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Tubule and neurofilament immunoreactivity in human hairy skin: Markers for intraepidermal nerve fibers

Muscle & nerve, 2004-09, Vol.30 (3), p.310-316

2004

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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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Sensory neuron diseases

Lancet neurology, 2005-06, Vol.4 (6), p.349-361

2005

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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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Epidermal nerve fiber density in sensory ganglionopathies: Clinical and neurophysiologic correlations

Muscle & nerve, 2001-08, Vol.24 (8), p.1034-1039

2001

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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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Clinical and radiological features of brain neurotoxicity caused by antitumor and immunosuppressant treatments

Neurological sciences, 2008-06, Vol.29 (3), p.131-137

2008

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Le complicazioni neurologiche in oncologia

1. Aufl., 2006

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MR Imaging and Proton MR Spectroscopy in Adult Krabbe Disease

American journal of neuroradiology : AJNR, 2000-09, Vol.21 (8), p.1478-1482

2000

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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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RESEARCH REPORT: Normal expression of myelin protein zero with frame-shift mutation correlates with mild phenotype

Journal of the peripheral nervous system, 2006-03, Vol.11 (1), p.61-66

2006

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Normal expression of myelin protein zero with frame-shift mutation correlates with mild phenotype

Journal of the peripheral nervous system, 2006-03, Vol.11 (1), p.61-66

2006

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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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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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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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Unrecognized Charcot-Marie-Tooth Disease: Diagnostic Difficulties in the Assessment of Recovery from Paralysis

Anesthesia and analgesia, 1995-07, Vol.81 (1), p.199-201

1995

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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 ?2 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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Unrecognized Charcot-Marie-Tooth Disease: Diagnostic Difficulties in the Assessment of Recovery from Paralysis

Anesthesia and analgesia, 1995-07, Vol.81 (1), p.199-201

1995

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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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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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Tubule and neurofilament immunoreactivity in human hairy skin: Markers for intraepidermal nerve fibers

Clinical and magnetic resonance imaging findings in chronic sensory ganglionopathies

Sensory neuron diseases

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

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

Epidermal nerve fiber density in sensory ganglionopathies: Clinical and neurophysiologic correlations

Neurophysiological Diagnosis of Acquired Sensory Ganglionopathies

Clinical and radiological features of brain neurotoxicity caused by antitumor and immunosuppressant treatments

Le complicazioni neurologiche in oncologia

MR Imaging and Proton MR Spectroscopy in Adult Krabbe Disease

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

RESEARCH REPORT: Normal expression of myelin protein zero with frame-shift mutation correlates with mild phenotype

Normal expression of myelin protein zero with frame-shift mutation correlates with mild phenotype

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

Case 38-2001: Paraneoplastic Encephalomyelitis and Sensory Ganglioneuropathy

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

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

Unrecognized Charcot-Marie-Tooth Disease: Diagnostic Difficulties in the Assessment of Recovery from Paralysis

Conduction velocities in Charcot-Marie-Tooth polyneuropathy type 1

Partial laminin ?2 chain deficiency in a patient with myopathy resembling inclusion body myositis

Unrecognized Charcot-Marie-Tooth Disease: Diagnostic Difficulties in the Assessment of Recovery from Paralysis

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

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

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