Detalhe da pesquisa
1.
Incidence and prevalence of NMOSD in Australia and New Zealand.
J Neurol Neurosurg Psychiatry
; 88(8): 632-638, 2017 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-28550069
2.
Modelling genetic susceptibility to multiple sclerosis with family data.
Neuroepidemiology
; 40(1): 1-12, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23075677
3.
MRI Patterns Distinguish AQP4 Antibody Positive Neuromyelitis Optica Spectrum Disorder From Multiple Sclerosis.
Front Neurol
; 12: 722237, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34566866
4.
Relapse Patterns in NMOSD: Evidence for Earlier Occurrence of Optic Neuritis and Possible Seasonal Variation.
Front Neurol
; 11: 537, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32612571
5.
The clinical profile of NMOSD in Australia and New Zealand.
J Neurol
; 267(5): 1431-1443, 2020 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-32006158
6.
Sequence variants of alpha-methylacyl-CoA racemase are associated with prostate cancer risk: a replication study in an ethnically homogeneous population.
Prostate
; 68(13): 1373-9, 2008 Sep 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-18537123
7.
Investigation of albinism genes in congenital esotropia.
Mol Vis
; 9: 710-4, 2003 Dec 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-14685142
8.
The association between hormonal and reproductive factors and hand osteoarthritis.
Maturitas
; 45(4): 257-65, 2003 Aug 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-12927312
9.
Identification of a prostate cancer susceptibility gene on chromosome 5p13q12 associated with risk of both familial and sporadic disease.
Eur J Hum Genet
; 17(3): 368-77, 2009 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-18830231
10.
Familial, structural, and environmental correlates of MRI-defined bone marrow lesions: a sibpair study.
Arthritis Res Ther
; 8(4): R137, 2006.
Artigo
em Inglês
| MEDLINE | ID: mdl-16887014
11.
Confirmation of the adult-onset primary open angle glaucoma locus GLC1B at 2cen-q13 in an Australian family.
Ophthalmologica
; 220(1): 23-30, 2006.
Artigo
em Inglês
| MEDLINE | ID: mdl-16374045
12.
The genetic contribution and relevance of knee cartilage defects: case-control and sib-pair studies.
J Rheumatol
; 32(10): 1937-42, 2005 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-16206350
13.
The genetic contribution to longitudinal changes in knee structure and muscle strength: a sibpair study.
Arthritis Rheum
; 52(9): 2830-4, 2005 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-16145664
14.
A cross sectional study of the association between sex, smoking, and other lifestyle factors and osteoarthritis of the hand.
J Rheumatol
; 29(8): 1719-24, 2002 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-12180736
15.
Cutaneous melanin density of Caucasians measured by spectrophotometry and risk of malignant melanoma, basal cell carcinoma, and squamous cell carcinoma of the skin.
Am J Epidemiol
; 155(7): 614-21, 2002 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-11914188
16.
The genetic contribution to muscle strength, knee pain, cartilage volume, bone size, and radiographic osteoarthritis: a sibpair study.
Arthritis Rheum
; 50(3): 805-10, 2004 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-15022322
17.
Does the addition of information on genotype improve prediction of the risk of melanoma and nonmelanoma skin cancer beyond that obtained from skin phenotype?
Am J Epidemiol
; 159(9): 826-33, 2004 May 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-15105175
18.
Mutations in a novel gene, NHS, cause the pleiotropic effects of Nance-Horan syndrome, including severe congenital cataract, dental anomalies, and mental retardation.
Am J Hum Genet
; 73(5): 1120-30, 2003 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-14564667