Works matching DE "FOCAL segmental glomerulosclerosis"
Results: 1531
Long-term efficacy of Rituximab in steroid dependent and frequent relapsing adult nephrotic syndrome.
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- BMC Nephrology, 2025, v. 26, n. 1, p. 1, doi. 10.1186/s12882-025-04035-0
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- Article
Overexpression of plasmalemmal vesicle-associated protein-1 in patient with cyanotic nephropathy: a case report.
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- 2025
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- Publication type:
- Case Study
Candidate Genetic Modifiers in Alport Syndrome: A Case Series.
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- Life (2075-1729), 2025, v. 15, n. 2, p. 298, doi. 10.3390/life15020298
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- Publication type:
- Article
Ethanol Extract of Centella asiatica (Gotu Kola) Attenuates Tubular Injury Through Inhibition of Inflammatory Cytokines and Enhancement of Anti-Fibrotic Factor in Mice with 5/6 Subtotal Nephrectomy.
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- Malaysian Journal of Medical Sciences, 2019, v. 26, n. 5, p. 53, doi. 10.21315/mjms2019.26.5.5
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- Article
Evaluation of screening with urine dipsticks and renal ultrasonography for 3-year-olds in Chiba City over 30 years.
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- Clinical & Experimental Nephrology, 2022, v. 26, n. 12, p. 1208, doi. 10.1007/s10157-022-02265-2
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- Publication type:
- Article
Activation of necroptosis pathway in podocyte contributes to the pathogenesis of focal segmental glomerular sclerosis.
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- Clinical & Experimental Nephrology, 2022, v. 26, n. 11, p. 1055, doi. 10.1007/s10157-022-02258-1
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- Publication type:
- Article
Decreased GM3 correlates with proteinuria in minimal change nephrotic syndrome and focal segmental glomerulosclerosis.
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- Clinical & Experimental Nephrology, 2022, v. 26, n. 11, p. 1078, doi. 10.1007/s10157-022-02249-2
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- Publication type:
- Article
Clinical, pathological, and genetic characteristics of cases with asymptomatic proteinuria not manifesting nephrotic syndrome at onset: a single-center retrospective study.
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- Clinical & Experimental Nephrology, 2022, v. 26, n. 5, p. 453, doi. 10.1007/s10157-021-02174-w
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- Article
A digest of the Evidence-Based Clinical Practice Guideline for Nephrotic Syndrome 2020.
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- Clinical & Experimental Nephrology, 2021, v. 25, n. 12, p. 1277, doi. 10.1007/s10157-021-02098-5
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- Publication type:
- Article
Overlapping obesity-related glomerulopathy and immunoglobulin A nephropathy: clinical and pathologic characteristics and prognosis.
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- Clinical & Experimental Nephrology, 2021, v. 25, n. 8, p. 865, doi. 10.1007/s10157-021-02045-4
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- Article
Association of serum lncRNA H19 expression with inflammatory and oxidative stress markers and routine biochemical parameters in chronic kidney disease.
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- Clinical & Experimental Nephrology, 2021, v. 25, n. 5, p. 522, doi. 10.1007/s10157-021-02023-w
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- Publication type:
- Article
A cross-sectional study in patients with IgA nephropathy of correlations between clinical data and pathological findings at the time of renal biopsy: a Japanese prospective cohort study.
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- Clinical & Experimental Nephrology, 2021, v. 25, n. 5, p. 509, doi. 10.1007/s10157-021-02022-x
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- Publication type:
- Article
Kidney biopsy guidebook 2020 in Japan.
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- Clinical & Experimental Nephrology, 2021, v. 25, n. 4, p. 325, doi. 10.1007/s10157-020-01986-6
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- Publication type:
- Article
Adult-onset minimal change disease: the significance of histological chronic changes for clinical presentation and outcome.
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- Clinical & Experimental Nephrology, 2021, v. 25, n. 3, p. 240, doi. 10.1007/s10157-020-01985-7
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- Publication type:
- Article
Efficacy of once-daily cyclosporine in Japanese children with steroid-dependent minimal change nephrotic syndrome.
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- 2021
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- Publication type:
- Letter
Serum levels of galactose-deficient IgA1 in Chinese children with IgA nephropathy, IgA vasculitis with nephritis, and IgA vasculitis.
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- Clinical & Experimental Nephrology, 2021, v. 25, n. 1, p. 37, doi. 10.1007/s10157-020-01968-8
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- Publication type:
- Article
Effects of LDL apheresis on proteinuria in patients with diabetes mellitus, severe proteinuria, and dyslipidemia.
