Ajmar F - Search Results

1

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: ajmar f. Am J Med Genet. 1991 Sep 1;40(3):374-6. doi: 10.1002/ajmg.1320400326. Am J Med Genet. 1991. PMID: 1683157

2

Parental origin of chromosome 4p deletion in Wolf-Hirschhorn syndrome.

Dallapiccola B, Mandich P, Bellone E, Selicorni A, Mokin V, Ajmar F, Novelli G. Dallapiccola B, et al. Among authors: ajmar f. Am J Med Genet. 1993 Nov 1;47(6):921-4. doi: 10.1002/ajmg.1320470622. Am J Med Genet. 1993. PMID: 7904122

3

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: ajmar f. Hum Mol Genet. 1994 Jul;3(7):1129-32. doi: 10.1093/hmg/3.7.1129. Hum Mol Genet. 1994. PMID: 7981682

4

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: ajmar f. Hum Mol Genet. 1994 Jan;3(1):93-8. doi: 10.1093/hmg/3.1.93. Hum Mol Genet. 1994. PMID: 8162059

5

Charcot-Marie-Tooth (CMT) 1a duplication at 17p11.2 in Italian families.

Bellone E, Mandich P, Mancardi GL, Schenone A, Uccelli A, Abbruzzese M, Sghirlanzoni A, Pareyson D, Ajmar F. Bellone E, et al. Among authors: ajmar f. J Med Genet. 1992 Jul;29(7):492-3. J Med Genet. 1992. PMID: 1640430 Free PMC article. No abstract available.

6

Genetic analysis of Huntington disease in Italy.

Ajmar F, Mandich P, Bellone E, Abbruzzese G. Ajmar F, et al. Am J Med Genet. 1991 May 1;39(2):211-4. doi: 10.1002/ajmg.1320390219. Am J Med Genet. 1991. PMID: 1829583

7

Autosomal dominant polycystic kidney disease: a linkage evaluation of heterogeneity in Italy. Italian Collaborative Group on Polycystic Kidney Disease.

Mandich P, Restagno G, Novelli G, Bellone E, Potenza L, Varetto O, Dallapiccola B, Carbonara A, Ajmar F. Mandich P, et al. Among authors: ajmar f. Am J Med Genet. 1990 Apr;35(4):579-81. doi: 10.1002/ajmg.1320350426. Am J Med Genet. 1990. PMID: 2333889

8

Molecular analysis of the IT15 gene in patients with apparently 'sporadic' Huntington's disease.

Mandich P, Di Maria E, Bellone E, Ajmar F, Abbruzzese G. Mandich P, et al. Among authors: ajmar f. Eur Neurol. 1996;36(6):348-52. doi: 10.1159/000117292. Eur Neurol. 1996. PMID: 8954302 Clinical Trial.

9

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: ajmar f. Ital J Neurol Sci. 1998 Apr;19(2):68-74. doi: 10.1007/BF02427559. Ital J Neurol Sci. 1998. PMID: 10935839

10

[Specific enzymatic amplification of a DNA region closely associated with Huntington chorea].

Novelli G, Mandich P, Ruzzo A, Mannello F, Ajmar F, Dallapiccola B. Novelli G, et al. Among authors: ajmar f. Boll Soc Ital Biol Sper. 1990 May;66(5):419-25. Boll Soc Ital Biol Sper. 1990. PMID: 2144430 Italian.

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