- Leigh Syndrome: Subgroup Aanalysis according to Mitochondrial DNA Mutation
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Jee NL, Her SM, Kim SH, Lee MJ, Lee CH, Lee YM
- KMID: 2435267
- J Korean Child Neurol Soc.
- 2018 Mar;26(1):7-12.
- doi: 10.26815/jkcns.2018.26.1.7
PURPOSE: Leigh syndrome (LS) is a rare, progressive neurodegenerative disorder with characteristic abnormalities in the central nervous system. Such patients present with heterogeneous clinical symptoms and genetic abnormalities; thus, prognosis... -
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- A Successfully Treated Case of Recurrent Focal Segmental Glomerulosclerosis (FSGS) with Plasmapheresis and High dose Methylprednisolone Pulse Therapy
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Her SM, Lee KH, Shin JI
- KMID: 2394458
- Child Kidney Dis.
- 2017 Oct;21(2):165-168.
- doi: 10.3339/jkspn.2017.21.2.165
Focal segmental glomerulosclerosis (FSGS) in children, which is a kind of nephrotic syndrome showing steroid resistance, usually progresses to a substantial number of end stage renal disease (ESRD). Although the... -
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- Therapeutic Plasma Exchange in Pediatric Kidney Disease: 23-year Experience at the Severance Children's Hospital in Korea
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Her SM, Lee KH, Kim JH, Lee JS, Kim PK, Shin JI
- KMID: 2394444
- Child Kidney Dis.
- 2017 Oct;21(2):81-88.
- doi: 10.3339/jkspn.2017.21.2.81
PURPOSE: The American Society for Apheresis provides clinical guidelines for therapeutic apheresis in adults, but there are no guidelines for children. This study aimed to analyze the effect of therapeutic... -
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