ScholarlyCommons
metadata only
Spatial Transcriptomics for Focal Cortical Dysplasia and Implications for Autism Spectrum Disorder
autism-spectrum-disordercell-and-developmental-biologydiseasesneuroscience-and-neurobiologyspatial-transcriptomics
Focal Cortical Dysplasia (FCD) is a neurodevelopmental disorder of the cerebral cortex and the leading cause of drug-resistant focal epilepsy in children and young adults. FCD type II presents with localized regions of dyslamination and abnormal cell types, specifically dysmorphic neurons (type IIa
Conceptio Open Archive
Analyze & explore related research in Conceptio
Connect this record directly into your research workflow or AI agent. Explore citations across open repositories, query full text, and export structured proof bundles.
This document is indexed with metadata only: full text is not available in the archive for this record. Open the official source ↗
Related documents
- Association of Brain Derived Neurotrophic Factor (BDNF) rs6265 Gene Polymorphism With Susceptibility to Epilepsy#1031037
- Cerebrospinal Fluid Proteome in Hydrocephalus#851904
- Effect of Lithium in Patients With Autism Spectrum Disorder and Phelan-McDermid Syndrome (SHANK3 Haploinsufficiency)#1114378
- Multi-cohort cerebrospinal fluid proteomics identifies robust molecular signatures across the Alzheimer disease continuum.#159830
- Global transcriptional changes across multiple isogenic <i>C9orf72</i> patient iPSC-derived neurons#253570
Record · ID 1092516
Retrieved via Conceptio: every document is proof-bundled with source, license, and retrieval metadata.
Retrieved via Conceptio: every document is proof-bundled with source, license, and retrieval metadata.
Bring this data into your agent: Connect via MCP or API · 20 free credits to start · no card required
Read the Docs → · View CLI source on GitHub · Conceptio Open Knowledge Archive
Read the Docs → · View CLI source on GitHub · Conceptio Open Knowledge Archive