- Metopic Craniosynostosis and Hydrocephalus in a Premature Opioid Dependent Baby
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Paul T, Makkar SS, Mohan S, Mohan P
- KMID: 2506916
- Ann Child Neurol.
- 2020 Oct;28(4):167-168.
- doi: 10.26815/acn.2020.00115
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- Cranial Bruits Associated with Internal Carotid Artery Stenosis Due to Focal Arterial Dissection in an Infant
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Cho KU, Kim SJ
- KMID: 2506915
- Ann Child Neurol.
- 2020 Oct;28(4):164-166.
- doi: 10.26815/acn.2020.00157
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- A Case of Extensive Cerebral Sinovenous Thrombosis Resulting from Neonatal Diabetes Mellitus
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Yoo C, Rhie S, Yoo EG, Choi HJ, Chae KY, Jung MK
- KMID: 2506913
- Ann Child Neurol.
- 2020 Oct;28(4):156-159.
- doi: 10.26815/acn.2020.00122
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- Riboflavin Transporter 1 Deficiency Caused by a Homozygous Single Exonal Deletion of SLC52A1
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Kang U, Yang DH, Nam SO, Lee Yj, Yeon GM
- KMID: 2506914
- Ann Child Neurol.
- 2020 Oct;28(4):160-163.
- doi: 10.26815/acn.2020.00136
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- Serum Uric Acid as a Predictive Factor for Rotaviral or Noroviral Benign Convulsions with Mild Gastroenteritis
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Yoo SY, Kim DH, Lee Y, Lee GH, Ha DJ, Kwon YS
- KMID: 2506911
- Ann Child Neurol.
- 2020 Oct;28(4):138-144.
- doi: 10.26815/acn.2020.00143
Purpose: This study investigated the relationship between serum uric acid levels and benign convulsions with mild gastroenteritis (CwGs) caused by rotavirus and norovirus. Methods: This retrospective study identified 89 patients with... -
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- Effectiveness of Intravenous Immunoglobulin Therapy for Pediatric Viral Encephalitis
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Byun JE, Lee KY
- KMID: 2506912
- Ann Child Neurol.
- 2020 Oct;28(4):145-155.
- doi: 10.26815/acn.2020.00164
Purpose: Intravenous immunoglobulin (IVIg) is considered as a first-line therapy for autoimmune encephalitis. However, its effectiveness in viral encephalitis has yet to be evaluated. Therefore, we investigated the effectiveness of... -
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- Deep Phenotyping in 1p36 Deletion Syndrome
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Shim Y, Go YJ, Kim SY, Kim H, Hwang H, Choi J, Lim BC, Kim KJ, Chae JH
- KMID: 2506910
- Ann Child Neurol.
- 2020 Oct;28(4):131-137.
- doi: 10.26815/acn.2020.00108
Purpose: Although 1p36 deletion syndrome is the most common terminal deletion syndrome, unexplained phenotypic variability still occurs. We aimed to delineate the phenotype of this syndrome in detail and to... -
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