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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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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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Risk of de novo cancers after transplantation: Results from a cohort of 7217 kidney transplant recipients, Italy 1997–2009

European journal of cancer (1990), 2013-01, Vol.49 (2), p.336-344

2013

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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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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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Imaging and outcome in severe complications of lumbar epidural anaesthesia : report of 16 cases

Neuroradiology, 2000-08, Vol.42 (8), p.564-571

2000

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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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Azathioprine as a single drug or in combination with steroids in the treatment of myasthenia gravis

Journal of neurology, 1988-11, Vol.235 (8), p.449-453

1988

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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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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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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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Neurophysiological Diagnosis of Acquired Sensory Ganglionopathies

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

2003

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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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Neurologic symptoms after epidural anaesthesia. Report of three cases

Acta anaesthesiologica Scandinavica, 1994-10, Vol.38 (7), p.742-743

1994

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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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Spinal arteriovenous fistula: a possible cause of paraparesis after epidural anaesthesia

Anaesthesia, 1989-10, Vol.44 (10), p.831-833

1989

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Epidural anaesthesia and spinal arachnoiditis

Anaesthesia, 1989-04, Vol.44 (4), p.317-321

1989

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Charcot-Marie-Tooth (CMT) 1a duplication at 17p11.2 in Italian families

Journal of medical genetics, 1992-07, Vol.29 (7), p.492-493

1992

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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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17p11.2 duplication is a common finding in sporadic cases of Charcot-Marie-Tooth type 1

European neurology, 1994, Vol.34 (3), p.135-139

1994

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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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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

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

Risk of de novo cancers after transplantation: Results from a cohort of 7217 kidney transplant recipients, Italy 1997–2009

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

MR Imaging and Proton MR Spectroscopy in Adult Krabbe Disease

Imaging and outcome in severe complications of lumbar epidural anaesthesia : report of 16 cases

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

Azathioprine as a single drug or in combination with steroids in the treatment of myasthenia gravis

Clinical and magnetic resonance imaging findings in chronic sensory ganglionopathies

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

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

Neurophysiological Diagnosis of Acquired Sensory Ganglionopathies

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

Neurologic symptoms after epidural anaesthesia. Report of three cases

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

Spinal arteriovenous fistula: a possible cause of paraparesis after epidural anaesthesia

Epidural anaesthesia and spinal arachnoiditis

Charcot-Marie-Tooth (CMT) 1a duplication at 17p11.2 in Italian families

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

17p11.2 duplication is a common finding in sporadic cases of Charcot-Marie-Tooth type 1

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

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