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- Clinical & Experimental Nephrology, 2021, v. 25, n. 1, p. 1, doi. 10.1007/s10157-020-01959-9
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- Article
Renal hypoplasia can be the cause of membranous nephropathy-like lesions.
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- Clinical & Experimental Nephrology, 2020, v. 24, n. 9, p. 813, doi. 10.1007/s10157-020-01902-y
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- Publication type:
- Article
Time-averaged proteinuria during follow-up and renal prognosis in patients with biopsy-proven benign nephrosclerosis.
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- Clinical & Experimental Nephrology, 2020, v. 24, n. 8, p. 688, doi. 10.1007/s10157-020-01885-w
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- Article
Pediatric glomerular hematuria: a clinicopathological study.
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- Clinical & Experimental Nephrology, 2020, v. 24, n. 7, p. 613, doi. 10.1007/s10157-020-01872-1
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- Publication type:
- Article
Incidence of remission and relapse of proteinuria, end-stage kidney disease, mortality, and major outcomes in primary nephrotic syndrome: the Japan Nephrotic Syndrome Cohort Study (JNSCS).
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- Clinical & Experimental Nephrology, 2020, v. 24, n. 6, p. 526, doi. 10.1007/s10157-020-01864-1
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- Publication type:
- Article
A clinicopathological comparison between IgA nephropathy and Henoch–Schönlein purpura nephritis in children: use of the Oxford classification.
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- Clinical & Experimental Nephrology, 2019, v. 23, n. 12, p. 1382, doi. 10.1007/s10157-019-01777-8
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- Publication type:
- Article
Urine exosomal ceruloplasmin: a potential early biomarker of underlying kidney disease.
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- Clinical & Experimental Nephrology, 2019, v. 23, n. 8, p. 1013, doi. 10.1007/s10157-019-01734-5
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- Publication type:
- Article
Successful management of post-transplant focal segmental glomerulosclerosis with therapeutic plasma exchange and rituximab.
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- Clinical & Experimental Nephrology, 2019, v. 23, n. 5, p. 700, doi. 10.1007/s10157-019-01690-0
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- Publication type:
- Article
Two different clinical aspects of Japanese children with asymptomatic nephrotic syndrome at onset.
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- 2019
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- Publication type:
- Letter
Mesangial C4d deposition is independently associated with poor renal survival in patients with primary focal segmental glomerulosclerosis.
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- Clinical & Experimental Nephrology, 2019, v. 23, n. 5, p. 650, doi. 10.1007/s10157-018-01688-0
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- Publication type:
- Article
Application of next-generation sequencing technology to diagnosis and treatment of focal segmental glomerulosclerosis.
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- Clinical & Experimental Nephrology, 2018, v. 22, n. 3, p. 491, doi. 10.1007/s10157-017-1449-y
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- Publication type:
- Article
Risk factors of venous thromboembolism in focal segmental glomerulosclerosis with nephrotic syndrome.
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- Clinical & Experimental Nephrology, 2016, v. 20, n. 2, p. 212, doi. 10.1007/s10157-015-1149-4
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- Publication type:
- Article
Reduced podocin expression in minimal change disease and focal segmental glomerulosclerosis is related to the level of proteinuria.
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- Clinical & Experimental Nephrology, 2013, v. 17, n. 6, p. 811, doi. 10.1007/s10157-013-0775-y
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- Publication type:
- Article
An explorative analysis of secretory receptor for advanced glycation endproducts in primary focal segmental glomerulosclerosis.
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- Clinical & Experimental Nephrology, 2012, v. 16, n. 4, p. 589, doi. 10.1007/s10157-012-0599-1
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- Publication type:
- Article
Nephrotic syndrome and renal failure in a patient with metastatic breast cancer.
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- Clinical & Experimental Nephrology, 2011, v. 15, n. 4, p. 567, doi. 10.1007/s10157-011-0425-1
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- Publication type:
- Article
A patient with Bartter syndrome accompanying severe growth hormone deficiency and focal segmental glomerulosclerosis.
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- Clinical & Experimental Nephrology, 2010, v. 14, n. 3, p. 278, doi. 10.1007/s10157-009-0262-7
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- Publication type:
- Article
Collapsing FSGS: a clinicopathologic study of 10 cases from Pakistan.
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- Clinical & Experimental Nephrology, 2010, v. 14, n. 3, p. 222, doi. 10.1007/s10157-010-0275-2
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- Publication type:
- Article
Sphingomyelin Phosphodiesterase Acid-Like 3b is Essential for Toll-Like Receptor 3 Signaling in Human Podocytes.
