Results 101 to 110 of about 11,554 (291)

Recurrent Hypothermia and Autonomic Dysfunction Secondary to Shapiro Syndrome

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT A 44‐year‐old man presented with recurrent hypothermia, diaphoresis and hypertension. Extensive investigation for infectious, inflammatory, metabolic and endocrine aetiologies was negative. MR scan of the brain demonstrated no lesions but revealed callosal dysgenesis, consistent with Shapiro syndrome.
Naveen Kumar, Jeremy Johnson, Susanne Watkins, Eoin Mulroy   +3 more
wiley   +1 more source

Spatial and Volumetric Characteristics of Glioblastoma: Associations With Clinical Presentation and Survival

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective We aim to comprehensively analyze how regional tumor and edema characteristics are associated with clinical presentations and survival outcomes in a large cohort of glioblastoma patients. Methods Patients with IDH‐wildtype glioblastoma who received brain MRI from 2010 to 2023 were included.
Daniel J. Zhou, Marc Jaskir, Julian Gal, Yombe Fonkeu, Christos Davatzikos, MacLean P. Nasrallah, Jose Garcia, Rubo Xing, Stephen J. Bagley, Arati Desai, Richard E. Phillips, Steven Tobochnik, Colin A. Ellis, James J. Gugger, Nishant Sinha, Joel M. Stein, Kathryn A. Davis   +16 more
wiley   +1 more source

Neuro-ophthalmic manifestations in a cohort of Ebola virus disease survivors from Sierra Leone: Ocular implications during convalescence

Heliyon
Background: We aim to characterize the spectrum of neuro-ophthalmic manifestations and their impact on visual acuity in a cohort of Ebola virus disease (EVD) survivors from the Western African outbreak from 2013 to 2016. Methods: Patients, who previously
Nam V. Nguyen, Tolulope Fashina, Ye Huang, Casey Randleman, Jean-Claude Mwanza, Jalikatu Mustapha, Matthew Jusu Vandy, Lloyd Harrison-Williams, Brent R. Hayek, Ian Crozier, Rod Foroozan, Jessica G. Shantha, Steven Yeh   +12 more
doaj   +1 more source

Test Your Knowledge - Disorders of Ocular Motility, Alignment, Pupils, and Lids - Case 35

Test your knowledge of disorders of ocular motility, alignment, pupils, and ...
Jonathan D. Trobe, MD
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Disorders of Ocular Motility in Childhood

, 1988
Ocular motility disturbances In childhood encompass a somewhat broader range of diagnostic posslblities than similar disturbances seen In adults.
Charles G. Maitland, MD
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Periodic Alternating Nystagmus Due to a Chiari Malformation - The Role of the Vestibulocerebellum in Ocular Motor Function

, 2023
We describe a 53-year-old woman presenting with oscillopsia and ocular motor abnormalities due to a Chiari I malformation, in the absence of headaches. The vestibulocerebellum can be thought of as two functional units: 1) flocculus/paraflocculus (tonsil)
Claire Allen; Daniel Gold
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MOGAD Is the Most Common Cause of Isolated Optic Neuritis in Children

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objectives The study aimed to characterize the clinical features, etiologies, and outcomes of isolated, first‐time pediatric ON in the post‐MOG‐IgG era. Methods This was a single‐center retrospective cohort study at Texas Children's Hospital of patients diagnosed with first‐time ON between 2018–2024, with follow‐up data collected through 2025.
Chaitanya Aduru, Akansha Chandrasekar, Kyla Blasingame, Jonathan Rosen, Jesse M. Levine, Karla Salazar, Madhuri Chilakapati, Rod Foroozan, Victoria Hardwick, Jonathan M. Yarimi, Nikita Shukla, Timothy E. Lotze, Kristen S. Fisher, Alexander J. Sandweiss   +13 more
wiley   +1 more source

Ocular Motility Disorders Due to Cerebral and Basal Ganglia Disease (abstract)

, 2016
Where we look determines what we see. Because human vision varies greatly with retinotopic location, with high spatial resolution limited to the fovea, humans have evolved a sophisticated ocular motor system, much of it aimed at stabilizing vision on ...
Jason J. S. Barton, MD PhD FRCP(C)
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Comprehensive Characterization of 98 Chinese Cases of Genetic Creutzfeldt‐Jakob Disease With T188K Mutation

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective To characterize the demographic, clinical, and laboratory features of the Chinese patients of genetic Creutzfeldt‐Jakob disease with T188K variant (T188K‐gCJD), the most common subtype of genetic prion diseases (gPrDs) in China. Methods In this nationwide retrospective study, data from 98 genetically confirmed T188K‐gCJD patients ...
Chun‐Jie Li, Dong‐Lin Liang, Li‐Ping Gao, Wei‐Wei Zhang, Wei Zhou, A. Ruhan, Bing Xu, Run‐Dong Cao, Kang Xiao, Cao Chen, Qi Shi, Xiao‐Ping Dong   +11 more
wiley   +1 more source

Ophthalmic complications of spina bifida and hydrocephalus

, 1986
This thesis represents an attempt to further our knowledge of the ophthalmic complications of spina bifida and hydrocephalus by means of literature review and a long term clinical study, and to determine whether regular ophthalmic supervision can assist ...
Gaston, Hannah
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