advertisement
Craig JE 48
Showing records 1 to 25 | Display all abstracts from Craig JE79816 Prevalence and type of artefact with spectral domain optical coherence tomography macular ganglion cell imaging in glaucoma surveillance
Awadalla MS
PLoS ONE 2018; 13: e0206684
79962 Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma
Siggs OM
JAMA ophthalmology 2019; 137: 348-355
79708 Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucoma
Lahola-Chomiak AA
Human Molecular Genetics 2019; 28: 1298-1311
79816 Prevalence and type of artefact with spectral domain optical coherence tomography macular ganglion cell imaging in glaucoma surveillance
Fitzgerald J
PLoS ONE 2018; 13: e0206684
79708 Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucoma
Footz T
Human Molecular Genetics 2019; 28: 1298-1311
79962 Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma
Souzeau E
JAMA ophthalmology 2019; 137: 348-355
79816 Prevalence and type of artefact with spectral domain optical coherence tomography macular ganglion cell imaging in glaucoma surveillance
Andrew NH
PLoS ONE 2018; 13: e0206684
79962 Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma
Pasutto F
JAMA ophthalmology 2019; 137: 348-355
79816 Prevalence and type of artefact with spectral domain optical coherence tomography macular ganglion cell imaging in glaucoma surveillance
Andrew NH
PLoS ONE 2018; 13: e0206684
79708 Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucoma
Nguyen-Phuoc K; Neil GJ
Human Molecular Genetics 2019; 28: 1298-1311
79816 Prevalence and type of artefact with spectral domain optical coherence tomography macular ganglion cell imaging in glaucoma surveillance
Zhou T
PLoS ONE 2018; 13: e0206684
79962 Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma
Dubowsky A; Smith JEH
JAMA ophthalmology 2019; 137: 348-355
79708 Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucoma
Fan B
Human Molecular Genetics 2019; 28: 1298-1311
79816 Prevalence and type of artefact with spectral domain optical coherence tomography macular ganglion cell imaging in glaucoma surveillance
Marshall H
PLoS ONE 2018; 13: e0206684
79708 Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucoma
Allen KF
Human Molecular Genetics 2019; 28: 1298-1311
79816 Prevalence and type of artefact with spectral domain optical coherence tomography macular ganglion cell imaging in glaucoma surveillance
Qassim A
PLoS ONE 2018; 13: e0206684
79962 Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma
Taranath D
JAMA ophthalmology 2019; 137: 348-355
79816 Prevalence and type of artefact with spectral domain optical coherence tomography macular ganglion cell imaging in glaucoma surveillance
Hassall M
PLoS ONE 2018; 13: e0206684
79962 Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma
Pater J
JAMA ophthalmology 2019; 137: 348-355
79708 Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucoma
Greenfield DS; Parrish RK
Human Molecular Genetics 2019; 28: 1298-1311
79816 Prevalence and type of artefact with spectral domain optical coherence tomography macular ganglion cell imaging in glaucoma surveillance
Casson RJ
PLoS ONE 2018; 13: e0206684
79962 Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma
Rait JL
JAMA ophthalmology 2019; 137: 348-355
79816 Prevalence and type of artefact with spectral domain optical coherence tomography macular ganglion cell imaging in glaucoma surveillance
Graham SL
PLoS ONE 2018; 13: e0206684
79708 Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucoma
Linkroum K
Human Molecular Genetics 2019; 28: 1298-1311
79962 Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma
Narita A
JAMA ophthalmology 2019; 137: 348-355
