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Journal Abstract Search

135 related items for PubMed ID: 17109732

  • 1. Recurrent nephrotic syndrome in homozygous truncating NPHS2 mutation is not due to anti-podocin antibodies.
    Becker-Cohen R, Bruschi M, Rinat C, Feinstein S, Zennaro C, Ghiggeri GM, Frishberg Y.
    Am J Transplant; 2007 Jan; 7(1):256-60. PubMed ID: 17109732
    [Abstract] [Full Text] [Related]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. 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
    [Abstract] [Full Text] [Related]

  • 4. Serum glomerular permeability activity in patients with podocin mutations (NPHS2) and steroid-resistant nephrotic syndrome.
    Carraro M, Caridi G, Bruschi M, Artero M, Bertelli R, Zennaro C, Musante L, Candiano G, Perfumo F, Ghiggeri GM.
    J Am Soc Nephrol; 2002 Jul; 13(7):1946-52. PubMed ID: 12089392
    [Abstract] [Full Text] [Related]

  • 5. 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
    [Abstract] [Full Text] [Related]

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  • 7. 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
    [Abstract] [Full Text] [Related]

  • 8. NPHS2 (podicin) mutations in Turkish children with idiopathic nephrotic syndrome.
    Berdeli A, Mir S, Yavascan O, Serdaroglu E, Bak M, Aksu N, Oner A, Anarat A, Donmez O, Yildiz N, Sever L, Tabel Y, Dusunsel R, Sonmez F, Cakar N.
    Pediatr Nephrol; 2007 Dec; 22(12):2031-40. PubMed ID: 17899208
    [Abstract] [Full Text] [Related]

  • 9. 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 15; 11(4):379-88. PubMed ID: 11854170
    [Abstract] [Full Text] [Related]

  • 10. 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 15; 12(12):2742-2746. PubMed ID: 11729243
    [Abstract] [Full Text] [Related]

  • 11. 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 15; 35(2):178-86. PubMed ID: 24227627
    [Abstract] [Full Text] [Related]

  • 12. 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 15; 25(4):854-7. PubMed ID: 24969201
    [Abstract] [Full Text] [Related]

  • 13. 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 15; 6(2):344-54. PubMed ID: 20947785
    [Abstract] [Full Text] [Related]

  • 14. NPHS2 mutation analysis and primary nephrotic syndrome in southern Indians.
    Jaffer A, Unnisa W, Raju DS, Jahan P.
    Nephrology (Carlton); 2014 Jul 15; 19(7):398-403. PubMed ID: 24674236
    [Abstract] [Full Text] [Related]

  • 15. Genetic forms of nephrotic syndrome.
    Niaudet P.
    Pediatr Nephrol; 2004 Dec 15; 19(12):1313-8. PubMed ID: 15503167
    [Abstract] [Full Text] [Related]

  • 16. 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, APN Study Group.
    J Am Soc Nephrol; 2008 Feb 15; 19(2):365-71. PubMed ID: 18216321
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  • 18. [A novel mutation of NPHS2 identified in a Chinese family with steroid-resistant nephrotic syndrome].
    Yu ZH, Ding J, Guan N, Shi Y, Zhang JJ, Huang JP, Yao Y, Yang JY.
    Zhonghua Er Ke Za Zhi; 2004 Feb 15; 42(2):108-12. PubMed ID: 15059485
    [Abstract] [Full Text] [Related]

  • 19. 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 Feb 15; 13(1):59-66. PubMed ID: 16572591
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