Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Sarah Elhadi"'
Publikováno v:
Case Reports in Nephrology, Vol 2017 (2017)
Goodpasture’s syndrome (GPS) remains a very rare disease entity in the pediatric population characterized by the presence of pulmonary hemorrhage and rapidly evolving glomerulonephritis. We hereby describe the case of a 2-year-old girl who presente
Externí odkaz:
https://doaj.org/article/ab0877087bc2457b83abc9a178b7e11d
Autor:
Madison Purvis, Heng Jin, Chongyu Ren, Massimo Attanasio, Yanfen Chai, Chao Cao, Prerna Rastogi, Anton M. Jetten, Qiong Ding, Dongmei Lu, Shan Shanshan Wang, Sarah Elhadi, Yan Zhang, Dingxiao Liu, Angela Wang, Peter Igarashi
Publikováno v:
Am J Pathol
Nephronophthisis (NPHP), the leading genetic cause of end-stage renal failure in children and young adults, is a group of autosomal recessive diseases characterized by kidney-cyst degeneration and fibrosis for which no therapy is currently available.
Autor:
Dao-Fu Dai, Diana Zepeda-Orozco, Yan Zhang, Heng Jin, Angela Wang, Madison Purvis, Prerna Rastogi, Judith Campisi, Yanfen Chai, Dingxiao Liu, Chao Cao, Ming Chang Hu, Qiong Ding, Dongmei Lu, Sarah Elhadi, Massimo Attanasio, Shan Shan Wang, Chongyu Ren
Publikováno v:
JCI Insight. 4
Acute kidney injury (AKI) is a common clinical condition of growing incidence. Patients who suffer severe AKI have a higher risk of developing interstitial fibrosis, chronic kidney disease, and end-stage renal disease later in life. Cellular senescen
Autor:
Kayla McEnery, Jili Zhu, Binghua Li, Peter Igarashi, Alysha Rauhauser, Komal Vadnagara, Dongmei Lu, Sarah Elhadi, Massimo Attanasio, Chongyu Ren, Moumita Chaki, Anton M. Jetten
Publikováno v:
Kidney International. 89:1307-1323
Enlargement of kidney tubules is a common feature of multiple cystic kidney diseases in humans and mice. However, while some of these pathologies are characterized by cyst expansion and organ enlargement, in others, progressive interstitial fibrosis
Autor:
Nicolas G. Bazan, Jili Zhu, Richard J. Quigg, Xin J. Zhou, Moumita Chaki, Dongmei Lu, Bokkyoo Jun, Susan E. Zimmerman, Alysha Rauhauser, Chandra Mohan, Sarah Elhadi, Komal Vadnagara, Shan Shan Wang, Chongyu Ren, Binghua Li, Denise K. Marciano, Fatih Ozaltin, Matthew K. Topham, Massimo Attanasio, Hanquin Wang, Yong Du
Publikováno v:
American Journal of Physiology-Renal Physiology. 310:F895-F908
Thrombotic microangiopathy (TMA) is a disorder characterized by microvascular occlusion that can lead to thrombocytopenia, hemolytic anemia, and glomerular damage. Complement activation is the central event in most cases of TMA. Primary forms of TMA