Detalhe da pesquisa
1.
Decision-making capacity assessment for confused patients in a regional hospital: A before and after study.
Aust J Rural Health
; 28(2): 132-140, 2020 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-32390205
2.
Assessing patients decision-making capacity in the hospital setting: A literature review.
Aust J Rural Health
; 28(2): 141-148, 2020 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-31960545
3.
Next-generation sequencing using microfluidic PCR enrichment for molecular autopsy.
BMC Cardiovasc Disord
; 19(1): 174, 2019 07 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-31337358
4.
Defining the genetic architecture of hypertrophic cardiomyopathy: re-evaluating the role of non-sarcomeric genes.
Eur Heart J
; 38(46): 3461-3468, 2017 Dec 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-28082330
5.
Whole-Gene Sequencing of CFTR Reveals a High Prevalence of the Intronic Variant c.3874-4522A>G in Cystic Fibrosis.
Am J Respir Crit Care Med
; 201(11): 1438-1441, 2020 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32017858
6.
Combined approaches, including long-read sequencing, address the diagnostic challenge of HYDIN in primary ciliary dyskinesia.
Eur J Hum Genet
; 2024 Apr 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-38605126
7.
Barriers in reaching new-borns and infants through home visits: A qualitative study using nexus planning framework.
Front Public Health
; 10: 956422, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36249255
8.
Decision-Making in People With Dementia or Mild Cognitive Impairment: A Narrative Review of Decision-Making Tools.
J Am Med Dir Assoc
; 22(10): 2056-2062.e4, 2021 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34314703
9.
Utilization of Postnatal Healthcare Services Delivered through Home Visitation and Health Facilities for Mothers and Newborns: An Integrative Review from Developing Countries.
Indian J Pediatr
; 87(3): 207-216, 2020 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-31900850
10.
Polymorphisms in the IL6 gene in Asian Indian families with premature coronary artery disease--the Indian Atherosclerosis Research Study.
Thromb Haemost
; 99(5): 944-50, 2008 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-18449426
11.
Genetic studies on the APOA1-C3-A5 gene cluster in Asian Indians with premature coronary artery disease.
Lipids Health Dis
; 7: 33, 2008 Sep 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-18801202
12.
Histiocytoid cardiomyopathy and microphthalmia with linear skin defects syndrome: phenotypes linked by truncating variants in NDUFB11.
Cold Spring Harb Mol Case Stud
; 3(1): a001271, 2017 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-28050600
13.
Development of a Comprehensive Sequencing Assay for Inherited Cardiac Condition Genes.
J Cardiovasc Transl Res
; 9(1): 3-11, 2016 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-26888179
14.
Integrated allelic, transcriptional, and phenomic dissection of the cardiac effects of titin truncations in health and disease.
Sci Transl Med
; 7(270): 270ra6, 2015 Jan 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-25589632
15.
Next generation diagnostics in inherited arrhythmia syndromes : a comparison of two approaches.
J Cardiovasc Transl Res
; 6(1): 94-103, 2013 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-22956155
16.
Towards clinical molecular diagnosis of inherited cardiac conditions: a comparison of bench-top genome DNA sequencers.
PLoS One
; 8(7): e67744, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23861798
17.
Usefulness of C-reactive protein as a marker for prediction of future coronary events in the asian Indian population: Indian atherosclerosis research study.
Int J Vasc Med
; 2010: 389235, 2010.
Artigo
em Inglês
| MEDLINE | ID: mdl-21152190
18.
Polymorphisms in the pituitary growth hormone gene and its receptor associated with coronary artery disease in a predisposed cohort from India.
J Genet
; 89(4): 437-47, 2010 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-21273694
19.
Genotype-phenotype relationship of F7 R353Q polymorphism and plasma factor VII coagulant activity in Asian Indian families predisposed to coronary artery disease.
J Genet
; 88(3): 291-7, 2009 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-20086294
20.
A common variant in chromosome 9p21 associated with coronary artery disease in Asian Indians.
J Genet
; 88(1): 113-8, 2009 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-19417554