Neonatal encephalopathy: Etiologies other than hypoxic-ischemic encephalopathy

AGS Karamian, S Mercimek-Andrews… - Seminars in Fetal and …, 2021 - Elsevier
Neonatal encephalopathy (NE) describes the clinical syndrome of a newborn with abnormal
brain function that may result from a variety of etiologies. HIE should be distinguished from …

How neurons maintain their axons long-term: an integrated view of axon biology and pathology

G Smith, ST Sweeney, CJ O'Kane… - Frontiers in Neuroscience, 2023 - frontiersin.org
Axons are processes of neurons, up to a metre long, that form the essential biological cables
wiring nervous systems. They must survive, often far away from their cell bodies and up to a …

[PDF][PDF] Centrosomal microtubule nucleation regulates radial migration of projection neurons independently of polarization in the developing brain

S Vinopal, S Dupraz, E Alfadil, T Pietralla, S Bendre… - Neuron, 2023 - cell.com
Cortical projection neurons polarize and form an axon while migrating radially. Even though
these dynamic processes are closely interwoven, they are regulated separately—the …

Pontocerebellar hypoplasia: a pattern recognition approach

CT Rüsch, BK Bölsterli, R Kottke, R Steinfeld… - The Cerebellum, 2020 - Springer
Pontocerebellar hypoplasias (PCH) represent a heterogeneous group of very rare disorders
with reduced volume of pons and cerebellum. The term is purely descriptive and does not …

Congenital brain malformations: an integrated diagnostic approach

BP Chaudhari, ML Ho - Seminars in pediatric neurology, 2022 - Elsevier
Congenital brain malformations are abnormalities present at birth that can result from
developmental disruptions at various embryonic or fetal stages. The clinical presentation is …

[HTML][HTML] Maintaining essential microtubule bundles in meter-long axons: a role for local tubulin biogenesis?

LM Pinho-Correia, A Prokop - Brain Research Bulletin, 2023 - Elsevier
Axons are the narrow, up-to-meter long cellular processes of neurons that form the
biological cables wiring our nervous system. Most axons must survive for an organism's …

The Reeler Mouse: A Translational Model of Human Neurological Conditions, or Simply a Good Tool for Better Understanding Neurodevelopment?

L Lossi, C Castagna, A Granato, A Merighi - Journal of Clinical Medicine, 2019 - mdpi.com
The first description of the Reeler mutation in mouse dates to more than fifty years ago, and
later, its causative gene (reln) was discovered in mouse, and its human orthologue (RELN) …

[HTML][HTML] The Neuron Navigators: Structure, function, and evolutionary history

RM Powers, RF Hevner, S Halpain - Frontiers in Molecular …, 2023 - frontiersin.org
Neuron navigators (Navigators) are cytoskeletal-associated proteins important for neuron
migration, neurite growth, and axon guidance, but they also function more widely in other …

DYNC1H1‐related epilepsy: Genotype–phenotype correlation

W Liu, M Cheng, Y Zhu, Y Chen, Y Yang… - … Medicine & Child …, 2023 - Wiley Online Library
Aim To explore the phenotypic spectrum and refine the genotype–phenotype correlation of
DYNC1H1‐related epilepsy. Method The clinical data of 15 patients with epilepsy in our …

Effects of altered tau expression on dentate granule cell excitability in mice

RA Cloyd, J Koren III, JF Abisambra, BN Smith - Experimental neurology, 2021 - Elsevier
Tauopathies, including Alzheimer's disease, are characterized by progressive accumulation
of hyperphosphorylated and pathologic tau protein in association with onset of cognitive and …