Absence of an increased wall thickness does not rule out cardiac amyloidosis [0.03%]
心肌壁厚度正常不能排除心脏淀粉样变性
Steven A Muller,Anouk Achten,Manon G van der Meer et al.
Steven A Muller et al.
Patient-reported satisfaction with telemedicine in light chain (AL) amyloidosis care [0.03%]
轻链(AL)淀粉样变性患者对远程医疗服务满意度的调查
Idayat Akinola,Kathryn E Flynn,Aniko Szabo et al.
Idayat Akinola et al.
Maria Ausilia Sciarrone,Rosa Lillo,Angela Romano et al.
Maria Ausilia Sciarrone et al.
Heterogeneity in families with ATTRV30M amyloidosis: a historical and longitudinal Portuguese case study impact for genetic counselling [0.03%]
葡萄牙ATTRV30M淀粉样变性的家族异质性：历史性和纵向性案例研究及其对遗传咨询的影响
Maria Pedroto,Teresa Coelho,Joana Fernandes et al.
Maria Pedroto et al.
Background: Hereditary transthyretin amyloidosis (ATTRv amyloidosis) is an inherited disease, where the study of family history holds importance. This study evaluates the changes of age-of-onset (AOO) and other age-relate...
Longitudinal analysis of serum neurofilament light chain levels as marker for neuronal damage in hereditary transthyretin amyloidosis [0.03%]
遗传性甲状腺素运载蛋白淀粉样变中神经丝轻链水平的纵向分析作为神经损伤标志物
Milou Berends,Anne F Brunger,Johan Bijzet et al.
Milou Berends et al.
Objective: To evaluate serum neurofilament light chain (sNfL) as biomarker of disease onset, progression and treatment effect in hereditary transthyretin (ATTRv) amyloidosis patients and TTR variant (TTRv) carriers. ...
Circulating transthyretin and retinol binding protein 4 levels among middle-age V122I TTR carriers in the general population [0.03%]
人群中携带V122I TTR基因的中年人血清甲状腺素运载蛋白和视黄醇结合蛋白4水平检测
Nicholas S Hendren,James A De Lemos,Jarett D Berry et al.
Nicholas S Hendren et al.
Background: Hereditary transthyretin cardiac amyloidosis (ATTRv-CA) has a long latency phase before clinical onset, creating a need to identify subclinical disease. We hypothesized circulating transthyretin (TTR) and reti...
Possible transmission of leukocyte chemotactic factor 2 amyloidosis after interpopulational liver transplantation [0.03%]
种间肝脏移植后白细胞趋化因子2淀粉样变性病可能的传播
Yuji Suzuki,Masayoshi Tasaki,Keisuke Kakisaka et al.
Yuji Suzuki et al.
Gait abnormalities in older adults with transthyretin cardiac amyloidosis [0.03%]
转甲状腺素蛋白心脏淀粉样变性老年患者步态异常分析
Fitsum E Petros,Alfonsina Mirabal Santos,Adedeji Adeniyi et al.
Fitsum E Petros et al.
Background: Transthyretin cardiac amyloidosis (ATTR cardiac amyloidosis) is caused by variant (ATTRv) or wild type (ATTRwt) transthyretin. While gait abnormalities have been studied in younger patients with ATTRv amyloido...
Serum neurofilament light chain in hereditary transthyretin amyloidosis: validation in real-life practice [0.03%]
遗传性转甲状腺素蛋白淀粉样变性病血清神经丝轻链的验证研究
Antonia S Carroll,Yousuf Razvi,Luke O&#x;Donnell et al.
Antonia S Carroll et al.
Background: Neurofilament light chain (NfL) has emerged as a sensitive biomarker in hereditary transthyretin amyloid polyneuropathy (ATTRv-PN). We hypothesise that NfL can identify conversion of gene carriers to symptomat...
Mass spectrometry-based proteomic analysis of proteins adsorbed by hexadecyl-immobilized cellulose bead column for the treatment of dialysis-related amyloidosis [0.03%]
十六烷基纤维素包埋珠柱吸附蛋白质的质谱蛋白质组学分析及其在透析相关淀粉样变性治疗中的应用研究
Suguru Yamamoto,Keiko Yamamoto,Yoshitoshi Hirao et al.
Suguru Yamamoto et al.
Background: Dialysis-related amyloidosis (DRA) is a severe complication in end-stage kidney disease (ESKD) patients undergoing long-term dialysis treatment, characterized by the deposition of β2-microglobulin-related amy...