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M. Ragno

University of Naples Federico II

20

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416

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Multimodal electrophysiologic follow-up study in 3 mutated but presymptomatic members of a spinocerebellar ataxia type 1 (SCA1) family

2005 Neurological Sciences
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Wide expressivity variation and high but no gender-related penetrance in two dopa-responsive dystonia families with a novel GCH-I mutation.

2004 Movement Disorders
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Abstracts of the 8th Meeting of the Italian Peripheral Nerve Study Group: 47

2003 Journal of The Peripheral Nervous System
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Relation between trinucleotide GAA repeat length and sensory neuropathy in Friedreich’s ataxia

1999 Journal of Neurology, Neurosurgery, and Psychiatry
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Broadened Friedreich's ataxia phenotype after gene cloning Minimal GAA expansion causes late-onset spastic ataxia

1997 Neurology
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Acute motor axonal neuropathy with high titer IgG and IgA anti-GD1 a antibodies following Campylobacter enteritis

1997 Journal of the Neurological Sciences
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Acute motor axonal neuropathy with high titer IgG and IgA anti-GD1 a antibodies following enteritis

1997 Journal of the Neurological Sciences
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Autosomal dominant cerebellar ataxia type I: multimodal electrophysiological study and comparison between SCA1 and SCA2 patients

1996 Journal of the Neurological Sciences
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Autosomal dominant cerebellar ataxia type I. Clinical and molecular study in 36 Italian families including a comparison between SCA1 and SCA2 phenotypes

1996 Journal of the Neurological Sciences
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Amiodarone-induced experimental acute neuropathy in rats

1992 Muscle & Nerve
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