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A. Sghirlanzoni

Vita-Salute San Raffaele University

54

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

2000 Neurology
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Partial laminin α2 chain deficiency in a patient with myopathy resembling inclusion body myositis

2000 Annals of Neurology
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Charcot-Marie-Tooth disease type 2 and P0 gene mutations

1999 Neurology
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CHARCOT-MARIE-TOOTH DISEASE TYPE 2 AND PO GENE MUTATIONS. AUTHORS' REPLY

1999 Neurology
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Heterozygous Null Mutation in the P0 Gene Associated with Mild Charcot‐Marie‐Tooth Disease

1999 Annals of the New York Academy of Sciences
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Detection of hereditary neuropathy with liability to pressure palsies among patients with acute painless mononeuropathy or plexopathy

1998 Muscle & Nerve
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Epidural anesthesia [2]

1997 Neurology
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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

1997 Neurology
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PMP22 frameshift mutation and hereditary neuropathy with liability to pressure palsies

1997 Neurology
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The phenotypic spectrum of tomaculous neuropathy

1997 Italian Journal of Neurological Sciences
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