190 related articles for article (PubMed ID: 38336226)
1. Ibrutinib-associated focal segmental glomerulosclerosis and the impact of podocin mutations in chronic lymphocytic leukemia.
Czogalla J; Schliffke S; Lu S; Schwerk M; Petereit H; Zhang T; Liu S; Dumoulin B; Gies S; Wu G; Hänzelmann S; Bode M; Grahammer F; Gödel M; Voigtländer M; Butt L; Bokemeyer C; Bergmann C; Benzing T; Wiech T; Puelles VG; Huber TB
Kidney Int; 2024 Apr; 105(4):877-881. PubMed ID: 38336226
[No Abstract] [Full Text] [Related]
2. NPHS2 gene, nephrotic syndrome and focal segmental glomerulosclerosis: a HuGE review.
Franceschini N; North KE; Kopp JB; McKenzie L; Winkler C
Genet Med; 2006 Feb; 8(2):63-75. PubMed ID: 16481888
[TBL] [Abstract][Full Text] [Related]
3. The p.R229Q variant of the NPHS2 (podocin) gene in focal segmental glomerulosclerosis and steroid-resistant nephrotic syndrome: a meta-analysis.
Lu L; Wan H; Yin Y; Feng WJ; Wang M; Zou YC; Huang B; Wang DT; Shi Y; Zhao Y; Wei LB
Int Urol Nephrol; 2014 Jul; 46(7):1383-93. PubMed ID: 24715228
[TBL] [Abstract][Full Text] [Related]
4. Broadening the spectrum of diseases related to podocin mutations.
Caridi G; Bertelli R; Di Duca M; Dagnino M; Emma F; Onetti Muda A; Scolari F; Miglietti N; Mazzucco G; Murer L; Carrea A; Massella L; Rizzoni G; Perfumo F; Ghiggeri GM
J Am Soc Nephrol; 2003 May; 14(5):1278-86. PubMed ID: 12707396
[TBL] [Abstract][Full Text] [Related]
5. Late onset of familial nephrotic syndrome associated with a compound heterozygous mutation of the podocin-encoding gene.
Ardiles LG; Carrasco AE; Carpio JD; Mezzano SA
Nephrology (Carlton); 2005 Dec; 10(6):553-6. PubMed ID: 16354237
[TBL] [Abstract][Full Text] [Related]
6. Prevalence, genetics, and clinical features of patients carrying podocin mutations in steroid-resistant nonfamilial focal segmental glomerulosclerosis.
Caridi G; Bertelli R; Carrea A; Di Duca M; Catarsi P; Artero M; Carraro M; Zennaro C; Candiano G; Musante L; Seri M; Ginevri F; Perfumo F; Ghiggeri GM
J Am Soc Nephrol; 2001 Dec; 12(12):2742-2746. PubMed ID: 11729243
[TBL] [Abstract][Full Text] [Related]
7. The podocin V260E mutation predicts steroid resistant nephrotic syndrome in black South African children with focal segmental glomerulosclerosis.
Govender MA; Fabian J; Gottlich E; Levy C; Moonsamy G; Maher H; Winkler CA; Ramsay M
Commun Biol; 2019; 2():416. PubMed ID: 31754646
[TBL] [Abstract][Full Text] [Related]
8. Clinical value of NPHS2 analysis in early- and adult-onset steroid-resistant nephrotic syndrome.
Santín S; Tazón-Vega B; Silva I; Cobo MÁ; Giménez I; Ruíz P; García-Maset R; Ballarín J; Torra R; Ars E;
Clin J Am Soc Nephrol; 2011 Feb; 6(2):344-54. PubMed ID: 20947785
[TBL] [Abstract][Full Text] [Related]
9. NPHS2 mutations in late-onset focal segmental glomerulosclerosis: R229Q is a common disease-associated allele.
Tsukaguchi H; Sudhakar A; Le TC; Nguyen T; Yao J; Schwimmer JA; Schachter AD; Poch E; Abreu PF; Appel GB; Pereira AB; Kalluri R; Pollak MR
J Clin Invest; 2002 Dec; 110(11):1659-66. PubMed ID: 12464671
[TBL] [Abstract][Full Text] [Related]
10. mRNA sequencing of a novel NPHS2 intronic mutation in a child with focal and segmental glomerulosclerosis.
