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10.11251/ojjscn.57.53
Mild encephalitis/encephalopathy with a reversible splenial lesion complicated by acute urinary retention in a 2-year-old boy
Jan 1, 2025
NO TO HATTATSU
Miki Akiyama + 2 more
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10.11251/ojjscn.57.56
Clinical and imaging findings useful for early diagnosis of molybdenum cofactor deficiency : a case report of siblings
Jan 1, 2025
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Eisuke Terasaki + 4 more
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10.11251/ojjscn.57.45
A case of hyperventilation-induced high-amplitude rhythmic slowing with altered awareness requiring differentiation from typical absence seizure
Jan 1, 2025
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Marie Noda + 4 more
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10.11251/ojjscn.57.62
Jan 1, 2025
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久保田 一生
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10.11251/ojjscn.57.19
Epigenetics and pediatric neurological disorders
Jan 1, 2025
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Shinji Saito
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10.11251/ojjscn.57.66
Jan 1, 2025
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椎原 隆
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10.11251/ojjscn.57.59
Microlissencephaly caused by a novel compound heterozygous variant in the <i>WDR81</i> gene : A case report
Jan 1, 2025
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Yohane Miyata + 8 more
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10.11251/ojjscn.57.64
Jan 1, 2025
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根岸 豊
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10.11251/ojjscn.57.24
The correlation between epileptic seizure types and symptom expressions of patients/caregivers in pediatric epilepsy
Jan 1, 2025
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Yuichi Tateishi + 5 more
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10.11251/ojjscn.57.34
Late-onset Aicardi-Goutières syndrome caused by an <i>ADAR</i> variant presented with spastic quadriplegia
Jan 1, 2025
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Yasuhiro Kawai + 16 more
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