Cacha D. Scholte-Peeters

's-hertogenbosch, NB, Netherlands

Last Updated: 09/26/2026

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Found 47 publications

Endovascular treatment in patients with renal dysfunction: results of the MR CLEAN Registry.

Endovascular treatment in patients with renal dysfunction: results of the MR CLEAN Registry.

Journal: European stroke journal
Published: January 22, 2026

Safety, Tolerability, and Pharmacokinetics of the Neuroprotectant 2-Iminobiotin in Patients With Large-Vessel Occlusion Ischemic Stroke Treated With Endovascular Thrombectomy.

Safety, Tolerability, and Pharmacokinetics of the Neuroprotectant 2-Iminobiotin in Patients With Large-Vessel Occlusion Ischemic Stroke Treated With Endovascular Thrombectomy.

Journal: Stroke
Published: April 24, 2025

Newborn with Refractory Seizures due to Hemimegalencephaly and Tuberous Sclerosis Complex: Case Report and Literature Review.

Newborn with Refractory Seizures due to Hemimegalencephaly and Tuberous Sclerosis Complex: Case Report and Literature Review.

Journal: Neuropediatrics
Published: January 15, 2025

Bi-allelic deleterious variants in SNAPIN, which encodes a retrograde dynein adaptor, cause a prenatal-onset neurodevelopmental disorder.

Bi-allelic deleterious variants in SNAPIN, which encodes a retrograde dynein adaptor, cause a prenatal-onset neurodevelopmental disorder.

Journal: American journal of human genetics
Published: July 24, 2024

Clinical Outcome and Risk Factors for Progression of Prenatally Diagnosed Fetal Ventriculomegaly: A Retrospective Multicenter Study.

Clinical Outcome and Risk Factors for Progression of Prenatally Diagnosed Fetal Ventriculomegaly: A Retrospective Multicenter Study.

Journal: Prenatal diagnosis
Published: February 13, 2024

Efficacy of Levetiracetam as Add-On Therapy in the Treatment of Seizures in Neonates.

Efficacy of Levetiracetam as Add-On Therapy in the Treatment of Seizures in Neonates.

Journal: Neonatology
Published: September 27, 2023

Clinical phenotype of FOXP1 syndrome: parent-reported medical signs and symptoms in 40 individuals.

Clinical phenotype of FOXP1 syndrome: parent-reported medical signs and symptoms in 40 individuals.

Journal: Journal of medical genetics
Published: July 26, 2023

Endovascular treatment of patients with stroke caused by anterior cerebral artery occlusions.

Endovascular treatment of patients with stroke caused by anterior cerebral artery occlusions.

Journal: Acta neurologica Belgica
Published: July 01, 2023

Early recognition of characteristic conventional and amplitude-integrated EEG patterns of seizures in SCN2A and KCNQ3-related epilepsy in neonates.

Early recognition of characteristic conventional and amplitude-integrated EEG patterns of seizures in SCN2A and KCNQ3-related epilepsy in neonates.

Journal: Seizure
Published: February 18, 2023

2-iminobiotin, a selective inhibitor of nitric oxide synthase, improves memory and learning in a rat model after four vessel occlusion, mimicking cardiac arrest.

2-iminobiotin, a selective inhibitor of nitric oxide synthase, improves memory and learning in a rat model after four vessel occlusion, mimicking cardiac arrest.

Journal: PloS one
Published: November 24, 2022

Social-emotional and behavioural issues after very preterm birth: Parental and teachers experiences.

Social-emotional and behavioural issues after very preterm birth: Parental and teachers experiences.

Journal: Journal of child health care : for professionals working with children in the hospital and community
Published: August 22, 2022

Clustered mutations in the GRIK2 kainate receptor subunit gene underlie diverse neurodevelopmental disorders.

Clustered mutations in the GRIK2 kainate receptor subunit gene underlie diverse neurodevelopmental disorders.

Journal: American journal of human genetics
Published: November 05, 2021
Showing 1-12 of 47

Last Updated: 09/26/2026