Detalhe da pesquisa
1.
Self-harm in adolescence and risk of crash: a 13-year cohort study of novice drivers in New South Wales, Australia.
Inj Prev
; 29(4): 302-308, 2023 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-36813554
2.
Acculturation and risk of traffic crashes in young Asian-born Australian drivers.
Inj Prev
; 29(1): 74-78, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36171076
3.
SLC38A8 mutations result in arrested retinal development with loss of cone photoreceptor specialization.
Hum Mol Genet
; 29(18): 2989-3002, 2020 11 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-32744312
4.
Genotypic and Phenotypic Spectrum of Foveal Hypoplasia: A Multicenter Study.
Ophthalmology
; 129(6): 708-718, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35157951
5.
Micro-fusion inhibition tests: quantifying antibody neutralization of virus-mediated cell-cell fusion.
J Gen Virol
; 102(1)2021 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33054904
6.
Prevalence and Epidemiology of Non-O157 Escherichia coli Serogroups O26, O103, O111, and O145 and Shiga Toxin Gene Carriage in Scottish Cattle, 2014-2015.
Appl Environ Microbiol
; 87(10)2021 04 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-33712425
7.
Early Recognition of Raised Intracranial Pressure in Craniosynostosis Using Optical Coherence Tomography.
J Craniofac Surg
; 32(1): 201-205, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-33185414
8.
Optic Nerve Head and Retinal Abnormalities Associated with Congenital Fibrosis of the Extraocular Muscles.
Int J Mol Sci
; 22(5)2021 Mar 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33806565
9.
Where are the missing gene defects in inherited retinal disorders? Intronic and synonymous variants contribute at least to 4% of CACNA1F-mediated inherited retinal disorders.
Hum Mutat
; 40(6): 765-787, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-30825406
10.
Albinism Associated With Torsional Nystagmus Masquerading as Spasmus Nutans.
J Neuroophthalmol
; 43(4): e313-e315, 2023 Dec 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34924531
11.
Abnormal retinal development associated with FRMD7 mutations.
Hum Mol Genet
; 23(15): 4086-93, 2014 Aug 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-24688117
12.
Retinal development in albinism: a prospective study using optical coherence tomography in infants and young children.
Lancet
; 385 Suppl 1: S14, 2015 Feb 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-26312836
13.
The Development of a Nystagmus-Specific Quality-of-Life Questionnaire.
Ophthalmology
; 123(9): 2023-7, 2016 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-27365177
14.
Optic Nerve Head Development in Healthy Infants and Children Using Handheld Spectral-Domain Optical Coherence Tomography.
Ophthalmology
; 123(10): 2147-57, 2016 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-27521172
15.
High-Resolution Imaging of the Optic Nerve and Retina in Optic Nerve Hypoplasia.
Ophthalmology
; 122(7): 1330-9, 2015 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-25939636
16.
Genetic and phenotypic diversity of NHE6 mutations in Christianson syndrome.
Ann Neurol
; 76(4): 581-93, 2014 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-25044251
17.
Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus.
Nat Genet
; 38(11): 1242-4, 2006 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-17013395
18.
A randomized controlled trial comparing soft contact lens and rigid gas-permeable lens wearing in infantile nystagmus.
Ophthalmology
; 121(9): 1827-36, 2014 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-24811959
19.
Using mobile technology to support lower-salt food choices for people with cardiovascular disease: protocol for the SaltSwitch randomized controlled trial.
BMC Public Health
; 14: 950, 2014 Sep 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-25217039
20.
Phenotypic Features Determining Visual Acuity in Albinism and the Role of Amblyogenic Factors.
Invest Ophthalmol Vis Sci
; 65(2): 14, 2024 Feb 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38319667