Results 51 to 60 of about 21,067 (213)

Immune-complex glomerulonephritis with a membranoproliferative pattern in Frasier syndrome: a case report and review of the literature

BMC Nephrology, 2020
Background Mutations in the Wilms tumor 1 gene cause a spectrum of podocytopathy ranging from diffuse mesangial sclerosis to focal segmental glomerulosclerosis.
Daisuke Matsuoka, Shunsuke Noda, Motoko Kamiya, Yoshihiko Hidaka, Hisashi Shimojo, Yasushi Yamada, Tsutomu Miyamoto, Kandai Nozu, Kazumoto Iijima, Hiroyasu Tsukaguchi   +9 more
doaj   +1 more source

Focal segmental glomerulosclerosis: Cellular variant and beyond

, 2006
The entity of focal segmental glomerulosclerosis (FSGS), oddly, includes several distinct changes involving glomeruli that need not be focal, segmental, or even sclerotic.
Nair, R.
core   +1 more source

Feasibility and outcomes of kidney transplantation in patients with end‐stage kidney disease after haemopoietic stem cell transplantation

Internal Medicine Journal, EarlyView.
Abstract Background Advances in haemopoietic stem cell transplantation (HSCT) have improved long‐term survival, but they have also led to late complications, such as nephropathy. However, the safety and feasibility of kidney transplantation (KT) in patients with HSCT‐related end‐stage kidney disease (ESKD) remain unclear.
Bioh Kim, Seunghyeok Choi, Hanbi Lee, Hye‐Eun Yoon, Hohyung Nam, Silvia Park, Byung Ha Chung   +6 more
wiley   +1 more source

Focal Segmental Glomerulosclerosis

Turkish Journal of Nephrology, 2019
Focal segmental glomerulosclerosis (FSGS) is a common histological aspect of glomerular injury due to diverse etiologies. It is the most common cause of end stage renal disease (ESRD) in primary glomerulonephritis.
Erkan ŞENGÜL, Tayfun EYİLETEN, Müjdat YENİCESU   +2 more
doaj  

Clinicopathological findings, correlations and outcomes in patients with renal disease and living with antiretroviral‐treated human immunodeficiency virus infection

Internal Medicine Journal, EarlyView.
Abstract Background and Aims Antiretroviral therapy (ART) has modified the incidence of renal complications and the patterns of renal disease in people living with Human Immunodeficiency Virus (PLWH). We reviewed (2011–2021) the progress and outcomes (follow‐up to mid‐2025) of 158 such individuals.
Jacqueline A. Evans, Christopher S. B. Sia, Gopal Basu, Orla O’Brien, Alan H. Pham, Rowan G. Walker   +5 more
wiley   +1 more source

MYO1E mutations and childhood familial focal segmental glomerulosclerosis

, 2011
BACKGROUND Focal segmental glomerulosclerosis is a kidney disease that is manifested as the nephrotic syndrome. It is often resistant to glucocorticoid therapy and progresses to end-stage renal disease in 50 to 70% of patients.
Andrea Calabria, Fatih Ozaltin, E. Otto, Fabio Macciardi, Paraskevas Iatropoulos, Sevinc Emre, Paola Cassis, Giuseppe Remuzzi, Edgar Otto, P. Cassis, S. Bettoni, M. Delledonne, M. Noris, M. Morigi, I. Abbate, Morigi, Marina, Abbate, Isabella, Ibsirlioglu, Tulin, P. Iatropoulos, T. Ibsirlioglu, Simona Buelli, Carmine Pecoraro, Franz Schaefer, F. Ozaltin, Otto, Edgar, Mira Krendel, R. Maranta, Benigni, Ariela, Piras, Rossella, G. Remuzzi, Isabella Abbate, C. Pecoraro, Maranta, Ramona, Marina Noris, F. Hildebrandt, Friedhelm Hildebrandt, Cassis, Paola, A. Benigni, M. Krendel, Capobianchi, Maria Rosaria, Caterina Mele, F. Schaefer, Delledonne, Massimo, Serena Bettoni, Roberta Donadelli, C. Mele, Iatropoulos, Paraskevas, A. Calabria, Hildebrandt, Friedhelm, Schaefer, Franz, Ramona Maranta, Ariela Benigni, R. Donadelli, S. Emre, Krendel, Mira, Rossella Piras, Emre, Sevinc, Buelli, Simona, R. Piras, Calabria, Andrea, Macciardi, Fabio, Mele, Caterina, Ozaltin, Fatih, Donadelli, Roberta, Maria Rosaria Capobianchi, S. Tomasoni, Remuzzi, Giuseppe, Bettoni, Serena, Susanna Tomasoni, M. R. Capobianchi, Pecoraro, Carmine, S. Buelli, Tomasoni, Susanna, Noris, Marina, Marina Morigi, Massimo Delledonne, F. Macciardi, Tulin Ibsirlioglu   +77 more
core   +1 more source

