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For: Rintell D, Heath D, Braga Mendendez F, Cross E, Cross T, Knobel V, Gagnon B, Turtle C, Cohen A, Kalmykov E, Fox J. Patient and family experience with transthyretin amyloid cardiomyopathy (ATTR-CM) and polyneuropathy (ATTR-PN) amyloidosis: results of two focus groups. Orphanet J Rare Dis 2021;16:70. [PMID: 33557882 DOI: 10.1186/s13023-021-01706-7] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
Number Citing Articles
1 Carry BJ, Young K, Fielden S, Kelly MA, Sturm AC, Avila JD, Martin CL, Kirchner HL, Fornwalt BK, Haggerty CM; Regeneron Genetics Center, Tarrytown, New York, USA. Genomic Screening for Pathogenic Transthyretin Variants Finds Evidence of Underdiagnosed Amyloid Cardiomyopathy From Health Records. JACC CardioOncol 2021;3:550-61. [PMID: 34746851 DOI: 10.1016/j.jaccao.2021.07.002] [Reference Citation Analysis]
2 Jang SC, Nam JH, Lee SA, An D, Kim HL, Kwon SH, Lee EK. Clinical manifestation, economic burden, and mortality in patients with transthyretin cardiac amyloidosis. Orphanet J Rare Dis 2022;17:262. [PMID: 35840997 DOI: 10.1186/s13023-022-02425-3] [Reference Citation Analysis]
3 Tschöpe C, Elsanhoury A. Treatment of Transthyretin Amyloid Cardiomyopathy: The Current Options, the Future, and the Challenges. J Clin Med 2022;11:2148. [PMID: 35456241 DOI: 10.3390/jcm11082148] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
4 Lauppe R, Liseth Hansen J, Fornwall A, Johansson K, Rozenbaum MH, Strand AM, Vakevainen M, Kuusisto J, Gude E, Smith JG, Gustafsson F. Healthcare resource use of patients with transthyretin amyloid cardiomyopathy. ESC Heart Fail 2022. [PMID: 35365974 DOI: 10.1002/ehf2.13913] [Reference Citation Analysis]
5 Daykin E, Fleischer N, Abdelwahab M, Hassib N, Schiffmann R, Ryan E, Sidransky E. Investigation of a dysmorphic facial phenotype in patients with Gaucher disease types 2 and 3. Mol Genet Metab 2021;134:274-80. [PMID: 34663554 DOI: 10.1016/j.ymgme.2021.09.008] [Reference Citation Analysis]