Mandich P - Search Results

1

Phenotypic spectrum of myelin protein zero-related neuropathies: a large cohort study from five mutation clusters across Italy.

Bertini A, Gentile L, Cavallaro T, Tozza S, Saveri P, Russo M, Massucco S, Falzone YM, Bellone E, Taioli F, Geroldi A, Occhipinti G, Ferrarini M, Cavalca E, Crivellari L, Mandich P, Balistreri F, Magri S, Taroni F, Previtali SC, Schenone A, Grandis M, Manganelli F, Fabrizi GM, Mazzeo A, Pareyson D, Pisciotta C. Bertini A, et al. Among authors: mandich p. J Neurol Neurosurg Psychiatry. 2024 Dec 16;96(1):47-53. doi: 10.1136/jnnp-2024-333842. J Neurol Neurosurg Psychiatry. 2024. PMID: 38839277 Free article.

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

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

6

Adult polycystic kidney disease: prenatal diagnosis with DNA polymorphic markers.

Bellone E, Mandich P, Costa P, Dalerba L, Ajmar F. Bellone E, et al. Among authors: mandich p. Boll Soc Ital Biol Sper. 1991 Oct-Nov;67(10-11):915-22. Boll Soc Ital Biol Sper. 1991. PMID: 1821132

7

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

8

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

9

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

10

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

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