未登录 Exploring population pharmacokinetic models in patients treated with vancomycin during continuous venovenous haemodiafiltration (CVVHDF) Kirwan, Marcus; Munshi, Reema; O'Keeffe, Hannah; Judge, Conor; Coyle, Mary; Deasy, Evelyn; Kelly, Yvelynne P.; Lavin, Peter J.; Donnelly, Maria; D'Arcy, Deirdre M. 分享 收藏
Utility of Genomic Testing after Renal Biopsy Murray, Susan L.; Dorman, Anthony; Benson, Katherine A.; Connaughton, Dervla M.; Stapleton, Caragh P.; Fennelly, Neil K.; Kennedy, Claire; McDonnell, Ciara A.; Kidd, Kendrah; Cormican, Sarah M.; Ryan, Louise A.; Lavin, Peter; Little, Mark A.; Bleyer, Anthony J.; Doyle, Brendan; Cavalleri, Gianpiero L.; Hildebrandt, Friedhelm; Conlon, Peter J. 分享 收藏
Autosomal dominant tubulointerstitial kidney disease (ADTKD) in Ireland 爱尔兰中的常染色体显性肾小管间质肾病 (ADTKD) Cormican, S.; Connaughton, D. M.; Kennedy, C.; Murray, S.; Zivna, M.; Kmoch, S.; Fennelly, N. K.; O'Kelly, P.; Benson, K. A.; Conlon, E. T.; Cavalleri, G.; Foley, C.; Doyle, B.; Dorman, A.; Little, M. A.; Lavin, P.; Kidd, K.; Bleyer, A. J.; Conlon, P. J. 分享 收藏
Monogenic causes of chronic kidney disease in adults 成人慢性肾脏疾病的单基因病因 Connaughton, Deryla M.; Kennedy, Claire; Shrill, Shirlee; Mann, Nina; Murray, Susan L.; Williams, Patrick A.; Conlon, Eoin; Nakayama, Makiko; van der Ven, Amelie T.; Ityel, Hadas; Kause, Franziska; Kolvenbach, Caroline M.; Dai, Rufeng; Vivante, Asaf; Braun, Daniela A.; Schneider, Ronen; Kitzler, Thomas M.; Moloney, Brona; Moran, Conor P.; Smyth, John S.; Kennedy, Alan; Benson, Katherine; Stapleton, Caragh; Denton, Mark; Magee, Coim; O'Seaghdha, Conall M.; Plant, William D.; Griffin, Matthew D.; Awan, Atif; Sweeney, Clodagh; Mane, Shrikant M.; Lifton, Richard P.; Griffin, Brenda; Leavey, Sean; Casserly, Liam; de Freitas, Declan G.; Holian, John; Dorman, Anthony; Doyle, Brendan; Lavin, Peter J.; Little, Mark A.; Conlon, Peter J.; Hildebrandt, Friedhelm 分享 收藏
Noninvasive Immunohistochemical Diagnosis and Novel MUC1 Mutations Causing Autosomal Dominant Tubulointerstitial Kidney Disease Zivna, Martina; Kidd, Kendrah; Pristoupilova, Anna; Baresova, Veronika; DeFelice, Mathew; Blumenstiel, Brendan; Harden, Maegan; Conlon, Peter; Lavin, Peter; Connaughton, Dervla M.; Hartmannova, Hana; Hodanova, Katerina; Stranecky, Viktor; Vrbacka, Alena; Vylet'al, Petr; Zivny, Jan; Votruba, Miroslav; Sovova, Jana; Hulkova, Helena; Robins, Victoria; Perry, Rebecca; Wenzel, Andrea; Beck, Bodo B.; Seeman, Tomas; Viklicky, Ondrej; Rajnochova-Bloudickova, Sylvie; Papagregoriou, Gregory; Deltas, Constantinos C.; Alper, Seth L.; Greka, Anna; Bleyer, Anthony J.; Kmoch, Stanislav 分享 收藏
Home haemodialysis in Ireland Kennedy, C.; Connaughton, D. M.; Murray, S.; Ormond, J.; Butler, A.; Phelan, E.; Young, J.; Durack, L.; Flavin, J.; O'Grady, M.; O'Kelly, P.; Lavin, P.; Leavey, S.; Lappin, D.; Giblin, L.; Casserly, L.; Plant, W. D.; Conlon, P. J. 分享 收藏
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A Novel Missense Mutation of Wilms' Tumor 1 Causes Autosomal Dominant FSGS 威尔姆斯肿瘤1的新型错义突变导致常染色体显性FSGS Hall, Gentzon; Gbadegesin, Rasheed A.; Lavin, Peter; Wu, Guanghong; Liu, Yangfan; Oh, Edwin C.; Wang, Liming; Spurney, Robert F.; Eckel, Jason; Lindsey, Thomas; Homstad, Alison; Malone, Andrew F.; Phelan, Paul J.; Shaw, Andrey; Howell, David N.; Conlon, Peter J.; Katsanis, Nicholas; Winn, Michelle P. 分享 收藏
Mutations in the Gene That Encodes the F-Actin Binding Protein Anillin Cause FSGS Gbadegesin, Rasheed A.; Hall, Gentzon; Adeyemo, Adebowale; Hanke, Nils; Tossidou, Irini; Burchette, James; Wu, Guanghong; Homstad, Alison; Sparks, Matthew A.; Gomez, Jose; Jiang, Ruiji; Alonso, Andrea; Lavin, Peter; Conlon, Peter; Korstanje, Ron; Stander, M. Christine; Shamsan, Ghaidan; Barua, Moumita; Spurney, Robert; Singhal, Pravin C.; Kopp, Jeffrey B.; Haller, Hermann; Howell, David; Pollak, Martin R.; Shaw, Andrey S.; Schiffer, Mario; Winn, Michelle P. 分享 收藏
