Li H - Search Results

1

A comprehensive safety profile of tafamidis in patients with transthyretin amyloid polyneuropathy.

Huber P, Flynn A, Sultan MB, Li H, Rill D, Ebede B, Gundapaneni B, Schwartz JH. Huber P, et al. Among authors: li h. Amyloid. 2019 Dec;26(4):203-209. doi: 10.1080/13506129.2019.1643714. Epub 2019 Jul 27. Amyloid. 2019. PMID: 31353964

2

Early intervention with tafamidis provides long-term (5.5-year) delay of neurologic progression in transthyretin hereditary amyloid polyneuropathy.

Waddington Cruz M, Amass L, Keohane D, Schwartz J, Li H, Gundapaneni B. Waddington Cruz M, et al. Among authors: li h. Amyloid. 2016 Sep;23(3):178-183. doi: 10.1080/13506129.2016.1207163. Epub 2016 Aug 5. Amyloid. 2016. PMID: 27494299 Free PMC article. Clinical Trial.

3

Long-term safety and efficacy of tafamidis for the treatment of hereditary transthyretin amyloid polyneuropathy: results up to 6 years.

Barroso FA, Judge DP, Ebede B, Li H, Stewart M, Amass L, Sultan MB. Barroso FA, et al. Among authors: li h. Amyloid. 2017 Sep;24(3):194-204. doi: 10.1080/13506129.2017.1357545. Epub 2017 Jul 31. Amyloid. 2017. PMID: 28758793 Clinical Trial.

4

Influence of baseline neurologic severity on disease progression and the associated disease-modifying effects of tafamidis in patients with transthyretin amyloid polyneuropathy.

Amass L, Li H, Gundapaneni BK, Schwartz JH, Keohane DJ. Amass L, et al. Among authors: li h. Orphanet J Rare Dis. 2018 Dec 17;13(1):225. doi: 10.1186/s13023-018-0947-7. Orphanet J Rare Dis. 2018. PMID: 30558645 Free PMC article. Clinical Trial.

5

Evaluation of Mortality During Long-Term Treatment with Tafamidis for Transthyretin Amyloidosis with Polyneuropathy: Clinical Trial Results up to 8.5 Years.

Merlini G, Coelho T, Waddington Cruz M, Li H, Stewart M, Ebede B. Merlini G, et al. Among authors: li h. Neurol Ther. 2020 Jun;9(1):105-115. doi: 10.1007/s40120-020-00180-w. Epub 2020 Feb 27. Neurol Ther. 2020. PMID: 32107748 Free PMC article.

6

Estimating the Effect of Tafamidis on Cardiovascular-Related Hospitalization in NYHA Class III Patients with Transthyretin Amyloid Cardiomyopathy in the Presence of Death.

Li H, Rozenbaum M, Casey M, Sultan MB. Li H, et al. Cardiology. 2022;147(4):398-405. doi: 10.1159/000525883. Epub 2022 Jul 19. Cardiology. 2022. PMID: 35853436 Free article. Clinical Trial.

7

Cardiac findings and events observed in an open-label clinical trial of tafamidis in patients with non-Val30Met and non-Val122Ile hereditary transthyretin amyloidosis.

Damy T, Judge DP, Kristen AV, Berthet K, Li H, Aarts J. Damy T, et al. Among authors: li h. J Cardiovasc Transl Res. 2015 Mar;8(2):117-27. doi: 10.1007/s12265-015-9613-9. Epub 2015 Mar 6. J Cardiovasc Transl Res. 2015. PMID: 25743445 Free PMC article. Clinical Trial.

8

Long-Term Efficacy and Safety of ARRY-371797 (PF-07265803) in Patients With Lamin A/C-Related Dilated Cardiomyopathy.

Judge DP, Lakdawala NK, Taylor MRG, Mestroni L, Li H, Oliver C, Angeli FS, Lee PA, MacRae CA. Judge DP, et al. Among authors: li h. Am J Cardiol. 2022 Nov 15;183:93-98. doi: 10.1016/j.amjcard.2022.08.001. Epub 2022 Sep 13. Am J Cardiol. 2022. PMID: 36114020 Free article.

9

Long-term effectiveness of ARRY-371797 in people with dilated cardiomyopathy and a faulty LMNA gene: a plain language summary.

Judge DP, Taylor MR, Li H, Oliver C, Angeli FS, Lee PA, MacRae CA. Judge DP, et al. Among authors: li h. Future Cardiol. 2023 Mar;19(3):117-126. doi: 10.2217/fca-2022-0125. Epub 2023 Apr 3. Future Cardiol. 2023. PMID: 37010012 Review.

10

Characterization and natural history of patients with LMNA-related dilated cardiomyopathy in the phase 3 REALM-DCM trial.

Garcia-Pavia P, Lakdawala NK, Sinagra G, Ripoll-Vera T, Afshar K, Priori SG, Ware JS, Owens A, Li H, Angeli FS, Elliott P, MacRae CA, Judge DP. Garcia-Pavia P, et al. Among authors: li h. ESC Heart Fail. 2024 Dec;11(6):4201-4208. doi: 10.1002/ehf2.14955. Epub 2024 Aug 15. ESC Heart Fail. 2024. PMID: 39145700 Free PMC article. Clinical Trial.

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