9 results on '"Suzuki-Muromoto, Sato"'
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2. Familial hemiplegic migraine with a PRRT2 mutation: Phenotypic variations and carbamazepine efficacy
3. Leucine-485 deletion variant of BRAF may exhibit the severe end of the clinical spectrum of CFC syndrome
4. A severe female case of arthrogryposis multiplex congenita with brain atrophy, spastic quadriplegia and intellectual disability caused by ZC4H2 mutation
5. Genomic analysis identifies masqueraders of full-term cerebral palsy
6. A case of new PCDH12 gene variants presented as dyskinetic cerebral palsy with epilepsy
7. Intra-individual cognitive imbalance in ASD between perceptual reasoning and ambiguity-solving related to tool use: Comparison among children exhibiting ASD, AD/HD, and typical development
8. A patient with Muenke syndrome manifesting migrating neonatal seizures
9. A case of 3p deletion syndrome associated with cerebellar hemangioblastoma
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