- A Rare Case of Anti-Ma2 Antibody-Mediated Autoimmune Encephalomyelitis in Childhood
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Kim H, Yum MS, Kim MJ, Ko TS
- KMID: 2548655
- Ann Child Neurol.
- 2022 Jul;30(3):148-151.
- doi: 10.26815/acn.2022.00150
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- Profound Biotinidase Deficiency: A Rare but Treatable Inborn Error of Metabolism in a Neonate with Recurrent Seizures
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Kim YN, Yum MS, Kim MJ, Ko TS
- KMID: 2549722
- Ann Child Neurol.
- 2024 Jan;32(1):57-61.
- doi: 10.26815/acn.2023.00192
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- Stroke-Like Episodes Associated with Coronavirus Disease 2019 in a Child with MELAS Syndrome
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Kim WJ, Yum MS, Kim MJ, Jang HN, Ko TS
- KMID: 2526109
- Ann Child Neurol.
- 2021 Oct;29(4):183-185.
- doi: 10.26815/acn.2021.00395
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- Epileptic Spasms, a Journey to Find Therapeutics Based on Pathophysiology
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Yum MS
- KMID: 2392545
- J Korean Child Neurol Soc.
- 2017 Sep;25(3):113-120.
- doi: 10.26815/jkcns.2017.25.3.113
After the first description of infantile spasms (IS) in 1841, extensive clinical and laboratory investigations have been done to find the pathophysiology and the optimal treatments. The concept of the... -
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- Erratum to: Epilepsy and Other Neuropsychiatric Manifestations in Children and Adolescents with 22q11.2 Deletion Syndrome
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Kim EH, Yum MS, Lee BH, Kim HW, Lee HJ, Kim GH, Lee YJ, Yoo HW, Ko TS
- KMID: 2354152
- J Clin Neurol.
- 2016 Apr;12(2):251-251.
- doi: 10.3988/jcn.2016.12.2.251
The publisher wishes to apologize for incorrectly displaying acknowledgement. -
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- A Case of Tuberous Sclerosis with Hemimegalencephaly
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Lee YJ, Lee EH, Jung MH, Yum MS, Ko TS
- KMID: 2329434
- J Korean Child Neurol Soc.
- 2009 Nov;17(2):231-236.
Hemimegalencephaly and tuberous sclerosis complex are distinct and rare conditions which are characterized by malformations of cortical developments. Hemimegalencephaly is a cerebral malformation of unknown pathophysiology characterized by asymmetry of... -
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- An Adolescent Case of Recurrent Episodes of Ophthalmoplegic Migraine
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Hwang S, Yum MS, Kim EH, Ko TS
- KMID: 1961834
- J Korean Child Neurol Soc.
- 2013 Sep;21(3):184-189.
Ophthalmoplegic migraine (OM) is a poorly understood neurological syndrome characterized by recurrent headaches with paresis of the ocular cranial nerves. The third cranial nerve is most commonly affected; the fourth... -
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- Topiramate can reduce the number of episodic attacks in cyclic vomiting syndrome:a case report
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Yum MS, Bae KW, You SJ, Ko TS
- KMID: 2140835
- Korean J Pediatr.
- 2007 Apr;50(4):386-389.
- doi: 10.3345/kjp.2007.50.4.386
Cyclic vomiting syndrome (CVS) is a paroxysmal, recurrent vomiting disorder of unknown pathophysiology and target organ. It has been hypothesized that CVS shares the same mechanism as migraine. We describe... -
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- Megalencephaly-capillary malformation-polymicrogyria syndrome: the first case report in Korea
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Choi YC, Yum MS, Kim MJ, Lee YJ, Ko TS
- KMID: 2362279
- Korean J Pediatr.
- 2016 Nov;59(Suppl 1):S152-S156.
- doi: 10.3345/kjp.2016.59.11.S152
Megalencephaly-capillary malformation-polymicrogyria syndrome (MCAP), previously known as macrocephaly-cutis marmorata telangiectatica congenita and macrocephaly-capillary malformation syndrome, is a rare multiple-malformation syndrome that is characterized by progressive megalencephaly, capillary malformations of the... -
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- The First Korean Case of KCNQ2 Mutation in a Family with Benign Familial Neonatal Convulsions
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Yum MS, Ko TS, Yoo HW
- KMID: 1779270
- J Korean Med Sci.
- 2010 Feb;25(2):324-326.
- doi: 10.3346/jkms.2010.25.2.324
Neonatal seizures represent a heterogeneous group of disorders with vastly different etiologies and outcomes. Benign familial neonatal convulsions (BFNC) are a distinctive epileptic syndrome of autosomal dominant inheritance with a... -
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- Status Epilepticus Induced by Respiratory Syncytial Virus Infection in Preterm Infants
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Jeong MH, Lee EH, Yum MS, Ko TS
- KMID: 2008758
- J Korean Epilepsy Soc.
