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Issue Date	Title	Journal Title
2014	A newly discovered LGI1 mutation in Korean family with autosomal dominant lateral temporal lobe epilepsy	SEIZURE-EUROPEAN JOURNAL OF EPILEPSY
2010	A nonsynonymous variation in MRP2/ABCC2 is associated with neurological adverse drug reactions of carbamazepine in patients with epilepsy.	PHARMACOGENETICS AND GENOMICS
2016	First Identification of Compound Heterozygous FKRP Mutations in a Korean Patient with Limb-Girdle Muscular Dystrophy	JOURNAL OF CLINICAL NEUROLOGY
2013	Genetic Variations of ABCC2 Gene Associated with Adverse Drug Reactions to Valproic Acid in Korean Epileptic Patients	Genomics & Informatics
2015	GWAS identifies two susceptibility loci for lamotrigine-induced skin rash in patients with epilepsy	EPILEPSY RESEARCH
2015	Low D4Z4 copy number and gender difference in Korean patients with facioscapulohumeral muscular dystrophy type 1	NEUROMUSCULAR DISORDERS
2015	Targeted next-generation sequencing for the genetic diagnosis of dysferlinopathy	NEUROMUSCULAR DISORDERS
2014	Whole-Genome Analysis in Korean Patients with Autoimmune Myasthenia Gravis	YONSEI MEDICAL JOURNAL