Danielle M. Veenma

Rotterdam, ZH, Netherlands

Last Updated: 09/26/2026

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Found 21 publications

Memantine treatment in individuals with GRIN gain-of-function variants is associated with improvements in behavior, development, and seizure frequency.

Memantine treatment in individuals with GRIN gain-of-function variants is associated with improvements in behavior, development, and seizure frequency.

Journal: Epilepsia

Published: September 11, 2025

Role of CAMK2D in neurodevelopment and associated conditions.

Role of CAMK2D in neurodevelopment and associated conditions.

Journal: American journal of human genetics

Published: August 12, 2025

Heterozygous alterations of GTF2I at the Williams-Beuren syndrome's locus cause a neurodevelopmental disorder.

Heterozygous alterations of GTF2I at the Williams-Beuren syndrome's locus cause a neurodevelopmental disorder.

Journal: Journal of medical genetics

Published: November 05, 2024

CAMK2; four genes, one syndrome? Delineation of genotype-phenotype correlations.

CAMK2; four genes, one syndrome? Delineation of genotype-phenotype correlations.

Journal: Current opinion in neurobiology

Published: June 28, 2024

Developmental epileptic encephalopathy in DLG4-related synaptopathy.

Developmental epileptic encephalopathy in DLG4-related synaptopathy.

Journal: Epilepsia

Published: October 13, 2023

Gain-of-function and loss-of-function variants in GRIA3 lead to distinct neurodevelopmental phenotypes.

Gain-of-function and loss-of-function variants in GRIA3 lead to distinct neurodevelopmental phenotypes.

Journal: Brain : a journal of neurology

Published: July 17, 2023

Incomplete spinal cord injury following minor trauma in two siblings with spondylocostal dysostis type 6.

Incomplete spinal cord injury following minor trauma in two siblings with spondylocostal dysostis type 6.

Journal: Spine deformity

Published: May 12, 2023

Role of CAMK2D in neurodevelopment and associated conditions.

Role of CAMK2D in neurodevelopment and associated conditions.

Journal: American journal of human genetics

Published: April 10, 2023

5q35 duplication syndrome: Narrowing the critical region on the distal side and further evidence of intrafamilial variability and expression.

5q35 duplication syndrome: Narrowing the critical region on the distal side and further evidence of intrafamilial variability and expression.

Journal: American journal of medical genetics. Part A

Published: June 03, 2022

Unraveling the Genetics of Congenital Diaphragmatic Hernia: An Ongoing Challenge.

Unraveling the Genetics of Congenital Diaphragmatic Hernia: An Ongoing Challenge.

Journal: Frontiers in pediatrics

Published: October 24, 2021

Case Report: Developmental Delay and Acute Neuropsychiatric Episodes Associated With a de novo Mutation in the CAMK2B Gene (c.328G>A p.Glu110Lys).

Case Report: Developmental Delay and Acute Neuropsychiatric Episodes Associated With a de novo Mutation in the CAMK2B Gene (c.328G>A p.Glu110Lys).

Journal: Frontiers in pharmacology

Published: October 12, 2021

Case Report and Review of the Literature: Congenital Diaphragmatic Hernia and Craniosynostosis, a Coincidence or Common Cause?

Case Report and Review of the Literature: Congenital Diaphragmatic Hernia and Craniosynostosis, a Coincidence or Common Cause?

Journal: Frontiers in pediatrics

Published: September 08, 2021

Showing 1-12 of 21

Last Updated: 09/26/2026