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R Grigg

Showing results (61-70 of 150) with videos related to

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Human Mutation|November 3, 2000
Identification of a novel mutation C144F in the Notch3 gene in an Australian CADASIL pedigreeR Grigg, R Lea, A A Sullivan, et al.
Clinical & Experimental Ophthalmology|May 6, 2023
Spectrum of ocular disease in children aged between 0 and 3 years at an Australian paediatric tertiary hospitalEdward Lo-Cao, Stephanie Crofts, Katie Geering, et al.
Translational Pediatrics|February 3, 2016
Retinal dystrophies, genomic applications in diagnosis and prospects for therapyBenjamin M Nash, Dale C Wright, John R Grigg, et al.
Clinical & Experimental Ophthalmology|March 2, 2016
Changing patterns in paediatric optic atrophy aetiology: 1979 to 2015Linda Zheng, Helen Hyun-Jin Do, Trent Sandercoe, et al.
Clinical Chemistry|May 1, 1980
Anomalous results with the CIS-Sorin corticotropin kitA Sharp, D Handelsman, R Ristuccia, et al.
Acta Ophthalmologica|December 1, 2020
Natural history and clinical biomarkers of progression in X-linked retinitis pigmentosa: a systematic reviewMark Zada, Elisa E Cornish, Clare L Fraser, et al.
Journal of Glaucoma|November 10, 2015
Uveal Effusion: Clinical Features, Management, and Visual Outcomes in a Retrospective Case SeriesParth R Shah, Jayshan Yohendran, Alex P Hunyor, et al.
The Journal of Urology|February 1, 1992
Renal function in unilateral nephrectomy subjectsP L Liu, E D Gallery, R Grigg, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|November 12, 2013
The importance of electrophysiology in revealing a complete homozygous deletion of KCNV2John R Grigg, Graham E Holder, Francis A Billson, et al.
Biorxiv : the Preprint Server for Biology|April 3, 2026
Linking reaction time variability to physiological markers of arousal across timescalesDeepa Issar, Emily E Skog, Madison R Grigg, et al.
Pageof 15

Showing results (61-70 of 150) with videos related to

Sort By:
Pageof 15
Human Mutation|November 3, 2000
Identification of a novel mutation C144F in the Notch3 gene in an Australian CADASIL pedigreeR Grigg, R Lea, A A Sullivan, et al.
Clinical & Experimental Ophthalmology|May 6, 2023
Spectrum of ocular disease in children aged between 0 and 3 years at an Australian paediatric tertiary hospitalEdward Lo-Cao, Stephanie Crofts, Katie Geering, et al.
Translational Pediatrics|February 3, 2016
Retinal dystrophies, genomic applications in diagnosis and prospects for therapyBenjamin M Nash, Dale C Wright, John R Grigg, et al.
Clinical & Experimental Ophthalmology|March 2, 2016
Changing patterns in paediatric optic atrophy aetiology: 1979 to 2015Linda Zheng, Helen Hyun-Jin Do, Trent Sandercoe, et al.
Clinical Chemistry|May 1, 1980
Anomalous results with the CIS-Sorin corticotropin kitA Sharp, D Handelsman, R Ristuccia, et al.
Acta Ophthalmologica|December 1, 2020
Natural history and clinical biomarkers of progression in X-linked retinitis pigmentosa: a systematic reviewMark Zada, Elisa E Cornish, Clare L Fraser, et al.
Journal of Glaucoma|November 10, 2015
Uveal Effusion: Clinical Features, Management, and Visual Outcomes in a Retrospective Case SeriesParth R Shah, Jayshan Yohendran, Alex P Hunyor, et al.
The Journal of Urology|February 1, 1992
Renal function in unilateral nephrectomy subjectsP L Liu, E D Gallery, R Grigg, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|November 12, 2013
The importance of electrophysiology in revealing a complete homozygous deletion of KCNV2John R Grigg, Graham E Holder, Francis A Billson, et al.
Biorxiv : the Preprint Server for Biology|April 3, 2026
Linking reaction time variability to physiological markers of arousal across timescalesDeepa Issar, Emily E Skog, Madison R Grigg, et al.
Pageof 15