Risk Factors and Management of Gingival Enlargement: A Systematic Review and Meta‐Analysis

Journal of Clinical Periodontology, EarlyView.
ABSTRACT Objective To identify risk factors/indicators of gingival enlargement (GE) and to summarise evidence for its management. Methods A systematic review was undertaken following PRISMA guidelines and divided into PECOTS and PICOTS questions, related to risk factors/indicators and treatment studies, respectively.
Luigi Nibali, Emily Ming‐Chieh Lu, Helvis E. S. Paz, Jing Kang, Nagihan Bostanci, Georgios N. Belibasakis   +5 more
wiley   +1 more source

Current distribution pattern of biopsy-proven glomerular disease in Salvador, Brazil, 40 years after an initial assessment

Brazilian Journal of Nephrology
Introduction: A report on the prevalence of glomerular disease diagnosed via renal biopsy in Salvador, BA, Brazil was published in 1973 and showed a predominance of membranoproliferative glomerulonephritis, which was frequently associated with ...
Washington Luis Conrado dos-Santos, Glória Maria Maranhão Sweet, Labene Gondim Azevêdo, Maria Brandão Tavares, Maria Fernanda Sanches Soares, Caroline Vilas Boas de Melo, Márcia Fernanda Melo Carneiro, Rilma Ferreira de Souza Santos, Márcia Cristina Conrado, Daniela Teixeira Leal Braga, Marcia Carvalho Bessa, Nathanael de Freitas Pinheiro Junior, Marília Bahiense-Oliveira   +12 more
doaj   +1 more source

Clinical and genetic heterogeneity in familial focal segmental glomerulosclerosis

, 1999
Clinical and genetic heterogeneity in familial focal segmental glomerulosclerosis.BackgroundFamilial forms of focal segmental glomerulosclerosis (FFSGS) that exhibit autosomal dominant or recessive patterns of inheritance have been described. The genetic
Winn, Michelle P., Bembe, Marylou, Gross, Deborah A, Rogala, Allison R, Smith, Anne H, Lynn, Kelvin L., Howell, David N, on behalf of the International Collaborative Group for the Study of Familial Focal Segmental Glomerulosclerosis, on behalf of the International Collaborative Group for the Study of Familial Focal Segmental, Graham, Felicia L., Conlon, Peter J., Vance, Jeffery M, Vance, Jeffery M., Gross, Deborah A., Winn, Michelle P, Conlon, Peter J, Quarles, L. Daryl, Graham, Felicia L, on behalf of the International Collaborative Group for the Study of Familial Focal Segmental Glomerulosclerosis,, Pericak-Vance, Margaret A., Pericak-Vance, Margaret A, Howell, David N., Rogala, Allison R., Lynn, Kelvin L, Smith, Anne H.   +23 more
core   +1 more source

5‐Methylcytosine Analysis of miRNAs in Minimal Change Disease

Biotechnology and Applied Biochemistry, Volume 73, Issue 3, Page 1137-1150, June 2026.
ABSTRACT Minimal change disease (MCD) is a glomerular disorder, which is the most common cause of nephrotic syndrome in children. Additionally, the prevalence of MCD in adults has been increasing in recent years. During protein synthesis, noncoding RNAs can be regulated through a variety of modifications, which helps preserve biological diversity and ...
Huiyi Zeng, Dandan Li, Yunyi Li, Chen Yun, Xinzhou Zhang, Wenyu Gong, Mengyun Xiao, Haitao Li, Zhipeng Zeng, Ruqi Tan, Yishen Yang, Shaodong Luan, Yong Dai, Lianghong Yin, Donge Tang   +14 more
wiley   +1 more source