- A Case of Joubert Syndrome
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Choi HW, Chun KU, Kim HM, Ho B
- KMID: 1582229
- J Korean Child Neurol Soc.
- 2004 May;12(1):105-110.
Joubert syndrome is a rare autosomal recessive condition characterized by dysgenesis of the cerebellar vermis, hypotonia, developmental delay, ataxia, abnormal eye movements, and a respiratory pattern of alternating tachypnea and... -
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- Atypical Teratoid Rhabdoid Tumour : From Tumours to Therapies
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Richardson EA, Ho B, Huang A
- KMID: 2417355
- J Korean Neurosurg Soc.
- 2018 May;61(3):302-311.
- doi: 10.3340/jkns.2018.0061
Atypical teratoid rhabdoid tumours (ATRTs) are the most common malignant central nervous system tumours in children ≤1 year of age and represent approximately 1–2% of all pediatric brain tumours. ATRT... -
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