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Journal Abstract Search

174 related items for PubMed ID: 35935761

  • 1. Association Between NPHS2 p.R229Q and Focal Segmental Glomerular Sclerosis/Steroid-Resistant Nephrotic Syndrome.
    Zhou Q, Weng Q, Zhang X, Liu Y, Tong J, Hao X, Shi H, Shen P, Ren H, Xie J, Chen N.
    Front Med (Lausanne); 2022; 9():937122. PubMed ID: 35935761
    [Abstract] [Full Text] [Related]

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

  • 3. 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; 6(2):344-54. PubMed ID: 20947785
    [Abstract] [Full Text] [Related]

  • 4. R229Q polymorphism of NPHS2 gene in patients with late-onset steroid-resistance nephrotic syndrome: a preliminary study.
    Fotouhi N, Ardalan M, Jabbarpour Bonyadi M, Abdolmohammadi R, Kamalifar A, Nasri H, Einollahi B.
    Iran J Kidney Dis; 2013 Sep; 7(5):399-403. PubMed ID: 24072153
    [Abstract] [Full Text] [Related]

  • 5. 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]

  • 6. Prevalence of the NPHS2 variants p.R229Q, p.A242V, and p.R138Q in patients with focal segmental glomerulosclerosis.
    de Almeida R, da Silva WC, Garbin HI, Itaquy TP, Dos Santos Pereira F, Garcia CD, Keitel E, Sales Luiz Vianna F, Veronese FV.
    Clin Nephrol; 2020 Oct; 94(4):187-196. PubMed ID: 32691731
    [Abstract] [Full Text] [Related]

  • 7. Analysis of NPHS2 Gene Mutations in Egyptian Children with Nephrotic Syndrome.
    Zaki M, El-Shaer S, Rady S, El-Salam MA, Abd-El-Salam R, Alkashlan IA, Saber M, Mohamed S, Hassaan M, Rabie E, Amr K.
    Open Access Maced J Med Sci; 2019 Oct 15; 7(19):3145-3148. PubMed ID: 31949506
    [Abstract] [Full Text] [Related]

  • 8. Mutational analysis of the NPHS2 gene in Czech patients with idiopathic nephrotic syndrome.
    Reiterová J, Safránková H, Obeidová L, Stěkrová J, Maixnerová D, Merta M, Tesař V.
    Folia Biol (Praha); 2012 Oct 15; 58(2):64-8. PubMed ID: 22578956
    [Abstract] [Full Text] [Related]

  • 9. [NPHS2 Mutation analysis study in children with steroid-resistant nephrotic syndrome].
    Azocar M, Vega Á, Farfán M, Cano F.
    Rev Chil Pediatr; 2016 Oct 15; 87(1):31-6. PubMed ID: 26455708
    [Abstract] [Full Text] [Related]

  • 10. Prevalence of NPHS2 gene R229Q polymorphism in Bangladeshi children with nephrotic syndrome.
    Jyoti SS, Islam F, Shrabonee II, Sultana TN, Chaity NI, Nahid NA, Islam MR, Islam MS, Apu MNH.
    Heliyon; 2020 Oct 15; 6(10):e05317. PubMed ID: 33102883
    [Abstract] [Full Text] [Related]

  • 11. 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 15; 110(11):1659-66. PubMed ID: 12464671
    [Abstract] [Full Text] [Related]

  • 12. Spectrum of NPHS1 and NPHS2 variants in egyptian children with focal segmental glomerular sclerosis: identification of six novel variants and founder effect.
    Thomas MM, Ahmed HM, El-Dessouky SH, Ramadan A, Botrous OE, Abdel-Hamid MS.
    Mol Genet Genomics; 2022 May 15; 297(3):689-698. PubMed ID: 35278126
    [Abstract] [Full Text] [Related]

  • 13. NPHS2 homozygous p.R229Q variant: potential modifier instead of causal effect in focal segmental glomerulosclerosis.
    Kerti A, Csohány R, Wagner L, Jávorszky E, Maka E, Tory K.
    Pediatr Nephrol; 2013 Oct 15; 28(10):2061-4. PubMed ID: 23800802
    [Abstract] [Full Text] [Related]

  • 14. 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 15; 3(6):1354-1362. PubMed ID: 30450462
    [Abstract] [Full Text] [Related]

  • 15. R229Q Polymorphism of NPHS2 Gene in Group of Iraqi Children with Steroid-Resistant Nephrotic Syndrome.
    Ali SH, Mohammed RK, Saheb HA, Abdulmajeed BA.
    Int J Nephrol; 2017 Nov 15; 2017():1407506. PubMed ID: 28529802
    [Abstract] [Full Text] [Related]

  • 16. Variability in phenotype induced by the podocin variant R229Q plus a single pathogenic mutation.
    Phelan PJ, Hall G, Wigfall D, Foreman J, Nagaraj S, Malone AF, Winn MP, Howell DN, Gbadegesin R.
    Clin Kidney J; 2015 Oct 15; 8(5):538-42. PubMed ID: 26413278
    [Abstract] [Full Text] [Related]

  • 17. Genetic basis of nephrotic syndrome--review.
    Obeidová H, Merta M, Reiterová J, Maixnerová D, Stekrová J, Rysavá R, Tesar V.
    Prague Med Rep; 2006 Oct 15; 107(1):5-16. PubMed ID: 16752799
    [Abstract] [Full Text] [Related]

  • 18. 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 15; 21(1):127-133. PubMed ID: 26820844
    [Abstract] [Full Text] [Related]

  • 19. 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 15; 73(3):400-403. PubMed ID: 30241959
    [Abstract] [Full Text] [Related]

  • 20. NPHS2 variation in focal and segmental glomerulosclerosis.
    Tonna SJ, Needham A, Polu K, Uscinski A, Appel GB, Falk RJ, Katz A, Al-Waheeb S, Kaplan BS, Jerums G, Savige J, Harmon J, Zhang K, Curhan GC, Pollak MR.
    BMC Nephrol; 2008 Sep 29; 9():13. PubMed ID: 18823551
    [Abstract] [Full Text] [Related]

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