Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Cheryl L. Tran"'
Autor:
Debbie S. Gipson, Howard Trachtman, Anne Waldo, Keisha L. Gibson, Sean Eddy, Katherine M. Dell, Tarak Srivastava, Kevin V. Lemley, Larry A. Greenbaum, Sangeeta Hingorani, Kevin E. Meyers, Frederick J. Kaskel, Kimberly J. Reidy, Christine B. Sethna, Cheryl L. Tran, Chia-shi Wang, Katherine R. Tuttle, Gia Oh, Alicia M. Neu, Elizabeth Brown, Jen-Jar Lin, Jennifer Lai Yee, Therese M. Roth, Jonathan P. Troost, Brenda W. Gillespie, Matthew G. Sampson, Matthias Kretzler, Wenjun Ju
Publikováno v:
Kidney International Reports, Vol 5, Iss 4, Pp 414-425 (2020)
Introduction: Childhood-onset nephrotic syndrome has a variable clinical course. Improved predictive markers of long-term outcomes in children with nephrotic syndrome are needed. This study tests the association between baseline urinary epidermal gro
Externí odkaz:
https://doaj.org/article/0ec9bfee819e47e6a0c27426843af311
Autor:
Chia-shi Wang, Jonathan P. Troost, Larry A. Greenbaum, Tarak Srivastava, Kimberly Reidy, Keisha Gibson, Howard Trachtman, John D. Piette, Christine B. Sethna, Kevin Meyers, Katherine M. Dell, Cheryl L. Tran, Suzanne Vento, Krishna Kallem, Emily Herreshoff, Sangeeta Hingorani, Kevin Lemley, Gia Oh, Elizabeth Brown, Jen-Jar Lin, Frederick Kaskel, Debbie S. Gipson
Publikováno v:
Kidney International Reports, Vol 4, Iss 8, Pp 1066-1074 (2019)
Introduction: There is limited information on effective disease monitoring for prompt interventions in childhood nephrotic syndrome. We examined the feasibility and effectiveness of a novel text messaging system (SMS) for disease monitoring in a mult
Externí odkaz:
https://doaj.org/article/ec7b9f47c989470490c2c567e54f7be7
Autor:
Cheryl L. Tran, David T. Selewski, Gia J. Oh, Jonathan P. Troost, Susan F. Massengill, Samhar I. Al-Akash, Shefali Mahesh, Rasheda Amin, Isa F. Ashoor, Rahul Chanchlani, Mahmoud Kallash, Robert P. Woroniecki, Debbie S. Gipson
Publikováno v:
Frontiers in Pediatrics, Vol 8 (2021)
Background: Children with nephrotic syndrome (NS) are at high risk for vaccine-preventable infections due to the immunological effects from the disease and concurrent treatment with immunosuppressive medications. Immunizations in these patients may b
Externí odkaz:
https://doaj.org/article/2168db9efaf3404cb520a421a989ce63
Autor:
Joseph G. Maliakkal, M. John Hicks, Mini Michael, David T. Selewski, Katherine Twombley, Michelle N. Rheault, Meredith Seamon, Jason M. Misurac, Cheryl L. Tran, Loretta Reyes, Joseph T. Flynn, Ali M. Onder, Alexandru R. Constantinescu, Vaishali Singh, Cynthia Pan, Abiodun Omoloja, Qiang Wu, William E. Smoyer, Guillermo Hidalgo, Scott E. Wenderfer
Publikováno v:
Journal of Clinical Medicine, Vol 9, Iss 8, p 2385 (2020)
There is no evidence-based definition for diagnosing crescentic glomerulonephritis. The prognostic implications of crescentic lesions on kidney biopsy have not been quantified. Our objective was to determine risk factors for end-stage kidney disease
Externí odkaz:
https://doaj.org/article/7c7e96a94dc64e33899ea6b74468e1df
Publikováno v:
Pediatrics In Review. 44:228-231
Autor:
