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Showing 1-20 of 9,528 results
  1. Modified histopathological classification with age-related glomerulosclerosis for predicting kidney survival in ANCA-associated glomerulonephritis

    Background

    The histopathological classification of ANCA-GN divides patients into four groups based on signs of glomerular injury. However, this...

    Mehmet Fethullah Aydın, Abdülmecit Yıldız, ... Alparslan Ersoy in International Urology and Nephrology
    Article 25 September 2022
  2. A case of idiopathic nodular glomerulosclerosis successfully treated by intensive blockade of the renin–angiotensin–aldosterone system

    Idiopathic nodular glomerulosclerosis has a poor renal prognosis and is characterized by diffuse nodular glomerulosclerotic lesions in the absence of...

    Hiroki Yamaguchi, Michihiro Hosojima, ... Ichiei Narita in CEN Case Reports
    Article 27 December 2022
  3. Hidden genetics behind glomerular scars: an opportunity to understand the heterogeneity of focal segmental glomerulosclerosis?

    Focal segmental glomerulosclerosis (FSGS) is a complex disease which describes different kinds of kidney defects, not exclusively linked with...

    Adele Mitrotti, Marica Giliberti, ... Loreto Gesualdo in Pediatric Nephrology
    Article Open access 20 September 2023
  4. Nephrotic syndrome due to focal segmental glomerulosclerosis complicating scleroderma: a case report

    Background

    Systemic scleroderma (SSc) is an insidious autoimmune connective tissue disorder with multiorgan involvement. Renal involvement is one of...

    Mahsa Mehdipour Dalivand, Asghar Hadjiabbasi, ... Habib Zayeni in Journal of Medical Case Reports
    Article Open access 15 January 2024
  5. A Case of Noncompaction Cardiomyopathy with Focal Segmental Glomerulosclerosis Treated with Combined Heart and Kidney Transplantation: a Case Report

    Left ventricular noncompaction cardiomyopathy (LVNC) is a rare condition and a cause of heart failure and sudden cardiac death in young adults. It is...

    Jennaire Lewars, Tsungyen Chen in SN Comprehensive Clinical Medicine
    Article 03 November 2023
  6. Familial focal segmental glomerulosclerosis with Alport-like glomerular basement changes caused by paired box protein 2 gene variant

    Paired box protein 2 ( PAX2 ) gene variant causes renal coloboma syndrome (MIM#120330). Further, they are associated with focal segmental...

    Yuko Yamada, Hiroki Yokoyama, ... Noriyuki Namba in CEN Case Reports
    Article Open access 28 October 2023
  7. Clinicopathological differences in focal segmental glomerulosclerosis depending on the accompanying pathophysiological conditions in renal allografts

    Primary focal segmental glomerulosclerosis (FSGS) is thought to be caused by circulating factors leading to podocytopathy, whereas segmental...

    Sekiko Taneda, Kazuho Honda, ... Yoji Nagashima in Virchows Archiv
    Article Open access 18 November 2023
  8. Ferroptosis-related genes, a novel therapeutic target for focal segmental glomerulosclerosis

    Recent studies have suggested that ferroptosis participates in various renal diseases. However, its effect on focal segmental glomerulosclerosis...

    Yanbin Lin, **xuan He, ... Lan Chen in BMC Nephrology
    Article Open access 17 February 2024
  9. A clinicopathological and prognostic study of 18 children with C1q nephropathy and focal segmental glomerulosclerosis: an 18-year experience from a single center

    Background

    C1q nephropathy is a relatively rare glomerulonephritis characterized by dominant mesangial deposition of C1q. Even though C1q nephropathy...

    Yingchao Peng, Tao Ju, ... Huangyu Chen in Journal of Nephrology
    Article 10 July 2023
  10. Focal segmental glomerulosclerosis in a patient with multiple sclerosis treated with Teriflunomide and Ocrelizumab

    We describe the case of a 24-year-old male patient with multiple sclerosis (MS) who was treated with Teriflunomide for eight months. However, due to...

