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201 related items for PubMed ID: 31754646

  • 1. 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
    [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
    [Abstract] [Full Text] [Related]

  • 3. APOL1 risk genotype in European steroid-resistant nephrotic syndrome and/or focal segmental glomerulosclerosis patients of different African ancestries.
    Gribouval O, Boyer O, Knebelmann B, Karras A, Dantal J, Fourrage C, Alibeu O, Hogan J, Dossier C, Tête MJ, Antignac C, Servais A.
    Nephrol Dial Transplant; 2019 Nov 01; 34(11):1885-1893. PubMed ID: 29992269
    [Abstract] [Full Text] [Related]

  • 4. 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, FSGS Spanish Study Group.
    Clin J Am Soc Nephrol; 2011 Feb 01; 6(2):344-54. PubMed ID: 20947785
    [Abstract] [Full Text] [Related]

  • 5. NPHS2 V260E Is a Frequent Cause of Steroid-Resistant Nephrotic Syndrome in Black South African Children.
    Asharam K, Bhimma R, David VA, Coovadia HM, Qulu WP, Naicker T, Gillies CE, Vega-Warner V, Johnson RC, Limou S, Kopp JB, Sampson M, Nelson GW, Winkler CA.
    Kidney Int Rep; 2018 Nov 01; 3(6):1354-1362. PubMed ID: 30450462
    [Abstract] [Full Text] [Related]

  • 6. HLA-DQA1 and APOL1 as Risk Loci for Childhood-Onset Steroid-Sensitive and Steroid-Resistant Nephrotic Syndrome.
    Adeyemo A, Esezobor C, Solarin A, Abeyagunawardena A, Kari JA, El Desoky S, Greenbaum LA, Kamel M, Kallash M, Silva C, Young A, Hunley TE, de Jesus-Gonzalez N, Srivastava T, Gbadegesin R.
    Am J Kidney Dis; 2018 Mar 01; 71(3):399-406. PubMed ID: 29277510
    [Abstract] [Full Text] [Related]

  • 7. 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 01; 13(2):400-405. PubMed ID: 11805168
    [Abstract] [Full Text] [Related]

  • 8. Association of HLA-DR/DQ alleles and haplotypes with nephrotic syndrome.
    Ramanathan AS, Senguttuvan P, Chinniah R, Vijayan M, Thirunavukkarasu M, Raju K, Mani D, Ravi PM, Rajendran P, Krishnan JI, Karuppiah B.
    Nephrology (Carlton); 2016 Sep 01; 21(9):745-52. PubMed ID: 26566811
    [Abstract] [Full Text] [Related]

  • 9. Low prevalence of NPHS2 mutations in African American children with steroid-resistant nephrotic syndrome.
    Chernin G, Heeringa SF, Gbadegesin R, Liu J, Hinkes BG, Vlangos CN, Vega-Warner V, Hildebrandt F.
    Pediatr Nephrol; 2008 Sep 01; 23(9):1455-60. PubMed ID: 18543005
    [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 01; 25(4):854-7. PubMed ID: 24969201
    [Abstract] [Full Text] [Related]

  • 11. 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 01; 12(12):2742-2746. PubMed ID: 11729243
    [Abstract] [Full Text] [Related]

  • 12. TRPC6 and NPHS2 gene variants in adult patients with steroid-resistant nephrotic syndrome in North-West of Iran.
    Zununi Vahed S, Moghaddas Sani H, Haghi M, Mohajel Shoja M, Ardalan M.
    Mol Biol Rep; 2019 Dec 01; 46(6):6339-6344. PubMed ID: 31529341
    [Abstract] [Full Text] [Related]

  • 13. WT1 and NPHS2 gene mutation analysis and clinical management of steroid-resistant nephrotic syndrome.
    Ramanathan AS, Vijayan M, Rajagopal S, Rajendiran P, Senguttuvan P.
    Mol Cell Biochem; 2017 Feb 01; 426(1-2):177-181. PubMed ID: 27885584
    [Abstract] [Full Text] [Related]

  • 14. 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 01; 21(1):127-133. PubMed ID: 26820844
    [Abstract] [Full Text] [Related]

  • 15. 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 01; 23(3):421-7. PubMed ID: 18058136
    [Abstract] [Full Text] [Related]

  • 16. 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 01; 43(4):727-32. PubMed ID: 15042551
    [Abstract] [Full Text] [Related]

  • 17. 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 01; 8(2):63-75. PubMed ID: 16481888
    [Abstract] [Full Text] [Related]

  • 18. 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 01; 21(4):677-684. PubMed ID: 27573339
    [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 01; 18(5):412-6. PubMed ID: 12687458
    [Abstract] [Full Text] [Related]

  • 20. Characterization of NPHS2 gene polymorphisms associated to steroid resistance nephrotic syndrome in Indian children.
    Joshi BB, Mistry KN, Gang S, Koringa PG, Joshi CG.
    Gene; 2017 Sep 10; 628():134-140. PubMed ID: 28712774
    [Abstract] [Full Text] [Related]

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