Published in Muscle Nerve on January 28, 2014
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Cornea nerve fiber quantification and construction of phenotypes in patients with fibromyalgia. Sci Rep (2016) 0.78
Lengthened Cutaneous Silent Period in Fibromyalgia Suggesting Central Sensitization as a Pathogenesis. PLoS One (2016) 0.75
Skin cytokine expression in patients with fibromyalgia syndrome is not different from controls. BMC Neurol (2014) 0.75
Discordant Dry Eye Disease (An American Ophthalmological Society Thesis). Trans Am Ophthalmol Soc (2016) 0.75
Routine use of punch biopsy to diagnose small fiber neuropathy in fibromyalgia patients. Clin Rheumatol (2014) 0.75
Autonomic Testing in Women with Chronic Pelvic Pain. J Urol (2016) 0.75
Lower Functional Connectivity of the Periaqueductal Gray Is Related to Negative Affect and Clinical Manifestations of Fibromyalgia. Front Neuroanat (2017) 0.75
Diagnostic value of blood tests for occult causes of initially idiopathic small-fiber polyneuropathy. J Neurol (2016) 0.75
OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes. Brain (2007) 3.35
Skin nerve α-synuclein deposits: a biomarker for idiopathic Parkinson disease. Neurology (2014) 2.31
Sympathetic skin response: basic mechanisms and clinical applications. Clin Auton Res (2003) 2.24
Efficient mitochondrial biogenesis drives incomplete penetrance in Leber's hereditary optic neuropathy. Brain (2013) 2.08
Ross syndrome: a rare or a misknown disorder of thermoregulation? A skin innervation study on 12 subjects. Brain (2006) 1.55
Idebenone treatment in Leber's hereditary optic neuropathy. Brain (2011) 1.39
Autosomal dominant lateral temporal epilepsy: clinical spectrum, new epitempin mutations, and genetic heterogeneity in seven European families. Epilepsia (2003) 1.27
Skin sympathetic adrenergic innervation: an immunofluorescence confocal study. Ann Neurol (2006) 1.26
Visual system involvement in patients with Friedreich's ataxia. Brain (2008) 1.25
Sleep disorders in patients with spinal cord injury. Sleep Med Rev (2013) 1.22
Pre-symptomatic diagnosis in fatal familial insomnia: serial neurophysiological and 18FDG-PET studies. Brain (2006) 1.18
Excessive fragmentary hypnic myoclonus: clinical and neurophysiological findings. Sleep Med (2002) 1.05
Arousal elicits exaggerated inhibition of sympathetic nerve activity in phobic syncope patients. Brain (2007) 1.00
Tremor in primary adult-onset dystonia: prevalence and associated clinical features. J Neurol Neurosurg Psychiatry (2012) 0.99
Pathophysiology inferred from electrodiagnostic nerve tests and classification of polyneuropathies. Suggested guidelines. Clin Neurophysiol (2005) 0.97
Rare primary mitochondrial DNA mutations and probable synergistic variants in Leber's hereditary optic neuropathy. PLoS One (2012) 0.96
Mitochondrial DNA nucleotide changes C14482G and C14482A in the ND6 gene are pathogenic for Leber's hereditary optic neuropathy. Ann Neurol (2002) 0.95
Autonomic disturbances in narcolepsy. Sleep Med Rev (2010) 0.95
Ross syndrome: a lesson from a monozygotic twin pair. Neurology (2013) 0.93
Small fiber neuropathy in female patients with fabry disease. Muscle Nerve (2010) 0.92
Sleep-related stridor due to dystonic vocal cord motion and neurogenic tachypnea/tachycardia in multiple system atrophy. Mov Disord (2007) 0.91
Defective mitochondrial adenosine triphosphate production in skeletal muscle from patients with dominant optic atrophy due to OPA1 mutations. Arch Neurol (2010) 0.91
