Bellone E - Search Results

1

Sural nerve biopsy and functional studies support the pathogenic role of a novel MPZ mutation.

Prada V, Capponi S, Ursino G, Alberti A, Callegari I, Passalacqua M, Marotta R, Mandich P, Bellone E, Schenone A, Grandis M. Prada V, et al. Among authors: bellone e. Neuropathology. 2015 Jun;35(3):254-9. doi: 10.1111/neup.12179. Epub 2014 Nov 11. Neuropathology. 2015. PMID: 25388615

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. Among authors: bellone e. 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: bellone e. 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. 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. Among authors: bellone e. Boll Soc Ital Biol Sper. 1991 Oct-Nov;67(10-11):907-13. Boll Soc Ital Biol Sper. 1991. PMID: 1687950

6

Genetic analysis of Huntington disease in Italy.

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

7

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: bellone e. Neurosci Lett. 1995 Jul 14;194(1-2):136-8. doi: 10.1016/0304-3940(95)11717-b. Neurosci Lett. 1995. PMID: 7478198

8

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: bellone e. J Neurol Sci. 1995 Jul;131(1):30-4. doi: 10.1016/0022-510x(95)00042-z. J Neurol Sci. 1995. PMID: 7561944

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. Among authors: bellone e. J Neurol. 1995 May;242(5):295-8. doi: 10.1007/BF00878871. J Neurol. 1995. PMID: 7643137

10

17p11.2 duplication is a common finding in sporadic cases of Charcot-Marie-Tooth type 1.

Mancardi GL, Uccelli A, Bellone E, Sghirlanzoni A, Mandich P, Pareyson D, Schenone A, Abbruzzese M, Ajmar F. Mancardi GL, et al. Among authors: bellone e. Eur Neurol. 1994;34(3):135-9. doi: 10.1159/000117026. Eur Neurol. 1994. PMID: 8033938

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