A. Perretti

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Cerebellar ataxia associated with subclinical celiac disease responding to gluten-free diet.

M. T. Pellecchia, P. Barone, L. Santoro, 1999, Neurology.

Is Ross syndrome a dysautonomic disorder only? An electrophysiologic and histologic study

G. Iannetti, G. Iannetti, L. Santoro, 2003, Clinical Neurophysiology.

Small fiber neuropathy in the chronic phase of Chagas disease: a case report

L. Santoro, M. Nolano, V. Provitera, 2013, Clinical Autonomic Research.

Postexercise facilitation of motor evoked potentials following transcranial magnetic stimulation: A study in normal subjects

L. Santoro, A. Perretti, M. Sannino, 2002, Muscle & nerve.

Patterns of motor control reorganization in a patient with mirror movements

P. Balbi, L. Santoro, L. Trojano, 2000, Clinical Neurophysiology.

Autosomal dominant cerebellar ataxia type I: multimodal electrophysiological study and comparison between SCA1 and SCA2 patients

G. Caruso, Francesco Barbieri, L. Santoro, 1996, Journal of the Neurological Sciences.

Has spinocerebellar ataxia type 2 a distinct phenotype? Genetic and clinical study of an Italian family

L. Santoro, L. Pianese, F. Cavalcanti, 1995, Neurology.

Clinical and genetic heterogeneity in early onset cerebellar ataxia with retained tendon reflexes.

L. Santoro, F. Cavalcanti, G. De Michele, 1990, Journal of neurology, neurosurgery, and psychiatry.

Levetiracetam in patients with cortical myoclonus: A clinical and electrophysiological study

P. Striano, A. Perretti, S. Striano, 2005, Movement disorders : official journal of the Movement Disorder Society.

Multimodal electrophysiologic follow-up study in 3 mutated but presymptomatic members of a spinocerebellar ataxia type 1 (SCA1) family

L. Santoro, A. Perretti, F. Manganelli, 2005, Neurological Sciences.

Electrophysiologic characterization in spinocerebellar ataxia 17

L. Santoro, M. Nolano, G. De Michele, 2006, Neurology.

A family with tomaculous neuropathy mimicking Charcot-Marie-Tooth disease

C. Crisci, L. Santoro, A. Perretti, 1990, Clinical Neurology and Neurosurgery.

The R495W mutation in SPG3A causes spastic paraplegia associated with axonal neuropathy

L. Santoro, A. Filla, A. Tessa, 2005, Journal of Neurology.

Neurophysiologic evaluation of central-peripheral sensory and motor pudendal pathways in primary premature ejaculation.

P. Balbi, A. Catalano, L. Santoro, 2003, Urology.

Correlations between clinical, electrophysiological and histological findings in patients with different diseases of the peripheral nervous system

G. Caruso, R. Massini, C. Crisci, 1983, The Italian Journal of Neurological Sciences.

Sensory (VEP, BAEP, SEP) and motor-evoked potentials, liquoral and magnetic resonance findings in multiple sclerosis.

P. Rossini, G. Bernardi, G. Caruso, 1989, European neurology.

A novel mutation in SACS gene in a family from southern Italy

L. Santoro, P. Gasparini, A. Monticelli, 2004, Neurology.

Evoked potentials in inherited ataxias: A multimodal electrophysiological study

G. Caruso, L. Pelosi, L. Santoro, 1994, The Italian Journal of Neurological Sciences.

Is early onset cerebellar ataxia with retained tendon reflexes identifiable by electrophysiologic and histologic profile? A comparison with Friedreich's ataxia

G. Caruso, Francesco Barbieri, C. Crisci, 1992, Journal of the Neurological Sciences.

Somatosensory evoked potentials and motor cortex stimulation in myelopathies.

G. Caruso, L. Pelosi, C. Crisci, 1990, Electroencephalography and clinical neurophysiology. Supplement.

Trigeminal Stimulation Elicits a Peripheral Vestibular Imbalance in Migraine Patients

E. Marciano, A. Perretti, F. Manganelli, 2005, Headache.

Study of Multimodal Evoked Potentials in Patients With Type 1 Gaucher's Disease

L. Santoro, G. Andria, L. Titomanlio, 2005, Journal of child neurology.

Motor cortex cholinergic dysfunction in CADASIL: A transcranial magnetic demonstration

L. Santoro, L. Trojano, A. Perretti, 2008, Clinical Neurophysiology.

Small‐fiber involvement in spinobulbar muscular atrophy (Kennedy's disease)

L. Santoro, M. Nolano, V. Provitera, 2007, Muscle & nerve.

Ross syndrome: a rare or a misknown disorder of thermoregulation? A skin innervation study on 12 subjects.

L. Santoro, M. Nolano, V. Provitera, 2006, Brain : a journal of neurology.

Autosomal dominant cerebellar ataxia type I. Clinical and molecular study in 36 Italian families including a comparison between SCA1 and SCA2 phenotypes

Sergio Cocozza, Giuseppe De Michele, Lucio Santoro, 1996, Journal of the Neurological Sciences.

Detection of early abnormalities in the mucopolysaccharidoses by the use of visual and brainstem auditory evoked potentials.

