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

Behavioral health technician delivered written exposure therapy for posttraumatic stress disorder in the military: Design of a hybrid implementation effectiveness trial

行为健康技师为军队中的创伤后应激障碍患者提供书面暴露疗法:混合实施效果试验的设计

McLean, Carmen P; Bell, Meghan M; Haddock, Christopher K; LoSavio, Stefanie T; Mann, Jeffrey; McCaslin, Shannon; Rahman, Nazia; Rodden, Lauren; Rogers, Timothy; Rosen, Craig S; Woodworth, Craig; Cook, Jeffrey

Algorithmic approach to finding people with multiple sclerosis using routine healthcare data in Wales

利用威尔士常规医疗保健数据寻找多发性硬化症患者的算法

Nicholas, Richard; Tallantyre, Emma Clare; Witts, James; Marrie, Ruth Ann; Craig, Elaine M; Knowles, Sarah; Pearson, Owen Rhys; Harding, Katherine; Kreft, Karim; Hawken, J; Ingram, Gillian; Morgan, Bethan; Middleton, Rodden M; Robertson, Neil; Research Group, Ukms Register

Sitting Less, Recovering Faster: Investigating the Relationship between Daily Sitting Time and Muscle Recovery following Intense Exercise: A Pilot Study

减少久坐,加快恢复:探究每日久坐时间与剧烈运动后肌肉恢复的关系:一项初步研究

Rodden, Jaime; Ortega, Dolores G; Costa, Pablo B

Imposter among us: field cancerization in the bladder

我们之中的冒名顶替者:膀胱癌变场

Rodden, Daniel J; Chung, Ella H; Pittie, Rea; Miyamoto, David T

Retinal hypoplasia and degeneration result in vision loss in Friedreich ataxia

弗里德赖希共济失调患者的视网膜发育不全和退化会导致视力丧失。

Rodden, Layne N; McIntyre, Kellie; Keita, Medina; Wells, Mckenzie; Park, Courtney; Profeta, Victoria; Waldman, Amy; Rummey, Christian; Balcer, Laura J; Lynch, David R

FXN gene methylation determines carrier status in Friedreich ataxia

FXN基因甲基化决定弗里德赖希共济失调的携带者状态。

Lam, Christina; Gilliam, Kaitlyn M; Rodden, Layne N; Schadt, Kimberly A; Lynch, David R; Bidichandani, Sanjay

Recovery From COVID-19 in Multiple Sclerosis: A Prospective and Longitudinal Cohort Study of the United Kingdom Multiple Sclerosis Register

英国多发性硬化症登记处开展的一项前瞻性纵向队列研究:新冠肺炎患者在多发性硬化症中的康复情况

Garjani, Afagh; Middleton, Rodden M; Nicholas, Richard; Evangelou, Nikos

A non-synonymous single nucleotide polymorphism in SIRT6 predicts neurological severity in Friedreich ataxia

SIRT6 中的非同义单核苷酸多态性可预测弗里德赖希共济失调的神经系统严重程度

Layne N Rodden, Christian Rummey, Yi Na Dong, Sarah Lagedrost, Sean Regner, Alicia Brocht, Khalaf Bushara, Martin B Delatycki, Christopher M Gomez, Katherine Mathews, Sarah Murray, Susan Perlman, Bernard Ravina, S H Subramony, George Wilmot, Theresa Zesiewicz, Alessandra Bolotta, Alain Domissy, Chri

DNA methylation in Friedreich ataxia silences expression of frataxin isoform E

弗里德赖希共济失调中的 DNA 甲基化抑制了 frataxin 异构体 E 的表达

Layne N Rodden, Kaitlyn M Gilliam, Christina Lam, Teerapat Rojsajjakul, Clementina Mesaros, Chiara Dionisi, Mark Pook, Massimo Pandolfo, David R Lynch, Ian A Blair, Sanjay I Bidichandani

Clinical Evidence for Variegated Silencing in Patients With Friedreich Ataxia

弗里德赖希共济失调患者中多种沉默现象的临床证据

Rodden, Layne N; Rummey, Christian; Dong, Yi Na; Lynch, David R