Mancardi G - Search Results

1

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: mancardi g. J Neurol. 1995 May;242(5):295-8. doi: 10.1007/BF00878871. J Neurol. 1995. PMID: 7643137

2

Direct immunofluorescence in sural nerve biopsies.

Schenone A, De Martini I, Tabaton M, Romagnoli P, Akkad Wattar AS, Bianchini D, Mancardi G. Schenone A, et al. Among authors: mancardi g. Eur Neurol. 1988;28(5):262-9. doi: 10.1159/000116281. Eur Neurol. 1988. PMID: 2852109

3

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

4

De novo duplication in Charcot-Marie-Tooth type 1A.

Mandich P, Bellone E, Schenone A, Mancardi G, Abbruzzese M, Ajmar F. Mandich P, et al. Among authors: mancardi g. Am J Hum Genet. 1996 Sep;59(3):739-40. Am J Hum Genet. 1996. PMID: 8751877 Free PMC article. No abstract available.

5

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: mancardi g. Neurosci Lett. 1996 Jul 26;213(1):71-3. doi: 10.1016/0304-3940(96)12825-1. Neurosci Lett. 1996. PMID: 8844715

6

Comments on Davar et al., Pain, 67 (1996) 135-139.

Mandich P, Bellone E, Montera M, Ajmar F, Schenone A, Nobbio L, Mancardi G, Pizzuti A, Ratti A, Windebank AJ. Mandich P, et al. Among authors: mancardi g. Pain. 1997 Aug;72(1-2):287-8. Pain. 1997. PMID: 9272817 Clinical Trial. No abstract available.

7

Correlation between PMP-22 messenger RNA expression and phenotype in hereditary neuropathy with liability to pressure palsies.

Schenone A, Nobbio L, Caponnetto C, Abbruzzese M, Mandich P, Bellone E, Ajmar F, Gherardi G, Windebank AJ, Mancardi G. Schenone A, et al. Among authors: mancardi g. Ann Neurol. 1997 Dec;42(6):866-72. doi: 10.1002/ana.410420607. Ann Neurol. 1997. PMID: 9403478

8

A study of lactoferrin and antibodies against lactoferrin in neurological diseases.

Penco S, Villaggio B, Mancardi G, Abbruzzese M, Garre C. Penco S, et al. Among authors: mancardi g. Adv Exp Med Biol. 1998;443:301-4. doi: 10.1007/978-1-4757-9068-9_37. Adv Exp Med Biol. 1998. PMID: 9781373 No abstract available.

9

PMP22 transgenic dorsal root ganglia cultures show myelin abnormalities similar to those of human CMT1A.

Nobbio L, Mancardi G, Grandis M, Levi G, Suter U, Nave KA, Windebank AJ, Abbruzzese M, Schenone A. Nobbio L, et al. Among authors: mancardi g. Ann Neurol. 2001 Jul;50(1):47-55. doi: 10.1002/ana.1034. Ann Neurol. 2001. PMID: 11456309

10

Central and peripheral nervous system complications following allogeneic bone marrow transplantation.

Solaro C, Murialdo A, Giunti D, Mancardi G, Uccelli A. Solaro C, et al. Among authors: mancardi g. Eur J Neurol. 2001 Jan;8(1):77-80. doi: 10.1046/j.1468-1331.2001.00160.x. Eur J Neurol. 2001. PMID: 11509085

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