L. Pelosi, P. Balbi, G. Parenti, 1990, Neuropediatrics.

Cervico-Oculo-Acoustic Syndrome in a Male with Consanguineous Parents

G. De Michele, A. Filla, E. Marciano, 2006, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

Friedreich's ataxia: Electrophysiologic and histologic findings in patients and relatives

G. Caruso, L. Pelosi, R. Massini, 1987, Muscle & nerve.

Friedreich's ataxia: electrophysiological and histological findings

G. Caruso, Francesco Barbieri, C. Crisci, 1983, Acta neurologica Scandinavica.

Myotonic dystrophy and pilomatricomas: an unusual association.

L. Pelosi, M. Delfino, A. Filla, 1982, Acta neurologica.

Brain damage in glycogen storage disease type I.

F. Di Salle, L. Santoro, L. Sequino, 2004, The Journal of pediatrics.

Autosomal recessive progressive myoclonus epilepsy with ataxia and mental retardation

P. Striano, G. Coppola, L. Santoro, 2005, Journal of Neurology.

Post-exercise facilitation and depression of motor evoked potentials to transcranial magnetic stimulation: a study in multiple sclerosis

P. Balbi, L. Santoro, L. Trojano, 2004, Clinical Neurophysiology.

Peripheral neuropathy in liver cirrhosis. A clinical and electrophysiological study.

G. Caruso, P. Balbi, M. Persico, 1995, The Italian journal of gastroenterology.

Neurophysiological evaluation of motor corticospinal pathways by TMS in idiopathic early-onset Parkinson’s disease

L. Santoro, A. Filla, G. Michele, 2011, Clinical Neurophysiology.

Neurophysiological evidence of corticospinal tract abnormality in patients with Parkin mutations

A. Brice, L. Santoro, G. De Michele, 2006, Journal of Neurology.

Excitatory and inhibitory mechanisms in Wilson's disease: investigation with magnetic motor cortex stimulation

Bernardo Lanzillo, Lucio Santoro, M. T. Pellecchia, 2001, Journal of the Neurological Sciences.

Clinical and computerized tomographic study of a case of Schilder's disease.

D. Grossi, A. Filla, A. Perretti, 1982, Acta neurologica.

A novel mutation of the β‐glucocererebrosidase gene associated with neurologic manifestations in three sibs

M. Filocamo, G. Andria, L. Titomanlio, 1998 .

Evaluation of the motor cortex by magnetic stimulation in patients with Alzheimer disease

G. Caruso, L. Santoro, M. Nolano, 1996, Journal of the Neurological Sciences.

Adult-onset familial laryngeal abductor paralysis, cerebellar ataxia, and pure motor neuropathy

M. T. Pellecchia, L. Santoro, G. De Michele, 2001, Neurology.

Why do some Friedreich’s ataxia patients retain tendon reflexes?

G. Caruso, G. Coppola, L. Santoro, 1999, Journal of Neurology.

Late onset recessive ataxia with Friedreich's disease phenotype.

L. Santoro, G. De Michele, A. Filla, 1989, Journal of neurology, neurosurgery, and psychiatry.

High frequency of exon 10 mutations in the NOTCH3 gene in Italian CADASIL families: phenotypic peculiarities

L. Pantoni, D. Inzitari, A. Federico, 2010, Journal of Neurology.

Why do some Friedreich's ataxia patients retain tendon reflexes? A clinical, neurophysiological and molecular study.

G. Caruso, G. Coppola, L. Santoro, 1999, Journal of neurology.

Influence of GAA expansion size and disease duration on central nervous system impairment in Friedreich's ataxia: contribution to the understanding of the pathophysiology of the disease

G. Caruso, G. Coppola, L. Santoro, 2000, Clinical Neurophysiology.

Cortico-spinal pathways and inhibitory mechanisms in hepatic encephalopathy.

M Nolano, M A Guardascione, L Amitrano, 1997, Electroencephalography and clinical neurophysiology.

Accuracy of clinical diagnostic criteria for Friedreich's ataxia

G. Caruso, P. Barone, G. Coppola, 2000, Movement disorders : official journal of the Movement Disorder Society.

Relation between trinucleotide GAA repeat length and sensory neuropathy in Friedreich’s ataxia

G. Caruso, C. Crisci, L. Santoro, 1999, Journal of Neurology Neurosurgery & Psychiatry.

Electrophysiological and histological follow‐up study in 15 Friedreich's ataxia patients

G. Caruso, R. Massini, C. Crisci, 1990, Muscle & nerve.

Motor and somatosensory evoked potentials in hereditary spastic paraplegia.

G. Caruso, L. Pelosi, L. Blumhardt, 1991, Journal of neurology, neurosurgery, and psychiatry.

Combination of mtDNA mutations in a patient with a mitochondrial multisystem syndrome

L. Santoro, F. Santorelli, C. Casali, 2000, Journal of Human Genetics.

The thymus and myasthenia gravis: immunological and neurophysiological aspects.

G. Caruso, P. Carrieri, A. Perretti, 1999, Annals medicus.

Botulinum toxin treatment in spasmodic torticollis.

A J Lees, A. Lees, Francesco Barbieri, 1990, Journal of neurology, neurosurgery, and psychiatry.

Benign adult familial myoclonic epilepsy

P. Balbi, P. Striano, F. Zara, 2003, Neurology.

Clinical Utility of Electrophysiological Evaluation in Crigler-Najjar Syndrome

A. Iolascon, P. Vajro, A. Perretti, 2007, Neuropediatrics.

Electrophysiological contribution to understanding the pathophysiology of Friedreich's ataxia

C. Crisci, L. Santoro, A. Perretti, 2001, Neurological Sciences.