Ciano C - Search Results

1

Charcot-Marie-Tooth disease type 2 and P0 gene mutations.

Pareyson D, Sghirlanzoni A, Bolti S, Ciano C, Fallica E, Mora M, Taroni F. Pareyson D, et al. Among authors: ciano c. Neurology. 1999 Mar 23;52(5):1110-1. doi: 10.1212/wnl.52.5.1106-f. Neurology. 1999. PMID: 10102454 No abstract available.

2

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: ciano c. Neurology. 1992 Nov;42(11):2201-4. doi: 10.1212/wnl.42.11.2201. Neurology. 1992. PMID: 1436537

3

Unrecognized Charcot-Marie-Tooth disease: diagnostic difficulties in the assessment of recovery from paralysis.

Fiacchino F, Grandi L, Ciano C, Sghirlanzoni A. Fiacchino F, et al. Among authors: ciano c. Anesth Analg. 1995 Jul;81(1):199-201. doi: 10.1097/00000539-199507000-00043. Anesth Analg. 1995. PMID: 7598259 No abstract available.

4

Combined central and peripheral acute demyelination.

Pareyson D, Ciano C, Fiacchino F, Gemma M, Savoiardo M, Sghirlanzoni A. Pareyson D, et al. Among authors: ciano c. Ital J Neurol Sci. 1993 Jan;14(1):83-6. doi: 10.1007/BF02339047. Ital J Neurol Sci. 1993. PMID: 8386146

5

Phenotypic heterogeneity in hereditary neuropathy with liability to pressure palsies associated with chromosome 17p11.2-12 deletion.

Pareyson D, Scaioli V, Taroni F, Botti S, Lorenzetti D, Solari A, Ciano C, Sghirlanzoni A. Pareyson D, et al. Among authors: ciano c. Neurology. 1996 Apr;46(4):1133-7. doi: 10.1212/wnl.46.4.1133. Neurology. 1996. PMID: 8780105

6

Detection of hereditary neuropathy with liability to pressure palsies among patients with acute painless mononeuropathy or plexopathy.

Pareyson D, Solari A, Taroni F, Botti S, Fallica E, Scaioli V, Ciano C, Sghirlanzoni A. Pareyson D, et al. Among authors: ciano c. Muscle Nerve. 1998 Dec;21(12):1686-91. doi: 10.1002/(sici)1097-4598(199812)21:12<1686::aid-mus10>3.0.co;2-z. Muscle Nerve. 1998. PMID: 9843070

7

Heterozygous null mutation in the P0 gene associated with mild Charcot-Marie-Tooth disease.

Pareyson D, Menichella D, Botti S, Sghirlanzoni A, Fallica E, Mora M, Ciano C, Shy ME, Taroni F. Pareyson D, et al. Among authors: ciano c. Ann N Y Acad Sci. 1999 Sep 14;883:477-80. Ann N Y Acad Sci. 1999. PMID: 10586278 No abstract available.

8

Cranial nerve involvement in CMT disease type 1 due to early growth response 2 gene mutation.

Pareyson D, Taroni F, Botti S, Morbin M, Baratta S, Lauria G, Ciano C, Sghirlanzoni A. Pareyson D, et al. Among authors: ciano c. Neurology. 2000 Apr 25;54(8):1696-8. doi: 10.1212/wnl.54.8.1696. Neurology. 2000. PMID: 10762521 Free article.

9

Chronic inflammatory demyelinating polyradiculoneuropathy: long-term course and treatment of 60 patients.

Sghirlanzoni A, Solari A, Ciano C, Mariotti C, Fallica E, Pareyson D. Sghirlanzoni A, et al. Among authors: ciano c. Neurol Sci. 2000 Feb;21(1):31-7. doi: 10.1007/s100720070116. Neurol Sci. 2000. PMID: 10938200 Clinical Trial.

10

Does CMT1A homozygosity cause more severe disease with root hypertrophy and higher CSF proteins?

Pareyson D, Testa D, Morbin M, Erbetta A, Ciano C, Lauria G, Milani M, Taroni F. Pareyson D, et al. Among authors: ciano c. Neurology. 2003 May 27;60(10):1721-2. doi: 10.1212/01.wnl.0000059262.34846.8a. Neurology. 2003. PMID: 12771282 Free article. No abstract available.

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