Mandich P - Search Results

1

Charcot-Marie-Tooth disease: frequency of genetic subtypes in a Southern Italy population.

Manganelli F, Tozza S, Pisciotta C, Bellone E, Iodice R, Nolano M, Geroldi A, Capponi S, Mandich P, Santoro L. Manganelli F, et al. Among authors: mandich p. J Peripher Nerv Syst. 2014 Dec;19(4):292-8. doi: 10.1111/jns.12092. J Peripher Nerv Syst. 2014. PMID: 25429913

2

Charcot-Marie-Tooth disease: evidence of a duplication at D17S122 locus.

Mandich P, Bellone E, Uccelli A, Pareyson D, Ajmar F. Mandich P, et al. Boll Soc Ital Biol Sper. 1992 Apr;68(4):225-30. Boll Soc Ital Biol Sper. 1992. PMID: 1281412

3

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

4

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: mandich p. J Med Genet. 1992 Jul;29(7):492-3. J Med Genet. 1992. PMID: 1640430 Free PMC article. No abstract available.

5

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

6

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

7

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

8

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

9

Molecular analysis of three cases with hereditary motor and sensory neuropathy with myelin outfolding.

James R, Bellone E, Nelis E, Mandich P, Schenone A, Mancardi G, Van Broeckhoven C, Abbruzzese M, Ajmar F. James R, et al. Among authors: mandich p. Neurosci Lett. 1995 Jul 14;194(1-2):136-8. doi: 10.1016/0304-3940(95)11717-b. Neurosci Lett. 1995. PMID: 7478198

10

Progressive sensory-motor polyneuropathy with tomaculous changes is associated to 17p11.2 deletion.

Mancardi GL, Mandich P, Nassani S, Schenone A, James R, Defferrari R, Bellone E, Giunchedi M, Ajmar F, Abbruzzese M. Mancardi GL, et al. Among authors: mandich p. J Neurol Sci. 1995 Jul;131(1):30-4. doi: 10.1016/0022-510x(95)00042-z. J Neurol Sci. 1995. PMID: 7561944

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