    Anne-Sofie Greve, Sivagini Prakash, ... Else Randers in Journal of Nephrology
    Article 21 November 2022
  11. Anterior and posterior ischemic optic neuropathy in a child with focal segmental glomerulosclerosis on hemodialysis

    Background

    Ischemic optic neuropathy (ION) is exceedingly rare in children on dialysis, resulting from poor perfusion of the optic nerve, and presents...

    Katherine Mai, Rina Su, ... Christine B. Sethna in Pediatric Nephrology
    Article 10 January 2024
  12. Non-glomerular Tip Lesion Focal Segmental Glomerulosclerosis as a Negative Predictor in Idiopathic Membranous Nephropathy

    Objective

    To assess the significance of focal segmental glomerulosclerosis (FSGS) variants on clinicopathological characteristics and short-term...

    Hui Wang, Cheng Wan, ... Chun Zhang in Current Medical Science
    Article Open access 30 September 2022
  13. Post-operative recurrence of focal segmental glomerulosclerosis according to pre-transplant treatment after kidney transplantation

    Background

    Recurrent focal segmental glomerulosclerosis (FSGS) after kidney transplantation (KT) is a serious complication and a significant risk...

    Hye Eun Kwon, Young Hoon Kim, ... Hyunwook Kwon in BMC Nephrology
    Article Open access 15 March 2023
  14. Ocular manifestations of the genetic causes of focal and segmental glomerulosclerosis

    Genetic forms of focal and segmental glomerulosclerosis (FSGS) often have extra-renal manifestations. This study examined FSGS-associated genes from...

    Victor Zhu, Tess Huang, ... Judy Savige in Pediatric Nephrology
    Article Open access 14 August 2023
  15. Kidney outcomes in children with primary focal segmental glomerulosclerosis from a low- and middle- income country

    Background

    Limited data exists regarding the clinical course and outcomes of children with primary focal segmental glomerulosclerosis (FSGS) from low-...

    Kolluri Priyanka, Bobbity Deepthi, ... Sriram Krishnamurthy in Pediatric Nephrology
    Article 23 April 2024
  16. WT1 exon 10 missense variant in a pediatric patient with focal segmental glomerulosclerosis with embryonal hyperplasia

    A 6-year-old boy was diagnosed with chromosomal abnormalities (48,XYY, + 21[11]/46,XY[19]) at 4 months of age after a physical examination revealed...

    Mari Kurokawa, Manao Nishimura, ... Yoshitsugu Kaku in Pediatric Nephrology
    Article 24 January 2024
  17. Development of a Conceptual Model for the Patient Experience of Focal Segmental Glomerulosclerosis (FSGS): A Qualitative Targeted Literature Review

    Introduction

    Focal segmental glomerulosclerosis (FSGS) is a leading cause of kidney disease and can progress to end stage kidney disease (ESKD). An...

    Natalie V. J. Aldhouse, Helen Kitchen, ... Christine L. Baker in Advances in Therapy
    Article Open access 11 October 2023
  18. Marked reduction of proteinuria after removal of a growth hormone-producing pituitary adenoma in a patient with focal segmental glomerulosclerosis: a case report and literature review

    Focal segmental glomerulosclerosis is a rare complication of acromegaly. A 74-year-old man was found to have acromegaly features such as enlargement...

    Shizuka Ishigaki, Yuji Oe, ... Mariko Miyazaki in CEN Case Reports
    Article 06 October 2022
  19. Anuria after kidney transplantation diagnosed as early recurrence of focal segmental glomerulosclerosis combined with acute calcineurin inhibitor nephrotoxicity: a case report and literature review

    Background

    Primary focal segmental glomerulosclerosis (FSGS) is a glomerular disease that sometimes recurs in patients after kidney transplantation...

    Yoon-Ju Kim, Seong-Wook Lee, ... Sun-Hee Park in BMC Nephrology
    Article Open access 05 April 2024
  20. CUBN gene mutations may cause focal segmental glomerulosclerosis (FSGS) in children

    Background

    Imerslund-Gräsbeck Syndrome (IGS) is mainly caused by CUBN gene biallelic mutations. Proteinuria accompanies IGS specific symptoms in about...

    **g Yang, Yongli Xu, ... Jianhua Zhou in BMC Nephrology
    Article Open access 03 January 2022
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