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

Examining the Clinical Usefulness of Urine Methylmalonic Acid for Diagnosis of Vitamin B-12 Deficiency in Older Adults: A Pilot Study

探讨尿甲基丙二酸在老年人维生素B12缺乏症诊断中的临床应用价值:一项初步研究

Bédard-Delisle, Charlotte; Leonard, Guillaume; Auray-Blais, Christiane; Reid, Isabelle; Gamrani, Mohamed; Chebbihi, Hassiba; Presse, Nancy

Lentivirus-mediated gene therapy for Fabry disease: 5-year End-of-Study results from the Canadian FACTs trial

慢病毒介导的基因疗法治疗法布里病:加拿大FACTs试验5年研究结束结果

Khan, Aneal; Barber, Dwayne L; McKillop, William M; Rupar, C Anthony; Auray-Blais, Christiane; Fraser, Graeme; Fowler, Daniel H; Berger, Alexandra; Foley, Ronan; Keating, Armand; West, Michael L; Medin, Jeffrey A

Unraveling porcine dendritic-cell diversity: welcome tDC and DC3

揭示猪树突状细胞的多样性:欢迎 tDC 和 DC3

Baillou, Ambre; Auray, Gaël; Brito, Francisco; Botos, Marius; Huber, Alizée; Summerfield, Artur; Talker, Stephanie C

Efficacy of genetically modified Mycoplasma hyopneumoniae strains and their effect on local and cell-mediated immune responses in pigs

基因改造猪肺炎支原体菌株的功效及其对猪局部和细胞介导免疫反应的影响

Beuckelaere, Lisa; Boyen, Filip; Auray, Gaël; Haspeslagh, Maarten; De Coensel, Eva; Trueeb, Bettina Salome; Meyer, Evelyne; Haesebrouck, Freddy; De Spiegelaere, Ward; Devriendt, Bert; Summerfield, Artur; Kuhnert, Peter; Maes, Dominiek

UPLC-MS/MS High-Risk Screening for Sphingolipidoses Using Dried Urine Spots.

利用干燥尿斑进行UPLC-MS/MS高风险鞘脂沉积症筛查

Martineau Tristan, Maranda Bruno, Auray-Blais Christiane

Prospective characterization of early symptom onset and progression in young pediatric patients with variants in the G LA gene across 5 years: Longitudinal data from the Fabry MOPPet Study

对携带 GLA 基因变异的年轻儿科患者早期症状出现和进展进行为期 5 年的前瞻性特征分析:来自 Fabry MOPPet 研究的纵向数据

Laney, D A; Houde, M F; Foley, A L; Peck, D S; Atherton, A M; Manwaring, L P; Grange, D K; Heese, B A; Holida, M D; Quillin, A L; Vinson, R; Auray-Blais, C; Hopkin, R J

Persistent hematopoietic polyclonality after lentivirus-mediated gene therapy for Fabry disease

法布里病慢病毒介导基因治疗后持续性造血多克隆性

Saleh, Amr H; Rothe, Michael; Barber, Dwayne L; McKillop, William M; Fraser, Graeme; Morel, Chantal F; Schambach, Axel; Auray-Blais, Christiane; West, Michael L; Khan, Aneal; Fowler, Daniel H; Rupar, C Anthony; Foley, Ronan; Medin, Jeffrey A; Keating, Armand

Late-onset and classic phenotypes of Fabry disease in males with the GLA-Thr410Ala mutation

携带 GLA-Thr410Ala 突变的男性法布里病患者表现出迟发型和经典表型。

Valtola, Kati; Hedman, Marja; Kantola, Ilkka; Walls, Susanne; Helisalmi, Seppo; Maria, Maleeha; Raivo, Joose; Auray-Blais, Christiane; Kuusisto, Johanna

American Society for Reconstructive Transplantation Biennial Meeting Abstracts 2022

美国重建移植学会2022年双年会摘要

Alarie, Christophe; Gagnon, Isabelle; Thao Huynh, Lily Trang; Doucet, Karine; Pichette-Auray, Adèle; Hinse-Joly, Cassandre; Swaine, Bonnie

A case of hyperlysinemia identified by urine newborn screening

通过新生儿尿液筛查发现一例高赖氨酸血症病例

Yeganeh, Mehdi; Auray-Blais, Christiane; Maranda, Bruno; Sabovic, Amanda; DeVita, Robert J; Lazarus, Michael B; Houten, Sander M