Results 161 to 170 of about 160,654 (303)

Neurodegenerative and functional signatures of the cerebellar cortex in m.3243A > G patients. [PDF]

Brain Commun, 2022
Haast RAM, De Coo IFM, Ivanov D, Khan AR, Jansen JFA, Smeets HJM, Uludağ K.   +6 more
europepmc   +1 more source

Review of Memristors for In‐Memory Computing and Spiking Neural Networks

Advanced Intelligent Systems, EarlyView.
Memristors uniquely enable energy‐efficient, brain‐inspired computing by acting as both memory and synaptic elements. This review highlights their physical mechanisms, integration in crossbar arrays, and role in spiking neural networks. Key challenges, including variability, relaxation, and stochastic switching, are discussed, alongside emerging ...
Mostafa Shooshtari, Teresa Serrano‐Gotarredona, Bernabé Linares‐Barranco   +2 more
wiley   +1 more source

Histopathology of the cerebellar cortex in essential tremor and other neurodegenerative motor disorders: comparative analysis of 320 brains. [PDF]

Acta Neuropathol, 2023
Louis ED, Martuscello RT, Gionco JT, Hartstone WG, Musacchio JB, Portenti M, McCreary M, Kuo SH, Vonsattel JG, Faust PL.   +9 more
europepmc   +1 more source

Candelabrum cells are ubiquitous cerebellar cortex interneurons with specialized circuit properties. [PDF]

Nat Neurosci, 2022
Osorno T, Rudolph S, Nguyen T, Kozareva V, Nadaf NM, Norton A, Macosko EZ, Lee WA, Regehr WG.   +8 more
europepmc   +1 more source

Infantile‐Onset Ascending Hereditary Spastic Paraplegia due to a Homozygous ALS2 Exons 24–25 Deletion: Expanding the Genotypic Spectrum

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT We describe a novel homozygous intragenic deletion in the ALS2 gene in an 8‐year‐old boy with Infantile‐onset Ascending Hereditary Spastic Paraplegia (IAHSP) and oculomotor apraxia, thereby contributing to the expanding genetic landscape of ALS2‐related disorders.
Vito Luigi Colona, Maria Gnazzo, Silvia Genovese, Gessica Vasco, Lorena Travaglini, Maurizio Sabbadini, Marina Macchiaiolo, Francesco Nicita, Jacopo Sartorelli, Carmelo Piscopo, Enrico Castelli, Enrico Bertini, Andrea Bartuli, Antonio Novelli, Gessica Della Bella, Davide Vecchio   +15 more
wiley   +1 more source

Moderate Exercise Stimulates PACAP-Mediated Neurogenesis in Rat Dentate Gyrus and Cerebellar Cortex. [PDF]

J Funct Morphol Kinesiol
Maugeri G, Di Bartolo S, Palmeri N, D'Amico AG, Brancato D, Federico C, D'Agata V, Musumeci G.   +7 more
europepmc   +1 more source

The Shape of Data: a Theory of the Representation of Information in the Cerebellar Cortex. [PDF]

Cerebellum, 2022
Gilbert M.
europepmc   +1 more source

Unveiling a New Link: Cholesterol Deficiency in Smith–Lemli–Opitz and Niemann–Pick C as a Driver of Ciliopathies

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT The ciliopathies are a group of genetic disorders caused by defective function of either the primary cilia (a large number) or the motile cilia (a much smaller number). These have been defined as diseases with mutations in genes encoding individual ciliary or cilia‐associated proteins.
Robert P. Erickson, Maria Teresa Fiorenza   +1 more
wiley   +1 more source

Author Correction: Patterns of cerebellar cortex hypermetabolism on motor and cognitive functions in PD. [PDF]

NPJ Parkinsons Dis
Ren WH, Chen B, He JQ, Qi YM, Yan YY, Jin SX, Chang Y.   +6 more
europepmc   +1 more source

A transcriptomic atlas of mouse cerebellar cortex comprehensively defines cell types. [PDF]

Nature, 2021
Kozareva V, Martin C, Osorno T, Rudolph S, Guo C, Vanderburg C, Nadaf N, Regev A, Regehr WG, Macosko E.   +9 more
europepmc   +1 more source