Lista de obras - Angelo Labate - Dominio Público Uruguay

3-T magnetic resonance imaging simultaneous automated multimodal approach improves detection of ambiguous visual hippocampal sclerosis.

artículo científico publicado en 2015

A familial t(4;8) translocation segregates with epilepsy and migraine with aura

artículo científico publicado en 2020

A functional genetic variation of the 5-HTR2A receptor affects age at onset in patients with temporal lobe epilepsy.

artículo científico publicado en 2012

A functional polymorphism in the SCN1A gene does not influence antiepileptic drug responsiveness in Italian patients with focal epilepsy

artículo científico publicado en 2011

A novel de novo HCN1 loss-of-function mutation in genetic generalized epilepsy causing increased neuronal excitability

artículo científico publicado en 2018

A possible case of natalizumab-dependent suicide attempt: A brief review about drugs and suicide.

artículo científico

A puzzling case without solution: isolated late-onset epileptic seizure

artículo científico publicado en 2015

AMPA receptors and perampanel behind selected epilepsies: current evidence and future perspectives

artículo científico publicado en 2017

Acute bulbar palsy without ophtalmoplegia associated with anti-GD3 IgM antibodies

scientific article published on 11 November 2016

Advanced MRI morphologic study shows no atrophy in healthy individuals with hippocampal hyperintensity.

artículo científico publicado en 2013

Advanced morphological neuroimaging study in lateral temporal lobe epilepsy: A multicentric study

artículo científico publicado en 2017

Age at onset predicts good seizure outcome in sporadic non-lesional and mesial temporal sclerosis based temporal lobe epilepsy

artículo científico publicado en 2010

Amygdala dysplasia with temporal lobe epilepsy and obsessive-compulsive disorder: an fMRI/EEG study.

artículo científico publicado en 2005

An SNP site in pri-miR-124, a brain expressed miRNA gene, no contribution to mesial temporal lobe epilepsy in an Italian sample.

artículo científico publicado en 2016

Anti-GM1 antibodies are not associated with cerebral atrophy in patients with multiple sclerosis.

artículo científico publicado en 2008

Anti-NMDA receptor encephalitis: a video case report

artículo científico publicado en 2009

ApoE epsilon4 allele and disease duration affect verbal learning in mild temporal lobe epilepsy

artículo científico publicado en 2005

Association between the M129V variant allele of PRNP gene and mild temporal lobe epilepsy in women.

artículo científico publicado en 2006

Autosomal dominant lateral temporal epilepsy (ADLTE): absence of chromosomal rearrangements in LGI1 gene

artículo científico publicado en 2013

Bell's palsy: a manifestation of prediabetes?

artículo científico publicado en 2011

Benign mesial temporal lobe epilepsy

artículo científico publicado en 2011

Benign partial epilepsies of adolescence: a report of 37 new cases

artículo científico publicado en 2001

Blocking out the real diagnosis

artículo científico publicado en 2011

Brand-to-generic levetiracetam switching: a 4-year prospective observational real-life study

artículo científico publicado en 2018

Cerebral venous thrombosis and isolated intracranial hypertension without papilledema in CDH

scientific article published on 01 July 2001

Combined use of cardiac m-i123-iodobenzylguanidine scintigraphy and ¹²³I-fp-cit single photon emission computed tomography in older adults with rapid eye movement sleep behavior disorder

artículo científico publicado en 2011

Comment on Brázdil (2012) "unveiling the mystery of dèjà-vù: the structural anatomy of dèjà-vù".

artículo científico publicado en 2012

Comparative risk of major congenital malformations with eight different antiepileptic drugs: a prospective cohort study of the EURAP registry

artículo científico publicado en 2018

Corrigendum to "Advanced morphological neuroimaging study in lateral temporal lobe epilepsy: A multicentric study" [Epilepsy Behav 74 (2017) Pages 69-72].

artículo científico publicado en 2017

DEPDC5 mutations are not a frequent cause of familial temporal lobe epilepsy

article

Deep Learning Representation from Electroencephalography of Early-Stage Creutzfeldt-Jakob Disease and Features for Differentiation from Rapidly Progressive Dementia.

artículo científico publicado en 2016

Detection of hippocampal atrophy in patients with temporal lobe epilepsy: A 3-Tesla MRI shape

scientific article published on 25 July 2013

Electroclinical features of a family with simple febrile seizures and temporal lobe epilepsy associated with SCN1A loss-of-function mutation.

artículo científico publicado en 2007

Epilepsy and sleep disorders improve in adolescents and adults with Angelman syndrome: A multicenter study on 46 patients

artículo científico publicado en 2017

Epilepsy associated with Leukoaraiosis mainly affects temporal lobe: a casual or causal relationship?

