Results 221 to 230 of about 1,760,110 (357)
ART. XVI. An Inquiry concerning the Diseases and Functions of the Brain, the Spinal Cord, and the Nerves. [PDF]
A. Brigham
openalex +1 more source
Abstract Objective Exploring the prevalence and association between intracranial atherosclerosis (ICAS) and cerebral small vessel diseases (CSVD), this study delved beyond the current scope, utilising high‐resolution vessel wall MRI (HRVW‐MRI) to investigate how subtle changes in intracranial atherosclerotic features influence the various burdens of ...
Joseph Amihere Ackah+6 more
wiley +1 more source
Direct generation of 1O2 in living tissues for the treatment of brain diseases. [PDF]
Semyachkina-Glushkovskaya O.
europepmc +1 more source
Progressive Myoclonus Epilepsy: Distinctive MRI Changes in Cerebellar and Motor Networks
ABSTRACT Objective Progressive myoclonus epilepsy (PME) is a rare generalized epilepsy syndrome with a well‐characterized genetic basis. The brain networks that are affected to give rise to the distinctive symptoms of PME are less well understood. Methods Eleven individuals with PME with a confirmed genetic diagnosis and 22 controls were studied.
Jillian M. Cameron+3 more
wiley +1 more source
AMPA Receptors in Synaptic Plasticity, Memory Function, and Brain Diseases. [PDF]
de León-López CAM+2 more
europepmc +1 more source
Iron homeostasis imbalance and ferroptosis in brain diseases. [PDF]
Long H, Zhu W, Wei L, Zhao J.
europepmc +1 more source
ABSTRACT Objective Certain frontotemporal lobar degeneration subtypes, including TDP‐A and B, can either occur sporadically or in association with specific genetic mutations. It is uncertain whether syndromic or imaging features previously associated with these patient groups are subtype or genotype specific.
Sean Coulborn+17 more
wiley +1 more source
The glymphatic system: a new perspective on brain diseases. [PDF]
Ding Z+7 more
europepmc +1 more source
FGF14 GAA Intronic Expansion in Unsolved Adult‐Onset Ataxia in the Care4Rare Canada Consortium
ABSTRACT Background and Objectives Spinocerebellar ataxias (SCA) represent a clinically and genetically heterogeneous group of progressive neurodegenerative diseases with prominent cerebellar atrophy. Recently, a novel pathogenic repeat expansion in intron 1 of FGF14 was identified, causing adult‐onset SCA (SCA27B). We aimed to determine the proportion
Alexanne Cuillerier+20 more
wiley +1 more source
Progress on the Mechanisms and Neuroprotective Benefits of Dexmedetomidine in Brain Diseases. [PDF]
Tao Z, Li P, Zhao X.
europepmc +1 more source