Neurons that regulate mouse torpor von Hrvatin, Sinisa, Sun, Senmiao, Wilcox, Oren F., Yao, Hanqi, Lavin-Peter, Aurora J., Cicconet, Marcelo, Assad, Elena G., Palmer, Michaela E., Aronson, Sage, Banks, Alexander S., Griffith, Eric C., Greenberg, Michael E.

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Exploring population pharmacokinetic models in patients treated with vancomycin during continuous venovenous haemodiafiltration (CVVHDF) von 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

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A hybrid CFHR3-1 gene causes familial C3 glomerulopathy von Malik, Talat H, Lavin, Peter J, Goicoechea de Jorge, Elena, Vernon, Katherine A, Rose, Kirsten L, Patel, Mitali P, de Leeuw, Marcel, Neary, John J, Conlon, Peter J, Winn, Michelle P, Pickering, Matthew C

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Pathogenesis and therapy of focal segmental glomerulosclerosis: an update von Gbadegesin, Rasheed, Lavin, Peter, Foreman, John, Winn, Michelle

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TRPC6 enhances angiotensin II-induced albuminuria von 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

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Inverted formin 2 mutations with variable expression in patients with sporadic and hereditary focal and segmental glomerulosclerosis von 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.

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A novel missense mutation of Wilms' Tumor 1 causes autosomal dominant FSGS von 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

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Unusual cause of loin pain von Wong, Limy, Kok, Hong Kuan, Akib, Radzi Rodzlan, Joseph Lavin, Peter, Torreggiani, William C.

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TNXB Mutations Can Cause Vesicoureteral Reflux von GBADEGESIN, Rasheed A, BROPHY, Patrick D, WESTREICH, Katherine, GUANGHONG WU, YUTAO LIU, HOLANDA, Danniele, CLARKE, Jason, LAVIN, Peter, SELIM, Angelica, MILLER, Sara, WIENER, John S, ROSS, Sherry S, ADEYEMO, Adebowale, FOREMAN, John, ROTIMI, Charles, WINN, Michelle P, HALL, Gentzon, GUPTA, Indra R, HAINS, David, BARTKOWIAK, Bartlomeij, EGLA RABINOVICH, C, CHANDRASEKHARAPPA, Settara, HOMSTAD, Alison

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A Hybrid CFHR3-1 Gene Causes Familial C3 Glomerulopathy von MALIK, Talat H, LAVIN, Peter J, PICKERING, Matthew C, GOICOECHEA DE JORGE, Elena, VERNON, Katherine A, ROSE, Kirsten L, PATEL, Mitali P, DE LEEUW, Marcel, NEARLY, John J, COLON, Peter J, WINN, Michelle P

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Hepatorenal Correction in Murine Glycogen Storage Disease Type I With a Double-stranded Adeno-associated Virus Vector von Luo, Xiaoyan, Hall, Gentzon, Li, Songtao, Bird, Andrew, Lavin, Peter J, Winn, Michelle P, Kemper, Alex R, Brown, Talmage T, Koeberl, Dwight D

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TRPC6 Enhances Angiotensin II-induced Albuminuria von ECKEL, Jason, LAVIN, Peter J, SPARKS, Matthew, ZHU SHAN ZHANG, HOMSTAD, Alison, BARISONI, Laura, BIRBAUMER, Lutz, ROSENBERG, Paul, WINN, Michelle P, FINCH, Elizabeth A, MUKERJI, Nirvan, BURCH, Jarrett, GBADEGESIN, Rasheed, GUANGHONG WU, BOWLING, Brandy, BYRD, Alison, HALL, Gentzon

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TORCing up the importance of calcium signaling von Lavin, Peter J, Winn, Michelle P

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Kidney transplant outcomes in familial C3 glomerulopathy von Wong, Limy, Moran, Sarah, Lavin, Peter J., Dorman, Anthony M., Conlon, Peter J.

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Object-Oriented PHP von Peter Lavin

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Object-oriented PHP: concepts, techniques, and code von Lavin, Peter

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Therapeutic targets in focal and segmental glomerulosclerosis von Lavin, Peter J, Gbadegesin, Rasheed, Damodaran, Tirupapuliyur V, Winn, Michelle P

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3089 Radiological assessment of suspected acute pyelonephritis in the management of urosepsis and prevention of acute kidney injury von Thornton, Johnny, Wall, Catherine, Mcevoy, Caitriona, Ward, Francis, Halpenny, Darragh, Lavin, Peter, Egan, Allyson C

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Exclusion of homozygous PLCE1 (NPHS3) mutations in 69 families with idiopathic and hereditary FSGS von Gbadegesin, Rasheed, Bartkowiak, Bartlomiej, Lavin, Peter J., Mukerji, Nirvan, Wu, Guanghong, Bowling, Brandy, Eckel, Jason, Damodaran, Tirupapuliyur, Winn, Michelle P.

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COMPUTING RESOURCE AND WORK ALLOCATIONS USING SOCIAL PROFILES von Peter, Lavin, Eamonn, Kenny, Brian, Coghlan

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