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Persistency rates for prostaglandin and other hypotensive eyedrops: population-based study using pharmacy claims data

Clinical & experimental ophthalmology, 2007-09, Vol.35 (7), p.602-611

2007

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Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma

JAMA ophthalmology, 2019-04, Vol.137 (4), p.348

2019

Volltextzugriff (PDF)

How best do we compensate for accidental medical injuries?

Medical journal of Australia, 2012-09, Vol.197 (5), p.299-300

Rait, Julian L

2012

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Glaucoma spectrum and age-related prevalence of individuals with FOXC1 and PITX2 variants

European journal of human genetics : EJHG, 2017-06, Vol.25 (7), p.839-847

2017

Volltextzugriff (PDF)

Informed consent in 2012

Clinical & experimental ophthalmology, 2012-12, Vol.40 (9), p.835-837

Rait, Julian L

2012

Volltextzugriff (PDF)

Glaucoma spectrum and age-related prevalence of individuals with FOXC1 and PITX2 variants

European journal of human genetics : EJHG, 2017-11, Vol.25 (11), p.1290-1290

2017

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Five-year incidence of open-angle glaucoma: The visual impairment project

Ophthalmology (Rochester, Minn.), 2002-06, Vol.109 (6), p.1047-1051

2002

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Legal aspects of open disclosure II: attitudes of health professionals — findings from a national survey

Medical journal of Australia, 2011-01, Vol.194 (1), p.48-48

2011

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Detection of undiagnosed glaucoma by eye health professionals

Ophthalmology (Rochester, Minn.), 2004-08, Vol.111 (8), p.1508-1514

2004

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Inner retinal neurons display differential responses to N-methyl-D-aspartate receptor activation

Journal of comparative neurology (1911), 2003-10, Vol.465 (1), p.38-56

2003

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Evidence for genetic heterogeneity within eight glaucoma families, with the GLC1A Gln368STOP mutation being an important phenotypic modifier

Ophthalmology (Rochester, Minn.), 2001-09, Vol.108 (9), p.1607-1620

2001

Volltextzugriff (PDF)

Progression of visual field loss in open angle glaucoma in the Melbourne Visual Impairment Project

Clinical & experimental ophthalmology, 2006-01, Vol.34 (1), p.20-26

2006

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Management of ocular hypertension and primary open angle glaucoma

Clinical and experimental optometry, 2000-05, Vol.83 (3), p.136-144

Rait, Julian L

2000

Volltextzugriff (PDF)

An evidence-based approach to glaucoma therapy

Clinical and experimental optometry, 2000-05, Vol.83 (3), p.111-112

Rait, Julian L

2000

Volltextzugriff (PDF)

Erratum: Glaucoma spectrum and age-related prevalence of individuals with FOXC1 and PITX2 variants

European journal of human genetics : EJHG, 2017-10, Vol.25 (11), p.1290-1290

2017

Volltextzugriff (PDF)

Glaucoma phenotype in pedigrees with the myocilin Thr377Met mutation

Archives of ophthalmology (1960), 2003-08, Vol.121 (8), p.1172

2003

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Accuracy and implications of a reported family history of glaucoma: experience from the Glaucoma Inheritance Study in Tasmania

Archives of ophthalmology (1960), 2000-07, Vol.118 (7), p.900

2000

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Systemic effects of topical ophthalmic β-adrenoceptor antagonists

Australian and New Zealand journal of ophthalmology, 1999-02, Vol.27 (1), p.57-64

Rait, Julian L

1999

Volltextzugriff (PDF)

Five-year incidence of open-angle glaucoma

Ophthalmology (Rochester, Minn.), 2002-06, Vol.109 (6), p.1047-1051

2002

Volltextzugriff (PDF)

Evidence for genetic heterogeneity within eight glaucoma families, with the GLC1A Gln368STOP mutation being an important phenotypic modifier11None of the authors has a financial interest relating to this article

Ophthalmology (Rochester, Minn.), 2001-09, Vol.108 (9), p.1607-1620

2001

Volltextzugriff (PDF)

Evidence for genetic heterogeneity within Eight Glaucoma families, with the GLC1A Gln368STOP mutation being an important phenotypic modifier. Discussion

Ophthalmology (Rochester, Minn.), 2001, Vol.108 (9), p.1607-1620

2001

Volltextzugriff (PDF)

The problem of overlapping glaucoma families in the Glaucoma Inheritance Study in Tasmania (GIST)

Ophthalmic genetics, 1996, Vol.17 (4), p.209-214

1996

Volltextzugriff (PDF)

Fastpac visual field screening

Ophthalmic epidemiology, 1995, Vol.2 (3), p.117-121

1995

Volltextzugriff (PDF)

Comparison between Fastpac and conventional Humphrey perimetry

Australian and New Zealand journal of ophthalmology, 1994-05, Vol.22 (2), p.95-99

1994

Volltextzugriff (PDF)

Public hospital day-case surgery in a dedicated facility

Australian and New Zealand journal of ophthalmology, 1989-11, Vol.17 (4), p.409-412

1989

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Persistency rates for prostaglandin and other hypotensive eyedrops: population-based study using pharmacy claims data

Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma

How best do we compensate for accidental medical injuries?

Glaucoma spectrum and age-related prevalence of individuals with FOXC1 and PITX2 variants

Informed consent in 2012

Glaucoma spectrum and age-related prevalence of individuals with FOXC1 and PITX2 variants

Five-year incidence of open-angle glaucoma: The visual impairment project

Legal aspects of open disclosure II: attitudes of health professionals — findings from a national survey

Detection of undiagnosed glaucoma by eye health professionals

Inner retinal neurons display differential responses to N-methyl-D-aspartate receptor activation

Evidence for genetic heterogeneity within eight glaucoma families, with the GLC1A Gln368STOP mutation being an important phenotypic modifier

Progression of visual field loss in open angle glaucoma in the Melbourne Visual Impairment Project

Management of ocular hypertension and primary open angle glaucoma

An evidence-based approach to glaucoma therapy

Erratum: Glaucoma spectrum and age-related prevalence of individuals with FOXC1 and PITX2 variants

Glaucoma phenotype in pedigrees with the myocilin Thr377Met mutation

Accuracy and implications of a reported family history of glaucoma: experience from the Glaucoma Inheritance Study in Tasmania

Systemic effects of topical ophthalmic β-adrenoceptor antagonists

Five-year incidence of open-angle glaucoma

Evidence for genetic heterogeneity within eight glaucoma families, with the GLC1A Gln368STOP mutation being an important phenotypic modifier11None of the authors has a financial interest relating to this article

Evidence for genetic heterogeneity within Eight Glaucoma families, with the GLC1A Gln368STOP mutation being an important phenotypic modifier. Discussion

The problem of overlapping glaucoma families in the Glaucoma Inheritance Study in Tasmania (GIST)

Fastpac visual field screening

Comparison between Fastpac and conventional Humphrey perimetry

Public hospital day-case surgery in a dedicated facility

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