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 *

603 related articles for article (PubMed ID: 26383224)

  • 41. Spectrum of steroid-resistant and congenital nephrotic syndrome in children: the PodoNet registry cohort.
    Trautmann A; Bodria M; Ozaltin F; Gheisari A; Melk A; Azocar M; Anarat A; Caliskan S; Emma F; Gellermann J; Oh J; Baskin E; Ksiazek J; Remuzzi G; Erdogan O; Akman S; Dusek J; Davitaia T; Özkaya O; Papachristou F; Firszt-Adamczyk A; Urasinski T; Testa S; Krmar RT; Hyla-Klekot L; Pasini A; Özcakar ZB; Sallay P; Cakar N; Galanti M; Terzic J; