FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

Isabelle Russell-Eggitt

Research Profile

Living Beings

Disorders

Physiology

Procedures

Concepts & Ideas

Anatomy

Co-author Network

Publications

TOP 3
Emma Glamuzina; Garry Brown; Ruth Brown; Carlos de Sousa; Kieran Hogarth; Matthew Pitt; Shamima Rahman; Isabelle Russell-Eggitt; Dawn Saunders; Stephanie Grunewald
Further delineation of pontocerebellar hypoplasia type 6 due to mutations in the gene encoding mitochondrial arginyl-tRNA synthetase, RARS2.
Shaheen P Shah; Jane C Sowden; Amy E Taylor; Clare E Gilbert; Nicola K Ragge; Jugnoo S Rahi; Isabelle Russell-Eggitt
Anophthalmos, microphthalmos, and Coloboma in the United kingdom: clinical features, results of investigations, and early management.
Mei Hong Tan; Dorothy A Thompson; Hoai Viet Tran; Andrew R Webster; Genevieve A Wright; Phillip Moradi; Anthony G Robson; Isabelle Russell-Eggitt; Alexander J Smith; Robin R Ali; Michael Cheetham; Jill Cowing; Arundhati Dev-Borman; Robert H Henderson; Mackay Donna; Robert E MacLaren; Michel Michaelides; Anthony T Moore
Leber congenital amaurosis associated with AIPL1: challenges in ascribing disease causation, clinical findings, and implications for gene therapy.

Register for free to view:

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the research activity
of experts around the globe

Geonetwork of Isabelle Russell-Eggitt (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

