Results 41 to 50 of about 13,290 (279)
EFFICACY OF TOPICAL ANAESTHESIA IN REDUCTION OF OCULOCARDIAC REFLEX DURING SQUINT SURGERY
Objective: To determine the efficacy of Topical Anaesthesiain reduction of oculocardiac reflex incidence and severity in patients undergoing squint surgery under general anaesthesia. Study Design: Quasi-Experimental Study.
Sana Abbas +5 more
doaj
Congenital cataracts presenting as a childhood squint
Aim: A timely reminder that a small posterior subcapsular cataract could present with a squint. Methods: A case series is reported of 4 patients who were referred to the paediatric ophthalmology service for management of a squint.
Shanel Sharma +2 more
doaj +1 more source
To reveal the dynamics of the development of the morphological changes in lateral geniculate nuclei caused by binocular vision impairment, we study the changes in density of SMI-32 immunopositive neurons in the frontal sections of the LGNd of both ...
Polina Y. Shkorbatova +2 more
doaj +1 more source
ABSTRACT ADNP‐related Helsmoortel–Van der Aa syndrome (ADNP‐related HVDAS) is a single gene form of autism spectrum disorder (ASD) caused by pathogenic sequence variants in the activity‐dependent neuroprotective protein (ADNP) gene. In addition to ASD, ADNP‐related HVDAS is associated with a wide range of cognitive, behavioral, and physical health ...
Jarrett Fastman +11 more
wiley +1 more source
Sidelobe reduction is a very primary task for synthetic aperture radar (SAR) images. Various methods have been proposed for broadside SAR, which can suppress the sidelobes effectively while maintaining high image resolution at the same time ...
Min Liu, Zhou Li, Lu Liu
doaj +1 more source
Spatial IDFT for Squint-Free Massive Arrays
This paper presents a novel technique to build squint-free massive phased arrays. This is accomplished by explicitly implementing a spatial IDFT to cancel out the DFT imposed by the array nature which causes beam squint.
Niknejad, Ali, Beshary, Hesham
core
A Novel Constitutional TUBB Variant Associated With Familial Malformations of Cortical Development
ABSTRACT Most pathogenic tubulin variants arise de novo in sporadic patients, causing severe brain malformations and significant neurodevelopmental impairment. The resulting reproductive disadvantage typically prevents these mutations from being transmitted to offspring.
Elena Cellini +9 more
wiley +1 more source
Expanding the Phenotypic Spectrum of TXNDC15‐Related Ciliopathies to Include Joubert Syndrome
ABSTRACT Biallelic loss‐of‐function variants in TXNDC15 are a known cause of the perinatally lethal ciliopathy Meckel syndrome (MKS). TXNDC15 encodes an endoplasmic reticulum (ER)‐resident thioredoxin‐domain protein required for ciliary transition zone integrity.
Zachary T. Sentell +16 more
wiley +1 more source

