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Axonal swellings predict the degeneration of epidermal nerve fibers in painful neuropathies

Neurology, 2003-09, Vol.61 (5), p.631-636

2003

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

Neurology, 2000-04, Vol.54 (8), p.1696-1698

2000

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

Neurology, 1996-04, Vol.46 (4), p.1133-1137

1996

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Impaired copper and iron metabolism in blood cells and muscles of patients affected by copper deficiency myeloneuropathy

Neuropathology and applied neurobiology, 2014-12, Vol.40 (7), p.888-898

2014

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

Neurological sciences, 2000-02, Vol.21 (1), p.31-37

2000

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Clinical and magnetic resonance imaging findings in chronic sensory ganglionopathies

Annals of neurology, 2000-01, Vol.47 (1), p.104-109

2000

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Neurophysiological Diagnosis of Acquired Sensory Ganglionopathies

European neurology, 2003-01, Vol.50 (3), p.146-152

2003

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HMSN III phenotype due to homozygous expression of a dominant HMSN II gene

Neurology, 1992-11, Vol.42 (11), p.2201-2201

1992

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

Journal of neurology, 1990-10, Vol.237 (6), p.339-344

1990

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Acute treatment of myasthenia gravis with intranasal neostigmine: clinical and electromyographic evaluation

Journal of neurology, neurosurgery and psychiatry, 1991-12, Vol.54 (12), p.1061-1062

1991

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The Course of Myasthenia Gravis in Patients Treated with Corticosteroids, Azathioprine, and Plasmapheresis

Annals of the New York Academy of Sciences, 1987, Vol.505 (1), p.517-525

1987

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The POEMS syndrome: report of six cases

Italian journal of neurological sciences, 1994-10, Vol.15 (7), p.353-358

1994

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

Muscle & nerve, 1998-12, Vol.21 (12), p.1686-1691

1998

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Neurological examination in patients recovering from general anesthesia

Italian journal of neurological sciences, 1992-12, Vol.13 (9), p.749-753

1992

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Homozygous hypertrophic hereditary motor and sensory neuropathies

Italian journal of neurological sciences, 1994-02, Vol.15 (1), p.5-14

1994

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Hereditary motor and sensory neuropathy type I and type II

Italian journal of neurological sciences, 1990-10, Vol.11 (5), p.471-479

1990

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Thymectomy for myasthenia gravis: a fourteen-year experience

Italian journal of neurological sciences, 1985-12, Vol.6 (4), p.425-428

1985

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Absence of decremental response in decentralized muscles of a myasthenic patient

Italian journal of neurological sciences, 1983-09, Vol.4 (3), p.355-357

1983

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Myasthenia gravis: prolonged treatment with steroids

Neurology, 1984-02, Vol.34 (2), p.170-170

1984

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Myasthenia gravis. Anti-acetylcholine receptor antibodies

Italian journal of neurological sciences, 1981-06, Vol.2 (2), p.165-171

1981

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Acoustic nerve in peripheral neuropathy: a BAEP study. Brainstem Auditory Evoked Potentials

Electromyography and clinical neurophysiology, 1995-10, Vol.35 (6), p.359

1995

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Cellular immune response against acetylcholine receptor in myasthenia gravis: I. Relevance to clinical course and pathogenesis

Neurology, 1979-04, Vol.29 (4), p.496-496

1979

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Kennedy's disease: clinical and molecular study of two Italian families

Italian journal of neurological sciences, 1995-10, Vol.16 (7), p.467-471

1995

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Effects of Rituximab on Morphofunctional Abnormalities of Membranous Glomerulopathy

Clinical journal of the American Society of Nephrology, 2008-11, Vol.3 (6), p.1652-1659

2008

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Axonal swellings predict the degeneration of epidermal nerve fibers in painful neuropathies

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

Effects of Manidipine and Delapril in Hypertensive Patients With Type 2 Diabetes Mellitus: The Delapril and Manidipine for Nephroprotection in Diabetes (DEMAND) Randomized Clinical Trial

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

Impaired copper and iron metabolism in blood cells and muscles of patients affected by copper deficiency myeloneuropathy

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

Clinical and magnetic resonance imaging findings in chronic sensory ganglionopathies

Neurophysiological Diagnosis of Acquired Sensory Ganglionopathies

HMSN III phenotype due to homozygous expression of a dominant HMSN II gene

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

Acute treatment of myasthenia gravis with intranasal neostigmine: clinical and electromyographic evaluation

The Course of Myasthenia Gravis in Patients Treated with Corticosteroids, Azathioprine, and Plasmapheresis

The POEMS syndrome: report of six cases

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

Neurological examination in patients recovering from general anesthesia

Homozygous hypertrophic hereditary motor and sensory neuropathies

Hereditary motor and sensory neuropathy type I and type II

Thymectomy for myasthenia gravis: a fourteen-year experience

Absence of decremental response in decentralized muscles of a myasthenic patient

Myasthenia gravis: prolonged treatment with steroids

Myasthenia gravis. Anti-acetylcholine receptor antibodies

Acoustic nerve in peripheral neuropathy: a BAEP study. Brainstem Auditory Evoked Potentials

Cellular immune response against acetylcholine receptor in myasthenia gravis: I. Relevance to clinical course and pathogenesis

Kennedy's disease: clinical and molecular study of two Italian families

Effects of Rituximab on Morphofunctional Abnormalities of Membranous Glomerulopathy

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