These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

147 related articles for article (PubMed ID: 28392951)

  • 41. Plasma exchange and retransplantation in recurrent nephrosis of patients with congenital nephrotic syndrome of the Finnish type (NPHS1).
    Kuusniemi AM; Qvist E; Sun Y; Patrakka J; Rönnholm K; Karikoski R; Jalanko H
    Transplantation; 2007 May; 83(10):1316-23. PubMed ID: 17519780
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Congenital nephrotic syndrome associated with 22q11.2 duplication syndrome in a Chinese family and functional analysis of the intronic NPHS1 c. 3286 + 5G > A mutation.
    Li L; Yi Z; Xi H; Ma L; Shao H; Wang W; Pan H; Li M; Jiang H
    Ital J Pediatr; 2019 Aug; 45(1):109. PubMed ID: 31443662
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Alport syndrome. Molecular genetic aspects.
    Hertz JM
    Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
    [TBL] [Abstract][Full Text] [Related]  

  • 44. [Analysis of a sib-pair with Finnish type congenital nephrotic syndrome due to variant of NPHS1 gene].
    Liu Z; Wang W; Zhang X; Fan S; Liu Y; Liu Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Dec; 37(12):1380-1383. PubMed ID: 33306827
    [TBL] [Abstract][Full Text] [Related]  

  • 45. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Glomerular sclerosis in kidneys with congenital nephrotic syndrome (NPHS1).
    Kuusniemi AM; Merenmies J; Lahdenkari AT; Holmberg C; Salmela K; Karikoski R; Rapola J; Jalanko H
    Kidney Int; 2006 Oct; 70(8):1423-31. PubMed ID: 16941028
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Positionally cloned gene for a novel glomerular protein--nephrin--is mutated in congenital nephrotic syndrome.
    Kestilä M; Lenkkeri U; Männikkö M; Lamerdin J; McCready P; Putaala H; Ruotsalainen V; Morita T; Nissinen M; Herva R; Kashtan CE; Peltonen L; Holmberg C; Olsen A; Tryggvason K
    Mol Cell; 1998 Mar; 1(4):575-82. PubMed ID: 9660941
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Phenotypic, metabolic, and molecular genetic characterization of six patients with congenital adrenal hyperplasia caused by novel mutations in the CYP11B1 gene.
    Nguyen HH; Eiden-Plach A; Hannemann F; Malunowicz EM; Hartmann MF; Wudy SA; Bernhardt R
    J Steroid Biochem Mol Biol; 2016 Jan; 155(Pt A):126-34. PubMed ID: 26476331
    [TBL] [Abstract][Full Text] [Related]  

  • 49. A Systematic Analysis of Major Susceptible Genes in Childhood-onset Steroid-resistant Nephrotic Syndrome.
    Li Y; He Q; Wang Y; Dang X; Wu X; Li X; Shuai L; Yi Z
    Ann Clin Lab Sci; 2019 May; 49(3):330-337. PubMed ID: 31308032
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Recurrence of proteinuria following renal transplantation in congenital nephrotic syndrome of the Finnish type.
    Srivastava T; Garola RE; Kestila M; Tryggvason K; Ruotsalainen V; Sharma M; Savin VJ; Jalanko H; Warady BA
    Pediatr Nephrol; 2006 May; 21(5):711-8. PubMed ID: 16518627
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Glomerular endothelium in kidneys with congenital nephrotic syndrome of the Finnish type (NPHS1).
    Kaukinen A; Kuusniemi AM; Lautenschlager I; Jalanko H
    Nephrol Dial Transplant; 2008 Apr; 23(4):1224-32. PubMed ID: 18048423
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Neonatal nephrotic presentation of a child with heterozygous NPHS1 mutation.
    Lemley KV
    Pediatr Nephrol; 2006 Jun; 21(6):864-6. PubMed ID: 16703378
    [TBL] [Abstract][Full Text] [Related]  

  • 53. [Changing c.106delG (p.Ala36fs*6) loss syndrome associated with congenital Finnish type: first case diagnosed in Togo].
    Sabi KA; Noto-Kadou-Kaza B; Gnionsahe DA; Amekoudi EY; Tsevi CM; Tsonya KD; Amedegnato D; Gnamey K
    Nephrol Ther; 2013 Dec; 9(7):494-6. PubMed ID: 23932794
    [TBL] [Abstract][Full Text] [Related]  

  • 54. [A case of severe congenital nephrotic syndrome secondary to NPHS1 mutation].
    Quiros A; Lefèbvre C; Collard L; Rigo V; Lombet J
    Rev Med Liege; 2020 Jul; 75(7-8):544-547. PubMed ID: 32779909
    [TBL] [Abstract][Full Text] [Related]  

  • 55. 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; 21(4):677-684. PubMed ID: 27573339
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Genetics of congenital and infantile nephrotic syndrome.
    Sharief SN; Hefni NA; Alzahrani WA; Nazer II; Bayazeed MA; Alhasan KA; Safdar OY; El-Desoky SM; Kari JA
    World J Pediatr; 2019 Apr; 15(2):198-203. PubMed ID: 30721404
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Cyclosporine A responsive congenital nephrotic syndrome with single heterozygous variants in NPHS1, NPHS2, and PLCE1.
    Eichinger A; Ponsel S; Bergmann C; Günthner R; Hoefele J; Amann K; Lange-Sperandio B
    Pediatr Nephrol; 2018 Jul; 33(7):1269-1272. PubMed ID: 29663071
    [TBL] [Abstract][Full Text] [Related]  

  • 58. A missense mutation in the nephrin gene impairs membrane targeting.
    Shimizu J; Tanaka H; Aya K; Ito S; Sado Y; Seino Y
    Am J Kidney Dis; 2002 Oct; 40(4):697-703. PubMed ID: 12324903
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Nephrin gene (NPHS1) in patients with minimal change nephrotic syndrome (MCNS).
    Lahdenkari AT; Kestilä M; Holmberg C; Koskimies O; Jalanko H
    Kidney Int; 2004 May; 65(5):1856-63. PubMed ID: 15086927
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Mutational analysis of podocyte genes in children with sporadic steroid-resistant nephrotic syndrome.
    Feng DN; Yang YH; Wang DJ; Meng DC; Fu R; Wang JJ; Yu ZH
    Genet Mol Res; 2014 Nov; 13(4):9514-22. PubMed ID: 25501161
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.