A Diagnostic Pitfall in the Emergency Department -Aortic Dissection Masquerading as Acute Paraplegia: A Case Report. [PDF]
Nagarajan S +4 more
europepmc +1 more source
ABSTRACT Real‐time monitoring of subtle muscle deformation remains of considerable importance for cooperative human‐exoskeleton control. Highly integrated flexible triboelectric nanogenerators (TENGs), owing to their self‐powered operation and high sensing resolution, are well suited for continuous physiological monitoring and human‐robot interaction ...
Heran Li +9 more
wiley +1 more source
Cervicodorsal Pott's Spine with Acute Onset Paraplegia Managed by Transmanubrial Anterior Decompression and Instrumentation: A Case Report. [PDF]
Kawade M +4 more
europepmc +1 more source
Opticus atrophy—Genetic testing with WES/WGS in 62 patients with optic atrophy provided a genetic diagnosis in 21 patients (33.9%). 42.9% of these involved non‐OPA1 genes, including WFS1, ACO2, NR2F1, UCHL1, CACNA1F, and COQ2, where the genetic diagnosis prompted additional clinical evaluation, surveillance, or therapeutic intervention.
Katrine M. Johannesen +9 more
wiley +1 more source
Hereditary neurodegenerative disorders with spastic-ataxic manifestations: genetic and clinical insights into previously reported variants. [PDF]
Ahmad R +4 more
europepmc +1 more source
Thoracic spinal cord injury is associated with significant remote degeneration of the uninjured cervical cord, even in the absence of direct cervical damage. Compared to able‐bodied controls, individuals with chronic thoracic injury showed reduced cervical cross‐sectional area and antero‐posterior/right–left diameters, along with increased eccentricity
Yann Quidé +8 more
wiley +1 more source
Late-Onset Rapidly Progressive Spastic Paraplegia with Extensive White Matter Abnormalities Associated with an MFN2 Variant. [PDF]
Yang J, Park HM, Lee YB.
europepmc +1 more source
Proteostasis of organelles in aging and disease
Cells rely on regulated proteostasis mechanisms to keep their internal compartments functioning properly. When these mechanisms fail, damaged proteins accumulate, disrupting organelles, such as the nucleus, mitochondria, endoplasmic reticulum, Golgi, and lysosomes, as well as membraneless organelles, such as stress granules, processing bodies, the ...
Yara Nabawi +5 more
wiley +1 more source
SPG4-Associated Hereditary Spastic Paraplegia and Dilated Cardiomyopathy: Coincidence or Clue? [PDF]
Panjrath G, Dakhakhni M.
europepmc +1 more source
Splice effect of a synonymous variant in <i>AP4B1</i>: multiomics approach establishes the diagnosis in two sisters with spastic paraplegia. [PDF]
Badmann S +14 more
europepmc +1 more source