artículo científico publicado en 2014

Epilepsy in cerebrovascular diseases: Review of experimental and clinical data with meta-analysis of risk factors.

artículo científico publicado en 2016

Failure to confirm association of a polymorphism in KCNMB4 gene with mesial temporal lobe epilepsy.

artículo científico publicado en 2013

Familial mesial temporal lobe epilepsies: clinical and genetic features.

artículo científico publicado en 2009

Family history and frontal lobe seizures predict long-term remission in newly diagnosed cryptogenic focal epilepsy

artículo científico publicado en 2013

Further evidence of genetic heterogeneity in families with autosomal dominant nocturnal frontal lobe epilepsy

artículo científico publicado en 2007

Gene conversion events in adult-onset spinal muscular atrophy

article

Generalized versus partial reflex seizures: a review.

artículo científico publicado en 2014

Gerstmann-Straussler-Scheinker disease with PRNP P102L heterozygous mutation presenting as progressive myoclonus epilepsy

artículo científico publicado en 2017

Hepatonecrosis and cholangitis related to long-term phenobarbital therapy: An autopsy report of two patients

artículo científico publicado en 2007

Hippocampal and thalamic atrophy in mild temporal lobe epilepsy: a VBM study

artículo científico publicado en 2008

Homozygous c.649dupC mutation in PRRT2 worsens the BFIS/PKD phenotype with mental retardation, episodic ataxia, and absences

artículo científico publicado en 2012

How reliable are fMRI-EEG studies of epilepsy? A nonparametric approach to analysis validation and optimization.

artículo científico publicado en 2005

Hypersomnia hiding a bipolar disorder

artículo científico publicado en 2017

Ictal 18F-FDG PET/MRI in a Patient With Cortical Heterotopia and Focal Epilepsy

artículo científico publicado en 2017

Identification of an Nav1.1 sodium channel (SCN1A) loss-of-function mutation associated with familial simple febrile seizures

artículo científico publicado en 2005

Impact of catechol-O-methyltransferase Val(108/158) Met genotype on hippocampal and prefrontal gray matter volume

artículo científico publicado en 2008

Insight into epileptic and physiological déjà vu: from a multicentric cohort study

scientific article published on 26 October 2018

Integrity of the corpus callosum in patients with benign temporal lobe epilepsy

artículo científico publicado en 2016

Is language lateralization in temporal lobe epilepsy patients related to the nature of the epileptogenic lesion?

artículo científico publicado en 2006

Juvenile Huntington's disease presenting as progressive myoclonic epilepsy.

artículo científico publicado en 2001

Lacosamide in patients with temporal lobe epilepsy: An observational multicentric open-label study.

artículo científico publicado en 2016

Late drug-resistance in mild MTLE: Can it be influenced by preexisting white matter alterations?

artículo científico publicado en 2020

Letter: Beyond and within CA1 subfield in magnetic resonance imaging negative temporal lobe epilepsy

artículo científico publicado en 2015

Levetiracetam in patients with generalised epilepsy and myoclonic seizures: an open label study.

artículo científico publicado en 2006

Long-term outcome of mild mesial temporal lobe epilepsy: A prospective longitudinal cohort study.

artículo científico publicado en 2016

Looking for indicative magnetic resonance imaging signs of hippocampal developmental abnormalities in patients with mesial temporal lobe epilepsy and healthy controls

artículo científico publicado en 2020

MAO A VNTR polymorphism and variation in human morphology: a VBM study.

artículo científico publicado en 2008

MRI evidence of mesial temporal sclerosis in sporadic "benign" temporal lobe epilepsy.

artículo científico publicado en 2006

Migraine attack triggering a generalised seizure: is this a case of migralepsy or ictal epileptic headache?

scientific article published on 08 November 2011

Mild Lafora disease: clinical, neurophysiologic, and genetic findings.

artículo científico publicado en 2014

Modulation of GABAergic dysfunction due to SCN1A mutation linked to Hippocampal Sclerosis

artículo científico publicado en 2020

Mutational analysis of EFHC1 gene in Italian families with juvenile myoclonic epilepsy.

artículo científico publicado en 2007

Mutations in PRRT2 result in familial infantile seizures with heterogeneous phenotypes including febrile convulsions and probable SUDEP

artículo científico publicado en 2013

Neocortical thinning in “benign” mesial temporal lobe epilepsy

artículo científico publicado en 2011

Neuro-anatomical differences among epileptic and non-epileptic déjà-vu

artículo científico publicado en 2014

Neuroanatomic correlates of psychogenic nonepileptic seizures: a cortical thickness and VBM study.

