Suchergebnisse - "Barrett, Brendan"

PubPharm (158)

101

Galectin-3 and new-onset CKD : marker or mediator?

enthalten in: Journal of the American Society of Nephrology : JASN | 2013

von Ravani, P. | Barrett, B.

CommentOn: J Am Soc Nephrol. 2013 Sep;24(9):1470-7. - PMID 23766533

102

The relationship between anisometropia and amblyopia

enthalten in: Progress in retinal and eye research | 2013

von Barrett, B. | Bradley, A. | Candy, T.

103

Reply to Fox et al--Contrast-induced nephropathy and dehydration

enthalten in: Canadian Association of Radiologists journal = Journal l'Association canadienne des radiologistes | 2013

von Carstensen, M. | Keer, D. | Rempel, J. | +2

CommentOn: Can Assoc Radiol J. 2012 Aug;63(3):177-82. - PMID 22030305

104

Cohort profile : Canadian study of prediction of death, dialysis and interim cardiovascular events (CanPREDDICT)

enthalten in: BMC nephrology | 2013

von Levin, A. | Rigatto, C. | Brendan, B. | +91

105

Test-retest reproducibility of accommodation measurements gathered in an unselected sample of UK primary school children

enthalten in: The British journal of ophthalmology | 2013

von Adler, P. | Scally, A. | Barrett, B.

CommentIn: Klin Monbl Augenheilkd. 2013 Nov;230(11):1076. - PMID 24383108

106

Bilateral changes in foveal structure in individuals with amblyopia

enthalten in: Ophthalmology | 2013

von Bruce, A. | Pacey, I. | Bradbury, J. | +2

107

Binocular summation and other forms of non-dominant eye contribution in individuals with strabismic amblyopia during habitual viewing

enthalten in: PloS one | 2013

von Barrett, B. | Panesar, G. | Scally, A. | +1

108

Using administrative databases in the surveillance of depressive disorders--case definitions

enthalten in: Population health management | 2012

von Alaghehbandan, R. | Macdonald, D. | Barrett, B. | +2

109

Adult siblings with homozygous G6PC3 mutations expand our understanding of the severe congenital neutropenia type 4 (SCN4) phenotype

enthalten in: BMC medical genetics | 2012

von Fernandez, B. | Green, J. | Bursey, F. | +20

110

Adult siblings with homozygous G6PC3 mutations expand our understanding of the severe congenital neutropenia type 4 (SCN4) phenotype

enthalten in: BMC medical genetics | 2012

von Fernandez, B. | Green, J. | Bursey, F. | +10