Results 1 to 10 of about 51,993 (293)

Pearls & Oy-sters: Isolated oculomotor nerve palsy due to pituitary apoplexy missed on CT scan [PDF]

Neurology, 2020
Pituitary apoplexy is an important differential diagnosis for acute headache, particularly accompanied by cranial nerve ...
Sina Marzoughi, A. Ganesh, A. Qaddoura, Pouya Motazedian, Simerpreet S. Bal   +4 more
semanticscholar   +2 more sources

Iron accumulation in the oculomotor nerve of the progressive supranuclear palsy brain

Scientific Reports, 2021
Abnormal iron accumulation around the substantia nigra (SN) is a diagnostic indicator of Parkinsonism. This study aimed to identify iron-related microarchitectural changes around the SN of brains with progressive supranuclear palsy (PSP) via postmortem ...
Hansol Lee, Myung Jun Lee, Eun-Joo Kim, G. Huh, Jae-Hyeok Lee, Hyungjoon Cho   +5 more
semanticscholar   +1 more source

Down and out: acquired oculomotor nerve palsy [PDF]

BMJ Case Reports, 2019
A 50-year-old male presented to the ophthalmology emergency room with a complaint of sudden drooping of his left eyelid and double vision in the left eye ([figure 1][1]). The patient had a history of diabetes mellitus for the past 9 years.
Rohan Bir Singh, Rohan Bir Singh, Sahil Thakur, Kanwar Partap Singh, Sukhman Shergill   +4 more
openaire   +2 more sources

Optimising reaction‐time analysis in eye movement perimetry using pooled promptness distributions

Ophthalmic and Physiological Optics, EarlyView.
Abstract Reaction‐time measurements play a crucial role in assessing cognitive and sensory processing, with applications in functional clinical diagnostics such as eye‐movement perimetry (EMP) for the detection of glaucoma. However, reaction‐time distributions are typically right‐skewed, complicating statistical analysis and requiring large numbers of ...
Ashwini Venkat Reddy Chanakya, Peter Bremen   +1 more
wiley   +1 more source

Recurrent isolated oculomotor nerve palsy after radiation of a mesencephalic metastasis. Case report and mini-review.

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, Jochen eLeonhardi, Carl Detlev Reimers   +2 more
doaj   +1 more source

Closing in on a Consensus in Identifying, Assessing and Diagnosing Children With Cerebral Visual Impairment

Acta Paediatrica, Volume 114, Issue 10, Page 2490-2498, October 2025.
ABSTRACT Aim Lack of global consensus regarding CVI makes assessment and research more difficult. Our aim is to describe current consensus and evident methods for how to identify, assess and diagnose CVI in children. Method Data‐based search on reviews and papers published 2014–2023. Result The seven reviews and 23 papers reviewed here jointly convey a
Barbro Lindquist, Christina Westerberg
wiley   +1 more source

Autosomal Recessive Cerebellar Ataxias: Translating Genes to Therapies

Annals of Neurology, Volume 98, Issue 3, Page 448-470, September 2025.
[Color figure can be viewed at www.annalsofneurology.org] Autosomal recessive cerebellar ataxias are disabling neurodegenerative genetic conditions affecting balance and coordination. Advancements in genomic testing have improved diagnosis, leading to a new focus on the development of targeted precision therapeutics addressing cellular, biochemical ...
Brent L. Fogel, Thomas Klopstock, David R. Lynch, Francesca Maltecca, Mayank Verma, Berge A. Minassian, Frances M. Platt, Débora Farina Gonçalves, Hélène Puccio, Andreas Roos, Matthis Synofzik   +10 more
wiley   +1 more source

Combined Ipsilateral Oculomotor Nerve Palsy and Contralateral Downbeat Nystagmus in a Case of Cerebral Infarction

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, Yasuhiro Manabe, Yoshiaki Takahashi, Hisashi Narai, Nobuhiko Omori, Koji Abe   +5 more
doaj   +1 more source

Hereditary Spastic Paraplegia in Alberta: Lessons from a Well‐Defined Cohort Including the Indigenous Population

Movement Disorders Clinical Practice, Volume 12, Issue 9, Page 1346-1356, September 2025.
Abstract Background Hereditary spastic paraplegias (HSP) are rare disorders sharing common features of leg spasticity with gait impairment. Simple and complex forms are recognized; over 50% of cases remain unsolved genetically. Little is known about the genetics of HSP among Indigenous Peoples. Objectives To describe clinical, radiological, and genetic
Ekhlas Assaedi, Setareh Ashtiani, Mehrdad A. Estiar, Ziv Gan‐Or, Erica D. McKenzie, Aakash Shetty, Guy Rouleau, Oksana Suchowersky   +7 more
wiley   +1 more source

Late‐onset multiple system atrophy: Neuropathological features associated with slow disease progression

Brain Pathology, Volume 35, Issue 5, September 2025.
Late‐onset multiple system atrophy (LO‐MSA; onset ≥75 years) shows milder degeneration of the striatonigral and olivopontocerebellar systems and serotonergic neurons in the ventrolateral medulla than usual‐age‐onset MSA with a similar disease duration. LO‐MSA may therefore exhibit slower pathological progression.
Misato Ozawa, Rie Saito, Takuya Konno, Yasuko Kuroha, Tetsuhiko Ikeda, Akio Yokoseki, Takashi Tani, Tomoe Sato, Jiro Idezuka, Reiji Koide, Shigeru Fujimoto, Osamu Onodera, Mari Tada, Akiyoshi Kakita   +13 more
wiley   +1 more source