Congenital Contractures of the Limbs and Face, Hypotonia, and Developmental Delay (CLIFAHDD) Associated with a De Novo Missense Variant in NALCN: The First Korean Case Report.
- Published in:
- 2025
- By:
- Publication type:
- Letter
Works matching IS 2635909X AND DT 2025 AND VI 33 AND IP 1
Results: 8
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2
A Surfer's Myelopathy in a 7-Year-Old Boy after His First Time Surfing.
- Published in:
- 2025
- By:
- Publication type:
- Letter
3
Identification of De Novo Radio-Tartaglia Syndrome and Comparison of Clinical and Molecular Characteristics with Those of 1p36 Deletion Syndrome.
- Published in:
- Annals of Child Neurology, 2025, v. 33, n. 1, p. 8, doi. 10.26815/acn.2024.00717
- By:
- Publication type:
- Article
4
Recurrent Painful Ophthalmoplegic Neuropathy in an 8-Year-Old Boy.
- Published in:
- 2025
- By:
- Publication type:
- Letter
5
Novel Mutation in the CACNA1B Gene Linked to Pediatric Focal Epilepsy.
- Published in:
- 2025
- By:
- Publication type:
- Letter
6
Prolonged-Release Melatonin for Sleep Disturbances in Autism Spectrum Disorder.
- Published in:
- Annals of Child Neurology, 2025, v. 33, n. 1, p. 1, doi. 10.26815/acn.2024.00682
- By:
- Publication type:
- Article
7
A Rare Pediatric Case of Top of the Basilar Syndrome.
- Published in:
- 2025
- By:
- Publication type:
- Letter
8
Unveiling the Uncommon: A Case of Postoperative Inflammatory Sciatic Neuropathy in a Child.
- Published in:
- 2025
- By:
- Publication type:
- Letter