Hyung-Jun Park, Ph.D.

2010 Syracuse University, Syracuse, NY, United States 
Chemical Engineering, Environmental Engineering, Nuclear Engineering
"Hyung-Jun Park"
Cross-listing: Envirotree


Sign in to add mentor
Lawrence L. Tavlarides grad student 2010 Syracuse
 (Sol-gel synthesis and characterization for metal ion separations from aqueous streams.)
BETA: Related publications


You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect.

Park HJ, Choi YC, Oh JW, et al. (2020) Prevalence, Mortality, and Cause of Death in Charcot-Marie-Tooth Disease in Korea: A Nationwide, Population-Based Study. Neuroepidemiology. 1-7
Choi YC, Hong JM, Park KD, et al. (2019) Proteomic analysis of the skeletal muscles from dysferlinopathy patients. Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia
Hong JM, Choi YC, Shin S, et al. (2019) Prevalence and Socioeconomic Status of Patients with Genetic Myopathy in Korea: A Nationwide, Population-Based Study. Neuroepidemiology. 1-6
Park HJ, Hong JM, Lee JH, et al. (2018) Comparative transcriptome analysis of skeletal muscle in ADSSL1 myopathy. Neuromuscular Disorders : Nmd
Kim K, Park HJ, Lee JH, et al. (2018) Two Korean Families with Limb-Girdle Muscular Dystrophy Type 1D Associated with DNAJB6 Mutations. Yonsei Medical Journal. 59: 698-701
Park HJ, Shin HY, Kim SH, et al. (2018) Partial Conduction Block as an Early Nerve Conduction Finding in Neurolymphomatosis. Journal of Clinical Neurology (Seoul, Korea). 14: 73-80
Jeong HN, Park HJ, Lee JH, et al. (2018) Clinical and Pathologic Findings of Korean Patients with RYR1-Related Congenital Myopathy. Journal of Clinical Neurology (Seoul, Korea). 14: 58-65
Park HJ, Lee MJ, Lee JE, et al. (2018) Pathogenic Variant of REEP1 in a Korean Family with Autosomal-Dominant Hereditary Spastic Paraplegia. Journal of Clinical Neurology (Seoul, Korea). 14: 248-250
Park HJ, Lee W, Kim SH, et al. (2018) FAT1 Gene Alteration in Facioscapulohumeral Muscular Dystrophy Type 1. Yonsei Medical Journal. 59: 337-340
Lee JH, Shin JH, Park HJ, et al. (2017) Targeted population screening of late onset Pompe disease in unspecified myopathy patients for Korean population. Neuromuscular Disorders : Nmd
See more...