Zobrazeno 1 - 10
of 110
pro vyhledávání: '"Serena M Bagnasco"'
Autor:
Kevin V Lemley, Serena M Bagnasco, Cynthia C Nast, Laura Barisoni, Catherine M Conway, Stephen M Hewitt, Peter X K Song
Publikováno v:
PLoS ONE, Vol 11, Iss 6, p e0157148 (2016)
OBJECTIVE:Most predictive models of kidney disease progression have not incorporated structural data. If structural variables have been used in models, they have generally been only semi-quantitative. METHODS:We examined the predictive utility of qua
Externí odkaz:
https://doaj.org/article/5a0226df1c314616a847c2674b2b826b
Sarcoidosis in native and transplanted kidneys: incidence, pathologic findings, and clinical course.
Autor:
Serena M Bagnasco, Srinivas Gottipati, Edward Kraus, Nada Alachkar, Robert A Montgomery, Lorraine C Racusen, Lois J Arend
Publikováno v:
PLoS ONE, Vol 9, Iss 10, p e110778 (2014)
Renal involvement by sarcoidosis in native and transplanted kidneys classically presents as non caseating granulomatous interstitial nephritis. However, the incidence of sarcoidosis in native and transplant kidney biopsies, its frequency as a cause o
Externí odkaz:
https://doaj.org/article/44d8c1a3976f4c079841ce7d8a4071fb
Publikováno v:
Biosensors, Vol 13, Iss 4, p 466 (2023)
Amyloids are proteins with characteristic beta-sheet secondary structures that display fibrillary ultrastructural configurations. They can result in pathologic lesions when deposited in human organs. Various types of amyloid protein can be routinely
Externí odkaz:
https://doaj.org/article/abb5d6c7a68f439aa90cac55fe8c7566
Publikováno v:
Case Reports in Nephrology, Vol 2022 (2022)
The involvement of hematological tumors such as lymphoma in the kidneys is a well-recognized phenomenon. Some of the distinct reported pathological processes resulting in kidney dysfunction include minimal change disease, lymphocytic invasion of the
Externí odkaz:
https://doaj.org/article/341f14fca41d40b9a5060d42dad7fffe
Autor:
Nada Alachkar, Marco Delsante, Ross S. Greenberg, Abbal Koirala, Tarek Alhamad, Basmah Abdalla, Manish Anand, Ben Boonpheng, Christopher Blosser, Umberto Maggiore, Serena M. Bagnasco
Publikováno v:
Transplantation.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a4e7d984b08422deb6d3232150baf35f
https://doi.org/10.1097/tp.0000000000004640
https://doi.org/10.1097/tp.0000000000004640
Autor:
Steven Menez, Steven G. Coca, Dennis G. Moledina, Yumeng Wen, Lili Chan, Heather Thiessen-Philbrook, Wassim Obeid, Brian T. Garibaldi, Evren U. Azeloglu, Ugochukwu Ugwuowo, C. John Sperati, Lois J. Arend, Avi Z. Rosenberg, Madhurima Kaushal, Sanjay Jain, F. Perry Wilson, Chirag R. Parikh, Jie Deng, Mo Atta, Serena M. Bagnasco, Albert Ko, Akiko Iwasaki, Shelli Farhadian, Allison Nelson, Arnau Casanovas-Massana, Elizabeth B. White, Wade Schulz, Andreas Coppi, Patrick Young, Angela Nunez, Denise Shepard, Irene Matos, Yvette Strong, Kelly Anastasio, Kristina Brower, Maxine Kuang, Michael Chiorazzi, Santos Bermejo, Pavithra Vijayakumar, Bertie Geng, John Fournier, Maksym Minasyan, M. Catherine Muenker, Adam J. Moore, Girish Nadkarni
Publikováno v:
American Journal of Kidney Diseases.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::84ffc026913dcfec33e0582b68b534e0
