Sghirlanzoni A - Search Results

1

Partial laminin alpha2 chain deficiency in a patient with myopathy resembling inclusion body myositis.

Di Blasi C, Mora M, Pareyson D, Farina L, Sghirlanzoni A, Vignier N, Blasevich F, Cornelio F, Guicheney P, Morandi L. Di Blasi C, et al. Among authors: sghirlanzoni a. Ann Neurol. 2000 Jun;47(6):811-6. Ann Neurol. 2000. PMID: 10852549

2

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

3

Clinical and magnetic resonance imaging findings in chronic sensory ganglionopathies.

Lauria G, Pareyson D, Grisoli M, Sghirlanzoni A. Lauria G, et al. Among authors: sghirlanzoni a. Ann Neurol. 2000 Jan;47(1):104-9. Ann Neurol. 2000. PMID: 10632108

4

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: sghirlanzoni a. Neurology. 2000 Apr 25;54(8):1696-8. doi: 10.1212/wnl.54.8.1696. Neurology. 2000. PMID: 10762521 Free article.

5

Neurogenic muscle hypertrophy. Report of two cases.

Pareyson D, Morandi L, Scaioli V, Marazzi R, Boiardi A, Sghirlanzoni A. Pareyson D, et al. Among authors: sghirlanzoni a. J Neurol. 1989 Jul;236(5):292-5. doi: 10.1007/BF00314459. J Neurol. 1989. PMID: 2760647

6

Chloroquine myopathy and myasthenia-like syndrome.

Sghirlanzoni A, Mantegazza R, Mora M, Pareyson D, Cornelio F. Sghirlanzoni A, et al. Muscle Nerve. 1988 Feb;11(2):114-9. doi: 10.1002/mus.880110205. Muscle Nerve. 1988. PMID: 3343986

7

Peripheral nerve involvement in Churg-Strauss syndrome.

Marazzi R, Pareyson D, Boiardi A, Corbo M, Scaioli V, Sghirlanzoni A. Marazzi R, et al. Among authors: sghirlanzoni a. J Neurol. 1992 Jul;239(6):317-21. doi: 10.1007/BF00867587. J Neurol. 1992. PMID: 1324984

8

Efficacy of intranasal administration of neostigmine in myasthenic patients.

Sghirlanzoni A, Pareyson D, Benvenuti C, Cei G, Cosi V, Lombardi M, Nicora M, Ricciardi R, Cornelio F. Sghirlanzoni A, et al. J Neurol. 1992 Mar;239(3):165-9. doi: 10.1007/BF00833919. J Neurol. 1992. PMID: 1573422 Clinical Trial.

9

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

10

Neurophysiological diagnosis of acquired sensory ganglionopathies.

Lauria G, Pareyson D, Sghirlanzoni A. Lauria G, et al. Among authors: sghirlanzoni a. Eur Neurol. 2003;50(3):146-52. doi: 10.1159/000073055. Eur Neurol. 2003. PMID: 14530620

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