All Publications

2012: Emma Glamuzina; Garry Brown; Ruth Brown; Carlos de Sousa; Kieran Hogarth; Matthew Pitt; Shamima Rahman; Isabelle Russell-Eggitt; Dawn Saunders; Stephanie Grunewald
Further delineation of pontocerebellar hypoplasia type 6 due to mutations in the gene encoding mitochondrial arginyl-tRNA synthetase, RARS2.
Journal of inherited metabolic disease 2012;35(3):459-67.
2012: Shaheen P Shah; Jane C Sowden; Amy E Taylor; Clare E Gilbert; Nicola K Ragge; Jugnoo S Rahi; Isabelle Russell-Eggitt
Anophthalmos, microphthalmos, and Coloboma in the United kingdom: clinical features, results of investigations, and early management.
Ophthalmology 2012;119(2):362-8.
2012: Mei Hong Tan; Dorothy A Thompson; Hoai Viet Tran; Andrew R Webster; Genevieve A Wright; Phillip Moradi; Anthony G Robson; Isabelle Russell-Eggitt; Alexander J Smith; Robin R Ali; Michael Cheetham; Jill Cowing; Arundhati Dev-Borman; Robert H Henderson; Mackay Donna; Robert E MacLaren; Michel Michaelides; Anthony T Moore
Leber congenital amaurosis associated with AIPL1: challenges in ascribing disease causation, clinical findings, and implications for gene therapy.
PloS one 2012;7(3):e32330.
2011: Robert H Henderson; Mackay Donna; Zheng Li; Phillip Moradi; Panagiotis Sergouniotis; Isabelle Russell-Eggitt; Dorothy A Thompson; Anthony G Robson; Graham E Holder; Andrew R Webster; Anthony T Moore
Phenotypic variability in patients with retinal dystrophies due to mutations in CRB1.
The British journal of ophthalmology 2011;95(6):811-7.
2011: Dorothy A Thompson; Sally Feather; Horia C Stanescu; Bernard Freudenthal; Anselm A Zdebik; Richard Warth; Milos Ognjanovic; Sally A Hulton; Evangeline Wassmer; William G Van't Hoff; Isabelle Russell-Eggitt; Angus Dobbie; Eamonn Sheridan; Robert Kleta; Detlef Bockenhauer
Altered electroretinograms in patients with KCNJ10 mutations and EAST syndrome.
The Journal of physiology 2011;589(Pt 7):1681-9.
2011: Shaheen P Shah; Amy E Taylor; Jane C Sowden; Nicola K Ragge; Isabelle Russell-Eggitt; Jugnoo S Rahi; Clare E Gilbert
Anophthalmos, microphthalmos, and typical coloboma in the United Kingdom: a prospective study of incidence and risk.
Investigative ophthalmology & visual science 2011;52(1):558-64.
2010: Göran Darius Hildebrand; Isabelle Russell-Eggitt; Dawn Saunders; William F Hoyt; David S I Taylor
Bow-tie cupping: a new sign of chiasmal compression.
Archives of ophthalmology 2010;128(12):1625-6.
2010: Ken K Nischal; Lola Solebo; Isabelle Russell-Eggitt
Paediatric IOL implantation and postoperative refractive state: what role do study methodology and surgical technique play?
The British journal of ophthalmology 2010;94(5):529-31.
2009: Peter J Minogue; Jun-Jie Tong; Anita Arora; Isabelle Russell-Eggitt; David Hunt; Anthony T Moore; Lisa Ebihara; Eric C Beyer; Viviana M Berthoud
A mutant connexin50 with enhanced hemichannel function leads to cell death.
Investigative ophthalmology & visual science 2009;50(12):5837-45.
2009: Ameeta Mehta; Peter C Hindmarsh; Hiten Mehta; James P G Turton; Isabelle Russell-Eggitt; David Taylor; W K Chong; Mehul T Dattani
Congenital hypopituitarism: clinical, molecular and neuroradiological correlates.
Clinical endocrinology 2009;71(3):376-82.
2008: Sérgio B Sousa; Isabelle Russell-Eggitt; Christine Hall; Bryan D Hall; Raoul Hennekam
Further delineation of spondylometaphyseal dysplasia with cone-rod dystrophy.
American journal of medical genetics. Part A 2008;146A(24):3186-94.
