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Intercropping with wheat suppressed Fusarium wilt in faba bean and modulated the composition of root exudates

Plant and soil, 2020-03, Vol.448 (1-2), p.153-164

2020

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Automatic Diagnosis of Epileptic Seizure in Electroencephalography Signals Using Nonlinear Dynamics Features

IEEE access, 2019, Vol.7, p.61046-61056

2019

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The relationship between the characteristics of burst suppression pattern and different etiologies in epilepsy

Scientific reports, 2021-08, Vol.11 (1), p.15903-15903, Article 15903

2021

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POLR3-related leukodystrophy caused by biallelic POLR3A and 1C pathogenic variants: a single-center experience

Frontiers in neurology, 2024-03, Vol.15, p.1355484-1355484

2024

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A long journey to treat epilepsy with the gut microbiota

Frontiers in cellular neuroscience, 2024-06, Vol.18, p.1386205

2024

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Case Report: Causative De novo Variants of KCNT2 for Developmental and Epileptic Encephalopathy

Frontiers in genetics, 2021-06, Vol.12

2021

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Genetic Etiologies in Developmental and/or Epileptic Encephalopathy With Electrical Status Epilepticus During Sleep: Cohort Study

Frontiers in genetics, 2021-04, Vol.12, p.607965-607965

2021

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Generation of a human iPSC line from an epileptic encephalopathy patient with electrical status epilepticus during sleep carrying KCNA2 (p.P405L) mutation

Stem cell research, 2020-12, Vol.49, p.102080-102080, Article 102080

2020

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Mosaicism and incomplete penetrance of PCDH19 mutations

Journal of medical genetics, 2019-02, Vol.56 (2), p.81

2019

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Long-term outcomes of epilepsy surgery in tuberous sclerosis complex

Journal of neurology, 2017-06, Vol.264 (6), p.1146-1154

2017

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CHD2‐related epilepsy: novel mutations and new phenotypes

Developmental medicine and child neurology, 2020-05, Vol.62 (5), p.647-653

2020

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A Feature Extraction Method for P2P Botnet Detection Using Graphic Symmetry Concept

Symmetry (Basel), 2019-03, Vol.11 (3), p.326

2019

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The clinical outcome and neuroimaging of acute encephalopathy after status epilepticus in Dravet syndrome

Developmental medicine and child neurology, 2018-06, Vol.60 (6), p.566-573

2018

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Clinical and genetic analysis of two Chinese infants with Mabry syndrome

Brain & development (Tokyo. 1979), 2016-10, Vol.38 (9), p.807-818

2016

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Case Report: A Case of Epileptic Disorder Associated With a Novel CNTN2 Frameshift Variant in Homozygosity due to Maternal Uniparental Disomy

Frontiers in genetics, 2021-10, Vol.12

2021

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A Rare Presentation Characterized by Epileptic Spasms in ALDH7A1 , Pyridox(am)ine-5'-Phosphate Oxidase, and PLPBP Deficiency

Frontiers in genetics, 2022-04, Vol.13, p.804461-804461

2022

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GABRB3-related epilepsy: novel variants, clinical features and therapeutic implications

Journal of neurology, 2022-05, Vol.269 (5), p.2649-2665

2022

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Complex Mosaicism of Two Distinct Mutations in a Female Patient With KCNA2-Related Encephalopathy: A Case Report

Frontiers in genetics, 2020-08, Vol.11

2020

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Analyzing clinical and genetic characteristics of a cohort with multiple congenital anomalies-hypotonia-seizures syndrome (MCAHS)

Orphanet journal of rare diseases, 2020-03, Vol.15 (1), p.78-78, Article 78

2020

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De novo variants in AGO1 recapitulate a heterogeneous neurodevelopmental disorder phenotype

Clinical genetics, 2022-04, Vol.101 (4), p.459-465

2022

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Analysis of the Phenotypic Variability as Well as Impact of Early Diagnosis and Treatment in Six Affected Families With ALDH7A1 Deficiency

Frontiers in genetics, 2021-04, Vol.12, p.644447-644447

2021

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Startle-Induced Epileptic Spasms: A Clinical and Video-EEG Study

Frontiers in neurology, 2022-06, Vol.13, p.878504-878504

2022

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GRIN2A mutations in epilepsy-aphasia spectrum disorders

Brain & development (Tokyo. 1979), 2018-03, Vol.40 (3), p.205-210

2018

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Temporal Onset Focal Seizures Induced by Intermittent Photic Stimulation

Frontiers in neurology, 2021-08, Vol.12, p.715236-715236

2021

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Phenotypes of GNAO1 Variants in a Chinese Cohort

Frontiers in neurology, 2021-05, Vol.12, p.662162-662162

2021

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Intercropping with wheat suppressed Fusarium wilt in faba bean and modulated the composition of root exudates

Automatic Diagnosis of Epileptic Seizure in Electroencephalography Signals Using Nonlinear Dynamics Features

The relationship between the characteristics of burst suppression pattern and different etiologies in epilepsy

POLR3-related leukodystrophy caused by biallelic POLR3A and 1C pathogenic variants: a single-center experience

A long journey to treat epilepsy with the gut microbiota

Case Report: Causative De novo Variants of KCNT2 for Developmental and Epileptic Encephalopathy

Genetic Etiologies in Developmental and/or Epileptic Encephalopathy With Electrical Status Epilepticus During Sleep: Cohort Study

Generation of a human iPSC line from an epileptic encephalopathy patient with electrical status epilepticus during sleep carrying KCNA2 (p.P405L) mutation

Mosaicism and incomplete penetrance of PCDH19 mutations

Long-term outcomes of epilepsy surgery in tuberous sclerosis complex

CHD2‐related epilepsy: novel mutations and new phenotypes

A Feature Extraction Method for P2P Botnet Detection Using Graphic Symmetry Concept

The clinical outcome and neuroimaging of acute encephalopathy after status epilepticus in Dravet syndrome

Clinical and genetic analysis of two Chinese infants with Mabry syndrome

Case Report: A Case of Epileptic Disorder Associated With a Novel CNTN2 Frameshift Variant in Homozygosity due to Maternal Uniparental Disomy

A Rare Presentation Characterized by Epileptic Spasms in ALDH7A1 , Pyridox(am)ine-5'-Phosphate Oxidase, and PLPBP Deficiency

GABRB3-related epilepsy: novel variants, clinical features and therapeutic implications

Complex Mosaicism of Two Distinct Mutations in a Female Patient With KCNA2-Related Encephalopathy: A Case Report

Analyzing clinical and genetic characteristics of a cohort with multiple congenital anomalies-hypotonia-seizures syndrome (MCAHS)

De novo variants in AGO1 recapitulate a heterogeneous neurodevelopmental disorder phenotype

Analysis of the Phenotypic Variability as Well as Impact of Early Diagnosis and Treatment in Six Affected Families With ALDH7A1 Deficiency

Startle-Induced Epileptic Spasms: A Clinical and Video-EEG Study

GRIN2A mutations in epilepsy-aphasia spectrum disorders

Temporal Onset Focal Seizures Induced by Intermittent Photic Stimulation

Phenotypes of GNAO1 Variants in a Chinese Cohort

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