- 2009 Dec;13(2):75-78.
Respiratory syncytial virus (RSV) is an extremely common cause of childhood respiratory infection resulting in significant morbidity and mortality especially in young infants and premature babies. There have been a... -
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- Three Cases of Hypercalcemia Due to Vitamin D Intoxication in Infancy
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Choi JH, Yum MS, Hahn H, Park YS
- KMID: 2278710
- Korean J Pediatr.
- 2004 Mar;47(3):332-337.
Hypercalcemia in infancy is an uncommon disorder but has a potential of serious sequelae. Therefore, infants with hypercalcemia must be promptly investigated and need urgent management. We report three cases... -
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- A Case of Spinal Cord Cavernoma Mimicking Transverse Myelitis
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Kim YA, Jeong MH, Lee EH, Yum MS, Ra YS, Ko TS
- KMID: 2329460
- J Korean Child Neurol Soc.
- 2010 May;18(1):153-157.
A 14-year-old girl presented with recurrent, progressive lower leg weakness and decrease in sensation. When the symptoms first appeared, she was misdiagnosed as transverse myelitis and was treated with methylprednisolone.... -
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- A Case of Omenn Syndrome in a Patient Treated for Chronic Diarrhea and Severe Exfoliative Erythrodermia
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Yum MS, Lee SY, Kim HB, Yoo HW, Ghim T, Hong SJ
- KMID: 2314377
- Pediatr Allergy Respir Dis.
- 2005 Jun;15(2):174-179.
Omenn syndrome (OS) is a peculiar, autosomal recessive severe combined immunodeficiency (SCID) associated with early-onset, generalized, exudative erythrodermia, lymphadenopathy, hepatosplenomegaly, hypereosinophilia, elevated serum IgE, and normal to highly activated, yet... -
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- Korean Infant and Child Developmental Test(KICDT) in Children with Epilepsy
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Choi HW, Jeong MH, Lee EH, Jeong SJ, Yum MS, Ko TS
- KMID: 2329444
- J Korean Child Neurol Soc.
- 2010 May;18(1):40-48.
PURPOSE: We assessed the usefulness of the Korean Infant and Child Developmental Screening Test(KICDT) by applying the test to children with epilepsy, identifying developmental delay and analyzing the results of... -
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- Sensory Guillain-Barre syndrome presenting as 'Burning Feet Syndrome': A case report
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Kim SB, Yum MS, Choi HW, Kim EH, Ko TS
- KMID: 2329272
- J Korean Child Neurol Soc.
- 2014 Mar;22(1):20-24.
The existence of purely sensory Guillain-Barre syndrome (GBS) is controversial, although diagnostic criteria have been established and several cases have been reported. Motor nerve conduction studies (NCS) have found that... -
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- A Case of Posterior Reversible Encephalopathy Syndrome during Cyclosporine Therapy in a Child with Steroid Resistant Nephrotic Syndrome
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Jeong MH, Lee JH, Yum MS, Ko TS, Park YS
- KMID: 1898241
- J Korean Soc Pediatr Nephrol.
- 2007 Apr;11(1):92-99.
The posterior reversible encephalopathy syndrome(PRES) is characterized clinically by a combination of acute or subacute confusion, lethargy, visual disturbance, and seizures. PRES has been described in various clinical settings, including... -
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- Treatment of Children and Adolescents with Epilepsy with Atomoxetine
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Park KJ, Ahn H, Yum MS, Ko TS, Kim HW
- KMID: 2501459
- Psychiatry Investig.
- 2020 May;17(5):412-416.
- doi: 10.30773/pi.2019.0287
Objective The objective of this study was to assess the effectiveness and safety of atomoxetine in Korean children and adolescents with epilepsy. Methods We retrospectively reviewed the electronic medical records of... -
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- Identification of two novel Duchenne muscular dystrophies mutations in patients with Becker muscular dystrophy
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Kim D, Kim YM, Seo GH, Kim GH, Yoo HW, Yum MS, Ko TS, Lee BH
- KMID: 2401810
- J Genet Med.
- 2017 Dec;14(2):75-79.
- doi: 10.5734/JGM.2017.14.2.75
Duchenne and Becker muscular dystrophies (DMD and BMD, respectively) are X-linked neuromuscular disorders characterized by progressive muscle weakness and severe skeletal muscle degeneration. BMD is a milder form with a... -
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- Two Cases of Hirayama Disease in a Pediatric Clinic
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Ahn H, Yum MS, Kim HJ, Yeh HR, Ko TS
- KMID: 2435275
- J Korean Child Neurol Soc.
- 2018 Mar;26(1):52-56.
- doi: 10.26815/jkcns.2018.26.1.52
We report two pediatric cases with Hirayama disease—a 16-year-old boy with a left wrist drop and a 14-year-old-boy with weakness and muscle atrophy of right hand. Motor nerve conduction study... -
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