2008: Cecilie Bredrup; Verena Matejas; Margaret Barrow; Kveta Bláhová; Detlef Bockenhauer; DJ Fowler; Richard M Gregson; Iwona Maruniak-Chudek; Ana Medeira; Erica Laima Mendonça; Mikhail Kagan; Jens Koenig; Hermann Krastel; Hester Y Kroes; Anand Saggar; Taylor Sawyer; Michael Schittkowski; Janusz Swietliński; Dorothy Thompson; Rene G VanDeVoorde; Dienke Wittebol-Post; Geoffrey Woodruff; Aleksandra Zurowska; Raoul Hennekam; Martin Zenker; Isabelle Russell-Eggitt
Ophthalmological aspects of Pierson syndrome.
American journal of ophthalmology 2008;146(4):602-611.
2008: R Goyal; D Thompson; Christine Timms; Louise C Wilson; Isabelle Russell-Eggitt
Review of cases presenting with microcephaly and bilateral congenital cataract in a paediatric cataract clinic.
Eye (London, England) 2008;22(2):273-81.
2007: Robert H Henderson; Naushin Waseem; Rowan Searle; Jacqueline van der Spuy; Isabelle Russell-Eggitt; Shomi S Bhattacharya; Dorothy A Thompson; Graham Holder; Michael Cheetham; Andrew R Webster; Anthony T Moore
An assessment of the apex microarray technology in genotyping patients with Leber congenital amaurosis and early-onset severe retinal dystrophy.
Investigative ophthalmology & visual science 2007;48(12):5684-9.
2007: Konal Saha; Christopher Lloyd; Isabelle Russell-Eggitt; David Samuel Irving Taylor
Chromosomal abnormalities and glaucoma: a case of congenital glaucoma associated with 9p deletion syndrome.
Ophthalmic genetics 2007;28(2):69-72.
2006: Kaan Boztug; Kwabena Frimpong-Ansah; Vasanta Rao Nanduri; Joanna Lawson; Isabelle Russell-Eggitt; Penelope Brock
Intraocular Langerhans cell histiocytosis in a neonate resulting in bilateral loss of vision.
Pediatric blood & cancer 2006;47(5):633-5.
2006: Christine Timms; Dorothy Thompson; Isabelle Russell-Eggitt; Richard Clement
Saccadic instabilities in albinism without nystagmus.
Experimental brain research. Experimentelle Hirnforschung. Expérimentation cérébrale 2006;175(1):45-9.
2005: D A Sami; D Saunders; Dorothy A Thompson; Isabelle Russell-Eggitt; Ken K Nischal; G Jeffrey; G Jeffery; M Dattani; R A Clement; Alki Liasis; A Liassis; David S I Taylor
The achiasmia spectrum: congenitally reduced chiasmal decussation.
The British journal of ophthalmology 2005;89(10):1311-7.
2005: James D McKay; B Patterson; Jamie E Craig; Isabelle Russell-Eggitt; M Gabriela Wirth; Kathryn P Burdon; Alex W Hewitt; Amy C Cohn; Y Kerdraon; David A Mackey
The telomere of human chromosome 1p contains at least two independent autosomal dominant congenital cataract genes.
The British journal of ophthalmology 2005;89(7):831-4.
2005: Nicola K Ragge; Alison G Brown; Charlotte M Poloschek; Birgit Lorenz; R Alex Henderson; Michael P Clarke; Isabelle Russell-Eggitt; Alistair Fielder; Dianne Gerrelli; Juan Pedro Martinez-Barbera; Piers Ruddle; Jane Hurst; J R O Collin; Alison Salt; Simon T Cooper; Pamela J Thompson; Sanjay M Sisodiya; Kathleen A Williamson; David R FitzPatrick; Veronica van Heyningen; Isabel M Hanson
Heterozygous mutations of OTX2 cause severe ocular malformations.
American journal of human genetics 2005;76(6):1008-22.
2005: Kunal Dansingani; Ayman al-Khaier; Isabelle Russell-Eggitt; Ken K Nischal
Management of intracorneal bleb after trabeculectomy for congenital glaucoma.
Cornea 2005;24(4):486-8.
2005: Jan D Marshall; Roderick T Bronson; Gayle B Collin; Anne D Nordstrom; Pietro Maffei; Richard B Paisey; Catherine Carey; Seamus Macdermott; Isabelle Russell-Eggitt; Sarah E Shea; Judy Davis; Sebastian Beck; Gocha Shatirishvili; Cristina Maria Mihai; Maria Hoeltzenbein; Giovanni Battista Pozzan; Ian Hopkinson; Nicola Sicolo; Jürgen K Naggert; Patsy M Nishina
