Results 161 to 170 of about 2,573,157 (336)

Automated detection of steps in videos of strabismus surgery using deep learning

BMC Ophthalmology
Background Learning to perform strabismus surgery is an essential aspect of ophthalmologists’ surgical training. Automated classification strategy for surgical steps can improve the effectiveness of training curricula and the efficient evaluation of ...
Ce Zheng, Wen Li, Siying Wang, Haiyun Ye, Kai Xu, Wangyi Fang, Yanli Dong, Zilei Wang, Tong Qiao   +8 more
doaj   +1 more source

The outcome of strabismus surgery in childhood exotropia [PDF]

, 1994
J M Keenan, H E Willshaw
openalex   +1 more source

Autoantibodies against TRIM46 identified in a dog suffering from suspected meningoencephalomyelitis of unknown origin

Journal of Small Animal Practice, EarlyView.
P. L. Heidemann, A. C. Nilsson, S. G. Schmidt, E. Lattwein, C. Allberg, M. Blaabjerg, H. Gredal   +6 more
wiley   +1 more source

Ocular Findings as the Most Striking Manifestation of a SMAD3 Variant

American Journal of Medical Genetics Part A, Volume 197, Issue 10, October 2025.
ABSTRACT Loeys‐Dietz syndrome (LDS) is a heritable connective tissue disorder with variable expressivity. It is a multisystemic condition mainly characterized by a propensity for arterial aneurysms and dissections, skeletal manifestations, hypertelorism, bifid uvula, craniosynostosis, and cutaneous features.
Noémie Villeneuve‐Cloutier, Christie A Boswell‐Patterson, Lucas Bronicki, Krista M. Vincent, Kalin Wilk, Andrea C. Yu, Gail E. Graham, Julie Richer   +7 more
wiley   +1 more source

Antiemetic prophylaxis with promethazine or droperidol in paediatric outpatient strabismus surgery [PDF]

, 1991
Victor Faria Blanc, Pierre Ruest, Jean Milot, Jean‐Louis Jacob, Alexander Tang   +4 more
openalex   +1 more source

A Case of Hereditary Spastic Paraplegia Type 50 With a Novel AP4M1 Variant and a Brief Review of the Literature

Clinical Case Reports, Volume 13, Issue 10, October 2025.
ABSTRACT We report a case of hereditary spastic paraplegia type 50, an extremely rare disease characterized by upper motor neuron dysfunction. This case underscores the importance of considering genetic etiologies in patients previously diagnosed with cerebral palsy, especially when clinical history, presentation, and imaging findings are inconsistent ...
Ana Teresa Guerra, André M. Travessa, José Paulo Monteiro   +2 more
wiley   +1 more source

Strabismus management in retinoblastoma survivors

BMC Ophthalmology
Purpose To report the result of strabismus surgery in eye-salvaged retinoblastoma (Rb) patients. Methods A retrospective case series including 18 patients with Rb and strabismus who underwent strabismus surgery after completing tumor treatment by a ...
Babak Masoomian, Carol L. Shields, Hamid Riazi Esfahani, Atefeh Khalili, Fariba Ghassemi, Pukhraj Rishi, Mohammad Reza Akbari, Masoud Khorrami-Nejad   +7 more
doaj   +1 more source

COL4A1‐Related Leukoencephalopathy and Microangiopathy: A Case Series of Two Palestinian Siblings

Clinical Case Reports, Volume 13, Issue 10, October 2025.
ABSTRACT We report two Palestinian siblings with a pathogenic COL4A1 mutation, presenting with congenital cataracts, seizures, developmental delay, and antenatal intracerebral hemorrhages. Despite sharing the same genetic variant, they exhibited striking phenotypic variability.
Thkra Meshal, Amal M. Shawabka, Kareem lbraheem, Rosol Iwaiwi, Nissreen E. Thafer, Jinan H. Afana, Ahmad G. Hammouri, Osama Atawneh   +7 more
wiley   +1 more source

تاثير ليدوکائين وريدی بر درد، آرامش و تهوع و استفراغ پس از اعمال جراحی استرابيسم [PDF]

, 2014
زمينه و هدف : اثرات ضد درد ليدوکايين وريدی در بعضی از مطالعات نشان داده شده است. بلوک‌کننده‌های کانال سديم نيز به‌صورت داخل وريدی برای درمان دردهای نوروپاتيک مورد قبول واقع شده‌اند.
حسنی, ابراهیم, ماهوری, علیرضا, مترجمی زاده, قادر, مجتهدی, شهرزاد   +3 more
core  

A Further Case Supporting PDCD6IP as the Gene Responsible for a Neurodevelopmental Disorder With Microcephaly

Clinical Genetics, Volume 108, Issue 4, Page 488-490, October 2025.
Summary of clinical and molecular findings in patients with biallelic variants in PDCD6IP.
Alfonso Manuel D'Alessio, Annalaura Torella, Manuela Morleo, Vincenzo Nigro, TUDP Study Group, Nicola Brunetti‐Pierri   +5 more
wiley   +1 more source