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

Plasma Metabolites Associated with CKD Stage in Autosomal Dominant Tubulointerstitial Kidney Disease

常染色体显性遗传性肾小管间质性肾病中与慢性肾脏病分期相关的血浆代谢物

Mušálková, Dita; Radina, Martin; Kidd, Kendrah; Hartmannová, Hana; Trešlová, Helena; Hodaňová, Kateřina; Vyleťal, Petr; Vrbacká, Alena; Votruba, Miroslav; Sanchez, Antonio; Martin, Lauren; Taylor, Abbigail; Kim, Alice; Rudl Kulhavá, Lucie; Hricko, Jiří; Čajka, Tomáš; Živná, Martina; Bleyer, Anthony J; Kmoch, Stanislav

MANF Clears Mutant Uromodulin in Human Kidney Organoids of Autosomal Dominant Tubulointerstitial Kidney Disease

MANF清除常染色体显性遗传性肾小管间质性肾病人类肾脏类器官中的突变尿调蛋白

Gu, Chenjian; Fang, Yili; Wang, Yixuan; Tycksen, Eric; Kondepati, Gayathri; Li, Chuang; Kidd, Kendrah; Liu, Jun; Urano, Fumihiko; Lindahl, Maria; Bleyer, Anthony J; Singamaneni, Srikanth; Sun, Zhao; Chen, Ying Maggie

Implementation of a Kidney Genetic Service Into the Diagnostic Pathway for Patients With Chronic Kidney Disease in Canada

在加拿大将肾脏遗传服务纳入慢性肾病患者的诊断流程

Schott, Clara; Arnaldi, Monica; Baker, Cadence; Wang, Jian; McIntyre, Adam D; Colaiacovo, Samantha; Relouw, Sydney; Offerni, Gabriela Almada; Campagnolo, Carla; Van Nynatten, Logan R; Pourtousi, Ava; Drago-Catalfo, Alexa; Lebedeva, Victoria; Chiu, Michael; Cowan, Andrea; Filler, Guido; Gunaratnam, Lakshman; House, Andrew A; Huang, Susan; Iyer, Hariharan; Jain, Arsh K; Jevnikar, Anthony M; Lotfy, Khaled; Moist, Louise; Rehman, Faisal; Roshanov, Pavel S; Sharma, Ajay P; Weir, Matthew A; Kidd, Kendrah; Bleyer, Anthony J; Hegele, Robert A; Connaughton, Dervla M

Genotype-phenotype correlations and clinical outcomes of genetic TRPC6 podocytopathies

基因型-表型相关性及遗传性TRPC6足细胞病临床结局

McAnallen, Susan M; Elhassan, Elhussein A E; Stoneman, Sinead; Pinto E Vairo, Filippo; Hogan, Marie C; Hoefele, Julia; Clince, Michelle; Mekraksakit, Poemlarp; Titan, Silvia M; Jorge, Sofia; Calado, Joaquim; Decramer, Stéphane; Colliou, Eloïse; Tellier, Stéphanie; Francisco, Telma; Servais, Aude; Cornet, Joséphine; de Fallois, Jonathan; Dossier, Claire; Fenoglio, Roberta; Renieri, Alessandra; Pinto, Anna Maria; Daga, Sergio; Loberti, Lorenzo; Fila, Marc; Quintana, Luis F; Becherucci, Francesca; Godefroid, Nathalie; Dubrasquet, Astrid; Kálmán, Tory; Dolan, Niamh; Alawi, Bushra Al; Sweeney, Clodagh; Riordan, Michael; Stack, Maria; Awan, Atif; Hui, Ng Kar; McCarthy, Hugh J; Biros, Erik; Harris, Trudie; Kidd, Kendrah; Haeberle, Stefanie; Bleyer, Anthony J; Mallett, Andrew J; Sayer, John A; Schafer, Franz; Benson, Katherine A; McCann, Emma; Conlon, Peter J

Genetic Testing in Adults over 50 Years with Chronic Kidney Disease: Diagnostic Yield and Clinical Implications in a Specialized Kidney Genetics Clinic

