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Lista de obras de Robert Henderson

A homozygous mutation in the TUB gene associated with retinal dystrophy and obesity

artículo científico publicado en 2013

A novel technique for high-density silicone oil removal

artículo científico publicado en 2012

Accuracy of scleral transillumination techniques to identify infant ciliary body for sclerostomy and intravitreal injections

scientific article published on 10 December 2018

An assessment of the apex microarray technology in genotyping patients with Leber congenital amaurosis and early-onset severe retinal dystrophy

artículo científico publicado en 2007

Clinical Characterization of CNGB1-Related Autosomal Recessive Retinitis Pigmentosa

artículo científico publicado en 2017

Early Onset Retinal Dystrophy Due to Mutations inLRAT: Molecular Analysis and Detailed Phenotypic Study

article

Effect of gene therapy on visual function in Leber's congenital amaurosis

artículo científico publicado en 2008

Group A streptococcal endophthalmitis complicating a sore throat in a 2-year-old child

artículo científico publicado en 2015

Immediate Sequential Bilateral Pediatric Vitreoretinal Surgery: An International Multicenter Study.

artículo científico publicado en 2016

Leber congenital amaurosis associated with AIPL1: challenges in ascribing disease causation, clinical findings, and implications for gene therapy.

artículo científico publicado en 2012

Misaligned foveal morphology and sector retinal dysfunction in AKT1-mosaic Proteus syndrome

artículo científico publicado en 2020

Missense variants in the X-linked gene PRPS1 cause retinal degeneration in females

artículo científico publicado en 2017

Novel mutations in MERTK associated with childhood onset rod-cone dystrophy

artículo científico publicado en 2010

Phenotypic variability in patients with retinal dystrophies due to mutations in CRB1.

artículo científico publicado en 2010

RDH12 retinopathy: novel mutations and phenotypic description.

artículo científico publicado en 2011

Screening of SPATA7 in patients with Leber congenital amaurosis and severe childhood-onset retinal dystrophy reveals disease-causing mutations.

artículo científico publicado en 2011

The Oculome Panel Test: Next-Generation Sequencing to Diagnose a Diverse Range of Genetic Developmental Eye Disorders

scientific article published on 14 January 2019

Wound-related complications and clinical outcomes following open globe injury repair

artículo científico publicado en 2015