Bellgard MI - Search Results

1

The role of patient registries for rare genetic lipid disorders.

Ng DM, Hooper AJ, Bellgard MI, Burnett JR. Ng DM, et al. Among authors: bellgard mi. Curr Opin Lipidol. 2018 Apr;29(2):156-162. doi: 10.1097/MOL.0000000000000485. Curr Opin Lipidol. 2018. PMID: 29351106 Review.

2

A modular approach to disease registry design: successful adoption of an internet-based rare disease registry.

Bellgard MI, Macgregor A, Janon F, Harvey A, O'Leary P, Hunter A, Dawkins H. Bellgard MI, et al. Hum Mutat. 2012 Oct;33(10):E2356-66. doi: 10.1002/humu.22154. Epub 2012 Jul 2. Hum Mutat. 2012. PMID: 22753342

3

Role of international registries in enhancing the care of familial hypercholesterolaemia.

Hammond E, Watts GF, Rubinstein Y, Farid W, Livingston M, Knowles JW, Lochmüller H, Bellgard M, Dawkins HJ. Hammond E, et al. Int J Evid Based Healthc. 2013 Jun;11(2):134-9. doi: 10.1111/1744-1609.12023. Int J Evid Based Healthc. 2013. PMID: 23750577 Free article.

4

Design of a framework for the deployment of collaborative independent rare disease-centric registries: Gaucher disease registry model.

Bellgard MI, Napier KR, Bittles AH, Szer J, Fletcher S, Zeps N, Hunter AA, Goldblatt J. Bellgard MI, et al. Blood Cells Mol Dis. 2018 Feb;68:232-238. doi: 10.1016/j.bcmd.2017.01.013. Epub 2017 Jan 27. Blood Cells Mol Dis. 2018. PMID: 28190666 Free PMC article.

5

A web-based, patient driven registry for Angelman syndrome: the global Angelman syndrome registry.

Napier KR, Tones M, Simons C, Heussler H, Hunter AA, Cross M, Bellgard MI. Napier KR, et al. Among authors: bellgard mi. Orphanet J Rare Dis. 2017 Aug 1;12(1):134. doi: 10.1186/s13023-017-0686-1. Orphanet J Rare Dis. 2017. PMID: 28764722 Free PMC article.

6

Rare disease registries: a call to action.

Lacaze P, Millis N, Fookes M, Zurynski Y, Jaffe A, Bellgard M, Winship I, McNeil J, Bittles AH. Lacaze P, et al. Intern Med J. 2017 Sep;47(9):1075-1079. doi: 10.1111/imj.13528. Intern Med J. 2017. PMID: 28891182

7

RD-RAP: beyond rare disease patient registries, devising a comprehensive data and analytic framework.

Bellgard MI, Snelling T, McGree JM. Bellgard MI, et al. Orphanet J Rare Dis. 2019 Jul 12;14(1):176. doi: 10.1186/s13023-019-1139-9. Orphanet J Rare Dis. 2019. PMID: 31300021 Free PMC article.

8

Design, development and deployment of a web-based patient registry for rare genetic lipid disorders.

Napier KR, Hooper AJ, Ng DM, Render L, Bell DA, Pang J, Watts GF, Bellgard MI, Burnett JR. Napier KR, et al. Among authors: bellgard mi. Pathology. 2020 Jun;52(4):447-452. doi: 10.1016/j.pathol.2020.02.002. Epub 2020 Apr 7. Pathology. 2020. PMID: 32276786

9

A Registry Framework Enabling Patient-Centred Care.

Bellgard MI, Napier K, Render L, Radochonski M, Lamont L, Graham C, Wilton SD, Fletcher S, Goldblatt J, Hunter AA, Weeramanthri T. Bellgard MI, et al. Stud Health Technol Inform. 2015;214:8-14. Stud Health Technol Inform. 2015. PMID: 26210411

10

A Web-Based Registry for Familial Hypercholesterolaemia.

Napier KR, Pang J, Lamont L, Walker CE, Dawkins HJ, Hunter AA, Bockxmeer FMV, Watts GF, Bellgard MI. Napier KR, et al. Among authors: bellgard mi. Heart Lung Circ. 2017 Jun;26(6):635-639. doi: 10.1016/j.hlc.2016.10.019. Epub 2016 Nov 30. Heart Lung Circ. 2017. PMID: 28065523

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