New Alström syndrome phenotypes based on the evaluation of 182 cases.
Archives of internal medicine 2005;165(6):675-83.
2004: Göran Darius Hildebrand; Christine Timms; Dorothy A Thompson; David J Atherton; Marian Malone; Gill A Levitt; D A H Laidlaw; Isabelle Russell-Eggitt; David S I Taylor
Juvenile xanthogranuloma with presumed involvement of the optic disc and retina.
Archives of ophthalmology 2004;122(10):1551-5.
2004: Peter R Hodgkins; Christopher M Harris; Fatima Shawkat; Dorothy A Thompson; Kling Chong; Christine Timms; Isabelle Russell-Eggitt; David S I Taylor; Anthony Kriss
Joubert syndrome: long-term follow-up.
Developmental medicine and child neurology 2004;46(10):694-9.
2004: Kathryn P Burdon; M Gabriela Wirth; David A Mackey; Isabelle Russell-Eggitt; Jamie E Craig; James E Elder; Joanne L Dickinson; Michèle M Sale
A novel mutation in the Connexin 46 gene causes autosomal dominant congenital cataract with incomplete penetrance.
Journal of medical genetics 2004;41(8):e106.
2004: M Vishwanath; R Cheong-Leen; D Taylor; Isabelle Russell-Eggitt; Jugnoo S Rahi
Is early surgery for congenital cataract a risk factor for glaucoma?
The British journal of ophthalmology 2004;88(7):905-10.
2004: Kathryn P Burdon; M Gabriela Wirth; David A Mackey; Isabelle Russell-Eggitt; Jamie E Craig; James E Elder; Joanne L Dickinson; Michèle M Sale
Investigation of crystallin genes in familial cataract, and report of two disease associated mutations.
The British journal of ophthalmology 2004;88(1):79-83.
2003: Klaus Werner; Jon Pritchard; Marjatta Lappi; Isabelle Russell-Eggitt; Mervi Taskinen; Markku Heikinheimo
Chronic papilloedema due to intra-orbital Langerhans cell histiocytosis.
Medical and pediatric oncology 2003;41(6):580-3.
2003: Margarita Indelman; Christian P Hamel; Reuven Bergman; Ken K Nischal; Dorothy Thompson; Marie-Odile Surget; Michal Ramon; Hatam Ganthos; Benjamin Miller; Gabriele Richard; raziel lurie; Rina Leibu; Isabelle Russell-Eggitt; Eli Sprecher
Phenotypic diversity and mutation spectrum in hypotrichosis with juvenile macular dystrophy.
The Journal of investigative dermatology 2003;121(5):1217-20.
2003: Kathryn P Burdon; James D McKay; Michèle M Sale; Isabelle Russell-Eggitt; David A Mackey; M Gabriela Wirth; James E Elder; Alan Nicoll; Michael P Clarke; Liesel M FitzGerald; Jim Stankovich; Marie A Shaw; Shiwani Sharma; Srecko Gajovic; Peter Gruss; Shelley Ross; Paul Thomas; Anne K Voss; Tim Thomas; Jozef Gécz; Jamie E Craig
Mutations in a novel gene, NHS, cause the pleiotropic effects of Nance-Horan syndrome, including severe congenital cataract, dental anomalies, and mental retardation.
American journal of human genetics 2003;73(5):1120-30.
2003: Richard A King; Jacy Pietsch; James P Fryer; Sarah Savage; Marcia J Brott; Isabelle Russell-Eggitt; C Gail Summers; William S Oetting
Tyrosinase gene mutations in oculocutaneous albinism 1 (OCA1): definition of the phenotype.
Human genetics 2003;113(6):502-13.
2003: Luis Amaya; David Taylor; Isabelle Russell-Eggitt; Ken K Nischal; Dora Lengyel
The morphology and natural history of childhood cataracts.
Survey of ophthalmology 2003;48(2):125-44.
2003: Isabelle Russell-Eggitt; James V Leonard; AM Lund; B Manoj; D A Thompson; A A M Morris
Cataract in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency (LCHADD).
