Zobrazeno 1 - 10
of 60
pro vyhledávání: '"Jean Hou"'
Autor:
Matthew B Palmer, Virginie Royal, J. Charles Jennette, Abigail R. Smith, Qian Liu, Josephine M. Ambruzs, Nicole K. Andeen, Vivette D. D’Agati, Agnes B. Fogo, Joseph Gaut, Rasheed A. Gbadegesin, Larry A. Greenbaum, Jean Hou, Margaret E Helmuth, Richard A. Lafayette, Helen Liapis, Bruce Robinson, Michael B. Stokes, Katherine Twombley, Hong Yin, Cynthia C. Nast
Publikováno v:
Glomerular Diseases, Vol 3, Iss 1, Pp 248-257 (2023)
Introduction: Cure Glomerulonephropathy (CureGN) is an observational cohort study of patients with minimal change disease (MCD), focal segmental glomerulosclerosis (FSGS), membranous nephropathy (MN), or IgA nephropathy. We developed a conventional,
Externí odkaz:
https://doaj.org/article/f1cb4212a72b410bafd61bc67ce53134
Autor:
Sasmit Roy MD, Jean Hou MD, Prabal Chourasia MD, Anish Yalamanchili BSc, Debargha Basuli MD, Praveen Kumar Errabelli MD, Samanvitha Sai Yarram BSc, Raul Ayala MD, Sreedhar Adapa MD
Publikováno v:
Journal of Investigative Medicine High Impact Case Reports, Vol 11 (2023)
Anti-glomerular basement membrane (GBM) antibody nephritis is defined by linear immunofluorescence staining of GBM by immunoglobulin G (IgG), typically associated with GBM rupture, fibrinoid necrosis, and crescent formation. Clinically, the patients
Externí odkaz:
https://doaj.org/article/c11323e026b24e678528004b97bec29a
Autor:
Nicole K. Andeen, Shahad Abdulameer, Vivek Charu, Jonathan E. Zuckerman, Megan Troxell, Neeraja Kambham, Charles E. Alpers, Behzad Najafian, Roberto F. Nicosia, Kelly D. Smith, Vanderlene L. Kung, Rupali S. Avasare, Anusha Vallurupalli, J. Ashley Jefferson, Douglas Hecox, Leah Swetnam, Michifumi Yamashita, Mercury Lin, Mei Lin Bissonnette, Shreeram Akilesh, Jean Hou
Publikováno v:
Kidney International Reports, Vol 7, Iss 3, Pp 568-579 (2022)
Introduction: There are limited reports on kidney biopsy findings in patients with mantle cell lymphoma (MCL). Methods: We initiated a multi-institutional, retrospective review of kidney biopsy findings in patients with active and treated MCL. Result
Externí odkaz:
https://doaj.org/article/8406b65d010b4e1cbefc568e24d60008
Autor:
Kevin Yi Mi Ren, Jean Hou
Publikováno v:
Glomerular Diseases, Pp 1-1 (2023)
Introduction: Membranous nephropathy (MN) is a common cause of adult nephrotic syndrome in the US. The typical ultrastructural finding is of global uniformly dense subepithelial electron-dense immune complex deposits along glomerular basement membran
Externí odkaz:
https://doaj.org/article/c56f8e059d724c4d99da953c81fdac7c
Autor:
Madeleine V. Pahl, Jean Hou
Publikováno v:
Glomerular Diseases, Pp 1-1 (2023)
Fabry Disease is an X-linked disorder due to a pathogenic variant of the GLA gene that codes for the alpha-galctosidase enzyme. The reduced or absent activity of the enzyme results in lysosomal accumulation of globotriosylceramide, and its derivative
Externí odkaz:
https://doaj.org/article/89088bbca75a4e2089e41db37b41d420
Publikováno v:
Glomerular Diseases (2022)
C3 glomerulopathy (C3G) is a rare disease resulting from dysregulation of the alternative complement pathway, resulting in the deposition of complement component 3 (C3) in the kidney. It encompasses two major subgroups: dense deposit disease (DDD) an
Externí odkaz:
https://doaj.org/article/39bddc98b920492a9339cb6928623fd9
Autor:
Sanjeev Sethi, Benjamin Madden, Marta Casal Moura, Raman Deep Singh, Samih H. Nasr, Jean Hou, Alok Sharma, Karl A. Nath, Ulrich Specks, Fernando C. Fervenza, Mark Haas
Publikováno v:
Journal of the American Society of Nephrology. 34:374-384
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::39522049ae8f2af2669fbcbb7eaf50af
https://doi.org/10.1681/asn.0000000000000061
https://doi.org/10.1681/asn.0000000000000061
Autor:
Ramy M. Hanna, Ngoc-Tram Tran, Sapna S. Patel, Jean Hou, Kenar D. Jhaveri, Rushang Parikh, Umut Selamet, Lena Ghobry, Olivia Wassef, Marina Barsoum, Vanesa Bijol, Kamyar Kalantar-Zadeh, Alex Pai, Alpesh Amin, Baruch Kupperman, Ira B. Kurtz
Publikováno v:
Frontiers in Medicine, Vol 7 (2020)
Vascular endothelial growth factor (VEGF) inhibition can cause worsening hypertension, proteinuria, chronic kidney injury, and glomerular disease. Thrombotic microangiopathy (TMA) and other nephrotic disorders have been reported with systemic VEGF bl
Externí odkaz:
https://doaj.org/article/6adab79bd83c45deb5c75cd4426d978b
Autor:
Ramy M. Hanna, Jean Hou, Huma Hasnain, Farid Arman, Umut Selamet, James Wilson, Samuel Olanrewaju, Jonathan E. Zuckerman, Marina Barsoum, Julie M. Yabu, Ira Kurtz
Publikováno v:
Frontiers in Medicine, Vol 7 (2020)
C3 dominant immunofluorescence staining is present in a subset of patients with idiopathic immune complex membranoproliferative glomerulonephritis (iMPGN). It is increasingly recognized that iMPGN may be complement driven, as are cases of “typical
Externí odkaz:
https://doaj.org/article/f0068d104fdc41bb97ddf27fc7e68809
Autor:
Ramy M. Hanna, Naomi So, Marian Kaldas, Jean Hou, Farid Arman, Michelle Sangalang, Bishoy Yanny, Umut Selamet, Sammy Saab, Niloofar Nobakht, Anjay Rastogi
Publikováno v:
Case Reports in Nephrology and Dialysis, Vol 8, Iss 2, Pp 161-170 (2018)
Hepatitis C (HCV) infection has a prevalence of 3 million infected individuals in the United States, according to recent Center for Disease Control reports, and can have various renal manifestations. Cryoglobulins, antibodies that precipitate at cold
Externí odkaz:
https://doaj.org/article/e5a1c61a316c478ba7aca25238e7662e