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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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Heterozygous Null Mutation in the P0 Gene Associated with Mild Charcot-Marie-Tooth Disease

Annals of the New York Academy of Sciences, 1999-10, Vol.883 (1), p.477-480

1999

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Heterozygous Null Mutation in the P 0 Gene Associated with Mild Charcot-Marie-Tooth Disease

Annals of the New York Academy of Sciences, 1999-10, Vol.883 (1), p.477-480

1999

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Charcot-Marie-Tooth disease type 2 and P0 gene mutations

Neurology, 1999-03, Vol.52 (5), p.1110

1999

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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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F response and somatosensory and brainstem auditory evoked potential studies in HMSN type I and II

Journal of neurology, neurosurgery and psychiatry, 1992-11, Vol.55 (11), p.1027-1031

1992

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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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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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Epidural anesthesia

Neurology, 1997-01, Vol.48 (1), p.293; author reply 294

1997

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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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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

Neurology, 1997-12, Vol.49 (6), p.1635-1640

1997

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

Annals of neurology, 2000-06, Vol.47 (6), p.811-816

2000

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Case 38-2001: Paraneoplastic Encephalomyelitis and Sensory Ganglioneuropathy

The New England journal of medicine, 2002-03, Vol.346 (13), p.1029-1030

2002

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Epidural anesthesia

Neurology, 1997-01, Vol.48 (1), p.293-294

1997

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A 1.5-Mb deletion in 17p11.2-p12 is frequently observed in Italian families with hereditary neuropathy with liability to pressure palsies

American journal of human genetics, 1995, Vol.56 (1), p.91-98

1995

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PMP22 frameshift mutation and hereditary neuropathy with liability to pressure palsies

Neurology, 1997-11, Vol.49 (5), p.1478-1478

1997

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Specific involvement of peripheral T lymphocytes against acetylcholine receptors in myasthenia gravis

Journal of neurology, neurosurgery and psychiatry, 1983-09, Vol.46 (9), p.832-836

1983

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Conduction velocities in Charcot-Marie-Tooth polyneuropathy type 1

Neurology, 1994-11, Vol.44 (11), p.2216-2216

1994

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

Annals of neurology, 2000-06, Vol.47 (6), p.811-816

2000

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Charcot-Marie-Tooth disease type 2 and P0 gene mutations

Neurology, 1999-03, Vol.52 (5), p.1106-1106

1999

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Immunosuppressive Treatments: Their Efficacy on Myasthenia Gravis Patients' Outcome and on the Natural Course of the Disease

Annals of the New York Academy of Sciences, 1993-06, Vol.681 (1), p.594-602

1993

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Myasthenia gravis: prolonged treatment with steroids

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

1984

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

Effect of longacting somatostatin analogue on kidney and cyst growth in autosomal dominant polycystic kidney disease (ALADIN): a randomised, placebo-controlled, multicentre trial

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

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

Heterozygous Null Mutation in the P0 Gene Associated with Mild Charcot-Marie-Tooth Disease

Heterozygous Null Mutation in the P 0 Gene Associated with Mild Charcot-Marie-Tooth Disease

Charcot-Marie-Tooth disease type 2 and P0 gene mutations

Clinical and magnetic resonance imaging findings in chronic sensory ganglionopathies

F response and somatosensory and brainstem auditory evoked potential studies in HMSN type I and II

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

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

Epidural anesthesia

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

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

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

Case 38-2001: Paraneoplastic Encephalomyelitis and Sensory Ganglioneuropathy

Epidural anesthesia

A 1.5-Mb deletion in 17p11.2-p12 is frequently observed in Italian families with hereditary neuropathy with liability to pressure palsies

PMP22 frameshift mutation and hereditary neuropathy with liability to pressure palsies

Specific involvement of peripheral T lymphocytes against acetylcholine receptors in myasthenia gravis

Conduction velocities in Charcot-Marie-Tooth polyneuropathy type 1

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

Charcot-Marie-Tooth disease type 2 and P0 gene mutations

Immunosuppressive Treatments: Their Efficacy on Myasthenia Gravis Patients' Outcome and on the Natural Course of the Disease

Myasthenia gravis: prolonged treatment with steroids

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