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Laura Licchetta

irccs institute of neurological sciences of bologna
H指数:34
被引数:5,447

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Early sodium channel blocker initiation is associated with better outcomes in KCNQ2 disorders

KCNQ2障碍中早期钠通道阻滞剂治疗与更优预后相关

Brain
IF11.7
2026-08-180
OAAI
Clinical and genetic landscape of epilepsies with absence seizures and single-gene etiology

伴有失神发作和单基因病因的癫痫的临床和遗传景观

2025-10-250
OAAI
Quantitative dried blood spot microsampling for therapeutic drug monitoring of -antiseizure medications by design of experiment and UHPLC-MS/MS

基于实验设计和UHPLC-MS/MS的定量干血斑微采样技术在抗癫痫药物治疗药物监测中的应用

TALANTA
IF6.1
2025-05-080
OAAI
CDK13-Related Disorder: Novel Insights From A Series of 27 Cases and Recommendations for Clinical Management

CDK13相关疾病:来自27例病例系列的新见解及临床管理建议

2025-02-190
OAAI
National survey on the prevalence of single-gene aetiologies for genetic developmental and epileptic encephalopathies in Italy

意大利关于遗传发育和癫痫性脑病的单基因病因患病率的全国调查

2024-11-281
PRE
Clinical features and genotype-phenotype correlations in epilepsy patients with de novo DYNC1H1 variants
2024-07-021
PRE
Fingerprick volumetric absorptive microsampling for therapeutic drug monitoring of antiseizure medications: Reliability and real-life feasibility in epilepsy patients
2024-05-011
PRE
GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture

超过29,000名癫痫患者的ghis荟萃分析确定了26个风险基因座和亚型特异性遗传结构

2023-08-3143
OAAI
Extended Glasgow Outcome Scale to Evaluate the Functional Impairment of Patients With Subcortical Band Heterotopia: A Multicentric Cross-sectional Study
2023-04-010
OAAI
Neurodevelopmental and Epilepsy Phenotypes in Individuals With Missense Variants in the Voltage-Sensing and Pore Domains of KCNH5
2023-02-0710
OA
Expanding the genetics and phenotypic spectrum of Lysine-specific demethylase 5C (KDM5C): a report of 13 novel variants
2022-11-2512
OA