Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Callen D. Giesen"'
Autor:
Jason N. Barreto, Erin F. Barreto, Kristin C. Mara, Andrew D. Rule, John C. Lieske, Callen D. Giesen, Carrie A. Thompson, Nelson Leung, Thomas E. Witzig, Kianoush B. Kashani
Publikováno v:
Kidney360. 4:673-679
Autor:
Casal Moura Marta, Sanjeev Sethi, Julie A. Vrana, Samar M. Said, John C. Lieske, Shane A. Bobart, An S. De Vriese, Samih H. Nasr, Mariam P. Alexander, Callen D. Giesen, Fernando C. Fervenza, Shahrzad Tehranian
Publikováno v:
Mayo Clinic Proceedings. 96:577-591
Objective To describe the clinical and pathological phenotype of membranous nephropathy (MN) associated with M-type-phospholipase–A2-receptor (PLA2R), thrombospondin-type-1-domain-containing-7A (THSD7A), semaphorin 3B (SEMA3B), neural-epidermal-gro
Autor:
Jason N. Barreto, Kianoush B. Kashani, Kristin C. Mara, Andrew D. Rule, John C. Lieske, Callen D. Giesen, Carrie A. Thompson, Nelson Leung, Thomas E. Witzig, Erin F. Barreto
Publikováno v:
Kidney international reports. 7(7)
Autor:
Shahrzad Tehranian, Callen D. Giesen, Shane A. Bobart, Heedeok Han, Juan Carlos León Román, Sanjeev Sethi, Ladan Zand, Cristina Andrades Gomez, An S. De Vriese, María José Soler, Andrew S. Bomback, Fernando C. Fervenza
Publikováno v:
Clin J Am Soc Nephrol
Background and objectives Kidney biopsy is the current gold standard to diagnose membranous nephropathy. Approximately 70%–80% of patients with primary membranous nephropathy have circulating anti-phospholipase A2 receptor antibodies. We previously
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8377b78d076f26bbf35ce5eccd4aa322
https://europepmc.org/articles/PMC8729491/
https://europepmc.org/articles/PMC8729491/
Autor:
Callen D. Giesen, Dimitar Gavrilov, Clayton T. Brady, John C. Lieske, Robin S. Chirackal, Nikolay Voskoboev, Ryan M. Flanagan
Publikováno v:
The Journal of Applied Laboratory Medicine. 2:55-64
Background Cystinuria is an autosomal recessive disorder resulting in poor proximal tubule reabsorption of cystine in the nephron, increasing the risk of cystine stone formation. A fast, inexpensive assay to screen for urinary cystine is needed becau
Autor:
Callen D. Giesen, Matthew M. Hanley, Darci R. Block, Jason J. Schilling, Sarah J. Cambern, Nikolay Voskoboev, John C. Lieske, Paul J. Jannetto
Publikováno v:
Clinical Biochemistry. 48:1126-1130
Background Validation of tests performed on body fluids other than blood or urine can be challenging due to the lack of a reference method to confirm accuracy. The aim of this study was to evaluate alternate assessments of accuracy that laboratories
Autor:
Katherine Thompson, John C. Lieske, Callen D. Giesen, Robin Patel, Amanda M. Greeno, Sarah M. Jenkins
Publikováno v:
Clinical Biochemistry. 46:810-813
Background The gold standard test for the diagnosis of urinary tract infection is bacterial culture. However, urine cultures are labor intensive and costly. Furthermore, since results take 1–2 days many patients are treated presumptively prior to c
Autor:
John C. Lieske, Callen D. Giesen
Because there is substantial biologic intraindividual variation in albumin excretion, randomized trials of albuminuria-reducing therapies may need multiple urine samples to estimate daily urinary albumin excretion. Mailing spot urine samples could of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10f29146819e9ad54a4c44026b29fab2
https://europepmc.org/articles/PMC5053796/
https://europepmc.org/articles/PMC5053796/