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

Risk of Subsequent Events in Patients With Minor Ischemic Stroke or High-Risk Transient Ischemic Attack

轻度缺血性卒中或高危短暂性脑缺血发作患者发生后续事件的风险

Lee, Keon-Joo; Shin, Dong Woo; Park, Hong-Kyun; Kim, Beom Joon; Park, Jong-Moo; Kang, Kyusik; Park, Tai Hwan; Lee, Kyung Bok; Hong, Keun-Sik; Cho, Yong-Jin; Kim, Dong-Eog; Ryu, Wi-Sun; Lee, Byung-Chul; Yu, Kyung-Ho; Oh, Mi-Sun; Lee, Soo Joo; Kim, Jae Guk; Lee, Jun; Cha, Jae-Kwan; Kim, Dae-Hyun; Kim, Joon-Tae; Choi, Kang-Ho; Choi, Jay Chol; Lesén, Eva; Hedberg, Jonatan; Tank, Amarjeet; Fita, Edmond G; Song, Ji Eun; Lee, Ji Sung; Lee, Juneyoung; Bae, Hee-Joon

Genomic Analysis of Mycobacterium abscessus Complex Isolates Collected in Ireland between 2006 and 2017

2006年至2017年间在爱尔兰收集的脓肿分枝杆菌复合群分离株的基因组分析

Redondo, Natalia; Mok, Simone; Montgomery, Lorraine; Flanagan, Peter R; McNamara, Eleanor; Smyth, Edmond G; O'Sullivan, Niamh; Schaffer, Kirsten; Rogers, Thomas R; Fitzgibbon, Margaret M

Efficacy and Safety of IDegAsp Versus BIAsp 30, Both Twice Daily, in Elderly Patients with Type 2 Diabetes: Post Hoc Analysis of Two Phase 3 Randomized Controlled BOOST Trials

IDegAsp 与 BIAsp 30(均每日两次)在老年 2 型糖尿病患者中的疗效和安全性:两项 3 期随机对照 BOOST 试验的事后分析

Fulcher, Greg; Mehta, Roopa; Fita, Edmond G; Ekelund, Magnus; Bain, Stephen C

A Review of Insulin Degludec/Insulin Aspart: Pharmacokinetic and Pharmacodynamic Properties and Their Implications in Clinical Use

胰岛素德谷/胰岛素门冬的药代动力学和药效学特性及其在临床应用中的意义综述

Haahr, Hanne; Fita, Edmond G; Heise, Tim

Disrupted auto-regulation of the spliceosomal gene SNRPB causes cerebro-costo-mandibular syndrome

剪接体基因SNRPB的自身调控紊乱导致脑肋下颌综合征

Lynch, Danielle C; Revil, Timothée; Schwartzentruber, Jeremy; Bhoj, Elizabeth J; Innes, A Micheil; Lamont, Ryan E; Lemire, Edmond G; Chodirker, Bernard N; Taylor, Juliet P; Zackai, Elaine H; McLeod, D Ross; Kirk, Edwin P; Hoover-Fong, Julie; Fleming, Leah; Savarirayan, Ravi; Majewski, Jacek; Jerome-Majewska, Loydie A; Parboosingh, Jillian S; Bernier, Francois P

Extreme intra-familial variability of congenital central hypoventilation syndrome: a case series

先天性中枢性低通气综合征的极端家族内变异性:病例系列研究

Bygarski, Elizabeth; Paterson, Melanie; Lemire, Edmond G

GPSM2 mutations cause the brain malformations and hearing loss in Chudley-McCullough syndrome

GPSM2基因突变会导致丘德利-麦卡洛综合征中的脑畸形和听力丧失。

Doherty, Dan; Chudley, Albert E; Coghlan, Gail; Ishak, Gisele E; Innes, A Micheil; Lemire, Edmond G; Rogers, R Curtis; Mhanni, Aizeddin A; Phelps, Ian G; Jones, Steven J M; Zhan, Shing H; Fejes, Anthony P; Shahin, Hashem; Kanaan, Moien; Akay, Hatice; Tekin, Mustafa; Triggs-Raine, Barbara; Zelinski, Teresa

Birt-Hogg-Dubé syndrome: an inherited cause of spontaneous pneumothorax

Birt-Hogg-Dubé综合征:一种遗传性自发性气胸病因

Pierce, Cameron W; Hull, Peter R; Lemire, Edmond G; Marciniuk, Darcy D

Further expansion of the phenotypic spectrum associated with mutations in ALDH18A1, encoding Δ¹-pyrroline-5-carboxylate synthase (P5CS)

与 ALDH18A1 突变相关的表型谱进一步扩展,编码 Δ¹-吡咯烷-5-羧酸合酶 (P5CS)

David L Skidmore, David Chitayat, Tim Morgan, Alek Hinek, Bjoern Fischer, Aikaterini Dimopoulou, Gino Somers, William Halliday, Susan Blaser, Yenge Diambomba, Edmond G Lemire, Uwe Kornak, Stephen P Robertson

Familial interstitial pulmonary fibrosis: a large family with atypical clinical features

家族性间质性肺纤维化:一个具有非典型临床特征的大家族

Chibbar, Ranji; Gjevre, John A; Shih, Francis; Neufeld, Heather; Lemire, Edmond G; Fladeland, Derek A; Cockcroft, Donald W