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Transient Cognitive Impairment in Epilepsy

Frontiers in molecular neuroscience, 2019-01, Vol.11, p.458-458

2019

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Classification of autism spectrum disorder using supervised learning of brain connectivity measures extracted from synchrostates

Journal of neural engineering, 2014-08, Vol.11 (4), p.046019-19

2014

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Epilepsy, Behavioral Abnormalities, and Physiological Comorbidities in Syntaxin-Binding Protein 1 (STXBP1) Mutant Zebrafish

PloS one, 2016-03, Vol.11 (3), p.e0151148-e0151148

2016

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Trehalose Treatment in Zebrafish Model of Lafora Disease

International journal of molecular sciences, 2022-06, Vol.23 (12), p.6874

2022

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Understanding Spreading Depression from Headache to Sudden Unexpected Death

Frontiers in neurology, 2018-02, Vol.9, p.19-19

2018

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Kir4.1 Dysfunction in the Pathophysiology of Depression: A Systematic Review

Cells (Basel, Switzerland), 2021-10, Vol.10 (10), p.2628

2021

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Autism with Seizures and Intellectual Disability: Possible Causative Role of Gain-of-function of the Inwardly-Rectifying K+ Channel Kir4.1

Neurobiology of disease, 2011-07, Vol.43 (1), p.239-247

2011

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Genetically induced dysfunctions of Kir2.1 channels: implications for short QT3 syndrome and autism-epilepsy phenotype

Human molecular genetics, 2014-09, Vol.23 (18), p.4875-4886

2014

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Safe and sound: Meta-analyzing the Mozart effect on epilepsy

Clinical neurophysiology, 2020-07, Vol.131 (7), p.1610-1620

2020

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On the application of quantitative EEG for characterizing autistic brain: a systematic review

Frontiers in human neuroscience, 2013, Vol.7, p.442-442

2013

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Mitochondrial epilepsy: a cross-sectional nationwide Italian survey

Neurogenetics, 2020-04, Vol.21 (2), p.87-96

2020

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Evolution of Epileptiform Activity in Zebrafish by Statistical-Based Integration of Electrophysiology and 2-Photon Ca2+ Imaging

Cells (Basel, Switzerland), 2020-03, Vol.9 (3), p.769

2020

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FOCAL CORTICAL DYSPLASIA, MICROCEPHALY AND EPILEPSY IN A BOY WITH 1q21.1-q21.3 DUPLICATION

European journal of medical genetics, 2016-05, Vol.59 (5), p.278-282

2016

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Somatic overgrowth predisposes to seizures in autism spectrum disorders

PloS one, 2013-09, Vol.8 (9), p.e75015-e75015

2013

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Expanding the clinical and genetic heterogeneity of SPAX5

Annals of clinical and translational neurology, 2020-04, Vol.7 (4), p.595-601

2020

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The Revolution in Migraine Genetics: From Aching Channels Disorders to a Next-Generation Medicine

Frontiers in cellular neuroscience, 2016-06, Vol.10, p.156-156

2016

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Loss of ap4s1 in zebrafish leads to neurodevelopmental defects resembling spastic paraplegia 52

Annals of clinical and translational neurology, 2020-04, Vol.7 (4), p.584-589

2020

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Sleep EEG microstructure in children and adolescents with attention deficit hyperactivity disorder: a systematic review and meta-analysis

Sleep (New York, N.Y.), 2021-07, Vol.44 (7), p.1

2021

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MECP2 duplication phenotype in symptomatic females: report of three further cases

Molecular cytogenetics, 2014-01, Vol.7 (1), p.10-10

2014

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Epilepsy and malformations of the cerebral cortex

Epileptic disorders, 2003-09, Vol.5 (S2), p.S9-S26

2003

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Epilepsy in LAMA2-related muscular dystrophy: A systematic review of the literature

Seizure (London, England), 2021-10, Vol.91, p.425-436

2021

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Morphometric network-based abnormalities correlate with psychiatric comorbidities and gene expression in PCDH19-related developmental and epileptic encephalopathy

Translational psychiatry, 2024-01, Vol.14 (1), p.35-35, Article 35

2024

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Clinical and genetic factors predicting Dravet syndrome in infants with SCN1A mutations

Neurology, 2017-03, Vol.88 (11), p.1037-1044

2017

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Maximum downward slope of sleep slow waves as a potential marker of attention-deficit/hyperactivity disorder clinical phenotypes

Journal of psychiatric research, 2022-12, Vol.156, p.679-689

2022

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Diagnostic Targeted Resequencing in 349 Patients with Drug‐Resistant Pediatric Epilepsies Identifies Causative Mutations in 30 Different Genes

Human mutation, 2017-02, Vol.38 (2), p.216-225

2017

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Transient Cognitive Impairment in Epilepsy

Classification of autism spectrum disorder using supervised learning of brain connectivity measures extracted from synchrostates

Epilepsy, Behavioral Abnormalities, and Physiological Comorbidities in Syntaxin-Binding Protein 1 (STXBP1) Mutant Zebrafish

Trehalose Treatment in Zebrafish Model of Lafora Disease

Understanding Spreading Depression from Headache to Sudden Unexpected Death

Kir4.1 Dysfunction in the Pathophysiology of Depression: A Systematic Review

Autism with Seizures and Intellectual Disability: Possible Causative Role of Gain-of-function of the Inwardly-Rectifying K+ Channel Kir4.1

Genetically induced dysfunctions of Kir2.1 channels: implications for short QT3 syndrome and autism-epilepsy phenotype

Safe and sound: Meta-analyzing the Mozart effect on epilepsy

On the application of quantitative EEG for characterizing autistic brain: a systematic review

Mitochondrial epilepsy: a cross-sectional nationwide Italian survey

Evolution of Epileptiform Activity in Zebrafish by Statistical-Based Integration of Electrophysiology and 2-Photon Ca2+ Imaging

FOCAL CORTICAL DYSPLASIA, MICROCEPHALY AND EPILEPSY IN A BOY WITH 1q21.1-q21.3 DUPLICATION

Somatic overgrowth predisposes to seizures in autism spectrum disorders

Expanding the clinical and genetic heterogeneity of SPAX5

The Revolution in Migraine Genetics: From Aching Channels Disorders to a Next-Generation Medicine

Loss of ap4s1 in zebrafish leads to neurodevelopmental defects resembling spastic paraplegia 52

Sleep EEG microstructure in children and adolescents with attention deficit hyperactivity disorder: a systematic review and meta-analysis

MECP2 duplication phenotype in symptomatic females: report of three further cases

Epilepsy and malformations of the cerebral cortex

Epilepsy in LAMA2-related muscular dystrophy: A systematic review of the literature

Morphometric network-based abnormalities correlate with psychiatric comorbidities and gene expression in PCDH19-related developmental and epileptic encephalopathy

Clinical and genetic factors predicting Dravet syndrome in infants with SCN1A mutations

Maximum downward slope of sleep slow waves as a potential marker of attention-deficit/hyperactivity disorder clinical phenotypes

Diagnostic Targeted Resequencing in 349 Patients with Drug‐Resistant Pediatric Epilepsies Identifies Causative Mutations in 30 Different Genes

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