Pearls & Oy-sters: rapidly progressive dementia: prions or immunomediated? Neurology (2014) 0.88
A de novo LGI1 mutation in sporadic partial epilepsy with auditory features. Ann Neurol (2004) 0.88
Does the prion protein gene 129 codon polymorphism influence sleep? Evidence from a fatal familial insomnia kindred. Clin Neurophysiol (2002) 0.87
Prognostic factors in patients with mesial temporal lobe epilepsy. Epilepsia (2009) 0.87
Atypical late-onset hereditary spastic paraplegia with thin corpus callosum due to novel compound heterozygous mutations in the SPG11 gene. J Neurol (2014) 0.87
Age at onset and symptom spread in primary adult-onset blepharospasm and cervical dystonia. Mov Disord (2012) 0.86
Habituation of sympathetic sudomotor and vasomotor skin responses: neural and non-neural components in healthy subjects. Clin Neurophysiol (2005) 0.86
A defective SERCA1 protein is responsible for congenital pseudomyotonia in Chianina cattle. Am J Pathol (2008) 0.86
A novel in-frame 18-bp microdeletion in MT-CYB causes a multisystem disorder with prominent exercise intolerance. Hum Mutat (2014) 0.86
Mitochondrial neurogastrointestinal encephalomyopathy: evidence of mitochondrial DNA depletion in the small intestine. Gastroenterology (2006) 0.86
Eye symptoms in relatives of patients with primary adult-onset dystonia. Mov Disord (2011) 0.85
Low penetrance of autosomal dominant lateral temporal epilepsy in Italian families without LGI1 mutations. Epilepsia (2013) 0.85
Autosomal dominant early-onset cortical myoclonus, photic-induced myoclonus, and epilepsy in a large pedigree. Epilepsia (2006) 0.85
Iodine-123 metaiodobenzylguanidine scintigraphy and iodine-123 ioflupane single photon emission computed tomography in Lewy body diseases: complementary or alternative techniques? J Neuroimaging (2012) 0.85
Anhidrosis in multiple system atrophy: a preganglionic sudomotor dysfunction? Mov Disord (2008) 0.84
Isolated noradrenergic failure in adult-onset autosomal dominant leukodystrophy. Auton Neurosci (2010) 0.84
Variation in lamotrigine plasma concentrations with hormonal contraceptive monthly cycles in patients with epilepsy. Epilepsia (2006) 0.84
Peripheral autonomic neuropathy: diagnostic contribution of skin biopsy. J Neuropathol Exp Neurol (2012) 0.84
Idiopathic central sleep apnoea syndrome treated with zolpidem. Neurol Sci (2008) 0.83
Cybrid studies establish the causal link between the mtDNA m.3890G>A/MT-ND1 mutation and optic atrophy with bilateral brainstem lesions. Biochim Biophys Acta (2012) 0.83
A clinically complex form of dominant optic atrophy (OPA8) maps on chromosome 16. Hum Mol Genet (2011) 0.83
A novel pedigree with familial cortical myoclonic tremor and epilepsy (FCMTE): clinical characterization, refinement of the FCMTE2 locus, and confirmation of a founder haplotype. Epilepsia (2013) 0.82
Oct-1 recruitment to the nuclear envelope in adult-onset autosomal dominant leukodystrophy. Biochim Biophys Acta (2012) 0.82
Axial myoclonus in Devic neuromyelitis optica. Mov Disord (2009) 0.82
Pseudomyotonia in Romagnola cattle caused by novel ATP2A1 mutations. BMC Vet Res (2012) 0.82
Sympathetic and cardiovascular activity during cataplexy in narcolepsy. J Sleep Res (2008) 0.81
Epidemiology of amyotrophic lateral sclerosis in Emilia Romagna Region (Italy): A population based study. Amyotroph Lateral Scler Frontotemporal Degener (2014) 0.81
Idebenone treatment in patients with OPA1-mutant dominant optic atrophy. Brain (2013) 0.81
