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Showing results 1 to 11 of 11

Issue Date	Title	Author(s)	Type
2015	A Pediatric Case of Neuromyelitis Optica Spectrum Disorder: Atypical Clinical Presentation like Multiphasic Demyelinating Encephalomyelitis	박기덕; 박형준	Meeting Abstract
2017	Clinical and Pathological Findings of a Korean Family with Pathogenic Variants of the TTN Gene	박기덕	Letter
2016	Clinical and Pathological Heterogeneity of Korean Patients with CAPN3 Mutations	박기덕; 박형준	Article
2019	CNT bundle-based thin intracochlear electrode array	전상범	Article
2019	Comparative transcriptome analysis of skeletal muscle in ADSSL1 myopathy	박기덕; 이정환	Article
2018	FAT1 Gene Alteration in Facioscapulohumeral Muscular Dystrophy Type 1	박기덕	Article
2015	Low D4Z4 copy number and gender difference in Korean patients with facioscapulohumetal muscular dystrophy type 1	박형준	Article
2019	Prevalence and Socioeconomic Status of Patients with Genetic Myopathy in Korea: A Nationwide, Population-Based Study	이정환	Article
2020	Proteomic analysis of the skeletal muscles from dysferlinopathy patients	박기덕	Article
2015	Targeted next-generation sequencing for the genetic diagnosis of dysferlinopathy	박형준	Article
2014	The Significance of Clinical and Laboratory Features in the Diagnosis of Glycogen Storage Disease Type V: A Case Report	박형준	Article

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