Focal or Multifocal Malformations in Neuronal Migration Latest Advances
Find the Latest Research About Focal or Multifocal Malformations in Neuronal Migration
Last Updated: 04/28/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 1600 publications
Miller-Dieker Syndrome: Genetic Etiology, Neurocognitive Impact, and Clinical Implications in a Neuronal Migration Disorder.
Journal: Developmental neuropsychology
Published: April 14, 2026
Bronchiectasis in a child with a homozygous DCDC2 gene mutation: A case report.
Journal: Journal of Taibah University Medical Sciences
Published: December 12, 2025
Histochemical characterization of muscularis macrophage loss and disruption of a miR-93-5p-AHNAK neuro-immune axis in Hirschsprung's disease.
Journal: Histochemistry and cell biology
Published: December 07, 2025
Ephrin and Eph family proteins: Molecular mechanisms of signaling pathways and their role in neural injury repair.
Journal: Neural regeneration research
Published: December 03, 2025
Subcortical band heterotopia in a child with new-onset seizures: A case report.
Journal: Epilepsy & behavior reports
Published: November 28, 2025
Microplastics and neurotoxicity: could prenatal exposure to microplastics boost congenital enteric neuropathies?
Journal: Frontiers in toxicology
Published: November 28, 2025
Gordonibacter-associated regulatory T cell dysfunction and S100A11-mediated neural impairment in Hirschsprung's disease: a microbiota-immune-neural axis.
Journal: Cell & bioscience
Published: November 09, 2025
Diagnostic Yield of Post-Mortem Fetal Micro-CT for Central Nervous System Abnormalities.
Journal: Prenatal diagnosis
Published: November 06, 2025
Conditional Deletion of Isl1 Disrupts Cochlear Sensory and Neuronal Development, Leading to Hearing Loss.
Journal: Molecular neurobiology
Published: October 15, 2025
Association of increased cortical thickness and cognitive impairment in patients with Kallmann syndrome.
Journal: European journal of endocrinology
Published: October 14, 2025
Dysfunctional CRPPA is responsible for recessively inherited Hereford hydrocephalus with muscular dystrophy and retinal dysplasia.
Journal: Veterinary pathology
Published: October 09, 2025
Last Updated: 04/28/2026