Brown E - Search Results

1

Phenotypes Associated With the Val122Ile, Leu58His, and Late-Onset Val30Met Variants in Patients With Hereditary Transthyretin Amyloidosis.

Zampino S, Sheikh FH, Vaishnav J, Judge D, Pan B, Daniel A, Brown E, Ebenezer G, Polydefkis M. Zampino S, et al. Among authors: brown e. Neurology. 2023 May 9;100(19):e2036-e2044. doi: 10.1212/WNL.0000000000207158. Epub 2023 Mar 20. Neurology. 2023. PMID: 36941075 Free PMC article.

2

Baseline Characteristics Predict the Presence of Amyloid on Endomyocardial Biopsy.

Ton VK, Bhonsale A, Gilotra NA, Halushka MK, Steenbergen C, Almansa J, Brown E, Tedford RJ, Wittstein I, Sharma K, Russell SD, Judge DP. Ton VK, et al. Among authors: brown e. J Card Fail. 2017 Apr;23(4):340-344. doi: 10.1016/j.cardfail.2016.12.006. Epub 2016 Dec 20. J Card Fail. 2017. PMID: 28011000

3

Genetic testing improves identification of transthyretin amyloid (ATTR) subtype in cardiac amyloidosis.

Brown EE, Lee YZJ, Halushka MK, Steenbergen C, Johnson NM, Almansa J, Tedford RJ, Cingolani O, Russell SD, Sharma K, Judge DP. Brown EE, et al. Amyloid. 2017 Jun;24(2):92-95. doi: 10.1080/13506129.2017.1324418. Epub 2017 May 11. Amyloid. 2017. PMID: 28494620 Clinical Trial.

4

Giant Ring Mitochondria in a Patient With Heart Failure and Cerebral White Matter Disease Resulting From an MT-TL1 Mitochondrial Gene Mutation.

Houston BA, Judge DP, Brown E, Halushka M, Barouch LA. Houston BA, et al. Among authors: brown e. J Card Fail. 2017 Aug;23(8):652-655. doi: 10.1016/j.cardfail.2017.06.001. Epub 2017 Jun 15. J Card Fail. 2017. PMID: 28624653

5

Protein molecular modeling techniques investigating novel TAB2 variant R347X causing cardiomyopathy and congenital heart defects in multigenerational family.

Caulfield TR, Richter JE Jr, Brown EE, Mohammad AN, Judge DP, Atwal PS. Caulfield TR, et al. Among authors: brown ee. Mol Genet Genomic Med. 2018 Apr 26;6(4):666-72. doi: 10.1002/mgg3.401. Online ahead of print. Mol Genet Genomic Med. 2018. PMID: 29700987 Free PMC article.

6

Bringing Autopsies Into the Molecular Genetic Era.

Judge DP, Brown EE. Judge DP, et al. Among authors: brown ee. Circulation. 2018 Jun 19;137(25):2727-2729. doi: 10.1161/CIRCULATIONAHA.118.033235. Circulation. 2018. PMID: 29915099 No abstract available.

7

Seven factors predict a delayed diagnosis of cardiac amyloidosis.

Bishop E, Brown EE, Fajardo J, Barouch LA, Judge DP, Halushka MK. Bishop E, et al. Among authors: brown ee. Amyloid. 2018 Sep;25(3):174-179. doi: 10.1080/13506129.2018.1498782. Epub 2018 Aug 31. Amyloid. 2018. PMID: 30169971

8

Genetic aetiologies should be considered in paediatric cases of acute heart failure presumed to be myocarditis.

Brown EE, McMilllan KN, Halushka MK, Ravekes WJ, Knight M, Crosson JE, Judge DP, Murphy AM. Brown EE, et al. Cardiol Young. 2019 Jul;29(7):917-921. doi: 10.1017/S1047951119001124. Epub 2019 Jun 14. Cardiol Young. 2019. PMID: 31198128

9

Clinical pathway to screen for cardiac amyloidosis in heart failure with preserved ejection fraction.

Fajardo J, Cummings A, Brown E, Cuomo K, Rhodes P, Woodbury S, Gilotra N, Russell S, Judge D. Fajardo J, et al. Among authors: brown e. Amyloid. 2019;26(sup1):166-167. doi: 10.1080/13506129.2019.1583178. Amyloid. 2019. PMID: 31343333 No abstract available.

10

Positive family history decreases diagnosis time by over 200.

Brown EE, Fajardo J, Judge DP. Brown EE, et al. Amyloid. 2019;26(sup1):17. doi: 10.1080/13506129.2019.1582484. Amyloid. 2019. PMID: 31343334 No abstract available.

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