Xiaoyan Liu

A single-center randomized controlled trial observing the safety and efficacy of modified step-up graded Valsalva manoeuver in patients with vasovagal syncope.

Acute Beneficial Effects of Sodium Nitroprusside in a Rabbit Model of Massive Pulmonary Embolism Associated with Circulatory Shock.

Bilateral sympathetic stellate ganglionectomy attenuates myocardial remodelling and fibrosis in a rat model of chronic volume overload.

Scalp-recorded high-frequency oscillations in childhood epileptic encephalopathy with continuous spike-and-wave during sleep with different etiologies.

T-type calcium channel gene alpha (1G) is not associated with childhood absence epilepsy in the Chinese Han population.

The gene encoding GABBR1 is not associated with childhood absence epilepsy in the Chinese Han population.

[Characteristic of children's EEG complexity at different ages and in different states].

[T-type calcium channel gene-CACNA1H is a susceptibility gene to childhood absence epilepsy].

CACNA1I is not associated with childhood absence epilepsy in the Chinese Han population.

A study on epileptic negative myoclonus in atypical benign partial epilepsy of childhood.

Nitric oxide-mediated neuronal apoptosis in rats with recurrent febrile seizures through endoplasmic reticulum stress pathway.

Partial seizures and atypical absence seizures as a single ictal event in a patient with Lennox-Gastaut syndrome.

Relationship among eye condition sensitivities, photosensitivity and epileptic syndromes.

[Effect of eyes closure, eyes closed and photic stimulation on the epileptiform discharges in children with epilepsies].

[Clinical and electrophysiologic studies on epileptic negative myoclonus in atypical benign partial epilepsy of childhood].

[Methylation-specific multiplex ligation-dependent probe amplification in diagnosis of Prader-Willi syndrome and Angelman syndrome].

Neck myoclonia with absence seizures: report of 3 cases.

Clinical and electrophysiological characteristics of startle epilepsy in childhood.

[Clinical and electroencephalographic characteristics of epilepsy with myoclonic absences].

Childhood absence epilepsy: Elctroclinical features and diagnostic criteria.

Analysis of SCN1A mutation and parental origin in patients with Dravet syndrome.

A role for Gcn5 in cardiomyocyte differentiation of rat mesenchymal stem cells.

Epilepsy in children with methylmalonic acidemia: electroclinical features and prognosis.

[Electroclinical features of myoclonic-atonic epilepsy].

NIPA2 located in 15q11.2 is mutated in patients with childhood absence epilepsy.

Epilepsy and narcolepsy-cataplexy in a child.

[Clinical and electroencephalographic characteristics of Jeavons syndrome].

[Genetic and phenotypic characteristics of SCN1A mutations in Dravet syndrome].

[Clinical and genetic characteristics of glucose transporter type 1 deficiency syndrome].

Early clinical features and diagnosis of Dravet syndrome in 138 Chinese patients with SCN1A mutations.

[Diagnosis and treatment of epilepsy and narcolepsy comorbid].

Phenotypes and PRRT2 mutations in Chinese families with benign familial infantile epilepsy and infantile convulsions with paroxysmal choreoathetosis.

ATP1A3 mutations and genotype-phenotype correlation of alternating hemiplegia of childhood in Chinese patients.

[Study on concordance of ictal and interictal epileptiform activity in patients with tuberous sclerosis complex].

[Clinical features and PRRT2 mutations in infantile convulsions with paroxysmal choreoathetosis].

[Phenotypes and PRRT2 mutation analysis in families with benign familial infantile epilepsy].

SCN8A mutations in Chinese children with early onset epilepsy and intellectual disability.

Gene Mutation Analysis in 253 Chinese Children with Unexplained Epilepsy and Intellectual/Developmental Disabilities.

A cohort study of pyridoxine-dependent epilepsy and high prevalence of splice site IVS11+1G>A mutation in Chinese patients.

[ATP1A3 gene mutations in patients with alternating hemiplegia of childhood].

[Clinical characteristics and prognosis analysis of vitamin B6 responsive infantile spasms].

[Electroencephalographic features of anti-N-methyl-D-aspartate receptor encephalitis in children].

Atonic elements combined or uncombined with epileptic spasms in infantile spasms.

Altered Channel Conductance States and Gating of GABA Receptors by a Pore Mutation Linked to Dravet Syndrome.

Electro-clinical-etiological associations of epilepsia partialis continua in 57 Chinese children.

[Surgery for pediatric intractable epilepsy due to posterior quadrantic cortical dysplasia].

Myoclonic epilepsy in infancy with preceding or concurrent afebrile generalized tonic-clonic seizures in Chinese children.

Early childhood myoclonic epilepsy: An independent genetic generalized epilepsy with myoclonic seizures as the main seizure type.

GRIN2A mutations in epilepsy-aphasia spectrum disorders.

GABA Receptor Coupling Junction and Pore GABRB3 Mutations are Linked to Early-Onset Epileptic Encephalopathy.

[Analysis of SCN1A deletions or duplications in patients with Dravet syndrome].

Genetic analysis of benign familial epilepsies in the first year of life in a Chinese cohort.

Upregulation of HMGB1-TLR4 inflammatory pathway in focal cortical dysplasia type II.

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

Genetic (idiopathic) epilepsy with photosensitive seizures includes features of both focal and generalized seizures.

Generalized seizures presurgically in a cohort of children with hemispherectomy: Predictors and a potential link to surgical outcome?

[Study of GRIN2A mutation in epilepsy-aphasia spectrum disorders].