Ophthalmic genetics 2003;24(1):49-57.
2003: Nicola K Ragge; C Hartley; A M Dearlove; J Walker; Isabelle Russell-Eggitt; Christopher M Harris
Familial vestibulocerebellar disorder maps to chromosome 13q31-q33: a new nystagmus locus.
Journal of medical genetics 2003;40(1):37-41.
2002: Jugnoo S Rahi; Stuart Logan; Mario Cortina Borja; Christine Timms; Isabelle Russell-Eggitt; David Taylor
Prediction of improved vision in the amblyopic eye after visual loss in the non-amblyopic eye.
Lancet 2002;360(9333):621-2.
2002: Jugnoo S Rahi; Stuart Logan; Christine Timms; Isabelle Russell-Eggitt; David Taylor
Risk, causes, and outcomes of visual impairment after loss of vision in the non-amblyopic eye: a population-based study.
Lancet 2002;360(9333):597-602.
2002: M Gabriela Wirth; Isabelle Russell-Eggitt; Jamie E Craig; James E Elder; David A Mackey
Aetiology of congenital and paediatric cataract in an Australian population.
The British journal of ophthalmology 2002;86(7):782-6.
2002: Tom Hearn; Glenn L Renforth; Cosma Spalluto; Neil A Hanley; Karen Piper; Sarah Brickwood; Chris White; Vincent Connolly; James F N Taylor; Isabelle Russell-Eggitt; Dominque Bonneau; Mark Walker; David I Wilson
Mutation of ALMS1, a large gene with a tandem repeat encoding 47 amino acids, causes Alström syndrome.
Nature genetics 2002;31(1):79-83.
2002: Gayle B Collin; Jan D Marshall; Akihiro Ikeda; W Venus So; Isabelle Russell-Eggitt; Pietro Maffei; Sebastian Beck; Cornelius F Boerkoel; Nicola Sicolo; Mitchell Martin; Patsy M Nishina; Jürgen K Naggert
Mutations in ALMS1 cause obesity, type 2 diabetes and neurosensory degeneration in Alström syndrome.
Nature genetics 2002;31(1):74-8.
2002: C Harrison; Kate Khair; B Baxter; Isabelle Russell-Eggitt; Ian Hann; Ri Liesner
Hermansky-Pudlak syndrome: infrequent bleeding and first report of Turkish and Pakistani kindreds.
Archives of disease in childhood 2002;86(4):297-301.
2001: Isabelle Russell-Eggitt
Albinism.
Ophthalmology clinics of North America 2001;14(3):533-46.
2001: David Taylor; K W Wright; L Amaya; L Cassidy; Ken K Nischal; Isabelle Russell-Eggitt; S Lightman; P McCluskey
Should we aggressively treat unilateral congenital cataracts?
The British journal of ophthalmology 2001;85(9):1120-6.
2001: Jugnoo S Rahi; G Adams; Isabelle Russell-Eggitt; Pat A Tookey
Epidemiological surveillance of rubella must continue.
BMJ (Clinical research ed.) 2001;323(7304):112.
2001: L Cassidy; Jugnoo S Rahi; Ken K Nischal; Isabelle Russell-Eggitt; David Taylor
Outcome of lens aspiration and intraocular lens implantation in children aged 5 years and under.
The British journal of ophthalmology 2001;85(5):540-2.
2000: Isabelle Russell-Eggitt
Non-syndromic posterior lenticonus a cause of childhood cataract: evidence for X-linked inheritance.
Eye (London, England) 2000;14(Pt 6):861-3.
2000: Isabelle Russell-Eggitt; D A Thompson; Kate Khair; Ri Liesner; Ian Hann
Hermansky-Pudlak syndrome presenting with subdural haematoma and retinal haemorrhages in infancy.
Journal of the Royal Society of Medicine 2000;93(11):591-2.
2000: Isabelle Russell-Eggitt; D A Mackey; David S I Taylor; Christine Timms; J W Walker
Vigabatrin-associated visual field defects in children.
Eye (London, England) 2000;14 ( Pt 3A)():334-9.
2000: A W Talbot; Isabelle Russell-Eggitt
Pharmaceutical management of the childhood glaucomas.
Expert opinion on pharmacotherapy 2000;1(4):697-711.
2000: Fatima Shawkat; Anthony Kriss; D Thompson; Isabelle Russell-Eggitt; David Taylor; C Harris
