Pareyson D - Search Results

1

Phenotypic Variability of Childhood Charcot-Marie-Tooth Disease.

Cornett KM, Menezes MP, Bray P, Halaki M, Shy RR, Yum SW, Estilow T, Moroni I, Foscan M, Pagliano E, Pareyson D, Laurá M, Bhandari T, Muntoni F, Reilly MM, Finkel RS, Sowden J, Eichinger KJ, Herrmann DN, Shy ME, Burns J; Inherited Neuropathies Consortium. Cornett KM, et al. Among authors: pareyson d. JAMA Neurol. 2016 Jun 1;73(6):645-51. doi: 10.1001/jamaneurol.2016.0171. JAMA Neurol. 2016. PMID: 27043305 Free PMC article.

2

A multicentre follow-up study of 1152 patients with myasthenia gravis in Italy.

Mantegazza R, Beghi E, Pareyson D, Antozzi C, Peluchetti D, Sghirlanzoni A, Cosi V, Lombardi M, Piccolo G, Tonali P, et al. Mantegazza R, et al. Among authors: pareyson d. J Neurol. 1990 Oct;237(6):339-44. doi: 10.1007/BF00315656. J Neurol. 1990. PMID: 2277266 Clinical Trial.

3

Conduction velocities in Charcot-Marie-Tooth polyneuropathy type 1.

Pareyson D, Sghirlanzoni A. Pareyson D, et al. Neurology. 1994 Nov;44(11):2216. doi: 10.1212/wnl.44.11.2216. Neurology. 1994. PMID: 7969998 No abstract available.

4

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

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. Neurology. 1996 Apr;46(4):1133-7. doi: 10.1212/wnl.46.4.1133. Neurology. 1996. PMID: 8780105

6

Gene dosage effects in hereditary peripheral neuropathy. Expression of peripheral myelin protein 22 in Charcot-Marie-Tooth disease type 1A and hereditary neuropathy with liability to pressure palsies nerve biopsies.

Gabriel JM, Erne B, Pareyson D, Sghirlanzoni A, Taroni F, Steck AJ. Gabriel JM, et al. Among authors: pareyson d. Neurology. 1997 Dec;49(6):1635-40. doi: 10.1212/wnl.49.6.1635. Neurology. 1997. PMID: 9409359

7

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. Neurology. 1999 Mar 23;52(5):1110-1. doi: 10.1212/wnl.52.5.1106-f. Neurology. 1999. PMID: 10102454 No abstract available.

8

Charcot-marie-tooth disease and related neuropathies: molecular basis for distinction and diagnosis.

Pareyson D. Pareyson D. Muscle Nerve. 1999 Nov;22(11):1498-509. doi: 10.1002/(sici)1097-4598(199911)22:11<1498::aid-mus4>3.0.co;2-9. Muscle Nerve. 1999. PMID: 10514227 Review.

9

Guidelines for the diagnosis of Charcot-Marie-Tooth disease and related neuropathies. Ad hoc Working Group of the Peripheral Nervous System Study Group, Italian Neurological Society.

Pareyson D. Pareyson D. Ital J Neurol Sci. 1999 Aug;20(4):207-16. doi: 10.1007/s100720050033. Ital J Neurol Sci. 1999. PMID: 10551906 No abstract available.

10

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. Ann N Y Acad Sci. 1999 Sep 14;883:477-80. Ann N Y Acad Sci. 1999. PMID: 10586278 No abstract available.

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