Phosphodiesterase 5 inhibition ameliorates angiontensin II-induced podocyte dysmotility via the protein kinase G-mediated downregulation of TRPC6 activity Hall, Gentzon; Rowell, Janelle; Farinelli, Federica; Gbadegesin, Rasheed A.; Lavin, Peter; Wu, Guanghong; Homstad, Alison; Malone, Andrew; Lindsey, Thomas; Jiang, Ruiji; Spurney, Robert; Tomaselli, Gordon F.; Kass, David A.; Winn, Michelle P. 分享 收藏
C3 glomerulopathy: consensus report C3肾小球病: 共识报告 Pickering, Matthew C.; D'Agati, Vivette D.; Nester, Carla M.; Smith, Richard J.; Haas, Mark; Appel, Gerald B.; Alpers, Charles E.; Bajema, Ingeborg M.; Bedrosian, Camille; Braun, Michael; Doyle, Mittie; Fakhouri, Fadi; Fervenza, Fernando C.; Fogo, Agnes B.; Fremeaux-Bacchi, Veronique; Gale, Daniel P.; de Jorge, Elena Goicoechea; Griffin, Gene; Harris, Claire L.; Holers, V. Michael; Johnson, Sally; Lavin, Peter J.; Medjeral-Thomas, Nicholas; Morgan, B. Paul; Nast, Cynthia C.; Noel, Laure-Helene; Peters, D. Keith; Rodriguez de Cordoba, Santiago; Servais, Aude; Sethi, Sanjeev; Song, Wen-Chao; Tamburini, Paul; Thurman, Joshua M.; Zavros, Michael; Cook, H. Terence 分享 收藏
TNXB Mutations Can Cause Vesicoureteral Reflux Gbadegesin, Rasheed A.; Brophy, Patrick D.; Adeyemo, Adebowale; Hall, Gentzon; Gupta, Indra R.; Hains, David; Bartkowiak, Bartlomeij; Rabinovich, C. Egla; Chandrasekharappa, Settara; Homstad, Alison; Westreich, Katherine; Wu, Guanghong; Liu, Yutao; Holanda, Danniele; Clarke, Jason; Lavin, Peter; Selim, Angelica; Miller, Sara; Wiener, John S.; Ross, Sherry S.; Foreman, John; Rotimi, Charles; Winn, Michelle P. 分享 收藏
A Hybrid CFHR3-1 Gene Causes Familial C3 Glomerulopathy Malik, Talat H.; Lavin, Peter J.; de Jorge, Elena Goicoechea; Vernon, Katherine A.; Rose, Kirsten L.; Patel, Mitali P.; de Leeuw, Marcel; Neary, John J.; Conlon, Peter J.; Winn, Michelle P.; Pickering, Matthew C. 分享 收藏
Inverted formin 2 mutations with variable expression in patients with sporadic and hereditary focal and segmental glomerulosclerosis 在散发性和遗传性局灶性和节段性肾小球硬化症患者中具有可变表达的反向formin 2突变 Gbadegesin, Rasheed A.; Lavin, Peter J.; Hall, Gentzon; Bartkowiak, Bartlomiej; Homstad, Alison; Jiang, Ruiji; Wu, Guanghong; Byrd, Alison; Lynn, Kelvin; Wolfish, Norman; Ottati, Carolina; Stevens, Paul; Howell, David; Conlon, Peter; Winn, Michelle P. 分享 收藏
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Arhgap24 inactivates Rac1 in mouse podocytes, and a mutant form is associated with familial focal segmental glomerulosclerosis Akilesh, Shreeram; Suleiman, Hani; Yu, Haiyang; Stander, M. Christine; Lavin, Peter; Gbadegesin, Rasheed; Antignac, Corinne; Pollak, Martin; Kopp, Jeffrey B.; Winn, Michelle P.; Shaw, Andrey S. 分享 收藏
TRPC6 Enhances Angiotensin II-induced Albuminuria Eckel, Jason; Lavin, Peter J.; Finch, Elizabeth A.; Mukerji, Nirvan; Burch, Jarrett; Gbadegesin, Rasheed; Wu, Guanghong; Bowling, Brandy; Byrd, Alison; Hall, Gentzon; Sparks, Matthew; Zhang, Zhu Shan; Homstad, Alison; Barisoni, Laura; Birbaumer, Lutz; Rosenberg, Paul; Winn, Michelle P. 分享 收藏
A New Locus for Familial FSGS on Chromosome 2P Gbadegesin, Rasheed; Lavin, Peter; Janssens, Louis; Bartkowiak, Bartlomiej; Homstad, Alison; Wu, Guanghong; Bowling, Brandy; Eckel, Jason; Potocky, Chris; Abbott, Diana; Conlon, Peter; Scott, William K.; Howell, David; Hauser, Elizabeth; Winn, Michelle P. 分享 收藏
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