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 *

142 related articles for article (PubMed ID: 31598951)

  • 21. [Prenatal diagnosis for congenital nephritic syndrome Finnish type: a case report].
    Zhu XL; Han B; Feng XW
    Zhonghua Fu Chan Ke Za Zhi; 2017 May; 52(5):342. PubMed ID: 28545272
    [No Abstract]   [Full Text] [Related]  

  • 22. [Prenatal diagnosis for a fetus with Walker-Warburg syndrome].
    Ma P; Chen X; Hui L; Zhang Q; Zhang C; Hao S; Yang L; Wang X; Xu F; Zhou B
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 May; 40(5):572-576. PubMed ID: 37102292
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Analysis of NPHS1, NPHS2, ACTN4, and WT1 in Japanese patients with congenital nephrotic syndrome.
    Sako M; Nakanishi K; Obana M; Yata N; Hoshii S; Takahashi S; Wada N; Takahashi Y; Kaku Y; Satomura K; Ikeda M; Honda M; Iijima K; Yoshikawa N
    Kidney Int; 2005 Apr; 67(4):1248-55. PubMed ID: 15780077
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Genetic heterogeneity and pathology of congenital nephrotic syndrome and its significance in prenatal diagnosis].
    Braga S; Moser H; Zimmermann A; Oetliker O
    J Genet Hum; 1985 Jun; 33(2):153-6. PubMed ID: 2410560
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Misleading findings of homozygosity mapping resulting from three novel mutations in NPHS1 encoding nephrin in a highly inbred community.
    Frishberg Y; Ben-Neriah Z; Suvanto M; Rinat C; Männikkö M; Feinstein S; Becker-Cohen R; Jalanko H; Zlotogora J; Kestilä M
    Genet Med; 2007 Mar; 9(3):180-4. PubMed ID: 17413422
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Genetic testing and prenatal diagnosis for a Chinese pedigree affected with Meckel-Gruber syndrome].
    Jiao Z; Zhao G; Liu L; Guo Y; Kong X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2021 Dec; 38(12):1204-1207. PubMed ID: 34839507
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. Prenatal diagnosis of congenital nephrotic syndrome of Finnish type.
    Srsnová K; Bencat M; Srsen S; Miháliková J; Slávik P; Svihrová V
    Funct Dev Morphol; 1992; 2(2):133-4. PubMed ID: 1450458
    [No Abstract]   [Full Text] [Related]  

  • 29. 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]  

  • 30. Simultaneous mutations of LAMB2 and NPHP1genes in a Chinese girl with isolated congenital nephrotic syndrome: a case report.
    Qiu L; Zhou J
    BMC Pediatr; 2016 Mar; 16():44. PubMed ID: 27004562
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Congenital nephrotic syndrome of the Finnish type in Italy: a molecular approach.
    Gigante M; Monno F; Roberto R; Laforgia N; Assael MB; Livolti S; Caringella A; La Manna A; Masella L; Iolascon A
    J Nephrol; 2002; 15(6):696-702. PubMed ID: 12495287
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Normalization of maternal serum alpha-fetoprotein levels after 23 weeks' gestation in an NPHS1 nephrotic syndrome carrier pregnancy.
    Brady TB; Mitra AG
    Prenat Diagn; 2011 Dec; 31(13):1314-6. PubMed ID: 22030743
    [No Abstract]   [Full Text] [Related]  

  • 33. Prenatal screening for congenital nephrosis in east Finland: results and impact on the birth prevalence of the disease.
    Heinonen S; Ryynänen M; Kirkinen P; Penttilä I; Syrjänen K; Seppälä M; Saarikoski S
    Prenat Diagn; 1996 Mar; 16(3):207-13. PubMed ID: 8710773
    [TBL] [Abstract][Full Text] [Related]  

  • 34. NPHS1 gene mutations confirm congenital nephrotic syndrome in four Brazilian cases: A novel mutation is described.
    Guaragna MS; Cleto TL; Souza ML; Lutaif AC; de Castro LC; Penido MG; Maciel-Guerra AT; Belangero VM; Guerra-Junior G; De Mello MP
    Nephrology (Carlton); 2016 Sep; 21(9):753-7. PubMed ID: 26560236
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Detection of the Finnish-type congenital nephrotic syndrome by restriction fragment length polymorphism and dual-color oligonucleotide ligation assays.
    Romppanen EL; Mononen I
    Clin Chem; 2000 Jun; 46(6 Pt 1):811-6. PubMed ID: 10839769
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Novel human pathological mutations. Gene symbol: NPHS1. Disease: congenital nephrotic syndrome, Finnish type.
    Tikhomirov E; Voznesenskaya T; Tsygin A
    Hum Genet; 2009 Apr; 125(3):334. PubMed ID: 19309778
    [No Abstract]   [Full Text] [Related]  

  • 37. A novel heterozygous mutation of the NPHS1 gene in a Chinese child with congenital nephrotic syndrome: A case report.
    Xie D; Wu J; Zhang W; Jin T; Wu P; An B; Huang S
    Medicine (Baltimore); 2023 Feb; 102(7):e32970. PubMed ID: 36800604
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Prenatal findings in four consecutive pregnancies with fetal Pierson syndrome, a newly defined congenital nephrosis syndrome.
    Mark K; Reis A; Zenker M
    Prenat Diagn; 2006 Mar; 26(3):262-6. PubMed ID: 16450351
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Clinical and genetic analysis for a Joubert syndrome family with CC2D2A gene mutations].
    Su Y; Xie J; Yu S; Luo H; Wu W; Xu Z
    Zhonghua Er Ke Za Zhi; 2015 Jun; 53(6):431-5. PubMed ID: 26310553
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Congenital nephrotic syndrome].
    Hattori M
    Nihon Rinsho; 2004 Oct; 62(10):1861-6. PubMed ID: 15500131
    [TBL] [Abstract][Full Text] [Related]  

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