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Journal Abstract Search

129 related items for PubMed ID: 36800604

  • 21. A case report of congenital nephrotic syndrome caused by new mutations of NPHS1.
    Li Z, Zhuang L, Han M, Li F.
    J Int Med Res; 2021 Aug; 49(8):3000605211038133. PubMed ID: 34396835
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  • 27. Congenital nephrotic syndrome with diffuse mesangial sclerosis caused by compound heterozygous mutation in LAMA5 gene.
    Deepthi B, Sivakumar RR, Krishnasamy S, Gochhait D, Mandal K, Krishnamurthy S.
    Pediatr Nephrol; 2024 May; 39(5):1421-1425. PubMed ID: 37985485
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  • 29. Congenital Nephrotic Syndrome - Finish Type.
    Spahiu L, Merovci B, Jashari H, Këpuska AB, Rugova BE.
    Med Arch; 2016 Jun; 70(3):232-4. PubMed ID: 27594755
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  • 34. Genetic Variations and Clinical Features of NPHS1-Related Nephrotic Syndrome in Chinese Children: A Multicenter, Retrospective Study.
    Rong L, Chen L, Rao J, Shen Q, Li G, Liu J, Mao J, Feng C, Wang X, Wang S, Kuang X, Huang W, Ma Q, Liu X, Ling C, Fu R, Gao X, Ding G, Yang H, Han M, Huang Z, Li Q, Zhang Q, Lin Y, Jiang X, Xu H.
    Front Med (Lausanne); 2021 Jun; 8():771227. PubMed ID: 34859019
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  • 39. Molecular Genetic Analysis of Steroid Resistant Nephrotic Syndrome, Detection of a Novel Mutation.
    Shojaei A, Serajpour N, Karimi B, Hooman N, Hosseini R, Khosravi P.
    Iran J Kidney Dis; 2019 May; 13(3):165-172. PubMed ID: 31209189
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  • 40. A spectrum of novel NPHS1 and NPHS2 gene mutations in pediatric nephrotic syndrome patients from Pakistan.
    Abid A, Khaliq S, Shahid S, Lanewala A, Mubarak M, Hashmi S, Kazi J, Masood T, Hafeez F, Naqvi SA, Rizvi SA, Mehdi SQ.
    Gene; 2012 Jul 10; 502(2):133-7. PubMed ID: 22565185
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