Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Suzanne Vento"'
APOL1 genotype-associated morphologic changes among patients with focal segmental glomerulosclerosis
Autor:
John F. O’Toole, Katherine R. Tuttle, Kevin V. Lemley, Matthew G. Sampson, Marie C. Hogan, Jarcy Zee, Michelle T McNulty, Sharon G. Adler, Vimal K. Derebail, Chia-shi Wang, Raed Bou Matar, Elizabeth J. Brown, Katherine MacRae Dell, Fernando C. Fervenza, Keisha L. Gibson, Gerald B. Appel, Cynthia C. Nast, Ambarish M. Athavale, Pamela Singer, Jonathan Ashley Jefferson, Richard A. Lafayette, Jeffrey B. Kopp, Larry A. Greenbaum, Kevin E.C. Meyers, Laura Barisoni, Alessia Fornoni, Jiten Patel, Kamalanathan K. Sambandam, Crystal A. Gadegbeku, Meredith A. Atkinson, Serena M. Bagnasco, Matthias Kretzler, Jonathan J. Hogan, Heather N. Reich, Suzanne Vento, Howard Trachtman, Jen Jar Lin, Jeffrey B. Hodgin, Lawrence B. Holzman, Tarak Srivastava, Sangeeta Hingorani, Frederick J. Kaskel, Michelle Hladunewich, Olga Zhdanova, Christine B. Sethna, Dhruti P. Chen, Debbie S. Gipson, John C. Lieske
Publikováno v:
Pediatr Nephrol
Background: The G1 and G2 alleles of apolipoprotein L1 (APOL1) are common in the Black population and associated with increased risk of focal segmental glomerulosclerosis (FSGS). The molecular mechanisms linking APOL1 risk variants with FSGS are not
Autor:
Shailee Lala, Laura Jane Pehrson, Laura Malaga-Dieguez, Joseph Connors, Rachel Aronov, Howard Trachtman, Suzanne Vento, Ming Wu
Publikováno v:
Radiology Case Reports
Radiology Case Reports, Vol 13, Iss 5, Pp 1003-1006 (2018)
Radiology Case Reports, Vol 13, Iss 5, Pp 1003-1006 (2018)
Interstitial nephritis (IN) is a relatively rare entity in children and adolescents that can be caused by a range of disorders including infection, medications, inflammatory bowel disease, and sarcoid. There is no proven therapy for this condition. W
Publikováno v:
Pediatric Nephrology. 21:584-587
Proteinuria is utilized to screen for underlying kidney disease and serves as a marker of disease progression. The aim of this study was to test the hypothesis that patients with proteinuria will have a higher frequency of urine dipstick positive for
Autor:
Xuzhen Hu, Peter S.T. Yuen, Rachel M. Frank, Hua Zhou, Robert A. Star, Howard Trachtman, Hiroshi Kajiyama, Suzanne Vento, Asada Leelahavanichkul, Takayuki Tsuji, Jeffrey B. Kopp
Renal Wilms' tumor-1 (WT-1) staining is used to detect podocyte loss in kidney biopsies. We aimed to determine if urinary exosomal WT-1 could serve as a noninvasive biomarker of podocyte injury. We examined WT-1 by Western blot in a human podocyte-li
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::334c3465e3c19b9b16a3eecf747e4a13
https://europepmc.org/articles/PMC3891263/
https://europepmc.org/articles/PMC3891263/
Autor:
Leslie M. Powell, Debbie S. Gipson, Suzanne Vento, Jacqueline MacHardy, Alexandra Peyser, Howard Trachtman, Nathaniel MacHardy, Cynthia G. Pan, Theresa Kump, Freya Tarapore, Virginia J. Savin
Publikováno v:
BMC Nephrology
BMC Nephrology, Vol 11, Iss 1, p 2 (2010)
BMC Nephrology, Vol 11, Iss 1, p 2 (2010)
Background Patients with resistant primary focal segmental glomerulosclerosis (FSGS) are at high risk of progression to chronic kidney disease stage V. Antifibrotic agents may slow or halt this process. We present outcomes of follow-up after a Phase
Autor:
Jeanne Choi-Rosen, Suzanne Vento, Stephanie Lasky, Kristy VanDervoort, Howard Trachtman, Beatrice Goilav, Christine B. Sethna, Rachel M. Frank
Publikováno v:
Clinical Medicine Insights: Pediatrics, Vol 3 (2009)
Clinical Medicine. Pediatrics
Clinical Medicine. Pediatrics
Background Infants with neonatal hydronephrosis and a normal voiding cystourethrogram (VCUG) are presumed to have ureteropelvic junction obstruction (UPJO). There is little current information about the natural history of children with hydronephrosis
Autor:
Suzanne Vento, Ashton Chen, Elsa Valderrama, Howard Trachtman, Bernard Gauthier, Virginia Crosby, Manju Chandra, Rachel M. Frank
Publikováno v:
BMC Nephrology
BMC Nephrology, Vol 8, Iss 1, p 11 (2007)
BMC Nephrology, Vol 8, Iss 1, p 11 (2007)
Background Idiopathic membranous nephropathy (IMN) is one of the most common causes of primary nephrotic syndrome in adults. However, it is a relatively rare entity in the pediatric population and there is a paucity of data about the incidence, progn