Developmental Delay - Nursing Science

Relevant Publications

Comparing the Pre-writing Skills of Diplegic Cerebral Palsy Children to Those of Normal Children.

Issue Release: 2024

Clinical characteristics and multimodal imaging can help diagnosing and treating mild malformation of cortical development with oligodendroglial hyperplasia and epilepsy.

Issue Release: 2024

All three MutL complexes are required for repeat expansion in a human stem cell model of CAG-repeat expansion mediated glutaminase deficiency.

Issue Release: 2024

Developmental milestones and daily living skills in individuals with Angelman syndrome.

Issue Release: 2024

Progressive spasticity and developmental delay in an infant with a mutation.

Issue Release: 2024

Novel KCNQ2 missense variant expands the genotype spectrum of DEE7.

Issue Release: 2024

Caregiver Narratives of Children with Autism Spectrum Disorder: Exploring Symptom Recognition, Diagnosis, and Interventions.

Issue Release: 2024

Short Report: 10-year follow-up of a boy with ARID1B-related disorder. Early intervention, longitudinal dimensional phenotype, brain imaging and outcome.

Issue Release: 2024

Epilepsy as a Novel Phenotype of BPTF-Related Disorders.

Issue Release: 2024

Cadmium and phthalate impacts developmental growth and mortality of Spodoptera littoralis, but not reproductive success.

Issue Release: 2024

Prevalence and socio-economic determinants of growth and developmental delays among Iranian children aged under five years: A cross sectional study.

Issue Release: 2024

Retinal detachment, vitreous hemorrhage, and foveal hypoplasia associated with 3q27.1q27.2 microdeletion: a case report.

Issue Release: 2024

It\'s all in the timing: Delayed feedback in autism may weaken predictive mechanisms during contour integration.

Issue Release: 2024

Frontiers in congenital disorders of glycosylation consortium, a cross-sectional study report at year 5 of 280 individuals in the natural history cohort.

Issue Release: 2024

The de novo missense mutation F224S in GABRB2, identified in epileptic encephalopathy and developmental delay, impairs GABAR function.

Issue Release: 2024

Genetic Diagnosis in Children with Developmental Delay.

Issue Release: 2024

Identification of the synonymous variant c.3141G > A in TNRC6B gene that altered RNA splicing by minigene assay.

Issue Release: 2024

Diagnostic Yield of Trio Whole-Genome Sequencing in Children with Undiagnosed Developmental Delay or Congenital Anomaly: A Prospective Cohort Study.

Issue Release: 2024

Skeletal pathology in mouse models of Gould syndrome is partially alleviated by genetically reducing TGFβ signaling.

Issue Release: 2024

A Case of Lateral Meningocele Syndrome without Lateral Meningoceles.

Issue Release: 2024

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