https://doi.org/10.1053/j.ajkd.2023.03.010
https://doi.org/10.1053/j.ajkd.2023.03.010
Autor:
Serena M. Bagnasco, Jeffrey J. Fadrowski, Francesca Costigliolo, Rebecca L. Ruebner, Hannah S. Kim
Publikováno v:
Pediatrics In Review. 42:266-269
1. Hannah S. Kim, MD* 2. Francesca Costigliolo, MD† 3. Serena Bagnasco, MD† 4. Jeffrey Fadrowski, MD, MHS* 5. Rebecca L. Ruebner, MD, MSCE* 1. *Division of Pediatric Nephrology and 2. †Division of Pathology, Johns Hopkins University, Baltimore,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::019381e41a64cebe9a4f9b4fcac84dea
https://doi.org/10.1542/pir.2020-0012
https://doi.org/10.1542/pir.2020-0012
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::82410ba54f15eef734e6f5132b4ae381
https://doi.org/10.1007/s00467-021-04990-4
https://doi.org/10.1007/s00467-021-04990-4
Autor:
Mohamed G. Atta, Giovanni Maria Rossi, Lois J. Arend, Serena M. Bagnasco, Derek M. Fine, Alice Chedid, Steven Menez, Francesco Peyronel, Avi Z. Rosenberg
Publikováno v:
Kidney International Reports
Introduction In patients with systemic lupus erythematosus (SLE) without concurrent active urinary sediment or unexplained acute kidney injury (AKI), current guidelines recommend performing a kidney biopsy in those with at least 500 mg/24-hour (Europ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::416a08c05dee7278407ef4a6b399f1ab
https://doi.org/10.1016/j.ekir.2020.09.007
https://doi.org/10.1016/j.ekir.2020.09.007
Autor:
Laura H. Mariani, Sean Eddy, Fadhl M. AlAkwaa, Phillip J. McCown, Jennifer L. Harder, Viji Nair, Felix Eichinger, Sebastian Martini, Adebowale D. Ademola, Vincent Boima, Heather N. Reich, Jamal El Saghir, Bradley Godfrey, Wenjun Ju, Emily C. Tanner, Virginia Vega-Warner, Noel L. Wys, Sharon G. Adler, Gerald B. Appel, Ambarish Athavale, Meredith A. Atkinson, Serena M. Bagnasco, Laura Barisoni, Elizabeth Brown, Daniel C. Cattran, Gaia M. Coppock, Katherine M. Dell, Vimal K. Derebail, Fernando C. Fervenza, Alessia Fornoni, Crystal A. Gadegbeku, Keisha L. Gibson, Laurence A. Greenbaum, Sangeeta R. Hingorani, Michelle A. Hladunewich, Jeffrey B. Hodgin, Marie C. Hogan, Lawrence B. Holzman, J. Ashley Jefferson, Frederick J. Kaskel, Jeffrey B. Kopp, Richard A. Lafayette, Kevin V. Lemley, John C. Lieske, Jen-Jar Lin, Rajarasee Menon, Kevin E. Meyers, Patrick H. Nachman, Cynthia C. Nast, Michelle M. O’Shaughnessy, Edgar A. Otto, Kimberly J. Reidy, Kamalanathan K. Sambandam, John R. Sedor, Christine B. Sethna, Pamela Singer, Tarak Srivastava, Cheryl L. Tran, Katherine R. Tuttle, Suzanne M. Vento, Chia-shi Wang, Akinlolu O. Ojo, Dwomoa Adu, Debbie S. Gipson, Howard Trachtman, Matthias Kretzler
Publikováno v:
Kidney international.
The diagnosis of nephrotic syndrome relies on clinical presentation and descriptive patterns of injury on kidney biopsies, but not specific to underlying pathobiology. Consequently, there are variable rates of progression and response to therapy with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de208f74baf467408c91da41f9fb8f45
https://pubmed.ncbi.nlm.nih.gov/36442540
https://pubmed.ncbi.nlm.nih.gov/36442540