Results 221 to 230 of about 79,223 (329)

Optic Nystagmus [PDF]

open access: bronze, 1927
E. Arnold Carmichael
openalex   +1 more source

Infant Death due to Cannabis Ingestion

open access: yesDrug Testing and Analysis, Volume 17, Issue 10, Page 2014-2021, October 2025.
ABSTRACT A child died in the emergency room of a local hospital a few hours after ingesting a substance the color of cork and the consistency of earth. At home, a modest amount of resinous substance was found. At the hospital, the child exhibited alterations in walking, balance, and consciousness.
Donata Favretto   +9 more
wiley   +1 more source

Eye movement features for assisting differentiation between posterior circulation infarction and vestibular neuritis in patients of acute vestibular syndrome. [PDF]

open access: yesEur J Med Res
Jin MM   +11 more
europepmc   +1 more source

Enterovirus A‐71 Associated Parainfectious Movement Disorders in Children

open access: yesMovement Disorders Clinical Practice, Volume 12, Issue 10, Page 1635-1639, October 2025.
Abstract Background Pediatric movement disorders can be challenging to characterize, given the phenotypic complexity and broad differential diagnosis. While genetic tests are often part of the diagnostic work‐up, it is important to consider acquired causes, which may require specific investigations.
Suus A. M. van Noort   +6 more
wiley   +1 more source

Clinical characteristics and caloric testing in patients with light or heavy cupula of the horizontal semicircular canal. [PDF]

open access: yesFront Neurol
Zhang X   +10 more
europepmc   +1 more source

Widespread Skin Telangiectasias in Spinocerebellar Ataxia Type 27B

open access: yes
Annals of Neurology, Volume 98, Issue 4, Page 762-763, October 2025.
Victor Alm   +3 more
wiley   +1 more source

Clinical characteristics, cerebellar MR spectroscopy and response to 3,4-diaminopyridine in spinocerebellar ataxia 27B: the Sheffield Ataxia Centre experience. [PDF]

open access: yesJ Neurol
Chukwuocha I   +10 more
europepmc   +1 more source

A Novel Missense Variant of the ABCD1 Gene in X‐Linked Adrenoleukodystrophy in Chinese Family

open access: yesMolecular Genetics &Genomic Medicine, Volume 13, Issue 10, October 2025.
This study identifies a novel ABCD1 gene variant (c.773T>G, p.Leu258Arg) linked to X‐linked adrenoleukodystrophy in a Chinese family, demonstrating its pathogenic impact via disrupted peroxisomal localization and impaired fatty acid metabolism, thus expanding the mutation spectrum and advancing molecular diagnosis and familial genetic counseling ...
Hongxia Fu   +5 more
wiley   +1 more source

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