Benetti E; Caridi G; Centi S; Vella MD; Ghiggeri GM; Artifoni L; Murer L
Saudi J Kidney Dis Transpl; 2014 Jul; 25(4):854-7. PubMed ID: 24969201
[TBL] [Abstract][Full Text] [Related]
11. The mutation-dependent pathogenicity of NPHS2 p.R229Q: A guide for clinical assessment.
Mikó Á; K Menyhárd D; Kaposi A; Antignac C; Tory K
Hum Mutat; 2018 Dec; 39(12):1854-1860. PubMed ID: 30260545
[TBL] [Abstract][Full Text] [Related]
12. Recurrence of focal segmental glomerulosclerosis after renal transplantation in patients with mutations of podocin.
Bertelli R; Ginevri F; Caridi G; Dagnino M; Sandrini S; Di Duca M; Emma F; Sanna-Cherchi S; Scolari F; Neri TM; Murer L; Massella L; Basile G; Rizzoni G; Perfumo F; Ghiggeri GM
Am J Kidney Dis; 2003 Jun; 41(6):1314-21. PubMed ID: 12776285
[TBL] [Abstract][Full Text] [Related]
13. The genetic basis of FSGS and steroid-resistant nephrosis.
Pollak MR
Semin Nephrol; 2003 Mar; 23(2):141-6. PubMed ID: 12704574
[TBL] [Abstract][Full Text] [Related]
14. Recurrence of proteinuria 10 years post-transplant in NPHS2-associated focal segmental glomerulosclerosis after conversion from cyclosporin A to sirolimus.
Höcker B; Knüppel T; Waldherr R; Schaefer F; Weber S; Tönshoff B
Pediatr Nephrol; 2006 Oct; 21(10):1476-9. PubMed ID: 16721582
[TBL] [Abstract][Full Text] [Related]
15. Chronic lymphocytic leukemia-associated nephrotic syndrome caused by focal segmental glomerulosclerosis.
Rosado MF; Morgensztern D; Abdullah S; Ruiz P; Lossos IS
Am J Hematol; 2004 Oct; 77(2):205-6. PubMed ID: 15389914
[No Abstract] [Full Text] [Related]
16. Nephrotic Syndrome With Mutations in NPHS2: The Role of R229Q and Implications for Genetic Counseling.
Rood IM; Deegens JKJ; Lugtenberg D; Bongers EMHF; Wetzels JFM
Am J Kidney Dis; 2019 Mar; 73(3):400-403. PubMed ID: 30241959
[TBL] [Abstract][Full Text] [Related]
17. Analysis of mutations in alpha-actinin 4 and podocin genes of patients with chronic renal failure due to sporadic focal segmental glomerulosclerosis.
Komatsuda A; Wakui H; Maki N; Kigawa A; Goto H; Ohtani H; Hamai K; Oyama Y; Makoto H; Sawada K; Imai H
Ren Fail; 2003 Jan; 25(1):87-93. PubMed ID: 12617336
[TBL] [Abstract][Full Text] [Related]
18. Rare functional variants of podocin (NPHS2) promoter in patients with nephrotic syndrome.
Oleggini R; Bertelli R; Di Donato A; Di Duca M; Caridi G; Sanna-Cherchi S; Scolari F; Murer L; Allegri L; Coppo R; Emma F; Camussi G; Perfumo F; Ghiggeri GM
Gene Expr; 2006; 13(1):59-66. PubMed ID: 16572591
[TBL] [Abstract][Full Text] [Related]
19. Infantile steroid-resistant nephrotic syndrome associated with double homozygous mutations of podocin.
Caridi G; Berdeli A; Dagnino M; Di Duca M; Mir S; Cura A; Ravazzolo R; Ghiggeri GM
Am J Kidney Dis; 2004 Apr; 43(4):727-32. PubMed ID: 15042551
[TBL] [Abstract][Full Text] [Related]
20. Genotype/phenotype correlations of NPHS1 and NPHS2 mutations in nephrotic syndrome advocate a functional inter-relationship in glomerular filtration.
Koziell A; Grech V; Hussain S; Lee G; Lenkkeri U; Tryggvason K; Scambler P
Hum Mol Genet; 2002 Feb; 11(4):379-88. PubMed ID: 11854170
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]