Daytime sympathetic hyperactivity in OSAS is related to excessive daytime sleepiness. J Sleep Res (2007) 0.81
Phenotypic overlap in familial and sporadic primary adult-onset extracranial dystonia. J Neurol (2012) 0.81
Somatic and autonomic small fiber neuropathy induced by bortezomib therapy: an immunofluorescence study. Neurol Sci (2011) 0.81
Subcutaneous immunoglobulin in CIDP and MMN: a short-term nationwide study. J Neurol (2014) 0.81
The empowerment of translational research: lessons from laminopathies. Orphanet J Rare Dis (2012) 0.80
Quality of life in patients with craniocervical dystonia: Italian validation of the "Cervical Dystonia Impact Profile (CDIP-58)" and the "Craniocervical Dystonia Questionnaire (CDQ-24)". Neurol Sci (2014) 0.80
Microneurographic evaluation of sympathetic activity in small fiber neuropathy. Clin Neurophysiol (2011) 0.79
Revisiting the issue of mitochondrial DNA content in optic mitochondriopathies. Neurology (2012) 0.79
Differential cerebro spinal fluid proteome investigation of Leber hereditary optic neuropathy (LHON) and multiple sclerosis. J Neuroimmunol (2007) 0.79
Topiramate therapeutic monitoring in patients with epilepsy: effect of concomitant antiepileptic drugs. Ther Drug Monit (2002) 0.78
The effect of entacapone on levodopa rate of absorption and latency to motor response in patients with Parkinson disease. Clin Neuropharmacol (2008) 0.77
Sleep-related periodic respiration with central sleep apnea in Leber Hereditary Optic Neuropathy (LHON). Sleep Med (2009) 0.77
A prospective multicentre study on sural nerve action potentials in ALS. Clin Neurophysiol (2008) 0.77
Skin sympathetic fiber α-synuclein deposits: a potential biomarker for pure autonomic failure. Neurology (2013) 0.77
Axial myoclonus in paraproteinemic polyneuropathy. Muscle Nerve (2008) 0.77
Partial epilepsy with prominent auditory symptoms not linked to chromosome 10q. Epileptic Disord (2002) 0.76
A case of fatal familial insomnia in Africa. J Neurol (2009) 0.76
Methods of sudomotor innervation quantification. Muscle Nerve (2011) 0.75
Author response. Neurology (2014) 0.75
Kinetic-dynamic monitoring of levetiracetam effects in patients with Parkinson disease and levodopa-induced dyskinesias. Clin Neuropharmacol (2007) 0.75
Possible contribution of vascular innervation to somatic sensory function. Pain (2010) 0.75
Continuous motor unit activity syndromes: a video-polysomnographic study. Clin Neurophysiol (2005) 0.75
Influence of peer review medical audit on pathophysiological interpretation of nerve conduction studies in polyneuropathies. Clin Neurophysiol (2006) 0.75
Differentiation of chromaffin cells in the developing adrenal gland of Testudo hermanni. Anat Embryol (Berl) (2006) 0.75
Electrophysiological findings in X-linked myopathy with excessive autophagy. Ann Neurol (2002) 0.75
Influence of medical audit on electrodiagnostic evaluation of polyneuropathy. A multicentre study. Clin Neurophysiol (2005) 0.75
Parallel changes in resting muscle sympathetic nerve activity and blood pressure in a hypertensive OSAS patient demonstrate treatment efficacy. Clin Auton Res (2006) 0.75
Molecular biology of channelopathies: impact on diagnosis and treatment. Expert Rev Neurother (2004) 0.75
Antibodies against hypocretin receptor 2 are rare in narcolepsy. Sleep (2016) 0.75
Variation in the neurophysiological examination of amyotrophic lateral sclerosis in Europe. Amyotroph Lateral Scler (2010) 0.75
Impact of medical audit on electrodiagnostic medicine in polyneuropathy. Clin Neurophysiol (2011) 0.75