학술논문
Profound Biotinidase Deficiency: A Rare but Treatable Inborn Error of Metabolism in a Neonate with Recurrent Seizures
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- 영문명
- Profound Biotinidase Deficiency: A Rare but Treatable Inborn Error of Metabolism in a Neonate with Recurrent Seizures
- 발행기관
- 대한소아신경학회
- 저자명
- Ye-Na Kim Mi-Sun Yum Min-Jee Kim Tae-Sung Ko
- 간행물 정보
- 『Annals of Child Neurology(구 대한소아신경학회지)』vol.32 no.1, 57~61쪽, 전체 5쪽
- 주제분류
- 의약학 > 소아과학
- 파일형태
- 발행일자
- 2023.12.31
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의약학 > 소아과학분야 NEW
- Acute Necrotizing Encephalopathy in Children with COVID-19 Accompanied by Multisystem Inflammatory Syndrome
- A Case of Cerebellar Infarction While Swimming in a Child Diagnosed by Ataxia and Gait Disturbance
- Profound Biotinidase Deficiency: A Rare but Treatable Inborn Error of Metabolism in a Neonate with Recurrent Seizures
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