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1.
Human Genetics Society of Australasia Position Statement: Use of Polygenic Scores in Clinical Practice and Population Health.
Twin Res Hum Genet
; 26(1): 40-48, 2023 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-36950972
2.
Becoming and being a parent with an inherited predisposition to diffuse gastric cancer: A qualitative study of young adults with a CDH1 pathogenic variant.
J Psychosoc Oncol
; 41(3): 286-302, 2023.
Artículo
en Inglés
| MEDLINE | ID: mdl-35959852
3.
Clinical impact of whole-genome sequencing in patients with early-onset dementia.
J Neurol Neurosurg Psychiatry
; 2022 Jul 29.
Artículo
en Inglés
| MEDLINE | ID: mdl-35906014
4.
Young people's experiences of a CDH1 pathogenic variant: Decision-making about gastric cancer risk management.
J Genet Couns
; 31(1): 242-251, 2022 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-34265132
5.
Assessing the acceptability, feasibility, and usefulness of a psychosocial screening tool to patients and clinicians in a clinical genetics service in Australia.
J Genet Couns
; 31(3): 653-662, 2022 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-34788484
6.
Streambanks: A net source of sediment and phosphorus to streams and rivers.
J Environ Manage
; 181: 602-614, 2016 Oct 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-27429360
7.
In vivo evidence of methamphetamine induced attenuation of brain tissue oxygenation as measured by EPR oximetry.
Toxicol Appl Pharmacol
; 275(2): 73-8, 2014 Mar 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-24412707
8.
Personalising genetic counselling (POETIC) trial: Protocol for a hybrid type II effectiveness-implementation randomised clinical trial of a patient screening tool to improve patient empowerment after cancer genetic counselling.
Trials
; 24(1): 712, 2023 Nov 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-37941026
9.
Rare germline variants in the AXIN2 gene in families with colonic polyposis and colorectal cancer.
Fam Cancer
; 21(4): 399-413, 2022 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-34817745
10.
Suicide in frontotemporal dementia and Huntington disease: analysis of family-reported pedigree data and implications for genetic healthcare for asymptomatic relatives.
Psychol Health
; 36(11): 1397-1402, 2021 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-33232178
11.
The clinical utility of exome sequencing and extended bioinformatic analyses in adolescents and adults with a broad range of neurological phenotypes: an Australian perspective.
J Neurol Sci
; 420: 117260, 2021 01 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-33310205
12.
Phenotypic confirmation of oligodontia, colorectal polyposis and cancer in a family carrying an exon 7 nonsense variant in the AXIN2 gene.
Fam Cancer
; 18(3): 311-315, 2019 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-30671715
13.
Comparison of neuroprotective effects induced by alpha-phenyl-N-tert-butyl nitrone (PBN) and N-tert-butyl-alpha-(2 sulfophenyl) nitrone (S-PBN) in lithium-pilocarpine status epilepticus.
Neurotoxicology
; 26(6): 969-79, 2005 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-15890407
14.
Differential neuroprotective effects of the NMDA receptor-associated glycine site partial agonists 1-aminocyclopropanecarboxylic acid (ACPC) and D-cycloserine in lithium-pilocarpine status epilepticus.
Neurotoxicology
; 25(5): 835-47, 2004 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-15288514
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