NPHS1 mutation and steroid resistancy in children with idiopathic nephrotic syndrome (INS)

被引:0
|
作者
Brodkiewicz, Andrzej
Binczak-Kuleta, Agnieszka
Adler, Grazyna
Szychot, Elwira
Peregud-Pogorzelsk, Jaroslaw
Jarmuzek, Wioletta
Litwin, Mieczyslaw
Grenda, Ryszard
机构
[1] Pomeranian Med Univ, Dept Pediat 1, Szczecin, Poland
[2] Pomeranian Med Univ, Dept Pathobiochem & Mol Biol, Szczecin, Poland
[3] Dept Nephrol & Transplantol, Warsaw, Poland
[4] Med Univ Warsaw, Dept Paediat & Nephrol, Warsaw, Poland
关键词
D O I
暂无
中图分类号
R3 [基础医学]; R4 [临床医学];
学科分类号
1001 ; 1002 ; 100602 ;
摘要
引用
收藏
页码:310 / 310
页数:1
相关论文
共 50 条
  • [31] A case report of congenital nephrotic syndrome caused by new mutations of NPHS1
    Li, Zhong
    Zhuang, Lanchun
    Han, Mei
    Li, Feng
    JOURNAL OF INTERNATIONAL MEDICAL RESEARCH, 2021, 49 (08)
  • [32] NPHS1 AND NPHS2 MUTATIONS IN CONGENITAL AND LATE-ONSET CHILDHOOD NEPHROTIC SYNDROME
    Lozupone, S.
    Tummolo, A.
    Aceto, G.
    Francioso, G.
    Gigante, M.
    Gesualdo, L.
    Messina, G.
    De Palo, T.
    Penza, R.
    PEDIATRIC NEPHROLOGY, 2009, 24 (09) : 1805 - 1805
  • [33] Heterozygous NPHS1 or NPHS2 mutations in responsive nephrotic syndrome and the multifactorial origin of proteinuria
    Caridi, G
    Bertelli, R
    Perfumo, F
    Ghiggeri, GM
    KIDNEY INTERNATIONAL, 2004, 66 (04) : 1715 - 1716
  • [34] Expanding the clinical spectrum of congenital nephrotic syndrome caused by NPHS1 mutations
    Godefroid, Nathalie
    Dahan, Karin
    NEPHROLOGY DIALYSIS TRANSPLANTATION, 2010, 25 (09) : 2837 - 2839
  • [35] Novel NPHS1 gene mutations in a Chinese family with congenital nephrotic syndrome
    FENGJIE YANG
    YAXIAN CHEN
    YU ZHANG
    LIRU QIU
    YU CHEN
    JIANHUA ZHOU
    Journal of Genetics, 2016, 95 : 161 - 166
  • [36] Two novel NPHS1 mutations in a Chinese family with congenital nephrotic syndrome
    Wu, L. Q.
    Hu, J. J.
    Xue, J. J.
    Liang, D. S.
    GENETICS AND MOLECULAR RESEARCH, 2011, 10 (04) : 2517 - 2522
  • [37] Novel NPHS1 gene mutations in a Chinese family with congenital nephrotic syndrome
    Yang, Fengjie
    Chen, Yaxian
    Zhang, Yu
    Qiu, Liru
    Chen, Yu
    Zhou, Jianhua
    JOURNAL OF GENETICS, 2016, 95 (01) : 161 - 166
  • [38] Glomerular endothelium in kidneys with congenital nephrotic syndrome of the Finnish type (NPHS1)
    Kaukinen, Anne
    Kuusniemi, Arvi-Matti
    Lautenschlager, Irmeli
    Jalanko, Hannu
    NEPHROLOGY DIALYSIS TRANSPLANTATION, 2008, 23 (04) : 1224 - 1232
  • [39] Nephrin gene (NPHS1) in patients with minimal change nephrotic syndrome (MCNS)
    Lahdenkari, AT
    Kestilä, M
    Holmberg, C
    Koskimies, O
    Jalanko, H
    KIDNEY INTERNATIONAL, 2004, 65 (05) : 1856 - 1863
  • [40] Fin major (121del CT), G1339A and C3418T NPHS1 mutations in polish children with idiopathic nephrotic syndrome (INS) -: A preliminary report
    Brodkiewicz, Andrzej
    Binczak-Kuleta, Agnieszka
    Adler, Grazyna
    Szychot, Elwira
    Peregud-Pogorzelski, Jaroslaw
    Jarmuzek, Wioletta
    Litwin, Mieczyslaw
    Grenda, Ryszard
    Panczyk-Tomaszewska, Malgorzata
    Kostro, Izabella
    Roszkowska-Blaim, Maria
    Ciechanowicz, Andrzej
    NEPHROLOGY DIALYSIS TRANSPLANTATION, 2006, 21 : 311 - 311