Microvascular pathology in the spinal cord of severe spinal muscular atrophy patients

Abstract Severe spinal muscular atrophy (SMA) is a life-limiting neurodegenerative disease of infancy and early childhood, caused by reduced expression of the ubiquitous survival motor neuron protein (SMN). While current therapies aim to increase SMN levels and preserve motor neurons, significant de...

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Hlavní autoři:	Hazel Allardyce, Heather Lanz, Benjamin D. Lawrence, Thomas O. Crawford, Charlotte J. Sumner, Simon H. Parson
Médium:	Artigo
Jazyk:	Inglês
Vydáno:	BMC 2026-02-01
Edice:	Acta Neuropathologica Communications
Témata:	von Willebrand Factor Endothelial cell BSCB Astrocytes Pericytes Microglia
On-line přístup:	https://doi.org/10.1186/s40478-026-02232-y
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