Results 81 to 90 of about 555,719 (297)
Activation of the mitochondrial protein OXR1 increases pSyn129 αSynuclein aggregation by lowering ATP levels and altering mitochondrial membrane potential, particularly in response to MSA‐derived fibrils. In contrast, ablation of the ER protein EMC4 enhances autophagic flux and lysosomal clearance, broadly reducing α‐synuclein aggregates.
Sandesh Neupane +11 more
wiley +1 more source
Medical students’ experience of emotions and success in neurological studies – What do they tell us?
Background There is a need to develop effective educational experience in neurology to improve the students’ skills in diagnosing and managing patients with neurological symptoms or disease.
Hanna Ansakorpi +2 more
doaj +1 more source
Psychogenic movement disorders present a diagnostically challenging entity that is often frightening for patients. Differentiating movement disorders, providing clear explanations, and addressing underlying conditions with a multidisciplinary approach ...
Andrew R. Hamm
doaj +1 more source
The combined issue (Numbers 1–2–3–4) of Volume 17 of the International Journal of Neurology (1983) was dedicated to developmental neurobiology, continuing the journal’s focus on the structural and molecular mechanisms underlying nervous system formation.
International Journal of Neurology
core +1 more source
Long‐term hippocampal alterations and cognitive impairment in a murine model of surgical sepsis
Using a mouse model of surgical sepsis, we tested long‐term memory and analyzed the transcriptome of single cells isolated from the hippocampus. Survivor mice showed worse memory, loss of certain brain cell subpopulations, and abnormal immune cell activity—suggesting that post‐sepsis brain alterations may be linked to cognitive deficits.
Dong Seong Cho +4 more
wiley +1 more source
ABSTRACT Objective Super‐Refractory Status Epilepticus (SRSE) is a rare, life‐threatening neurological emergency with unclear etiology in many cases. Mitochondrial dysfunction, often due to disease‐causing genetic variants, is increasingly recognized as a cause, with each gene producing distinct pathophysiological mechanisms.
Pouria Mohammadi +2 more
wiley +1 more source
ABSTRACT Introduction Spinal cord infarction (SCI) is a rare but devastating myelopathy, characterized by a high disability rate and an unfavorable prognosis. It has often been underdiagnosed and misdiagnosed as idiopathic transverse myelitis (ITM). This study aimed to describe the clinical features, radiological biomarkers, treatments, and functional ...
Zeqiang Ji +13 more
wiley +1 more source
The combined issue (Numbers 1–2–3–4) of Volume 18 of the International Journal of Neurology (1984) was dedicated to brain metabolism, presenting a comprehensive and multidisciplinary exploration of biochemical, neurophysiological, and imaging advances ...
International Journal of Neurology
core +1 more source
ABSTRACT Background SOX1 antibody‐positive paraneoplastic neurological syndromes (PNS) exhibit significant population‐specific clinical heterogeneity. While Western cohorts predominantly manifest Lambert‐Eaton myasthenic syndrome (65%–80%), comprehensive clinical characterization and treatment response data in Asian populations remain critically ...
Jin‐Long Ye +11 more
wiley +1 more source
The combined issue (Numbers 1–2–3–4) of Volume 21 of the International Journal of Neurology (1987) was dedicated to Memory, offering one of the most comprehensive interdisciplinary examinations of the biological, cognitive, and clinical mechanisms ...
International Journal of Neurology
core +1 more source

