Agenesis Of The Corpus Callosum - Histology

Relevant Publications

Developmental surface dyslexia and dysgraphia in a child with corpus callosum agenesis: an approach to diagnosis and treatment.

Issue Release: 2024

Sleep disorders in pediatric patients with agenesis of the corpus callosum.

Issue Release: 2024

A rare case report: The value of fetal MRI to detect diprosopus twins.

Issue Release: 2024

Imagawa-Matsumoto Syndrome: The First Case From Turkey.

Issue Release: 2024

Neurosurgical intervention for the Meckel-Gruber Syndrome: A systematic review.

Issue Release: 2024

A selective defect in the glial wedge as part of the neuroepithelium disruption in hydrocephalus development in the mouse hyh model is associated with complete corpus callosum dysgenesis.

Issue Release: 2024

Retrospective analysis of the prognostic factors of fetal corpus callosum dysplasia.

Issue Release: 2024

A case of Wilson\'s disease combined with intracranial lipoma and dysplasia of the corpus callosum with review of the literature.

Issue Release: 2024

Prenatal and Postnatal Diagnosis and Genetic Background of Corpus Callosum Malformations and Neonatal Follow-Up.

Issue Release: 2024

The postnatal injection of AAV9-FOXG1 rescues corpus callosum agenesis and other brain deficits in the mouse model of FOXG1 syndrome.

Issue Release: 2024

Fetal agenesis of corpus callosum: chromosomal copy number abnormalities and postnatal follow-up.

Issue Release: 2024

Language and communication functioning in children and adolescents with agenesis of the corpus callosum.

Issue Release: 2024

Adaptive behavior in primary agenesis of the corpus callosum.

Issue Release: 2024

Case report: Twice-daily tolvaptan dosing regimen in a challenging case of hyponatremia due to SIAD.

Issue Release: 2024

Single Nucleotide Polymorphism in Cell Adhesion Molecule L1 Affects Learning and Memory in a Mouse Model of Traumatic Brain Injury.

Issue Release: 2024

Assessment of fetal corpus callosum biometry by 3D super-resolution reconstructed T2-weighted magnetic resonance imaging.

Issue Release: 2024

Perinatal clinical course of Vici syndrome associated with novel variants: unique cardiac changes and difficulty with foetal diagnosis.

Issue Release: 2024

Genotype-phenotype correlation in CLCN4-related developmental and epileptic encephalopathy.

Issue Release: 2024

Demystifying the Mystery of Genes: A Case Report on Constitutional Mismatch Repair Deficiency.

Issue Release: 2024

SRPK3 Is Essential for Cognitive and Ocular Development in Humans and Zebrafish, Explaining X-Linked Intellectual Disability.

Issue Release: 2024

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