Results 151 to 160 of about 70,653 (310)

Ocular Motor Abnormalities in Functional Neurological Disorder: A Video‐Oculography Study

open access: yesMovement Disorders Clinical Practice, Volume 13, Issue 3, Page 711-722, March 2026.
Abstract Background Functional neurological disorders (FND) can include various sensory, motor or cognitive symptoms. Eye movement recordings, measured through video‐oculography, could serve as biomarkers for characterizing these dysfunctions in FND.
Aude Sangare   +13 more
wiley   +1 more source

The Prevalence and Severity of Acquired Blepharoptosis in US Eye Care Clinic Patients and Their Receptivity to Treatment

open access: yesClinical Ophthalmology
Cynthia Matossian Matossian Eye Associates, Doylestown, PA, USACorrespondence: Cynthia Matossian, 3096 Comfort Road, New Hope, Doylestown, PA, 18938, USA, Tel +1 215-208-6944, Email cmatossianmd@icloud.comPurpose: To assess the presence and severity of ...
Matossian C
doaj  

What the Eyelid Can Tell You: The Unexpected Initial Presentation of De Novo Stage IV Breast Carcinoma

open access: yesJournal of Cutaneous Pathology, Volume 53, Issue 3, Page 248-253, March 2026.
ABSTRACT A 66‐year‐old female presented with seven months of progressive right upper eyelid (RUL) drooping and thickening of her right lower eyelid (RLL). MRI revealed soft tissue enhancement of the RUL and RLL pre‐septal planes without posterior extension.
Grace L. Casado   +4 more
wiley   +1 more source

PTOSIS OPERATION [PDF]

open access: yesBritish Journal of Ophthalmology, 1926
openaire   +2 more sources

Mersilene mesh sling as an alternative to autogenous fascia lata in the management of ptosis [PDF]

open access: bronze, 2001
Essam El-Toukhy   +4 more
openalex   +1 more source

Wernicke Encephalopathy Complicating a Distinctive POLG Phenotype With MNGIE‐Like Features

open access: yesEuropean Journal of Neurology, Volume 33, Issue 3, March 2026.
ABSTRACT Background Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE) is an extremely rare autosomal recessive disease caused by variants in the thymidine phosphorylase gene (TYMP), primarily characterized by severe gastrointestinal and neurological symptoms.
Giuliana Capece   +13 more
wiley   +1 more source

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