset distribution in Huntington's chorea using the EM algorithm.

Brambilla C, Frontali M, Malaspina P, Rossi C. Brambilla C, et al. Among authors: frontali m. Ann Hum Genet. 1990 Jul;54(3):225-33. doi: 10.1111/j.1469-1809.1990.tb00380.x. Ann Hum Genet. 1990. PMID: 2145799

10

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL). Clinical, neuroimaging, pathological and genetic study of a large Italian family.

Sabbadini G, Francia A, Calandriello L, Di Biasi C, Trasimeni G, Gualdi GF, Palladini G, Manfredi M, Frontali M. Sabbadini G, et al. Among authors: frontali m. Brain. 1995 Feb;118 ( Pt 1):207-15. doi: 10.1093/brain/118.1.207. Brain. 1995. PMID: 7895005

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