List of works - Patrizia Avoni

A de novo LGI1 mutation in sporadic partial epilepsy with auditory features

scientific article

Abnormal sympathetic skin responses in thalamic lesions

scientific article published in June 1992

Absence of sleep EEG markers in fatal familial insomnia healthy carriers: a spectral analysis study.

scientific article published in October 2001

Atypical late-onset hereditary spastic paraplegia with thin corpus callosum due to novel compound heterozygous mutations in the SPG11 gene.

scientific article published on 25 July 2014

Autonomic innervation in multiple system atrophy and pure autonomic failure

scientific article published on 26 July 2010

Autosomal dominant lateral temporal epilepsy: clinical spectrum, new epitempin mutations, and genetic heterogeneity in seven European families

scientific article

Differential cerebro spinal fluid proteome investigation of Leber hereditary optic neuropathy (LHON) and multiple sclerosis.

scientific article

Dissociated 24-Hour Patterns of Somatotropin and Prolactin in Fatal Familial Insomnia ⬇️

scientific article published on June 1, 1995

Does the prion protein gene 129 codon polymorphism influence sleep? Evidence from a fatal familial insomnia kindred

scientific article published in December 2002

Epilepsy with auditory features: Long-term outcome and predictors of terminal remission

scientific article published on 21 February 2018

Headache in epilepsy: prevalence and clinical features

scientific article

Idebenone treatment in Leber's hereditary optic neuropathy.

scientific article published on 2 August 2011

Idiopathic partial epilepsy with auditory features (IPEAF): a clinical and genetic study of 53 sporadic cases.

scientific article

Immunotherapy of oneiric stupor in Morvan syndrome: Efficacy documented by actigraphy

scientific article published on 15 May 2015

Kinetic-dynamic monitoring of levetiracetam effects in patients with Parkinson disease and levodopa-induced dyskinesias

scientific article published on 01 March 2007

Levodopa therapy monitoring in patients with Parkinson disease: a kinetic-dynamic approach

scientific article published on 01 December 2001

Low penetrance of autosomal dominant lateral temporal epilepsy in Italian families without LGI1 mutations.

scientific article published on 26 April 2013

Mitochondrial DNA nucleotide changes C14482G and C14482A in the ND6 gene are pathogenic for Leber's hereditary optic neuropathy.

scientific article

Molecular biology of channelopathies: impact on diagnosis and treatment.

scientific article

Non-paraneoplastic ataxia in a patient with contactin-associated protein-2 antibodies and benign course

scientific article published on 01 May 2015

Partial epilepsy of long duration: changing semiology with age.

scientific article published in February 1996

Pre-symptomatic diagnosis in fatal familial insomnia: serial neurophysiological and 18FDG-PET studies.

scientific article published on 6 January 2006

Primary progressive narcolepsy type 1: the other side of the coin

scientific article

Prognostic factors in patients with mesial temporal lobe epilepsy

article

Skin nerve α-synuclein deposits: a biomarker for idiopathic Parkinson disease

scientific article published on 14 March 2014

Sleep disorders in patients with spinal cord injury

scientific article published on 22 April 2013

Sleep-wake cycle abnormalities in fatal familial insomnia. Evidence of the role of the thalamus in sleep regulation.

scientific article published in June 1995

Small nerve fiber involvement in patients referred for fibromyalgia

scientific article published on 28 January 2014

Syndromic parkinsonism and dementia associated with OPA1 missense mutations

scientific article

The effect of entacapone on levodopa rate of absorption and latency to motor response in patients with Parkinson disease

scientific article published in September 2008

Topiramate therapeutic monitoring in patients with epilepsy: effect of concomitant antiepileptic drugs

scientific article published in June 2002

List of works by Patrizia Avoni

A de novo LGI1 mutation in sporadic partial epilepsy with auditory features

Abnormal sympathetic skin responses in thalamic lesions

Absence of sleep EEG markers in fatal familial insomnia healthy carriers: a spectral analysis study.

Atypical late-onset hereditary spastic paraplegia with thin corpus callosum due to novel compound heterozygous mutations in the SPG11 gene.

Autonomic innervation in multiple system atrophy and pure autonomic failure

Autosomal dominant lateral temporal epilepsy: clinical spectrum, new epitempin mutations, and genetic heterogeneity in seven European families

Differential cerebro spinal fluid proteome investigation of Leber hereditary optic neuropathy (LHON) and multiple sclerosis.

Dissociated 24-Hour Patterns of Somatotropin and Prolactin in Fatal Familial Insomnia ⬇️

Does the prion protein gene 129 codon polymorphism influence sleep? Evidence from a fatal familial insomnia kindred

Epilepsy with auditory features: Long-term outcome and predictors of terminal remission

Headache in epilepsy: prevalence and clinical features

Idebenone treatment in Leber's hereditary optic neuropathy.

Idiopathic partial epilepsy with auditory features (IPEAF): a clinical and genetic study of 53 sporadic cases.

Immunotherapy of oneiric stupor in Morvan syndrome: Efficacy documented by actigraphy

Kinetic-dynamic monitoring of levetiracetam effects in patients with Parkinson disease and levodopa-induced dyskinesias

Levodopa therapy monitoring in patients with Parkinson disease: a kinetic-dynamic approach

Low penetrance of autosomal dominant lateral temporal epilepsy in Italian families without LGI1 mutations.

Mitochondrial DNA nucleotide changes C14482G and C14482A in the ND6 gene are pathogenic for Leber's hereditary optic neuropathy.

Molecular biology of channelopathies: impact on diagnosis and treatment.

Non-paraneoplastic ataxia in a patient with contactin-associated protein-2 antibodies and benign course

Partial epilepsy of long duration: changing semiology with age.

Pre-symptomatic diagnosis in fatal familial insomnia: serial neurophysiological and 18FDG-PET studies.

Primary progressive narcolepsy type 1: the other side of the coin

Prognostic factors in patients with mesial temporal lobe epilepsy

Skin nerve α-synuclein deposits: a biomarker for idiopathic Parkinson disease

Sleep disorders in patients with spinal cord injury

Sleep-wake cycle abnormalities in fatal familial insomnia. Evidence of the role of the thalamus in sleep regulation.

Small nerve fiber involvement in patients referred for fibromyalgia

Syndromic parkinsonism and dementia associated with OPA1 missense mutations

The effect of entacapone on levodopa rate of absorption and latency to motor response in patients with Parkinson disease

Topiramate therapeutic monitoring in patients with epilepsy: effect of concomitant antiepileptic drugs

Variation in lamotrigine plasma concentrations with hormonal contraceptive monthly cycles in patients with epilepsy