BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

242 related articles for article (PubMed ID: 37578539)

  • 1. Ocular manifestations of the genetic causes of focal and segmental glomerulosclerosis.
    Zhu V; Huang T; Wang D; Colville D; Mack H; Savige J
    Pediatr Nephrol; 2024 Mar; 39(3):655-679. PubMed ID: 37578539
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Causal and putative pathogenic mutations identified in 39% of children with primary steroid-resistant nephrotic syndrome in South Africa.
    Nandlal L; Winkler CA; Bhimma R; Cho S; Nelson GW; Haripershad S; Naicker T
    Eur J Pediatr; 2022 Oct; 181(10):3595-3606. PubMed ID: 35920919
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genetic basis of nephrotic syndrome--review.
    Obeidová H; Merta M; Reiterová J; Maixnerová D; Stekrová J; Rysavá R; Tesar V
    Prague Med Rep; 2006; 107(1):5-16. PubMed ID: 16752799
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mutations in INF2 may be associated with renal histology other than focal segmental glomerulosclerosis.
    Büscher AK; Celebi N; Hoyer PF; Klein HG; Weber S; Hoefele J
    Pediatr Nephrol; 2018 Mar; 33(3):433-437. PubMed ID: 29038887
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Retrospective mutational analysis of NPHS1, NPHS2, WT1 and LAMB2 in children with steroid-resistant focal segmental glomerulosclerosis - a single-centre experience.
    Bińczak-Kuleta A; Rubik J; Litwin M; Ryder M; Lewandowska K; Taryma-Leśniak O; Clark JS; Grenda R; Ciechanowicz A
    Bosn J Basic Med Sci; 2014 May; 14(2):89-93. PubMed ID: 24856380
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Bigenic heterozygosity and the development of steroid-resistant focal segmental glomerulosclerosis.
    Löwik M; Levtchenko E; Westra D; Groenen P; Steenbergen E; Weening J; Lilien M; Monnens L; van den Heuvel L
    Nephrol Dial Transplant; 2008 Oct; 23(10):3146-51. PubMed ID: 18443213
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Eye involvement in children with primary focal segmental glomerulosclerosis.
    Ozaltin F; Heeringa S; Poyraz CE; Bilginer Y; Kadayifcilar S; Besbas N; Topaloglu R; Ozen S; Hildebrandt F; Bakkaloglu A
    Pediatr Nephrol; 2008 Mar; 23(3):421-7. PubMed ID: 18058136
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mutations in podocyte genes are a rare cause of primary FSGS associated with ESRD in adult patients.
    Büscher AK; Konrad M; Nagel M; Witzke O; Kribben A; Hoyer PF; Weber S
    Clin Nephrol; 2012 Jul; 78(1):47-53. PubMed ID: 22732337
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Dominant PAX2 mutations may cause steroid-resistant nephrotic syndrome and FSGS in children.
    Vivante A; Chacham OS; Shril S; Schreiber R; Mane SM; Pode-Shakked B; Soliman NA; Koneth I; Schiffer M; Anikster Y; Hildebrandt F
    Pediatr Nephrol; 2019 Sep; 34(9):1607-1613. PubMed ID: 31001663
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Collapsing Glomerulopathy in a Patient with a TRPC6 Mutation Presenting as Rapidly Progressive Glomerulonephritis: A Case Report and Review of the Literature.
    Gokce I; Kaya M; Cicek N; Guven S; Ercetin Y; Yildiz N; Kaya H; Alpay H
    Saudi J Kidney Dis Transpl; 2023 May; 34(3):254-258. PubMed ID: 38231721
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Clinical, Pathological, and Genetic Characteristics in Patients with Focal Segmental Glomerulosclerosis.
    Nagano C; Hara S; Yoshikawa N; Takeda A; Gotoh Y; Hamada R; Matsuoka K; Yamamoto M; Fujinaga S; Sakuraya K; Kamei K; Hamasaki Y; Oguchi H; Araki Y; Ogawa Y; Okamoto T; Ito S; Tanaka S; Kaito H; Aoto Y; Ishiko S; Rossanti R; Sakakibara N; Horinouchi T; Yamamura T; Nagase H; Iijima K; Nozu K
    Kidney360; 2022 Aug; 3(8):1384-1393. PubMed ID: 36176665
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Targeted next-generation sequencing in steroid-resistant nephrotic syndrome: mutations in multiple glomerular genes may influence disease severity.
    Bullich G; Trujillano D; Santín S; Ossowski S; Mendizábal S; Fraga G; Madrid Á; Ariceta G; Ballarín J; Torra R; Estivill X; Ars E
    Eur J Hum Genet; 2015 Sep; 23(9):1192-9. PubMed ID: 25407002
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Advances in molecular diagnosis and therapeutics in nephrotic syndrome and focal and segmental glomerulosclerosis.
    Sharif B; Barua M
    Curr Opin Nephrol Hypertens; 2018 May; 27(3):194-200. PubMed ID: 29465426
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Clinical, pathological, and genetic characteristics of cases with asymptomatic proteinuria not manifesting nephrotic syndrome at onset: a single-center retrospective study.
    Watanabe Y; Fujinaga S; Sakuraya K; Ikeda H; Nozu K
    Clin Exp Nephrol; 2022 May; 26(5):453-459. PubMed ID: 35113255
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genetic Study in Korean Pediatric Patients with Steroid-Resistant Nephrotic Syndrome or Focal Segmental Glomerulosclerosis.
    Park E; Lee C; Kim NKD; Ahn YH; Park YS; Lee JH; Kim SH; Cho MH; Cho H; Yoo KH; Shin JI; Kang HG; Ha IS; Park WY; Cheong HI
    J Clin Med; 2020 Jun; 9(6):. PubMed ID: 32604935
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Podocyte-associated gene mutation screening in a heterogeneous cohort of patients with sporadic focal segmental glomerulosclerosis.
    Laurin LP; Lu M; Mottl AK; Blyth ER; Poulton CJ; Weck KE
    Nephrol Dial Transplant; 2014 Nov; 29(11):2062-9. PubMed ID: 24500309
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A Systematic Analysis of Major Susceptible Genes in Childhood-onset Steroid-resistant Nephrotic Syndrome.
    Li Y; He Q; Wang Y; Dang X; Wu X; Li X; Shuai L; Yi Z
    Ann Clin Lab Sci; 2019 May; 49(3):330-337. PubMed ID: 31308032
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Racial and ethnic differences in the incidence and progression of focal segmental glomerulosclerosis in children.
    Andreoli SP
    Adv Ren Replace Ther; 2004 Jan; 11(1):105-9. PubMed ID: 14730545
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Precise clinicopathologic findings for application of genetic testing in pediatric kidney transplant recipients with focal segmental glomerulosclerosis/steroid-resistant nephrotic syndrome.
    Miura K; Kaneko N; Hashimoto T; Ishizuka K; Shirai Y; Hisano M; Chikamoto H; Akioka Y; Kanda S; Harita Y; Yamamoto T; Hattori M
    Pediatr Nephrol; 2023 Feb; 38(2):417-429. PubMed ID: 35655039
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Spectrum of NPHS1 and NPHS2 variants in egyptian children with focal segmental glomerular sclerosis: identification of six novel variants and founder effect.
    Thomas MM; Ahmed HM; El-Dessouky SH; Ramadan A; Botrous OE; Abdel-Hamid MS
    Mol Genet Genomics; 2022 May; 297(3):689-698. PubMed ID: 35278126
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.