日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Cardiac phenotype in hereditary transthyretin amyloidosis: correlations between fibril types and 99mTc-DPD uptake

遗传性转甲状腺素蛋白淀粉样变性的心脏表型:纤维类型与 99mTc-DPD 摄取之间的相关性

Löfbacka, Viktor; Wixner, Jonas; Westermark, Per; Vesterlund, Justina Damjanovic; Anan, Intissar; Pilebro, Björn

A real-world study of tafamidis in people with transthyretin amyloid cardiomyopathy (ATTR-CM) with heart and nerve symptoms: a plain language summary

一项关于他法米地治疗伴有心脏和神经症状的转甲状腺素蛋白淀粉样变性心肌病(ATTR-CM)患者的真实世界研究:简明语言摘要

Wixner, Jonas; Dispenzieri, Angela; Amass, Leslie; Carlsson, Martin; Riley, Steve; Powers, Evan; Kelly, Jeffery W

Five-Year Results With Patisiran for Hereditary Transthyretin Amyloidosis With Polyneuropathy: A Randomized Clinical Trial With Open-Label Extension

帕替西兰治疗伴有多发性神经病变的遗传性转甲状腺素蛋白淀粉样变性五年结果:一项开放标签扩展的随机临床试验

Adams, David; Wixner, Jonas; Polydefkis, Michael; Berk, John L; Conceição, Isabel M; Dispenzieri, Angela; Peltier, Amanda; Ueda, Mitsuharu; Bender, Shaun; Capocelli, Kelley; Jay, Patrick Y; Yureneva, Elena; Obici, Laura

Sixty years of experience with hereditary transthyretin amyloidosis: Insights from the Swedish transthyretin amyloidosis registry

六十年来遗传性转甲状腺素蛋白淀粉样变性的经验:来自瑞典转甲状腺素蛋白淀粉样变性登记处的启示

Stenberg, Lotta; Pilebro, Björn; Anan, Intissar; Baranda, Jorge Mejia; Samuelsson, Kristin; Eldhagen, Per; Backlund, Rolf; Wixner, Jonas

Introducing a revised version of the Kumamoto scale as an easy-to-use clinical tool for monitoring multisystemic changes in hereditary transthyretin amyloidosis

介绍修订版的熊本量表,作为一种易于使用的临床工具,用于监测遗传性转甲状腺素蛋白淀粉样变性的多系统变化。

Wixner, Jonas; Pilebro, Björn; Wien, Tale N; Eldhagen, Per; Mölgaard, Henning; Hedström, Björn; Terkelsen, Astrid J

Estimating Meaningful Differences in Measures of Neuropathic Impairment, Health-Related Quality of Life, and Nutritional Status in Patients With Hereditary Transthyretin Amyloidosis

评估遗传性转甲状腺素蛋白淀粉样变性患者神经病理性损伤、健康相关生活质量和营养状况指标的显著差异

Folkvaljon, Folke; Gertz, Morie; Gillmore, Julian D; Khella, Sami; Masri, Ahmad; Maurer, Mathew S; Cruz, Márcia Waddington; Wixner, Jonas; Chen, Jersey; Reicher, Barry; Kwoh, Jesse; Yarlas, Aaron; Berk, John L

Survival in a Contemporary, Real-World Cohort of Patients with Mixed-Phenotype Transthyretin Amyloid Cardiomyopathy Treated with Tafamidis: An Analysis from THAOS

THAOS 研究分析了接受 Tafamidis 治疗的混合表型转甲状腺素蛋白淀粉样变性心肌病患者的生存情况:一项当代真实世界队列研究的结果。

Wixner, Jonas; Dispenzieri, Angela; Amass, Leslie; Carlsson, Martin; Riley, Steve; Powers, Evan; Kelly, Jeffery W

Clinical and Genotype Characteristics and Symptom Migration in Patients With Mixed Phenotype Transthyretin Amyloidosis from the Transthyretin Amyloidosis Outcomes Survey

来自转甲状腺素蛋白淀粉样变性结局调查的混合表型转甲状腺素蛋白淀粉样变性患者的临床和基因型特征及症状迁移

González-Moreno, Juan; Dispenzieri, Angela; Grogan, Martha; Coelho, Teresa; Tournev, Ivailo; Waddington-Cruz, Márcia; Wixner, Jonas; Diemberger, Igor; Garcia-Pavia, Pablo; Chapman, Doug; Gupta, Pritam; Glass, Oliver; Amass, Leslie

Eplontersen for Hereditary Transthyretin Amyloidosis With Polyneuropathy

Eplontersen 用于治疗伴有多发性神经病变的遗传性转甲状腺素蛋白淀粉样变性

Coelho, Teresa; Marques, Wilson Jr; Dasgupta, Noel R; Chao, Chi-Chao; Parman, Yesim; França, Marcondes Cavalcante Jr; Guo, Yuh-Cherng; Wixner, Jonas; Ro, Long-Sun; Calandra, Cristian R; Kowacs, Pedro A; Berk, John L; Obici, Laura; Barroso, Fabio A; Weiler, Markus; Conceição, Isabel; Jung, Shiangtung W; Buchele, Gustavo; Brambatti, Michela; Chen, Jersey; Hughes, Steven G; Schneider, Eugene; Viney, Nicholas J; Masri, Ahmad; Gertz, Morie R; Ando, Yukio; Gillmore, Julian D; Khella, Sami; Dyck, P James B; Waddington Cruz, Márcia

Characteristics of Patients with Hereditary Transthyretin Amyloidosis-Polyneuropathy (ATTRv-PN) in NEURO-TTRansform, an Open-label Phase 3 Study of Eplontersen

NEURO-TTRansform(一项Eplontersen开放标签3期研究)中遗传性转甲状腺素淀粉样变性-多发性神经病(ATTRv-PN)患者的特征

Coelho, Teresa; Waddington Cruz, Márcia; Chao, Chi-Chao; Parman, Yeşim; Wixner, Jonas; Weiler, Markus; Barroso, Fabio A; Dasgupta, Noel R; Jung, Shiangtung W; Schneider, Eugene; Viney, Nicholas J; Dyck, P James B; Ando, Yukio; Gillmore, Julian D; Khella, Sami; Gertz, Morie A; Obici, Laura; Berk, John L