218 related articles for article (PubMed ID: 24227627)
1. NPHS2 mutations in steroid-resistant nephrotic syndrome: a mutation update and the associated phenotypic spectrum.
Bouchireb K; Boyer O; Gribouval O; Nevo F; Huynh-Cong E; Morinière V; Campait R; Ars E; Brackman D; Dantal J; Eckart P; Gigante M; Lipska BS; Liutkus A; Megarbane A; Mohsin N; Ozaltin F; Saleem MA; Schaefer F; Soulami K; Torra R; Garcelon N; Mollet G; Dahan K; Antignac C
Hum Mutat; 2014 Feb; 35(2):178-86. PubMed ID: 24227627
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. NPHS2 mutation analysis shows genetic heterogeneity of steroid-resistant nephrotic syndrome and low post-transplant recurrence.
Weber S; Gribouval O; Esquivel EL; Morinière V; Tête MJ; Legendre C; Niaudet P; Antignac C
Kidney Int; 2004 Aug; 66(2):571-9. PubMed ID: 15253708
[TBL] [Abstract][Full Text] [Related]
4. Mutations in NPHS2 (podocin) in Mexican children with nephrotic syndrome who respond to standard steroid treatment.
Carrasco-Miranda JS; Garcia-Alvarez R; Sotelo-Mundo RR; Valenzuela O; Islas-Osuna MA; Sotelo-Cruz N
Genet Mol Res; 2013 Jun; 12(2):2102-7. PubMed ID: 23913389
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Clinical and epidemiological assessment of steroid-resistant nephrotic syndrome associated with the NPHS2 R229Q variant.
Machuca E; Hummel A; Nevo F; Dantal J; Martinez F; Al-Sabban E; Baudouin V; Abel L; Grünfeld JP; Antignac C
Kidney Int; 2009 Apr; 75(7):727-35. PubMed ID: 19145239
[TBL] [Abstract][Full Text] [Related]
7. Mutational analysis in podocin-associated hereditary nephrotic syndrome in Polish patients: founder effect in the Kashubian population.
Lipska BS; Balasz-Chmielewska I; Morzuch L; Wasielewski K; Vetter D; Borzecka H; Drozdz D; Firszt-Adamczyk A; Gacka E; Jarmolinski T; Ksiazek J; Kuzma-Mroczkowska E; Litwin M; Medynska A; Silska M; Szczepanska M; Tkaczyk M; Wasilewska A; Schaefer F; Zurowska A; Limon J
J Appl Genet; 2013 Aug; 54(3):327-33. PubMed ID: 23645318
[TBL] [Abstract][Full Text] [Related]
8. Specific podocin mutations correlate with age of onset in steroid-resistant nephrotic syndrome.
Hinkes B; Vlangos C; Heeringa S; Mucha B; Gbadegesin R; Liu J; Hasselbacher K; Ozaltin F; Hildebrandt F;
J Am Soc Nephrol; 2008 Feb; 19(2):365-71. PubMed ID: 18216321
[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. 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]
11. [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]
12. NPHS2 variation in Chinese southern infants with late steroid-resistant nephrotic syndrome.
Dai Y; Yang H; Gao P; Liu WD
Ren Fail; 2014 Oct; 36(9):1395-8. PubMed ID: 25112471
[TBL] [Abstract][Full Text] [Related]
13. Genetic screening in adolescents with steroid-resistant nephrotic syndrome.
Lipska BS; Iatropoulos P; Maranta R; Caridi G; Ozaltin F; Anarat A; Balat A; Gellermann J; Trautmann A; Erdogan O; Saeed B; Emre S; Bogdanovic R; Azocar M; Balasz-Chmielewska I; Benetti E; Caliskan S; Mir S; Melk A; Ertan P; Baskin E; Jardim H; Davitaia T; Wasilewska A; Drozdz D; Szczepanska M; Jankauskiene A; Higuita LM; Ardissino G; Ozkaya O; Kuzma-Mroczkowska E; Soylemezoglu O; Ranchin B; Medynska A; Tkaczyk M; Peco-Antic A; Akil I; Jarmolinski T; Firszt-Adamczyk A; Dusek J; Simonetti GD; Gok F; Gheissari A; Emma F; Krmar RT; Fischbach M; Printza N; Simkova E; Mele C; Ghiggeri GM; Schaefer F;
Kidney Int; 2013 Jul; 84(1):206-13. PubMed ID: 23515051
[TBL] [Abstract][Full Text] [Related]
14. NPHS2 mutations in Indian children with sporadic early steroid resistant nephrotic syndrome.
Vasudevan A; Siji A; Raghavendra A; Sridhar TS; Phadke KD
Indian Pediatr; 2012 Mar; 49(3):231-3. PubMed ID: 22080622
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. NPHS2 gene in steroid-resistant nephrotic syndrome: prevalence, clinical course, and mutational spectrum in South-West Iranian children.
Basiratnia M; Yavarian M; Torabinezhad S; Erjaee A
Iran J Kidney Dis; 2013 Sep; 7(5):357-62. PubMed ID: 24072147
[TBL] [Abstract][Full Text] [Related]
17. NPHS2 mutation analysis and primary nephrotic syndrome in southern Indians.
Jaffer A; Unnisa W; Raju DS; Jahan P
Nephrology (Carlton); 2014 Jul; 19(7):398-403. PubMed ID: 24674236
[TBL] [Abstract][Full Text] [Related]
18. Genotype-phenotype correlations in non-Finnish congenital nephrotic syndrome.
Machuca E; Benoit G; Nevo F; Tête MJ; Gribouval O; Pawtowski A; Brandström P; Loirat C; Niaudet P; Gubler MC; Antignac C
J Am Soc Nephrol; 2010 Jul; 21(7):1209-17. PubMed ID: 20507940
[TBL] [Abstract][Full Text] [Related]
19. NPHS2 mutations in sporadic steroid-resistant nephrotic syndrome in Japanese children.
Maruyama K; Iijima K; Ikeda M; Kitamura A; Tsukaguchi H; Yoshiya K; Hoshii S; Wada N; Uemura O; Satomura K; Honda M; Yoshikawa N
Pediatr Nephrol; 2003 May; 18(5):412-6. PubMed ID: 12687458
[TBL] [Abstract][Full Text] [Related]
20. A novel mutation in NPHS2 gene identified in a Chinese pedigree with autosomal recessive steroid-resistant nephrotic syndrome.
Sun H; Zhou W; Wang J; Yin L; Lu Y; Fu Q
Pathology; 2009; 41(7):661-5. PubMed ID: 20001346
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