针对50岁以上慢性肾病成年患者的基因检测:肾脏遗传专科诊所的诊断率和临床意义

Schott, Clara; Alajmi, Mohammad; Bukhari, Mohammad; Relouw, Sydney; Wang, Jian; McIntyre, Adam D; Baker, Cadence; Colaiacovo, Samantha; Campagnolo, Carla; Almada Offerni, Gabriela; Blake, Peter G; Chiu, Micheal; Cowan, Andrea; Garg, Amit X; Gunaratnam, Lakshman; House, Andrew A; Huang, Shih-Han Susan; Iyer, Hariharan; Jain, Arsh K; Jevnikar, Anthony M; Johnson, John; Lotfy, Khaled; Moist, Louise; Rehman, Faisal; Roshanov, Pavel S; Sultan, Nabil; Weir, Matthew A; Basharat, Pari; Florendo-Cumbermack, Anita; Khan, Tayyab; Thain, Jenny; Kidd, Kendrah; Kmoch, Stanislav; Bleyer, Anthony J; Bhangu, Jaspreet; Hegele, Robert A; Connaughton, Dervla M

An Observational Study of SGLT2 Inhibitors and Their Use in Autosomal Dominant Tubulointerstitial Kidney Disease

SGLT2抑制剂及其在常染色体显性遗传性肾小管间质性肾病中的应用观察性研究

Kidd, Kendrah O; Williams, Adrienne H; Elhassan, Elhussein A E; Taylor, Abbigail; Martin, Lauren; Kim, Alice; Rocco, Michael V; Choi, Michael J; Zivna, Martina; Kmoch, Stanislav; Conlon, Peter J; Bleyer, Anthony J

Description of a New Simple and Cost-Effective Molecular Testing That Could Simplify MUC1 Variant Detection

一种新型简便且经济高效的分子检测方法简介,该方法可简化MUC1变异体的检测。

Fages, Victor; Bourre, Florentin; Larrue, Romain; Wenzel, Andrea; Gibier, Jean-Baptiste; Bonte, Fabrice; Dhaenens, Claire-Marie; Kidd, Kendrah; Kmoch, Stanislav; Bleyer, Anthony; Glowacki, François; Grunewald, Olivier

A Novel Monoallelic ALG5 Variant Causing Late-Onset ADPKD and Tubulointerstitial Fibrosis

一种新型单等位基因ALG5变异导致晚发性ADPKD和肾小管间质纤维化

Elhassan, Elhussein A E; Kmochová, Tereza; Benson, Katherine A; Fennelly, Neil K; Barešová, Veronika; Kidd, Kendrah; Doyle, Brendan; Dorman, Anthony; Morrin, Martina M; Kyne, Niamh C; Vyleťal, Petr; Hartmannová, Hana; Hodaňová, Kateřina; Sovová, Jana; Mušálková, Dita; Vrbacká, Alena; Přistoupilová, Anna; Živný, Jan; Svojšová, Klára; Radina, Martin; Stránecký, Viktor; Loginov, Dmitry; Pompach, Petr; Novák, Petr; Vaníčková, Zdislava; Hansíková, Hana; Rajnochová-Bloudíčková, Silvie; Viklický, Ondřej; Hůlková, Helena; Cavalleri, Gianpiero L; Hnízda, Aleš; Bleyer, Anthony J; Kmoch, Stanislav; Conlon, Peter J; Živná, Martina

Eight-fold increased COVID-19 mortality in autosomal dominant tubulointerstitial kidney disease due to MUC1 mutations: an observational study

常染色体显性遗传性肾小管间质性肾病患者因MUC1基因突变导致COVID-19死亡率增加8倍:一项观察性研究

Kidd, Kendrah O; Williams, Adrienne H; Taylor, Abbigail; Martin, Lauren; Robins, Victoria; Sayer, John A; Olinger, Eric; Mabillard, Holly R; Papagregoriou, Gregory; Deltas, Constantinos; Stavrou, Christoforos; Conlon, Peter J; Hogan, Richard Edmund; Elhassan, Elhussein A E; Springer, Drahomíra; Zima, Tomáš; Izzi, Claudia; Vrbacká, Alena; Piherová, Lenka; Pohludka, Michal; Radina, Martin; Vylet'al, Petr; Hodanova, Katerina; Zivna, Martina; Kmoch, Stanislav; Bleyer, Anthony J Sr

Mammographically and sonographically occult male DCIS seen only on breast MRI

乳腺X线摄影和超声检查均无法发现的男性导管原位癌,仅在乳腺MRI检查中可见。

Osei, Kendrah; Panigrahi, Babita