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

Distinctive clinical features in biopsy-proven nerve large-arteriole vasculitis and microvasculitis

经活检证实的神经大动脉血管炎和微血管炎的独特临床特征

Soontrapa, Pannathat; Pinto, Marcus V; Shouman, Kamal; Mandrekar, Jay; Engelstad, JaNean K; Aragon Pinto, Catarina; Taylor, Sean; Mauermann, Michelle L; Berini, Sarah E; Bosch, E Peter; Rubin, Devon I; Koster, Matthew J; Weyand, Cornelia M; Warrington, Kenneth J; Klein, Christopher J; Dyck, Peter J; Dyck, P James B

Long-term efficacy and safety of inotersen for hereditary transthyretin amyloidosis: NEURO-TTR open-label extension 3-year update

inotersen治疗遗传性转甲状腺素蛋白淀粉样变性的长期疗效和安全性:NEURO-TTR开放标签扩展研究3年更新

Brannagan, Thomas H; Coelho, Teresa; Wang, Annabel K; Polydefkis, Michael J; Dyck, Peter J; Berk, John L; Drachman, Brian; Gorevic, Peter; Whelan, Carol; Conceição, Isabel; Plante-Bordeneuve, Violaine; Merlini, Giampaolo; Obici, Laura; Plana, Josep Maria Campistol; Gamez, Josep; Kristen, Arnt V; Mazzeo, Anna; Gentile, Luca; Narayana, Arvind; Olugemo, Kemi; Aquino, Peter; Benson, Merrill D; Gertz, Morie

Lumbosacral Radiculoplexus Neuropathy: Neurologic Outcomes and Survival in a Population-Based Study

腰骶神经根丛病变:基于人群的研究中的神经系统结局和生存情况

Pinto, Marcus V; Ng, Peng-Soon; Howe, Benjamin M; Laughlin, Ruple S; Thapa, Prabin; Dyck, Peter J; Dyck, P James B

Design and Rationale of the Global Phase 3 NEURO-TTRansform Study of Antisense Oligonucleotide AKCEA-TTR-L(Rx) (ION-682884-CS3) in Hereditary Transthyretin-Mediated Amyloid Polyneuropathy

针对遗传性转甲状腺素蛋白介导的淀粉样多发性神经病,开展反义寡核苷酸AKCEA-TTR-L(Rx) (ION-682884-CS3)的全球3期NEURO-TTRansform研究的设计和原理

Coelho, Teresa; Ando, Yukio; Benson, Merrill D; Berk, John L; Waddington-Cruz, Márcia; Dyck, Peter J; Gillmore, Julian D; Khella, Sami L; Litchy, William J; Obici, Laura; Monteiro, Cecilia; Tai, Li-Jung; Viney, Nicholas J; Buchele, Gustavo; Brambatti, Michela; Jung, Shiangtung W; St L O'Dea, Louis; Tsimikas, Sotirios; Schneider, Eugene; Geary, Richard S; Monia, Brett P; Gertz, Morie

Determinants of Bone Material Strength and Cortical Porosity in Patients with Type 2 Diabetes Mellitus

2型糖尿病患者骨骼材料强度和皮质孔隙率的决定因素

Samakkarnthai, Parinya; Sfeir, Jad G; Atkinson, Elizabeth J; Achenbach, Sara J; Wennberg, Paul W; Dyck, Peter J; Tweed, Amanda J; Volkman, Tammie L; Amin, Shreyasee; Farr, Joshua N; Vella, Adrian; Drake, Matthew T; Khosla, Sundeep

Spectrum of diabetic neuropathies

糖尿病神经病变谱

Sasaki, Hideyuki; Kawamura, Nobutoshi; Dyck, Peter J; Dyck, P James B; Kihara, Mikihiro; Low, Phillip A

Inotersen Treatment for Patients with Hereditary Transthyretin Amyloidosis

Inotersen治疗遗传性转甲状腺素蛋白淀粉样变性患者

Benson, Merrill D; Waddington-Cruz, Márcia; Berk, John L; Polydefkis, Michael; Dyck, Peter J; Wang, Annabel K; Planté-Bordeneuve, Violaine; Barroso, Fabio A; Merlini, Giampaolo; Obici, Laura; Scheinberg, Morton; Brannagan, Thomas H 3rd; Litchy, William J; Whelan, Carol; Drachman, Brian M; Adams, David; Heitner, Stephen B; Conceição, Isabel; Schmidt, Hartmut H; Vita, Giuseppe; Campistol, Josep M; Gamez, Josep; Gorevic, Peter D; Gane, Edward; Shah, Amil M; Solomon, Scott D; Monia, Brett P; Hughes, Steven G; Kwoh, T Jesse; McEvoy, Bradley W; Jung, Shiangtung W; Baker, Brenda F; Ackermann, Elizabeth J; Gertz, Morie A; Coelho, Teresa

Genomic analysis reveals frequent TRAF7 mutations in intraneural perineuriomas

基因组分析揭示神经内膜瘤中TRAF7基因突变频繁发生

Klein, Christopher J; Wu, Yanhong; Jentoft, Mark E; Mer, Georges; Spinner, Robert J; Dyck, P James B; Dyck, Peter J; Mauermann, Michelle L

Trial design and rationale for APOLLO, a Phase 3, placebo-controlled study of patisiran in patients with hereditary ATTR amyloidosis with polyneuropathy

APOLLO 试验的设计和原理:一项评估帕替西兰治疗伴有多发性神经病变的遗传性 ATTR 淀粉样变性患者的 3 期安慰剂对照研究。

Adams, David; Suhr, Ole B; Dyck, Peter J; Litchy, William J; Leahy, Raina G; Chen, Jihong; Gollob, Jared; Coelho, Teresa

Vasculitic neuropathy following exposure to minocycline

接触米诺环素后发生的血管炎性神经病变

Baratta, John M; Dyck, P James B; Brand, Patricio; Thaisetthawatkul, Pariwat; Dyck, Peter J; Engelstad, JaNean K; Goodman, Brent; Karam, Chafic