Results 121 to 130 of about 432,986 (215)

Focal Segmental Glomerulosclerosis: Histopathology Discussion

European Medical Journal Nephrology, 2022
Brian Mark Churchill, Mahesha Vankalakunti, Pallavi Patri, Sankaran Sundar   +3 more
doaj   +1 more source

Disease Recurrence—The Sword of Damocles in Kidney Transplantation for Primary Focal Segmental Glomerulosclerosis

Frontiers in Immunology, 2019
A major obstacle in kidney transplantation for primary focal segmental glomerulosclerosis (FSGS) is the risk of disease recurrence. Recurrent FSGS affects up to 60% of first kidney grafts and exceeds 80% in patients who have lost their first graft due to
K. Kienzl-Wagner, S. Waldegger, S. Schneeberger   +2 more
semanticscholar   +1 more source

Clinical and pathological characteristics of primary focal segmental glomerulosclerosis in adult [PDF]

, 2017
Background and objective: Focal segmental glomerulosclerosis shares overlapping patterns of injury with segmental consolidation and obliteration of glomerular architecture by the accumulation of collagenous extracellular matrix or by increased ...
Al-Mukhtar, Safa Ezzidin, Wadee, Salam Fareed   +1 more
core  

Adaptations métaboliques des podocytes à différents stress imitant la hyalinose segmentaire et focale [PDF]

Focal segmental glomerulosclerosis (FSGS) is a complex and diverse subset of renal glomerular disorder. Podocytes, crucial for maintaining the glomerular filtration barrier architecture are the primary sites of the injury in FSGS. Various stresses lead
Tagliatti, Vanessa, Esteve, Emmanuel, Thirion, Marine, Hecq, Aurore, Colet, Jean-Marie, Nortier, Antoine, Decleves, Anne-Emilie   +6 more
core   +1 more source

A mutation in transcription factor MAFB causes Focal Segmental Glomerulosclerosis with Duane Retraction Syndrome.

Kidney International, 2018
Focal segmental glomerulosclerosis (FSGS) is a leading cause of end-stage renal disease in children and adults. Genetic factors significantly contribute to early-onset FSGS, but the etiologies of most adult cases remain unknown.
Yoshinori Sato, H. Tsukaguchi, H. Morita, K. Higasa, M. Tran, Michito Hamada, Toshiaki Usui, Naoki Morito, S. Horita, Takao Hayashi, J. Takagi, I. Yamaguchi, H. T. Nguyen, M. Harada, Kiyoko Inui, Yuichi Maruta, Y. Inoue, F. Koiwa, Hiroshi Sato, F. Matsuda, S. Ayabe, Seiya Mizuno, F. Sugiyama, Satoru Takahashi, A. Yoshimura   +24 more
semanticscholar   +1 more source

Drug discovery in focal and segmental glomerulosclerosis

, 2016
Despite the high medical burden experienced by patients with focal segmental glomerulosclerosis, the etiology of the condition remains largely unknown. Focal segmental glomerulosclerosis is highly heterogeneous in clinical and morphologic manifestations.
Pullen, Nick, Fornoni, Alessia
core   +1 more source

Demographic, Clinicopathological and Laboratory Features of Focal Segmental Glomerulosclerosis Patients

, 2020
Aim: Focal segmental glomerulosclerosis (FSGS) is one of the common glomerulonephritis in Turkey and the world. The aim of our study was to determine demographic and clinical features and biopsy results of patients who were followed up with primary FSGS ...
Ozturk, Savaş, Bashan, Yagmur, Ozkan, Oktay, Cebeci, Egemen, Uzun, Sami, Karadag, Serhat, Ozler, Tuba Elif, Karaali, Zeynep, Ceylan, Ozge Can, Dag, Hatice Burcu   +9 more
core   +1 more source

Focal segmental glomerulosclerosis; collapsing variant [PDF]

Journal of Nephropathology, 2012
Peyman Mohammadi Torbati
doaj   +1 more source

A Rare Cause of the Acute Renal Failure: Glomerular Tip Lesion

Turkish Journal of Nephrology, 2019
Glomerular tip lesion is frequently used to defi ne a histological variant of focal segmental glomerulosclerosis. Most patients with glomerular tip lesion have nephrotic syndrome and show a good response to steroid treatment.
Serhan PİŞKİNPAŞA, Nihal ÖZKAYAR, Ezgi YENİGÜN ÇOŞKUN, Hadim AKOĞLU, Eyüp KOÇ, İpek Işık GÖNÜL, Fatih DEDE   +6 more
doaj  

WT-1 and NPHS2 mutation analysis in patients with non-familial steroid-resistant focal-segmental glomerulosclerosis.

, 2003
Item does not contain fulltextBACKGROUND: Familial forms of steroid-resistant nephrotic syndrome with the histologic findings of focal-segmental glomerulosclerosis have frequently a genetic basis.
Lowik, M.M., Heuvel, L.P.W.J. van den, Monnens, L.A.H., M.M. Löwik, L.A.H. Monnens, Levtchenko, E.N., E.N. Levtchenko, L.P.W.J. van den Heuvel   +7 more
core   +1 more source