[HTML][HTML] Monosomy of chromosome 3 and an inflammatory phenotype occur together in uveal melanoma

W Maat, LV Ly, ES Jordanova… - … & visual science, 2008 - tvst.arvojournals.org
purpose. In uveal melanoma, different predictors of poor prognosis have been identified,
including monosomy of chromosome 3, HLA expression, and the presence of infiltrating …

Long term follow up of premature infants: detection of strabismus, amblyopia, and refractive errors

NE Schalij-Delfos, MEL de Graaf, WF Treffers… - British journal of …, 2000 - bjo.bmj.com
AIM To establish recommendations for long term ophthalmological follow up of prematurely
born infants. METHODS 130 infants with a gestational age (GA)< 37 weeks and born …

The phenotypic spectrum of albinism

CC Kruijt, GC de Wit, AA Bergen, RJ Florijn… - Ophthalmology, 2018 - Elsevier
Purpose To describe the phenotypic spectrum of a large cohort of albino patients, to
investigate the relationship between the ocular abnormalities and the visual acuity (VA), and …

Genotypic and phenotypic characteristics of CRB1-associated retinal dystrophies: a long-term follow-up study

M Talib, MJ van Schooneveld, MM van Genderen… - Ophthalmology, 2017 - Elsevier
Purpose To describe the phenotype, long-term clinical course, clinical variability, and
genotype of patients with CRB1-associated retinal dystrophies. Design Retrospective cohort …

Screening for refractive errors in children: the plusoptiX S08 and the Retinomax K-plus2 performed by a lay screener compared to cycloplegic retinoscopy

T Paff, AM Oudesluys-Murphy, R Wolterbeek… - Journal of American …, 2010 - Elsevier
PURPOSE: To evaluate the performance of the autorefractor Retinomax K-plus2 and the
photoscreener plusoptiX S08 in measuring refractive errors by comparing them with …

Visual outcome in Sturge–Weber syndrome: a systematic review and Dutch multicentre cohort

Y Koenraads, MB van Egmond‐Ebbeling… - Acta …, 2016 - Wiley Online Library
Abstract Visual functions in Sturge–Weber syndrome (SWS) may be impaired by glaucoma,
diffuse choroidal haemangioma (DCH) or leptomeningeal angioma. The aim of this study …

Clinical and genetic characteristics of male patients with RPGR-associated retinal dystrophies: a long-term follow-up study

M Talib, MJ Van Schooneveld, AA Thiadens, M Fiocco… - Retina, 2019 - journals.lww.com
Purpose: To describe the phenotype and clinical course of patients with RPGR-associated
retinal dystrophies, and to identify genotype–phenotype correlations. Methods: A multicenter …

The heterogeneous distribution of monosomy 3 in uveal melanomas: implications for prognostication based on fine-needle aspiration biopsies

W Maat, ES Jordanova… - … of pathology & …, 2007 - meridian.allenpress.com
Context.—The detection of monosomy 3 in uveal melanomas has repeatedly been
associated with adverse outcome. Fine-needle aspiration biopsy is being used to detect …

[HTML][HTML] CRB1-associated retinal dystrophies: a prospective natural history study in anticipation of future clinical trials

M Talib, MJ van Schooneveld, J Wijnholds… - American Journal of …, 2022 - Elsevier
PURPOSE To investigate the natural disease course of retinal dystrophies associated with
crumbs cell polarity complex component 1 (CRB1) and identify clinical end points for future …

Long-term outcomes of eye-conserving treatment with Ruthenium106 brachytherapy for choroidal melanoma

KMS Verschueren, CL Creutzberg… - Radiotherapy and …, 2010 - Elsevier
PURPOSE: To evaluate long-term outcomes of eye-conserving treatment using Ruthenium-
106 plaque brachytherapy with or without transpupillary thermotherapy (TTT) for small to …