Vertical or asymmetric nystagmus need not imply neurological disease.
The British journal of ophthalmology 2000;84(2):175-80.
2000: Peter R Hodgkins; Anthony Kriss; S Boyd; Kling Chong; D Thompson; David S I Taylor; Isabelle Russell-Eggitt; Christopher M Harris
A study of EEG, electroretinogram, visual evoked potential, and eye movements in classical lissencephaly.
Developmental medicine and child neurology 2000;42(1):48-52.
1999: Dorothy A Thompson; Anthony Kriss; Kling Chong; C Harris; Isabelle Russell-Eggitt; Fatima Shawkat; B G Neville; W Aclimandos; David S I Taylor
Visual-evoked potential evidence of chiasmal hypoplasia.
Ophthalmology 1999;106(12):2354-61.
1999: David Goldblatt; J Butcher; Adrian J Thrasher; Isabelle Russell-Eggitt
Chorioretinal lesions in patients and carriers of chronic granulomatous disease.
The Journal of pediatrics 1999;134(6):780-3.
1999: Louis Tong; Peter R Hodgkins; J Denyer; D Brosnahan; J Harper; Isabelle Russell-Eggitt; David S I Taylor; David J Atherton
The eye in epidermolysis bullosa.
The British journal of ophthalmology 1999;83(3):323-6.
1999: O Backhouse; R J Leitch; D Thompson; Anthony Kriss; D Charris; P Clayton; Isabelle Russell-Eggitt
A case of reversible blindness in maple syrup urine disease.
The British journal of ophthalmology 1999;83(2):250-1.
1998: L F Smith; Isabelle Russell-Eggitt; J Harper
Familial pseudoxanthoma elasticum.
Ophthalmic genetics 1998;19(3):169-71.
1998: Isabelle Russell-Eggitt; P T Clayton; R Coffey; Anthony Kriss; David S I Taylor; J F Taylor
Alström syndrome. Report of 22 cases and literature review.
Ophthalmology 1998;105(7):1274-80.
1998: Dorothy A Thompson; Anthony Kriss; D Taylor; Isabelle Russell-Eggitt; Peter R Hodgkins; G Morgan; A Vellodi; E J Gerritsen
Early VEP and ERG evidence of visual dysfunction in autosomal recessive osteopetrosis.
Neuropediatrics 1998;29(3):137-44.
1998: Isabelle Russell-Eggitt; Christopher M Harris; Anthony Kriss
Delayed visual maturation: an update.
Developmental medicine and child neurology 1998;40(2):130-6.
1997: Isabelle Russell-Eggitt; P Zamiri
Review of aphakic glaucoma after surgery for congenital cataract.
Journal of cataract and refractive surgery 1997;23 Suppl 1():664-8.
1996: R J Leitch; D Thompson; C M Harris; K Chong; Isabelle Russell-Eggitt; Anthony Kriss
Achiasmia in a case of midline craniofacial cleft with seesaw nystagmus.
The British journal of ophthalmology 1996;80(11):1023-4.
1996: D A Thompson; H Møller; Isabelle Russell-Eggitt; Anthony Kriss
Visual acuity in unilateral cataract.
The British journal of ophthalmology 1996;80(9):794-8.
1996: A S Narita; Isabelle Russell-Eggitt
Bilateral epiretinal membranes: a new finding in Hunter syndrome.
Ophthalmic genetics 1996;17(2):75-8.
1996: Christopher M Harris; Fatima Shawkat; Isabelle Russell-Eggitt; J Wilson; D Taylor
Intermittent horizontal saccade failure ('ocular motor apraxia') in children.
The British journal of ophthalmology 1996;80(2):151-8.
1996: Christopher M Harris; Anthony Kriss; Fatima Shawkat; D Taylor; Isabelle Russell-Eggitt
Delayed visual maturation in infants: a disorder of figure-ground separation?
Brain research bulletin 1996;40(5-6):365-9.
1996: Isabelle Russell-Eggitt; Anthony Kriss; M Restori; L Speedwell; D Thompson; Christine Timms; C Yu
Severe microcornea with anterior segment malformation in a mother and her son.
Acta ophthalmologica Scandinavica. Supplement 1996;(219):27-9.
