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Journal Abstract Search

193 related items for PubMed ID: 19099861

  • 21. TRPC6 mutations in children with steroid-resistant nephrotic syndrome and atypical phenotype.
    Gigante M, Caridi G, Montemurno E, Soccio M, d'Apolito M, Cerullo G, Aucella F, Schirinzi A, Emma F, Massella L, Messina G, De Palo T, Ranieri E, Ghiggeri GM, Gesualdo L.
    Clin J Am Soc Nephrol; 2011 Jul; 6(7):1626-34. PubMed ID: 21734084
    [Abstract] [Full Text] [Related]

  • 22. Mutational analysis of podocyte genes in children with sporadic steroid-resistant nephrotic syndrome.
    Feng DN, Yang YH, Wang DJ, Meng DC, Fu R, Wang JJ, Yu ZH.
    Genet Mol Res; 2014 Nov 11; 13(4):9514-22. PubMed ID: 25501161
    [Abstract] [Full Text] [Related]

  • 23. Analysis of NPHS1, NPHS2, ACTN4, and WT1 in Japanese patients with congenital nephrotic syndrome.
    Sako M, Nakanishi K, Obana M, Yata N, Hoshii S, Takahashi S, Wada N, Takahashi Y, Kaku Y, Satomura K, Ikeda M, Honda M, Iijima K, Yoshikawa N.
    Kidney Int; 2005 Apr 11; 67(4):1248-55. PubMed ID: 15780077
    [Abstract] [Full Text] [Related]

  • 24. 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 11; 91(4):937-947. PubMed ID: 28117080
    [Abstract] [Full Text] [Related]

  • 25. Clinical utility of genetic testing in children and adults with steroid-resistant nephrotic syndrome.
    Santín S, Bullich G, Tazón-Vega B, García-Maset R, Giménez I, Silva I, Ruíz P, Ballarín J, Torra R, Ars E.
    Clin J Am Soc Nephrol; 2011 May 11; 6(5):1139-48. PubMed ID: 21415313
    [Abstract] [Full Text] [Related]

  • 26. Genetic basis of nephrotic syndrome--review.
    Obeidová H, Merta M, Reiterová J, Maixnerová D, Stekrová J, Rysavá R, Tesar V.
    Prague Med Rep; 2006 May 11; 107(1):5-16. PubMed ID: 16752799
    [Abstract] [Full Text] [Related]

  • 27. Donor splice-site mutations in WT1 are responsible for Frasier syndrome.
    Barbaux S, Niaudet P, Gubler MC, Grünfeld JP, Jaubert F, Kuttenn F, Fékété CN, Souleyreau-Therville N, Thibaud E, Fellous M, McElreavey K.
    Nat Genet; 1997 Dec 11; 17(4):467-70. PubMed ID: 9398852
    [Abstract] [Full Text] [Related]

  • 28. Broad and unexpected phenotypic expression in Greek children with steroid-resistant nephrotic syndrome due to mutations in the Wilms' tumor 1 (WT1) gene.
    Megremis S, Mitsioni A, Fylaktou I, Tzeli SK, Komianou F, Stefanidis CJ, Kanavakis E, Traeger-Synodinos J.
    Eur J Pediatr; 2011 Dec 11; 170(12):1529-34. PubMed ID: 21499692
    [Abstract] [Full Text] [Related]

  • 29. Molecular basis of steroid-resistant nephrotic syndrome.
    Antignac C.
    Nefrologia; 2005 Dec 11; 25 Suppl 2():25-8. PubMed ID: 16050398
    [Abstract] [Full Text] [Related]

  • 30. Mutations in WT1 in boys with sporadic isolated steroid-resistant nephrotic syndrome.
    Yang Y, Zhao F, Tu X, Yu Z.
    Genet Mol Res; 2016 Mar 11; 15(1):15017559. PubMed ID: 26985958
    [Abstract] [Full Text] [Related]

