Results 121 to 130 of about 26,469 (241)
Paroxysmal Dystonia: An Etiology Not to Be Missed in an Older Adult Patient
Movement Disorders Clinical Practice, EarlyView.
Valentin Mira +2 more
wiley +1 more source
Changes in corticospinal excitability in response to mediolateral gait instability
Abstract Unpredictable gait disturbances, particularly in the mediolateral direction, pose a significant challenge to stability and are a common contributor to falls. Although the corticospinal tract is critical for gait and postural control, its response to such instabilities remains unclear.
Raven O. Huiberts +2 more
wiley +1 more source
Abstract figure There is positive covariation in the amplitudes of motor evoked potentials (MEPs) generated by (near simultaneous) stimulation of the two motor cortices. That is, larger responses to stimulation of the left motor cortex tend to be accompanied by larger responses to stimulation of the right motor cortex, and smaller responses to ...
Richard G. Carson
wiley +1 more source
ObjectiveThe current research aimed to analyze the alterations within the motor cortex and pyramidal pathways and their association with the degree of damage within the peripheral nerve fibers in patients with chronic inflammatory demyelinating ...
Edyta Dziadkowiak +5 more
doaj +1 more source
Abstract figure legend During infection, prostaglandin E2 (PGE2) is produced and elicits warmth‐seeking behaviour and involuntary febrile responses by acting on prostaglandin EP3 receptors (EP3Rs) in two distinct brain sites. PGE2 acting on EP3Rs on neurons in the external lateral part of the lateral parabrachial nucleus (LPBel) augments cold sensory ...
Takaki Yahiro +2 more
wiley +1 more source
Progressive memory loss for one year and visual changes for three months
A 49-year-old Chinese male presented with memory loss and vision disturbances. Neurological examination revealed bilateral positive Babinski signs. Cognitive assessments showed cognitive impairments.
Si-yuan FAN +5 more
doaj
ABSTRACT Arginase 1 deficiency (ARG1D) is the least common urea cycle disorder. Neonatal onset is rarely described, and hyperammonemic coma is less common in patients with ARG1D compared to other urea cycle disorders. In recent years, we diagnosed a high number of ARG1D patients in Mayotte, an insular (Comoro Islands) department of France.
Aurélie de Bruyne +16 more
wiley +1 more source
ABSTRACT Objective Neurological soft signs (NSS) are minor, non‐localizable neurological abnormalities. This study aimed to investigate the factor structure of the Neurological Evaluation Scale. Material and Methods A total of 355 subjects (233 patients and 122 general population subjects). NSS were assessed using the NES.
Konstantinos N. Fountoulakis +4 more
wiley +1 more source
Distal urethral obstruction in an eight‐week‐old colt with struvite urolithiasis
Summary An 8‐week‐old Thoroughbred colt presented with acute colic signs. Physical examination and transcutaneous ultrasound of the abdomen and penis revealed a urinary tract obstruction in the distal urethra due to urolithiasis. A distal urethrotomy over the site of obstruction was performed to remove the urolith and relieve the obstruction.
M. T. Connaughton +2 more
wiley +1 more source
ABSTRACT Pathogenic variants in KIF1C cause Spastic Paraplegia 58 (SPG58), typically presenting with cerebellar ataxia and spastic paraparesis. We report two unrelated patients with spastic paraparesis, cerebellar ataxia, and tremor. Whole‐exome sequence analysis identified novel homozygous variants in the motor domain of KIF1C (NM_006612.6): c.921G>A (
Akihiko Mitsutake +12 more
wiley +1 more source

