Serpil Alkan
Liege, WAL 4000, Belgium
Last Updated: 09/26/2026
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Found 10 publications
Association between CACNA1A and ATP1A2 Variants are Responsible for Severe Neurodevelopmental Disorder.
Journal: Neuropediatrics
Published: December 12, 2024
Autistic behavior is a common outcome of biallelic disruption of PDZD8 in humans and mice.
Journal: Molecular autism
Published: December 02, 2024
Widening the infantile hypotonia with psychomotor retardation and characteristic Facies-1 Syndrome's clinical and molecular spectrum through NALCN in-silico structural analysis.
Journal: Frontiers in genetics
Published: August 08, 2024
Rapid Whole Genome Sequencing Diagnoses and Guides Treatment in Critically Ill Children in Belgium in Less than 40 Hours.
Journal: International journal of molecular sciences
Published: December 30, 2022
Atypical Hemifacial Spasm and Myoclonus Related to AIFM1 Variant.
Journal: Neuropediatrics
Published: March 09, 2022
How I explore… a disorder of intellectual development in a child
Journal: Revue medicale de Liege
Published: October 08, 2020
Image of the month. Delayed and isolated basal ganglia damage after methadone intoxication
Journal: Revue medicale de Liege
Published: October 19, 2018
Showing 1-10 of 10
Last Updated: 09/26/2026