Sirolimus for treatment of verrucous venous malformation: A retrospective cohort study.

Distinctive epileptogenic networks for parietal operculum seizures.

Large De Novo Microdeletion in Epilepsy with Intellectual and Developmental Disabilities, with a Systems Biology Analysis.

Remodeling of myocardial energy and metabolic homeostasis in a sheep model of persistent atrial fibrillation.

Clinical features and surgical outcomes in young children with focal cortical dysplasia type II.

Seizure Outcome and Its Prognostic Predictors After Hemispherotomy in Children With Refractory Epilepsy in a Chinese Pediatric Epileptic Center.

Somatic variants in new candidate genes identified in focal cortical dysplasia type II.

Semiologic subgroups of insulo-opercular seizures based on connectional architecture atlas.

Surgical treatment in children with intractable epilepsy after viral encephalitis.

Surgical treatment of children with drug-resistant epilepsy involving the Rolandic area.

Postoperative seizure and developmental outcomes of children with hemimegalencephaly and drug-resistant epilepsy.

Epilepsy centers in China: Current status and ways forward.

The National Comprehensive Governance for epilepsy prevention and control in China.

Subtotal hemispherotomy for intractable lesional hemispheric epilepsy without hemiparesis in children.

Seizures and EEG characteristics in a cohort of pediatric patients with dystroglycanopathies.

A prediction model integrating synchronization biomarkers and clinical features to identify responders to vagus nerve stimulation among pediatric patients with drug-resistant epilepsy.

Sensorimotor outcomes after resection for perirolandic drug-resistant epilepsy: a systematic review and individual patient data meta-analysis.

Lesional Intractable Epileptic Spasms in Children: Electroclinical Localization and Postoperative Outcomes.

Safety and efficacy of rapid withdrawal of antiseizure medications during long-term video-electroencephalogram monitoring in children with drug-resistant epilepsy: A retrospective study.

Pediatric epilepsy surgery in patients with Lennox-Gastaut syndrome after viral encephalitis.

Late sodium current in synergism with Ca/calmodulin-dependent protein kinase II contributes to β-adrenergic activation-induced atrial fibrillation.

Clinical characteristics and surgical outcomes in children with mild malformation of cortical development and oligodendroglial hyperplasia in epilepsy.

The association of BRAF V600E gene mutation with proliferative activity and histopathological characteristics of congenital melanocytic nevi in children.

Disconnection Surgery in Pediatric Epilepsy: A Single Center's Experience With 185 Cases.

Long-term seizure and developmental outcomes of epilepsy surgery in children under 3 years old: A single-center study of 113 patients.

Melatonin decreases GSDME mediated mesothelial cell pyroptosis and prevents peritoneal fibrosis and ultrafiltration failure.

Surgical treatment for drug-resistant epilepsy due to early brain injury in children.

Osimertinib versus comparator first-generation epidermal growth factor receptor tyrosine kinase inhibitors as first-line treatment in patients with advanced -mutated non-small cell lung cancer: a Chinese, multicenter, real-world cohort study.

Clinical features of unilateral multilobar and hemispheric polymicrogyria (PMG)-related epilepsy and seizure outcome with different treatment options.

Establishment of a normal control model of children's brain 18-fluorodeoxyglucose positron emission tomography and analysis of the changing pattern in patients aged 0-14 years.

Regional variation in diagnostic intensity of dementia among older U.S. adults: An observational study.

An Epidemiological Study of Physical-Mental Multimorbidity in Youth: Une étude épidémiologique de la morbidité physique-mentale chez les jeunes.

Profiling the Roles and Responsibilities of Professionals and Non-Professionals Providing Speech Language Services for Individuals with CLP in Resource-Limited Regions.

A Love Letter to Sexually Transmitted Diseases.

Cellular Schwannoma Mimicking a Nodular Melanoma on the Sole of the Foot, an Avoidable Diagnostic Pitfall.

Changes in Time Perception and Coping Strategies in Young Adults With Cancer: A Qualitative Study.

Exam reform: an opportunity for the redistribution of academic power.

Complex Fractures of the Radial and Ulnar Shaft.

Long-term comparison of rotational and directional atherectomy outcomes in patients with femoropopliteal lesions.

Diagnostic Value of Serum Procalcitonin, CSF Neutrophil-to-lymphocyte ratio, and CSF Lactate in Pediatric Bacterial Meningoencephalitis.

Accumulation of branched-chain amino acids deteriorates the neuroinflammatory response of Müller cells in diabetic retinopathy via leucine/Sestrin2-mediated sensing of mTOR signaling.

Structural Evolution of Photoexcited Methylcobalamin toward a CarH-like Metastable State: Evidence from Time-Resolved X-ray Absorption and X-ray Emission.

Assessment of ventilatory functions and associated inflammatory markers among workers in slaughterhouses.

Soluble tumor necrosis factor alpha receptors in generalized vitiligo.

The Promise and Perils of Transcatheter Aortic Valve Replacement (TAVR) in Low Surgical Risk Patients with Severe Aortic Stenosis in the Current Era.

A single-cell analysis of the NK-cell landscape reveals that dietary restriction boosts NK cell antitumor immunity via Eomesdermin.

Depolymerization of Waste Polycarbonates to Value Added Products.

Association between human leukocyte antigen class II-DR-DQ and narcolepsy: a case control study.

Management of Sideline Medical Emergencies.

The Brussels Breast Surgery Fellowship | A Three-Month Experience in Advancing Skills in Breast Surgery.