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Atrial fibrillation and coexisting cerebral amyloid angiopathy: safety and efficacy of transcatheter left atrial appendage occlusion
Atrial fibrillation and coexisting cerebral amyloid angiopathy: safety and efficacy of transcatheter left atrial appendage occlusion
To investigate the safety and efficacy of transcatheter left atrial appendage occlusion (LAAO) in patients with concomitan...
Is levodopa induced freezing of gait a paradox or an expected phenomenon?: a clinico-pathophysiological hypothesis
Is levodopa induced freezing of gait a paradox or an expected phenomenon?: a clinico-pathophysiological hypothesis
Freezing of Gait (FOG) is the most disabling and puzzling symptom of Parkinson’s Disease (PD). FOG is strongly assoc...
Real-world challenges in primary central nervous system lymphoma: a case series
Real-world challenges in primary central nervous system lymphoma: a case series
Primary central nervous system lymphoma (PCNSL) belongs to the group of the large B-cell lymphomas of immune-privileged si...
Efficacy and safety of ketogenic diet in glioblastoma: an updated systematic review and meta-analysis
Efficacy and safety of ketogenic diet in glioblastoma: an updated systematic review and meta-analysis
Glioblastoma (GBM) remains the most common and lethal primary central nervous system tumor, with a median survival of only...
Enlarging the phenotypical spectrum of -related epilepsy
Enlarging the phenotypical spectrum of -related epilepsy
Epilepsy is a frequent feature of genetic neurodevelopmental disorders and is increasingly recognized as a disorder of dis...
Slowly progressive amyotrophic lateral sclerosis associated with a rare SOD1 Pro67Arg mutation: a case report
Slowly progressive amyotrophic lateral sclerosis associated with a rare SOD1 Pro67Arg mutation: a case report
Cite this articleHu, N., Liu, M. & Cui, L. Slowly progressive amyotrophic lateral sclerosis associated with a rare SOD...
A novel biallelic mutation in the  gene as a cause of Miyoshi myopathy
A novel biallelic mutation in the gene as a cause of Miyoshi myopathy
Miyoshi myopathy is an autosomal recessive distal myopathy resulting from pathogenic variants in the DYSF gene encoding dy...
The role of angiotensin receptor blockers in treating epilepsy: a review
The role of angiotensin receptor blockers in treating epilepsy: a review
Epilepsy is a chronic brain disease with a global prevalence of 70 million people. According to the World Health Organizat...
Adult-onset leukoencephalopathy with persistent diffusion restriction dot lesions
Adult-onset leukoencephalopathy with persistent diffusion restriction dot lesions
A 31-year-old nonconsanguineous man without any obvious clinical manifests exhibited leukoencephalopathy lesions on brain ...
Sex-specific grey matter abnormalities in individuals with chronic insomnia
Sex-specific grey matter abnormalities in individuals with chronic insomnia
Previous studies have reported sex differences in altered brain function in patients with chronic insomnia (CI). However, ...
Corpus callosum bilateral infarction in Sneddon disease
Corpus callosum bilateral infarction in Sneddon disease
Ethical approval and Informed consent Written informed consent for ...
Development and internal validation of a prognostic model for loss of balance and falls in mid- to late-stage Parkinson’s disease
Development and internal validation of a prognostic model for loss of balance and falls in mid- to late-stage Parkinson’s disease
Mid- to late-stage Parkinson’s disease (PD) is often linked with worsened and significant impairment of motor activi...
Unique association of anti-GABAA receptor encephalitis and myasthenia gravis in a patient with type A thymoma
Unique association of anti-GABAA receptor encephalitis and myasthenia gravis in a patient with type A thymoma
Association between anti-GABAAR encephalitis and myasthenia gravis is extremely rare with few reported cases. Herein, we r...
PIGW-related glycosylphosphatidylinositol deficiency: A case report and literature review
PIGW-related glycosylphosphatidylinositol deficiency: A case report and literature review
PIGW-related glycosylphosphatidylinositol deficiency is a rare disease that manifests heterogeneous clinical phenotypes. W...
Association between motor symptoms of Parkinson’s disease and swallowing disorders
Association between motor symptoms of Parkinson’s disease and swallowing disorders
Parkinson’s disease (PD) presents with motor symptoms that hinder physical activity. This study aimed to thoroughly ...
Drug refractory epilepsy in MOGAD: an evolving spectrum
Drug refractory epilepsy in MOGAD: an evolving spectrum
Liu K, Sun S, Cui J, Zhang L, Zhang K, Zhang L (2021) Seizures in myelin oligodendrocyte glycoprotein antibody-associated ...
Efficacy of transcranial direct current stimulation in patients with dysphagia after stroke: a systematic review
Efficacy of transcranial direct current stimulation in patients with dysphagia after stroke: a systematic review
Swallowing is a complex function that can be disrupted after stroke. Transcranial Direct Current Stimulation (tDCS) is a n...
Posterior reversible encephalopathy syndrome and acute ischemic stroke: an underreported association
Posterior reversible encephalopathy syndrome and acute ischemic stroke: an underreported association
Posterior reversible encephalopathy syndrome (PRES) is a rare and complex disorder with variable clinical presentation and...
Altered brain function and structure pre- and post- COVID-19 infection: a longitudinal study
Altered brain function and structure pre- and post- COVID-19 infection: a longitudinal study
Evidence indicates that the SARS-CoV-2 virus can infect the brain, resulting in central nervous system symptoms. However, ...
Stroke in a young adult: looking beyond the diffusion-weighted imaging sequence
Stroke in a young adult: looking beyond the diffusion-weighted imaging sequence
A 37-year-old migrainous woman was referred several hours after a sudden dysarthria lasting less than 1 min. Brai...