BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

172 related articles for article (PubMed ID: 37670083)

  • 1. Copy number variation analysis in 138 families with steroid-resistant nephrotic syndrome identifies causal homozygous deletions in PLCE1 and NPHS2 in two families.
    Pantel D; Mertens ND; Schneider R; Hölzel S; Kari JA; Desoky SE; Shalaby MA; Lim TY; Sanna-Cherchi S; Shril S; Hildebrandt F
    Pediatr Nephrol; 2024 Feb; 39(2):455-461. PubMed ID: 37670083
    [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. Whole exome sequencing identifies monogenic forms of nephritis in a previously unsolved cohort of children with steroid-resistant nephrotic syndrome and hematuria.
    Xiao H; Hildebrandt F
    Pediatr Nephrol; 2022 Jul; 37(7):1567-1574. PubMed ID: 34762194
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Whole Exome Sequencing of Patients with Steroid-Resistant Nephrotic Syndrome.
    Warejko JK; Tan W; Daga A; Schapiro D; Lawson JA; Shril S; Lovric S; Ashraf S; Rao J; Hermle T; Jobst-Schwan T; Widmeier E; Majmundar AJ; Schneider R; Gee HY; Schmidt JM; Vivante A; van der Ven AT; Ityel H; Chen J; Sadowski CE; Kohl S; Pabst WL; Nakayama M; Somers MJG; Rodig NM; Daouk G; Baum M; Stein DR; Ferguson MA; Traum AZ; Soliman NA; Kari JA; El Desoky S; Fathy H; Zenker M; Bakkaloglu SA; Müller D; Noyan A; Ozaltin F; Cadnapaphornchai MA; Hashmi S; Hopcian J; Kopp JB; Benador N; Bockenhauer D; Bogdanovic R; Stajić N; Chernin G; Ettenger R; Fehrenbach H; Kemper M; Munarriz RL; Podracka L; Büscher R; Serdaroglu E; Tasic V; Mane S; Lifton RP; Braun DA; Hildebrandt F
    Clin J Am Soc Nephrol; 2018 Jan; 13(1):53-62. PubMed ID: 29127259
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Copy Number Variation Analysis Facilitates Identification of Genetic Causation in Patients with Congenital Anomalies of the Kidney and Urinary Tract.
    Wu CW; Lim TY; Wang C; Seltzsam S; Zheng B; Schierbaum L; Schneider S; Mann N; Connaughton DM; Nakayama M; van der Ven AT; Dai R; Kolvenbach CM; Kause F; Ottlewski I; Stajic N; Soliman NA; Kari JA; El Desoky S; Fathy HM; Milosevic D; Turudic D; Al Saffar M; Awad HS; Eid LA; Ramanathan A; Senguttuvan P; Mane SM; Lee RS; Bauer SB; Lu W; Hilger AC; Tasic V; Shril S; Sanna-Cherchi S; Hildebrandt F
    Eur Urol Open Sci; 2022 Oct; 44():106-112. PubMed ID: 36185583
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genetic analysis and outcomes of Omani children with steroid-resistant nephrotic syndrome.
    Al Riyami MS; Al Alawi I; Al Gaithi B; Al Maskari A; Al Kalbani N; Al Hashmi N; Al Balushi A; Al Shahi M; Al Saidi S; Al Bimani M; Al Hatali F; Mabillard H; Sayer JA
    Mol Genet Genomic Med; 2023 Sep; 11(9):e2201. PubMed ID: 37204080
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Spectrum of mutations in Chinese children with steroid-resistant nephrotic syndrome.
    Wang F; Zhang Y; Mao J; Yu Z; Yi Z; Yu L; Sun J; Wei X; Ding F; Zhang H; Xiao H; Yao Y; Tan W; Lovric S; Ding J; Hildebrandt F
    Pediatr Nephrol; 2017 Jul; 32(7):1181-1192. PubMed ID: 28204945
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Analysis of 24 genes reveals a monogenic cause in 11.1% of cases with steroid-resistant nephrotic syndrome at a single center.
    Tan W; Lovric S; Ashraf S; Rao J; Schapiro D; Airik M; Shril S; Gee HY; Baum M; Daouk G; Ferguson MA; Rodig N; Somers MJG; Stein DR; Vivante A; Warejko JK; Widmeier E; Hildebrandt F
    Pediatr Nephrol; 2018 Feb; 33(2):305-314. PubMed ID: 28921387
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Patients with mutations in NPHS2 (podocin) do not respond to standard steroid treatment of nephrotic syndrome.
