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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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Speciated fine particulate matter in Northern Italy: A whole year chemical and transport modelling reconstruction

Atmospheric research, 2010-03, Vol.95 (4), p.496-514

2010

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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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Sensory neuron diseases

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

2005

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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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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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Measuring and estimating GFR and treatment effect in ADPKD patients: results and implications of a longitudinal cohort study

PloS one, 2012-02, Vol.7 (2), p.e32533-e32533

2012

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De novo malignancies after organ transplantation: focus on viral infections

Current molecular medicine, 2013-08, Vol.13 (7), p.1217-1227

2013

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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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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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Le complicazioni neurologiche in oncologia

1. Aufl., 2006

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

Speciated fine particulate matter in Northern Italy: A whole year chemical and transport modelling reconstruction

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

Sensory neuron diseases

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

MR Imaging and Proton MR Spectroscopy in Adult Krabbe Disease

Measuring and estimating GFR and treatment effect in ADPKD patients: results and implications of a longitudinal cohort study

De novo malignancies after organ transplantation: focus on viral infections

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

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

Le complicazioni neurologiche in oncologia

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

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

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