1995: Fatima Shawkat; D Kingsley; B Kendall; Isabelle Russell-Eggitt; David S I Taylor; Christopher M Harris
Neuroradiological and eye movement correlates in children with intermittent saccade failure: "ocular motor apraxia".
Neuropediatrics 1995;26(6):298-305.
1995: Fatima Shawkat; Christopher M Harris; David S I Taylor; Dorothy A Thompson; Isabelle Russell-Eggitt; Anthony Kriss
The optokinetic response differences between congenital profound and nonprofound unilateral visual deprivation.
Ophthalmology 1995;102(11):1615-22.
1995: Christopher Lloyd; J G Dowler; Anthony Kriss; L Speedwell; D A Thompson; Isabelle Russell-Eggitt; D Taylor
Modulation of amblyopia therapy following early surgery for unilateral congenital cataracts.
The British journal of ophthalmology 1995;79(9):802-6.
1995: L Speedwell; Isabelle Russell-Eggitt
Improvement in visual acuity in children with ectopia lentis.
Journal of pediatric ophthalmology and strabismus 1995;32(2):94-7.
1995: M J Peters; H U Moeller; Isabelle Russell-Eggitt; V Novelli
Cytomegalovirus retinitis in AIDS.
Archives of disease in childhood 1995;72(1):54-5.
1993: C K Patel; David S I Taylor; Isabelle Russell-Eggitt; Anthony Kriss; P Demaerel
Congenital third nerve palsy associated with mid-trimester amniocentesis.
The British journal of ophthalmology 1993;77(8):530-3.
1993: Christopher M Harris; J Walker; Fatima Shawkat; J Wilson; Isabelle Russell-Eggitt
Eye movements in a familial vestibulocerebellar disorder.
Neuropediatrics 1993;24(3):117-22.
1993: C M Harris; Anthony Kriss; Isabelle Russell-Eggitt
Autosomal recessive cerebellar hypoplasia.
Pediatric neurology 1993;9(3):247.
1992: Anthony Kriss; Isabelle Russell-Eggitt; C M Harris; Christopher Lloyd; D Taylor
Aspects of albinism.
Ophthalmic paediatrics and genetics 1992;13(2):89-100.
1992: Isabelle Russell-Eggitt; N S Rice; B Jay; R K Wyse
Relapse following goniotomy for congenital glaucoma due to trabecular dysgenesis.
Eye (London, England) 1992;6 ( Pt 2)():197-200.
1992: Christopher Lloyd; M Goss-Sampson; Brett G Jeffrey; Anthony Kriss; Isabelle Russell-Eggitt; D Taylor
Neonatal cataract: aetiology, pathogenesis and management.
Eye (London, England) 1992;6 ( Pt 2)():184-96.
1992: Anthony Kriss; Isabelle Russell-Eggitt
Electrophysiological assessment of visual pathway function in infants.
Eye (London, England) 1992;6 ( Pt 2)():145-53.
1990: Anthony Kriss; Isabelle Russell-Eggitt; D Taylor
Childhood albinism. Visual electrophysiological features.
Ophthalmic paediatrics and genetics 1990;11(3):185-92.
1990: Isabelle Russell-Eggitt; K D Blake; David S I Taylor; R K Wyse
The eye in the CHARGE association.
The British journal of ophthalmology 1990;74(7):421-6.
1990: R K Wyse; M Mars; S al-Mahdawi; Isabelle Russell-Eggitt; K D Blake
Congenital heart anomalies in patients with clefts of the lip and/or palate.
The Cleft palate journal 1990;27(3):258-64; discussion 264-5.
1990: Isabelle Russell-Eggitt; Anthony Kriss; David S I Taylor
Albinism in childhood: a flash VEP and ERG study.
The British journal of ophthalmology 1990;74(3):136-40.
1990: K D Blake; Isabelle Russell-Eggitt; D W Morgan; J M Ratcliffe; R K Wyse
Who's in CHARGE? Multidisciplinary management of patients with CHARGE association.
Archives of disease in childhood 1990;65(2):217-23.
1989: Isabelle Russell-Eggitt; David S I Taylor; P T Clayton; A Garner; Anthony Kriss; J F Taylor
Leber's congenital amaurosis--a new syndrome with a cardiomyopathy.
The British journal of ophthalmology 1989;73(4):250-4.