    Ruf RG; Lichtenberger A; Karle SM; Haas JP; Anacleto FE; Schultheiss M; Zalewski I; Imm A; Ruf EM; Mucha B; Bagga A; Neuhaus T; Fuchshuber A; Bakkaloglu A; Hildebrandt F;
    J Am Soc Nephrol; 2004 Mar; 15(3):722-32. PubMed ID: 14978175
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Novel NPHS2 variant in patients with familial steroid-resistant nephrotic syndrome with early onset, slow progression and dominant inheritance pattern.
    Suvanto M; Patrakka J; Jahnukainen T; Sjöström PM; Nuutinen M; Arikoski P; Kataja J; Kestilä M; Jalanko H
    Clin Exp Nephrol; 2017 Aug; 21(4):677-684. PubMed ID: 27573339
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A single-gene cause in 29.5% of cases of steroid-resistant nephrotic syndrome.
    Sadowski CE; Lovric S; Ashraf S; Pabst WL; Gee HY; Kohl S; Engelmann S; Vega-Warner V; Fang H; Halbritter J; Somers MJ; Tan W; Shril S; Fessi I; Lifton RP; Bockenhauer D; El-Desoky S; Kari JA; Zenker M; Kemper MJ; Mueller D; Fathy HM; Soliman NA; ; Hildebrandt F
    J Am Soc Nephrol; 2015 Jun; 26(6):1279-89. PubMed ID: 25349199
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Factors predicting the occurrence of disease-causing variants on next-generation sequencing in children with steroid-resistant nephrotic syndrome - implications for resource-constrained settings.
    Kaur A; Banday AZ; Dawman L; Rawat A; Tiewsoh K
    Pediatr Nephrol; 2023 Nov; 38(11):3663-3670. PubMed ID: 37335381
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mutations in NPHS2 encoding podocin are a prevalent cause of steroid-resistant nephrotic syndrome among Israeli-Arab children.
    Frishberg Y; Rinat C; Megged O; Shapira E; Feinstein S; Raas-Rothschild A
    J Am Soc Nephrol; 2002 Feb; 13(2):400-405. PubMed ID: 11805168
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Rapid detection of monogenic causes of childhood-onset steroid-resistant nephrotic syndrome.
    Lovric S; Fang H; Vega-Warner V; Sadowski CE; Gee HY; Halbritter J; Ashraf S; Saisawat P; Soliman NA; Kari JA; Otto EA; Hildebrandt F;
    Clin J Am Soc Nephrol; 2014 Jun; 9(6):1109-16. PubMed ID: 24742477
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17. Genomic and clinical profiling of a national nephrotic syndrome cohort advocates a precision medicine approach to disease management.
    Bierzynska A; McCarthy HJ; Soderquest K; Sen ES; Colby E; Ding WY; Nabhan MM; Kerecuk L; Hegde S; Hughes D; Marks S; Feather S; Jones C; Webb NJ; Ognjanovic M; Christian M; Gilbert RD; Sinha MD; Lord GM; Simpson M; Koziell AB; Welsh GI; Saleem MA
    Kidney Int; 2017 Apr; 91(4):937-947. PubMed ID: 28117080
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Report of novel genetic variation in NPHS2 gene associated with idiopathic nephrotic syndrome in South Indian children.
    Dhandapani MC; Venkatesan V; Rengaswamy NB; Gowrishankar K; Ekambaram S; Sengutavan P; Perumal V
    Clin Exp Nephrol; 2017 Feb; 21(1):127-133. PubMed ID: 26820844
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [NPHS2 Mutation analysis study in children with steroid-resistant nephrotic syndrome].
    Azocar M; Vega Á; Farfán M; Cano F
    Rev Chil Pediatr; 2016; 87(1):31-6. PubMed ID: 26455708
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genetic variants in the LAMA5 gene in pediatric nephrotic syndrome.
    Braun DA; Warejko JK; Ashraf S; Tan W; Daga A; Schneider R; Hermle T; Jobst-Schwan T; Widmeier E; Majmundar AJ; Nakayama M; Schapiro D; Rao J; Schmidt JM; Hoogstraten CA; Hugo H; Bakkaloglu SA; Kari JA; El Desoky S; Daouk G; Mane S; Lifton RP; Shril S; Hildebrandt F
    Nephrol Dial Transplant; 2019 Mar; 34(3):485-493. PubMed ID: 29534211
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.