artículo científico publicado en 2011

Neuropsychological profile of mild temporal lobe epilepsy

artículo científico publicado en 2018

No evidence for a role of the coding variant of the Toll-like receptor 4 gene in temporal lobe epilepsy.

artículo científico publicado en 2013

No evidence of a role for cystatin B gene in juvenile myoclonic epilepsy

artículo científico publicado en 2015

Orolingual tremor as unusual presentation of anti-Hu paraneoplastic syndrome.

artículo científico publicado en 2008

PCDH19 mutations in female patients from Southern Italy

artículo científico publicado en 2014

PRIMA1 mutation: a new cause of nocturnal frontal lobe epilepsy

artículo científico publicado en 2015

Perampanel as first add-on choice on the treatment of mesial temporal lobe epilepsy: an observational real-life study

artículo científico publicado en 2020

Pharmacological modulation in mesial temporal lobe epilepsy: Current status and future perspectives.

artículo científico publicado en 2016

Polymorphism of the multidrug resistance 1 gene MDR1/ABCB1 C3435T and response to antiepileptic drug treatment in temporal lobe epilepsy

article

Positivity to p-ANCA in patients with status epilepticus

artículo científico publicado en 2014

Prodynorphin Gene Promoter Polymorphism and Temporal Lobe Epilepsy

article

Prognostic factors in patients with mesial temporal lobe epilepsy

article

Psychiatric Assessment in Patients with Mild Temporal Lobe Epilepsy

scientific article published on 14 January 2019

Psychopathological constellation in patients with PNES: A new hypothesis

artículo científico publicado en 2017

Rating scale for psychogenic nonepileptic seizures: scale development and clinimetric testing.

artículo científico publicado en 2011

Recommendations for the use of structural magnetic resonance imaging in the care of patients with epilepsy: A consensus report from the International League Against Epilepsy Neuroimaging Task Force

artículo científico publicado en 2019

Reflex periodic spasms induced by eating

artículo científico publicado en 2006

Relationship between genetic variant in pre-microRNA-146a and genetic predisposition to temporal lobe epilepsy: A case–control study

artículo científico publicado en 2012

Relevance of clinical context in the diagnostic-therapeutic approach to status epilepticus.

artículo científico publicado en 2016

Response to commentary on recommendations for the use of structural MRI in the care of patients with epilepsy: A consensus report from the ILAE Neuroimaging Task Force

scientific article published on 29 August 2019

Reversible symmetrical external capsule hyperintensity as an early finding of autoimmune encephalitis

artículo científico publicado en 2014

Role of pharmacogenomics in antiepileptic drug therapy: current status and future perspectives.

artículo científico publicado en 2017

Rosacea-like facial rash related to metformin administration in a young woman.

artículo científico publicado en 2014

SUNCT and high nocturnal prolactin levels: some new unusual characteristics

artículo científico publicado en 2007

Septo-optic dysplasia plus bilateral perisylvian polymicrogyria: a case report

artículo científico publicado en 2012

Serotonin transporter gene (5-Htt): Association analysis with temporal lobe epilepsy

article

Silent celiac disease in patients with childhood localization-related epilepsies

artículo científico publicado en 2001

Spontaneous obliteration of MRI-silent cerebral angiomatosis revealed by CT angiography in a patient with Sturge–Weber syndrome

scientific article published on 27 August 2007

Startle epilepsy complicating aspartylglucosaminuria.

artículo científico publicado en 2004

Structural brain abnormalities in the common epilepsies assessed in a worldwide ENIGMA study.

artículo científico publicado en 2018

Temporal lobe abnormalities on brain MRI in healthy volunteers: A prospective case-control study

scientific article published on 20 January 2010

Thalamotemporal impairment in benign temporal lobe epilepsy: same hypotheses?

artículo científico publicado en 2014

The DRD2 TaqIA polymorphism associated with changed midbrain volumes in healthy individuals.

artículo científico publicado en 2009

The ENIGMA-Epilepsy working group: Mapping disease from large data sets

artículo científico publicado en 2020

The impact of sexual abuse on psychopathology of patients with psychogenic nonepileptic seizures

scientific article published on 13 August 2020

The mystery of unexplained traumatic sudden falls. A clinical case that adds a new feasible cause.

artículo científico publicado en 2017

The parkin gene is not involved in late-onset Parkinson's disease

artículo científico publicado en 2001

The role of calcium channel mutations in human epilepsy.

artículo científico

Topiramate and temporal lobe epilepsy: an open-label study.

