Ewelina Wolanska
Wroclaw, DS 50368, Poland
Last Updated: 09/26/2026
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Found 8 publications
Neurodevelopmental Disorder with Psychomotor Delay, Hearing Loss, and Spasticity Caused by Compound Heterozygous SPATA5L1 Variants-Expanding Phenotype.
Journal: Journal of clinical medicine
Published: November 07, 2025
Case Report: Expanded delineation of phenotype of TRPM3-related neurodevelopmental disorders.
Journal: Frontiers in pediatrics
Published: May 19, 2024
FINCA syndrome-Defining neurobehavioral phenotype in survivors into late childhood.
Journal: Molecular genetics & genomic medicine
Published: July 09, 2021
Primitive Reflex Activity in Relation to Motor Skills in Healthy Preschool Children.
Journal: Brain sciences
Published: May 11, 2021
The Role of the Reanalysis of Genetic Test Results in the Diagnosis of Dysmorphic Syndrome Caused by Inherited xq24 Deletion including the UBE2A and CXorf56 Genes.
Journal: Genes
Published: February 06, 2021
Case Report: Further Delineation of Neurological Symptoms in Young Children Caused by Compound Heterozygous Mutation in the PIEZO2 Gene.
Journal: Frontiers in genetics
Published: October 23, 2020
Primitive Reflex Activity in Relation to the Sensory Profile in Healthy Preschool Children.
Journal: International journal of environmental research and public health
Published: September 07, 2020
A Child's Perception of Their Developmental Difficulties in Relation to Their Adult Assessment. Analysis of the INPP Questionnaire.
Journal: Journal of personalized medicine
Published: August 05, 2020
Showing 1-8 of 8
Last Updated: 09/26/2026