  • 31. Spectrum of steroid-resistant and congenital nephrotic syndrome in children: the PodoNet registry cohort.
    Trautmann A, Bodria M, Ozaltin F, Gheisari A, Melk A, Azocar M, Anarat A, Caliskan S, Emma F, Gellermann J, Oh J, Baskin E, Ksiazek J, Remuzzi G, Erdogan O, Akman S, Dusek J, Davitaia T, Özkaya O, Papachristou F, Firszt-Adamczyk A, Urasinski T, Testa S, Krmar RT, Hyla-Klekot L, Pasini A, Özcakar ZB, Sallay P, Cakar N, Galanti M, Terzic J, Aoun B, Caldas Afonso A, Szymanik-Grzelak H, Lipska BS, Schnaidt S, Schaefer F, PodoNet Consortium.
    Clin J Am Soc Nephrol; 2015 Apr 07; 10(4):592-600. PubMed ID: 25635037
    [Abstract] [Full Text] [Related]

  • 32. Nephrotic syndrome in the first year of life: two thirds of cases are caused by mutations in 4 genes (NPHS1, NPHS2, WT1, and LAMB2).
    Hinkes BG, Mucha B, Vlangos CN, Gbadegesin R, Liu J, Hasselbacher K, Hangan D, Ozaltin F, Zenker M, Hildebrandt F, Arbeitsgemeinschaft für Paediatrische Nephrologie Study Group.
    Pediatrics; 2007 Apr 07; 119(4):e907-19. PubMed ID: 17371932
    [Abstract] [Full Text] [Related]

  • 33. Screening of WT1 mutations in exon 8 and 9 in children with steroid resistant nephrotic syndrome from a single centre and establishment of a rapid screening assay using high-resolution melting analysis in a clinical setting.
    Siji A, Pardeshi VC, Ravindran S, Vasudevan A, Vasudevan A.
    BMC Med Genet; 2017 Jan 10; 18(1):3. PubMed ID: 28068926
    [Abstract] [Full Text] [Related]

  • 34. Early recognition of gonadal dysgenesis in congenital nephrotic syndrome
.
    Ukarapong S, Berkovitz G, McElreavey K, Bashamboo A, Bao Y.
    Clin Nephrol; 2016 Dec 10; 86 (2016)(12):341-344. PubMed ID: 27719739
    [Abstract] [Full Text] [Related]

  • 35. The relationship among nephrin, podocin, CD2AP, and alpha-actinin might not be a true 'interaction' in podocyte.
    Fan Q, Xing Y, Ding J, Guan N, Zhang J.
    Kidney Int; 2006 Apr 10; 69(7):1207-15. PubMed ID: 16501493
    [Abstract] [Full Text] [Related]

  • 36. In vivo expression of podocyte slit diaphragm-associated proteins in nephrotic patients with NPHS2 mutation.
    Zhang SY, Marlier A, Gribouval O, Gilbert T, Heidet L, Antignac C, Gubler MC.
    Kidney Int; 2004 Sep 10; 66(3):945-54. PubMed ID: 15327385
    [Abstract] [Full Text] [Related]

  • 37. [Clinical and pathological features and mutational types of WT1 mutation-associated nephropathy].
    Sun LZ, Wang HY, Li M, Lin HR, Wu JL, Tang W, Li YJ, Yue ZH, Liu T, Chen HM, Hu MY.
    Zhonghua Er Ke Za Zhi; 2018 Oct 02; 56(10):769-774. PubMed ID: 30293282
    [Abstract] [Full Text] [Related]

  • 38. Use of genomic and functional analysis to characterize patients with steroid-resistant nephrotic syndrome.
    Kitzler TM, Kachurina N, Bitzan MM, Torban E, Goodyer PR.
    Pediatr Nephrol; 2018 Oct 02; 33(10):1741-1750. PubMed ID: 29982877
    [Abstract] [Full Text] [Related]

  • 39. WT1 gene mutations in Chinese children with early onset nephrotic syndrome.
    Li J, Ding J, Zhao D, Yu Z, Fan Q, Chen Y, Zhang H, Zhong X, Huang J, Yao Y, Xiao H.
    Pediatr Res; 2010 Aug 02; 68(2):155-8. PubMed ID: 20442690
    [Abstract] [Full Text] [Related]

  • 40. Mother-to-child transmitted WT1 splice-site mutation is responsible for distinct glomerular diseases.
    Denamur E, Bocquet N, Mougenot B, Da Silva F, Martinat L, Loirat C, Elion J, Bensman A, Ronco PM.
    J Am Soc Nephrol; 1999 Oct 02; 10(10):2219-23. PubMed ID: 10505700
    [Abstract] [Full Text] [Related]

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