Results 91 to 100 of about 46,292 (256)
Movement Disorders, Volume 40, Issue 5, Page 928-937, May 2025.Abstract Background Antidopaminergic medications (ADM) are often used for symptom management of Huntington's disease (HD). Evidence from past research suggests that ADMs are associated with worse clinical outcomes in HD, but their impact on various domains remains underexplored.
Michal Geva +5 more
wiley +1 more source
Muscle &Nerve, Volume 71, Issue 5, Page 869-888, May 2025.Abstract Hand function is important in every aspect of our lives. Across a wide range of neuromuscular disorders—inherited ataxias, motor neuron diseases, polyneuropathies, and myopathies—people can experience losses in hand strength, tone, movement, dexterity, joint range, and sensation.
Colleen O'Connell +5 more
wiley +1 more source
Clinical and Experimental Neuroimmunology, Volume 16, Issue 2, Page 174-187, May 2025.ABSTRACT Autoimmune glial fibrillary acidic protein (GFAP) astrocytopathy (GFAP‐A) is an autoimmune inflammatory central nervous system disease. Recent neuropathological findings indicate that GFAP‐specific cluster of differentiation (CD)8+ T cells are likely the effectors of GFAP‐A.
Akio Kimura
wiley +1 more source
Neurovascular compression of the oculomotor nerve presenting with aberrant reinnervation
American Journal of Ophthalmology Case Reports, 2021 Purpose: To report a case of neurovascular compression in a patient presenting with ophthalmic evidence of aberrant reinnervation. Observation: A 68-year-old woman diagnosed with right partial third nerve palsy with aberrant regeneration.
Mary Maher +3 more
doaj
Frontiers in Neurology, 2014 Introduction: Recurrent oculomotor nerve palsies are extremely rare clinical conditions. Case report: Here, we report on a unique case of a short-lasting recurrent unilateral incomplete external and complete internal oculomotor nerve palsy.
Olga eGrabau +2 more
doaj +1 more source
Immune Dysregulation in a Child With SOD1‐Related Neurological Disease
American Journal of Medical Genetics Part A, Volume 197, Issue 4, April 2025.ABSTRACT Spastic tetraplegia and axial hypotonia (STAHP) associated with biallelic SOD1 deficiency is a recently described neurological disorder affecting children. Five studies have described a total of nine cases thus far, all characterized by the onset of progressive spastic tetraplegia beginning before 2 years of age. All but two of these cases are
Rozlyn Claire Thomas Boutin +5 more
wiley +1 more source
Oculomotor Nerve Palsy in a Patient with a Ruptured Middle Cerebral Artery Aneurysm [PDF]
, 2018 We describe a case of acute oculomotor nerve palsy caused by a ruptured middle cerebral artery (MCA) aneurysm. A 59-year-old female presenting with headache and nausea was admitted to our hospital.
Ikeda, Toshiki +4 more
core
Case Reports in Neurology, 2014 We report a patient with acute cerebral infarction of the left paramedian thalamus, upper mesencephalon and cerebellum who exhibited ipsilateral oculomotor nerve palsy and contralateral downbeat nystagmus.
Kosuke Matsuzono +5 more
doaj +1 more source
Ocular Neuromyotonia—A Rare but Reversible Cause of Intermittent Diplopia
Movement Disorders Clinical Practice, EarlyView.
Parthvi Ravat +4 more
wiley +1 more source
Natural history of cerebral visual impairment in children with cerebral palsy
Developmental Medicine &Child Neurology, Volume 67, Issue 4, Page 486-495, April 2025.This original article is commented by Williams on pages 424–425 of this issue. Plain language summary: https://onlinelibrary.wiley.com/doi/10.1111/dmcn.16143 Abstract Aim To longitudinally evaluate the natural history of cerebral visual impairment (CVI) in children with cerebral palsy (CP) and identify which early visual signs or symptoms are ...
Jessica Galli +9 more
wiley +1 more source