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 *

131 related articles for article (PubMed ID: 31598951)

  • 41. Congenital nephrotic syndrome: prenatal diagnosis and genetic counselling by estimation of aminotic-fluid and maternal serum alpha-fetoprotein.
    Seppälä M; Rapola J; Huttunen NP; Aula P; Karjalainen O; Ruoslahti E
    Lancet; 1976 Jul; 2(7977):123-5. PubMed ID: 59186
    [TBL] [Abstract][Full Text] [Related]  

  • 42. 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; 11(4):379-88. PubMed ID: 11854170
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Renal pathology of fetuses with congenital nephrotic syndrome of the Finnish type. A qualitative and quantitative light microscopic study.
    Autio-Harmainen H; Rapola J
    Nephron; 1981; 29(3-4):158-63. PubMed ID: 7329491
    [TBL] [Abstract][Full Text] [Related]  

  • 44. NPHS1 gene mutations in children with Nephrotic Syndrome in northwest Iran.
    Behbahan AG; Poorshiri B; Mortazavi F; Khaniani MS; Derakhshan SM
    Pak J Biol Sci; 2013 Sep; 16(17):882-6. PubMed ID: 24498843
    [TBL] [Abstract][Full Text] [Related]  

  • 45. [Congenital nephrotic syndrome].
    Stajić N; Putnik J; Paripović A; Djurić S; Bogdanović R
    Srp Arh Celok Lek; 2008 Dec; 136 Suppl 4():307-11. PubMed ID: 20804100
    [TBL] [Abstract][Full Text] [Related]  

  • 46. [Congenital nephrotic syndrome - Finnish type].
    Mihatsch MJ; Rapola J
    Verh Dtsch Ges Pathol; 1982; 66():307-11. PubMed ID: 7184252
    [No Abstract]   [Full Text] [Related]  

  • 47. Structure of the gene for congenital nephrotic syndrome of the finnish type (NPHS1) and characterization of mutations.
    Lenkkeri U; Männikkö M; McCready P; Lamerdin J; Gribouval O; Niaudet PM; Antignac C K; Kashtan CE; Homberg C; Olsen A; Kestilä M; Tryggvason K
    Am J Hum Genet; 1999 Jan; 64(1):51-61. PubMed ID: 9915943
    [TBL] [Abstract][Full Text] [Related]  

  • 48. 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]  

  • 49. Recurrence of nephrotic syndrome in kidney grafts of patients with congenital nephrotic syndrome of the Finnish type: role of nephrin.
    Patrakka J; Ruotsalainen V; Reponen P; Qvist E; Laine J; Holmberg C; Tryggvason K; Jalanko H
    Transplantation; 2002 Feb; 73(3):394-403. PubMed ID: 11884936
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Congenital nephrotic syndrome of NPHS1 associated with cardiac malformation.
    Uysal B; Dönmez O; Uysal F; Akacı O; Vuruşkan BA; Berdeli A
    Pediatr Int; 2015; 57(1):177-9. PubMed ID: 25711261
    [TBL] [Abstract][Full Text] [Related]  

  • 51. 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]  

  • 52. [Mutational analysis and prenatal diagnosis of
    Ren SM; Wu QH; Chen C; Kong XD
    Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2020 Apr; 55(4):344-349. PubMed ID: 32306631
    [No Abstract]   [Full Text] [Related]  

  • 53. Endometrial and fetoplacental markers in pregnancies with fetal congenital nephrosis.
    Heinonen S; Ryynänen M; Kirkinen P; Saarikoski S
    Acta Obstet Gynecol Scand; 1996 Jul; 75(6):526-30. PubMed ID: 8693927
    [TBL] [Abstract][Full Text] [Related]  

  • 54. The thickness of the glomerular basement membrane in congenital nephrotic syndrome of the Finnish type.
    Autio-Harmainen H; Rapola J
    Nephron; 1983; 34(1):48-50. PubMed ID: 6855995
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Mutation spectrum of genes associated with steroid-resistant nephrotic syndrome in Chinese children.
    Wang Y; Dang X; He Q; Zhen Y; He X; Yi Z; Zhu K
    Gene; 2017 Aug; 625():15-20. PubMed ID: 28476686
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Haplotype analysis of congenital nephrotic syndrome of the Finnish type in non-Finnish families.
    Männikkö M; Lenkkeri U; Kashtan CE; Kestilä M; Holmberg C; Tryggvason K
    J Am Soc Nephrol; 1996 Dec; 7(12):2700-3. PubMed ID: 8989752
    [TBL] [Abstract][Full Text] [Related]  

  • 57. 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]  

  • 58. [Diagnosis of a fetus with atelosteogenesis type 2 through combined prenatal ultrasonography and whole exome sequencing].
    Li J; Meng Y; Li M; Liu C; Li-Ling J; Lyu Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Jul; 37(7):767-770. PubMed ID: 32619261
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Targeted next-generation sequencing identifies novel compound heterozygous mutations of DYNC2H1 in a fetus with short rib-polydactyly syndrome, type III.
    Mei L; Huang Y; Pan Q; Su W; Quan Y; Liang D; Wu L
    Clin Chim Acta; 2015 Jul; 447():47-51. PubMed ID: 25982780
    [TBL] [Abstract][Full Text] [Related]  

  • 60. CRB2 mutations produce a phenotype resembling congenital nephrosis, Finnish type, with cerebral ventriculomegaly and raised alpha-fetoprotein.
    Slavotinek A; Kaylor J; Pierce H; Cahr M; DeWard SJ; Schneidman-Duhovny D; Alsadah A; Salem F; Schmajuk G; Mehta L
    Am J Hum Genet; 2015 Jan; 96(1):162-9. PubMed ID: 25557780
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.