Pooja Patel, Marietta de Guzman, M. John Hicks, Joseph G. Maliakkal, Michelle N. Rheault, David T. Selewski, Katherine Twombley, Jason M. Misurac, Cheryl L. Tran, Alexandru R. Constantinescu, Ali M. Onder, Meredith Seamon, Wacharee Seeherunvong, Vaishali Singh, Cynthia Pan, Daryl M. Okamura, Abiodun Omoloja, Mahmoud Kallash, William E. Smoyer, Guillermo Hidalgo, Scott E. Wenderfer
Publikováno v:
Pediatric Nephrology. 37:3139-3145
The revised 2018 ISN/RPS Classification System for lupus nephritis (LN) includes calculations for both activity index (A.I.) and chronicity index (C.I.). Unchanged were the thresholds of 25%, 25-50%, and 50% crescents to distinguish between mild, mod
Autor:
David J. Sas, Daniella Magen, Wesley Hayes, Hadas Shasha-Lavsky, Mini Michael, Indra Schulte, Anne-Laure Sellier-Leclerc, Jiandong Lu, Ali Seddighzadeh, Bahru Habtemariam, Tracy L. McGregor, Kenji P. Fujita, Yaacov Frishberg, Justine Bacchetta, Véronique Baudouin, Rachel Becker-Cohen, Shimrit Tzvi Behr, Efrat Ben-Shalom, Maria Berdaguer, Detlef Bockenhauer, Pierre Cochat, Martin Coenen, Carl H. Cramer, Georges Deschênes, Claire Dossier, Emilie Doye, Liat Feraru Feldman, Maximilian Hohenadel, Florentia Kaguelidou, Irina Libinson Zebegret, John C. Lieske, Anne Maisin, Dawn S. Milliner, Moran Plonsky Toder, Shirley Pollack, Aurélie Portefaix, Bruno Ranchin, Choni Rinat, Adnan Safdar, Gesa Schalk, Poyyapakkam R. Srivaths, Cheryl L. Tran, William Van't Hoff, Jenny Weinbrand-Goichberg, Irith Weissman
Publikováno v:
Genetics in Medicine. 24:654-662
Primary hyperoxaluria type 1 (PH1) is a rare, progressive, genetic disease with limited treatment options. We report the efficacy and safety of lumasiran, an RNA interference therapeutic, in infants and young children with PH1.This single-arm, open-l
Autor:
Nianzhou Xiao, Adrienne Stolfi, Rossana Malatesta-Muncher, Reshma Bholah, Amy Kogon, Angelica Eddington, Deepa Chand, Larry A. Greenbaum, Coral Hanevold, Cheryl L Tran, Aftab Chishti, Keefe Davis, Robyn Matloff, Robert Woroniecki, Colleen Klosterman, Kera Luckritz, Abiodun Omoloja
Publikováno v:
International Journal of Nephrology, Vol 2019 (2019)
Introduction. There is a paucity of information about risk behaviors in adolescents with chronic kidney disease (CKD). We designed this study to assess the prevalence of risk behaviors among teens with CKD in the United States and to investigate any
Externí odkaz:
https://doaj.org/article/db626b42f4a94ccd8da42416f872bdec
Autor:
Lilian Monteiro P. Palma, Maria Helena Vaisbich-Guimarães, Meera Sridharan, Cheryl L. Tran, Sanjeev Sethi
Publikováno v:
Pediatric Nephrology (Berlin, Germany)
The syndrome of thrombotic microangiopathy (TMA) is a clinical-pathological entity characterized by microangiopathic hemolytic anemia, thrombocytopenia, and end organ involvement. It comprises a spectrum of underlying etiologies that may differ in ch
Autor:
Cheryl L. Tran, Dorota M Marchel, Isabelle Ayoub, Michelle R. Denburg, Jessica Greco, Michael E. Matheny, Laura H. Mariani, Hailey Desmond, Andrea L. Oliverio, Chad Dorn, Debbie S. Gipson, Salem Almaani, Jonathan P. Troost, Susan F. Massengill
Publikováno v:
Kidney360
Background: Primary nephrotic syndromes are rare diseases which impedes adequate sample size for observational patient-oriented research and clinical trial enrollment. A computable phenotype may be powerful in identifying patients with these diseases