Mandich P - Search Results

1

A misleading presentation of Mohr-Tranebjaerg syndrome: What is hidden behind an axonal neuropathy?

Geroldi A, Trevisan L, Gaudio A, Gotta F, Patrone S, Origone P, Grandis M, Gemelli C, Schenone A, Accogli A, Zara F, Mandich P, Bellone E. Geroldi A, et al. Among authors: mandich p. Parkinsonism Relat Disord. 2022 Sep;102:54-56. doi: 10.1016/j.parkreldis.2022.07.021. Epub 2022 Aug 5. Parkinsonism Relat Disord. 2022. PMID: 35947939 No abstract available.

2

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.

3

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

4

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

5

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

6

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

7

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: mandich p. Eur Neurol. 1994;34(3):135-9. doi: 10.1159/000117026. Eur Neurol. 1994. PMID: 8033938

8

Hereditary motor and sensory neuropathy with myelin outfolding: clinical, genetic and neuropathological study of three cases.

Schenone A, Abbruzzese M, Uccelli A, Mandich P, James R, Bellone E, Giunchedi M, Rolando S, Capello E, Mandich R [corrected to Mandich P], et al. Schenone A, et al. Among authors: mandich p, mandich r corrected to mandich p. J Neurol Sci. 1994 Mar;122(1):20-7. doi: 10.1016/0022-510x(94)90047-7. J Neurol Sci. 1994. PMID: 8195799

9

Identification of a 4 bp deletion (1560del4) in po gene in a family with severe Charcot-Marie-Tooth disease.

Bellone E, Mandich P, James R, Nelis E, Lamba LD, Van Broeckhoven C, Ajmar F. Bellone E, et al. Among authors: mandich p. Hum Mutat. 1996;7(4):377-8. doi: 10.1002/humu.1380070403. Hum Mutat. 1996. PMID: 8723697 No abstract available.

10

Use of cosH1 probe in hereditary neuropathy with liability to pressure palsies: a reliable genetic test for demonstration of identical size of 17p11.2 deletion in unrelated patients.

Bellone E, Schenone A, Mancardi G, Nicholson GA, Abbruzzese M, Ajmar F, Mandich P. Bellone E, et al. Among authors: mandich p. Neurosci Lett. 1996 Jul 26;213(1):71-3. doi: 10.1016/0304-3940(96)12825-1. Neurosci Lett. 1996. PMID: 8844715

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