artículo científico publicado en 2012

Tremor pattern differentiates drug-induced resting tremor from Parkinson disease.

artículo científico publicado en 2016

Two novel SCN1A missense mutations in generalized epilepsy with febrile seizures plus

artículo científico publicado en 2003

Unexpected detection of melanoma brain metastasis by PET with iodine-124 betaCIT.

artículo científico publicado en 2009

Unilateral basal ganglia atrophy in a patient with tuberous sclerosis complex and hemichorea.

artículo científico publicado en 2011

Usefulness of a morning routine EEG recording in patients with juvenile myoclonic epilepsy

artículo científico publicado en 2007

Usefulness of rectal biopsy for the diagnosis of Kufs disease: a controlled study and review of the literature.

artículo científico publicado en 2012

Validation Study of Italian Version of Inventory for Déjà Vu Experiences Assessment (I-IDEA): A Screening Tool to Detect Déjà Vu Phenomenon in Italian Healthy Individuals

artículo científico

Value of Clinical Features to Differentiate Refractory Epilepsy from Mimics A prospective longitudinal cohort study

artículo científico publicado en 2018

Value of Multimodal Imaging Approach to Diagnosis of Neurosarcoidosis

scientific article published on 21 September 2019

Voxel-based morphometry of sporadic epileptic patients with mesiotemporal sclerosis

artículo científico publicado en 2009

White matter abnormalities differentiate severe from benign temporal lobe epilepsy.

artículo científico publicado en 2015

Why should we change the term psychogenic nonepileptic seizures?

artículo científico publicado en 2015

Lista de obras de Angelo Labate

3-T magnetic resonance imaging simultaneous automated multimodal approach improves detection of ambiguous visual hippocampal sclerosis.

A familial t(4;8) translocation segregates with epilepsy and migraine with aura

A functional genetic variation of the 5-HTR2A receptor affects age at onset in patients with temporal lobe epilepsy.

A functional polymorphism in the SCN1A gene does not influence antiepileptic drug responsiveness in Italian patients with focal epilepsy

A novel de novo HCN1 loss-of-function mutation in genetic generalized epilepsy causing increased neuronal excitability

A possible case of natalizumab-dependent suicide attempt: A brief review about drugs and suicide.

A puzzling case without solution: isolated late-onset epileptic seizure

AMPA receptors and perampanel behind selected epilepsies: current evidence and future perspectives

Acute bulbar palsy without ophtalmoplegia associated with anti-GD3 IgM antibodies

Advanced MRI morphologic study shows no atrophy in healthy individuals with hippocampal hyperintensity.

Advanced morphological neuroimaging study in lateral temporal lobe epilepsy: A multicentric study

Age at onset predicts good seizure outcome in sporadic non-lesional and mesial temporal sclerosis based temporal lobe epilepsy

Amygdala dysplasia with temporal lobe epilepsy and obsessive-compulsive disorder: an fMRI/EEG study.

An SNP site in pri-miR-124, a brain expressed miRNA gene, no contribution to mesial temporal lobe epilepsy in an Italian sample.

Anti-GM1 antibodies are not associated with cerebral atrophy in patients with multiple sclerosis.

Anti-NMDA receptor encephalitis: a video case report

ApoE epsilon4 allele and disease duration affect verbal learning in mild temporal lobe epilepsy

Association between the M129V variant allele of PRNP gene and mild temporal lobe epilepsy in women.

Autosomal dominant lateral temporal epilepsy (ADLTE): absence of chromosomal rearrangements in LGI1 gene

Bell's palsy: a manifestation of prediabetes?

Benign mesial temporal lobe epilepsy

Benign partial epilepsies of adolescence: a report of 37 new cases

Blocking out the real diagnosis

Brand-to-generic levetiracetam switching: a 4-year prospective observational real-life study

Cerebral venous thrombosis and isolated intracranial hypertension without papilledema in CDH

Combined use of cardiac m-i123-iodobenzylguanidine scintigraphy and ¹²³I-fp-cit single photon emission computed tomography in older adults with rapid eye movement sleep behavior disorder

Comment on Brázdil (2012) "unveiling the mystery of dèjà-vù: the structural anatomy of dèjà-vù".

Comparative risk of major congenital malformations with eight different antiepileptic drugs: a prospective cohort study of the EURAP registry

Corrigendum to "Advanced morphological neuroimaging study in lateral temporal lobe epilepsy: A multicentric study" [Epilepsy Behav 74 (2017) Pages 69-72].

DEPDC5 mutations are not a frequent cause of familial temporal lobe epilepsy

Deep Learning Representation from Electroencephalography of Early-Stage Creutzfeldt-Jakob Disease and Features for Differentiation from Rapidly Progressive Dementia.

