Mandich P - Search Results

1

DRD3 Ser9Gly variant is not associated with essential tremor in a series of Italian patients.

Vitale C, Gulli R, Ciotti P, Scaglione C, Bellone E, Avanzino L, Lantieri F, Abbruzzese G, Martinelli P, Barone P, Mandich P. Vitale C, et al. Among authors: mandich p. Eur J Neurol. 2008 Sep;15(9):985-7. doi: 10.1111/j.1468-1331.2008.02164.x. Epub 2008 May 15. Eur J Neurol. 2008. PMID: 18484990

2

HMSN III phenotype due to homozygous expression of a dominant HMSN II gene.

Sghirlanzoni A, Pareyson D, Balestrini MR, Bellone E, Berta E, Ciano C, Mandich P, Marazzi R. Sghirlanzoni A, et al. Among authors: mandich p. Neurology. 1992 Nov;42(11):2201-4. doi: 10.1212/wnl.42.11.2201. Neurology. 1992. PMID: 1436537

3

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

4

Polymerase chain reaction (PCR) amplification of hypervariable genomic sequences.

Mandich P, Bellone E, Massari A, Ajmar F. Mandich P, et al. Boll Soc Ital Biol Sper. 1991 Oct-Nov;67(10-11):907-13. Boll Soc Ital Biol Sper. 1991. PMID: 1687950

5

Genetic analysis of Huntington disease in Italy.

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

6

Forensic applications of molecular genetic analysis: an Italian collaborative study on paternity testing by the determination of variable number of tandem repeat DNA polymorphisms.

Gasparini P, Mandich P, Novelli G, Bellone E, Sangiuolo F, De Stefano F, Potenza L, Trabetti E, Marigo M, Pignatti PF, et al. Gasparini P, et al. Among authors: mandich p. Hum Hered. 1991;41(3):174-81. doi: 10.1159/000153997. Hum Hered. 1991. PMID: 1937491

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. Am J Med Genet. 1990 Apr;35(4):579-81. doi: 10.1002/ajmg.1320350426. Am J Med Genet. 1990. PMID: 2333889

8

DNA marker analysis of adult polycystic kidney disease in Italian families. Italian Cooperative Group on ADPKD.

Potenza L, Mandich P, Restagno G, Bellone E, Novelli G, Dallapiccola B, Ajmar F, Carbonara A. Potenza L, et al. Among authors: mandich p. Prog Clin Biol Res. 1989;305:77-81. Prog Clin Biol Res. 1989. PMID: 2569744 No abstract available.

9

Molecular diagnosis of hereditary neuropathy with liability to pressure palsies (HNPP) by detection of 17p11.2 deletion in Italian patients.

Mandich P, James R, Nassani S, Defferrari R, Bellone E, Mancardi G, Schenone A, Abbruzzese M, Rocchi M, Ajmar F, et al. Mandich P, et al. J Neurol. 1995 May;242(5):295-8. doi: 10.1007/BF00878871. J Neurol. 1995. PMID: 7643137

10

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

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