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- Journal of Membrane Biology, 2022, v. 255, n. 1, p. 117, doi. 10.1007/s00232-021-00206-w
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- Article
Clinicopathological characteristics and renal outcomes of adult patients with pauci-immune necrotizing glomerulonephritis according to ANCA status.
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- Clinical Rheumatology, 2024, v. 43, n. 8, p. 2669, doi. 10.1007/s10067-024-07047-7
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- Article
Analysis of the clinical characteristics of arthritis with renal disease caused by a NPHS2 gene mutation.
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- Clinical Rheumatology, 2021, v. 40, n. 8, p. 3335, doi. 10.1007/s10067-020-05574-7
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- Article
Kidney transplantation as a treatment of choice for AA amyloidosis due to periodic fever syndrome.
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- Clinical Rheumatology, 2021, v. 40, n. 2, p. 763, doi. 10.1007/s10067-020-05283-1
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- Article
Validation of a renal risk score in a cohort of ANCA-associated vasculitis patients with severe kidney damage.
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- Clinical Rheumatology, 2020, v. 39, n. 6, p. 1935, doi. 10.1007/s10067-020-04936-5
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- Publication type:
- Article
New method for the assessment of perineural invasion from perihilar cholangiocarcinoma.
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- Surgery Today, 2021, v. 51, n. 1, p. 136, doi. 10.1007/s00595-020-02071-x
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- Publication type:
- Article
Clinicopathological Evaluation of Elderly Biopsies in Turkish Society.
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- Namık Kemal Tıp Dergisi, 2024, v. 12, n. 2, p. 78, doi. 10.4274/nkmj.galenos.2024.67689
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- Publication type:
- Article
Demographic and Clinical Features and Factors Associated with Survival in Patients with Primary Glomerulonephritis: Single Tertiary Center Experience.
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- Namık Kemal Tıp Dergisi, 2023, v. 11, n. 1, p. 27, doi. 10.4274/nkmj.galenos.2023.06078
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- Publication type:
- Article
Journal scan.
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- Asian Journal of Pediatric Nephrology, 2023, v. 6, n. 2, p. 70, doi. 10.4103/ajpn.ajpn_22_23
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- Publication type:
- Article
Focal Segmental Glomerulosclerosis in Primary Sjogren Syndrome.
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- Asian Journal of Pediatric Nephrology, 2023, v. 6, n. 1, p. 24, doi. 10.4103/ajpn.ajpn_19_22
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- Publication type:
- Article
Childhood Nephrotic Syndrome: A Single Center Experience.
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- Asian Journal of Pediatric Nephrology, 2022, v. 5, n. 2, p. 78, doi. 10.4103/ajpn.ajpn_39_21
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- Publication type:
- Article
A rare case of Focal Segmental glomerulosclerosis in Mixed connective tissue disease.
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- Indian Journal of Basic & Applied Medical Research, 2019, v. 8, n. 2, p. 10
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- Publication type:
- Article
Dysregulated levels of glycogen synthase kinase-3β (GSK-3β) and miR-135 in peripheral blood samples of cases with nephrotic syndrome.
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- PeerJ, 2020, p. 1, doi. 10.7717/peerj.10377
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- Publication type:
- Article
Spectrum of biopsy-proven renal disease in geriatric patients: Clinical Presentation, Histological Diagnosis and Biopsy Indications, A Single-Centre Experience.
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- Revista de Nefrología Diálisis y Trasplante, 2024, v. 44, n. 2, p. 71
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- Publication type:
- Article
THE TREATMENT WITH MYCOPHENOLATE MOFETIL OF CORTICORESISTENT NEPHROTIC SYNDROME BY IDIOPATHIC FOCAL SEGMENTAL GLOMERULOSCLEROSIS: ANALYSIS OF TWENTY CASES.
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- Contributions / Prilozi (1857-9345), 2019, v. 40, n. 3, p. 135, doi. 10.2478/prilozi-2020-0013
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- Publication type:
- Article
EVALUATION OF CLINICAL, LABORATORY AND TREATMENT MODALITIES IN C3 GLOMERULOPATHY: SINGLE CENTER EXPERIENCE.
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- Contributions / Prilozi (1857-9345), 2019, v. 40, n. 2, p. 15, doi. 10.2478/prilozi-2019-0010
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- Publication type:
- Article
Health-related quality of life in Egyptian children with nephrotic syndrome.
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- Quality of Life Research, 2020, v. 29, n. 8, p. 2185, doi. 10.1007/s11136-020-02438-0
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- Publication type:
- Article