Detection of hippocampal atrophy in patients with temporal lobe epilepsy: A 3-Tesla MRI shape

Electroclinical features of a family with simple febrile seizures and temporal lobe epilepsy associated with SCN1A loss-of-function mutation.

Epilepsy and sleep disorders improve in adolescents and adults with Angelman syndrome: A multicenter study on 46 patients

Epilepsy associated with Leukoaraiosis mainly affects temporal lobe: a casual or causal relationship?

Epilepsy in cerebrovascular diseases: Review of experimental and clinical data with meta-analysis of risk factors.

Failure to confirm association of a polymorphism in KCNMB4 gene with mesial temporal lobe epilepsy.

Familial mesial temporal lobe epilepsies: clinical and genetic features.

Family history and frontal lobe seizures predict long-term remission in newly diagnosed cryptogenic focal epilepsy

Further evidence of genetic heterogeneity in families with autosomal dominant nocturnal frontal lobe epilepsy

Gene conversion events in adult-onset spinal muscular atrophy

Generalized versus partial reflex seizures: a review.

Gerstmann-Straussler-Scheinker disease with PRNP P102L heterozygous mutation presenting as progressive myoclonus epilepsy

Hepatonecrosis and cholangitis related to long-term phenobarbital therapy: An autopsy report of two patients

Hippocampal and thalamic atrophy in mild temporal lobe epilepsy: a VBM study

Homozygous c.649dupC mutation in PRRT2 worsens the BFIS/PKD phenotype with mental retardation, episodic ataxia, and absences

How reliable are fMRI-EEG studies of epilepsy? A nonparametric approach to analysis validation and optimization.

Hypersomnia hiding a bipolar disorder

Ictal 18F-FDG PET/MRI in a Patient With Cortical Heterotopia and Focal Epilepsy

Identification of an Nav1.1 sodium channel (SCN1A) loss-of-function mutation associated with familial simple febrile seizures

Impact of catechol-O-methyltransferase Val(108/158) Met genotype on hippocampal and prefrontal gray matter volume

Insight into epileptic and physiological déjà vu: from a multicentric cohort study

Integrity of the corpus callosum in patients with benign temporal lobe epilepsy

Is language lateralization in temporal lobe epilepsy patients related to the nature of the epileptogenic lesion?

Juvenile Huntington's disease presenting as progressive myoclonic epilepsy.

Lacosamide in patients with temporal lobe epilepsy: An observational multicentric open-label study.

Late drug-resistance in mild MTLE: Can it be influenced by preexisting white matter alterations?

Letter: Beyond and within CA1 subfield in magnetic resonance imaging negative temporal lobe epilepsy

Levetiracetam in patients with generalised epilepsy and myoclonic seizures: an open label study.

Long-term outcome of mild mesial temporal lobe epilepsy: A prospective longitudinal cohort study.

Looking for indicative magnetic resonance imaging signs of hippocampal developmental abnormalities in patients with mesial temporal lobe epilepsy and healthy controls

MAO A VNTR polymorphism and variation in human morphology: a VBM study.

MRI evidence of mesial temporal sclerosis in sporadic "benign" temporal lobe epilepsy.

Migraine attack triggering a generalised seizure: is this a case of migralepsy or ictal epileptic headache?

Mild Lafora disease: clinical, neurophysiologic, and genetic findings.

Modulation of GABAergic dysfunction due to SCN1A mutation linked to Hippocampal Sclerosis

Mutational analysis of EFHC1 gene in Italian families with juvenile myoclonic epilepsy.

Mutations in PRRT2 result in familial infantile seizures with heterogeneous phenotypes including febrile convulsions and probable SUDEP

Neocortical thinning in “benign” mesial temporal lobe epilepsy

Neuro-anatomical differences among epileptic and non-epileptic déjà-vu

Neuroanatomic correlates of psychogenic nonepileptic seizures: a cortical thickness and VBM study.

Neuropsychological profile of mild temporal lobe epilepsy

No evidence for a role of the coding variant of the Toll-like receptor 4 gene in temporal lobe epilepsy.

No evidence of a role for cystatin B gene in juvenile myoclonic epilepsy

Orolingual tremor as unusual presentation of anti-Hu paraneoplastic syndrome.

PCDH19 mutations in female patients from Southern Italy

PRIMA1 mutation: a new cause of nocturnal frontal lobe epilepsy

Perampanel as first add-on choice on the treatment of mesial temporal lobe epilepsy: an observational real-life study

Pharmacological modulation in mesial temporal lobe epilepsy: Current status and future perspectives.