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Article

Electroencephalographic findings in KBG syndrome: a child with novel mutation in ANKRD11 gene.

Acta neurologica Belgica - 1 Dec 2015

Samanta Debopam, Willis Erin

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PMID: 25543316
DOI: 10.1007/s13760-014-0413-9

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Electroencephalographic findings in KBG syndrome: a child with novel mutation in ANKRD11 gene.PMID 25543316Read ↗

Electroclinical features and outcome of ANKRD11-related KBG syndrome: A novel report and literature review.Semantic proximity Read ↗

Novel Variant ANKRD11 Gene Mutation Associated With Drug-Resistant Epilepsy in KBG Syndrome Phenotype.Semantic proximity Read ↗

KBG syndrome: case report of a novel variant ANKR11 gene mutation and literature review.Semantic proximity Read ↗

KBG syndrome involving a single-nucleotide duplication in ANKRD11.Semantic proximity Read ↗

Audiological findings in a de novo mutation of ANKRD11 gene in KBG syndrome: Report of a case and review of the literature.Semantic proximity Read ↗

Epilepsy in KBG syndrome.Semantic proximity Read ↗

Long-term changes in electroencephalogram findings in a girl with a nonsense SMC1A variant: A case reportSemantic proximity Read ↗

Clinical feature and genetic mutation of KBG syndrome diagnosed in neonatal period: A case report.Semantic proximity Read ↗

[Analysis of three patients with KBG syndrome and epileptic seizures due to variants of ANKRD11 gene].Semantic proximity Read ↗

[Audiological phenotypes of KBG syndrome: a case report and literatures review].Semantic proximity Read ↗

Heterogeneity of Epileptic Phenotypes in KBG Syndrome: A Series of Four Cases and Literature ReviewSemantic proximity Read ↗

Clinical and genetic aspects of KBG syndrome.Semantic proximity Read ↗

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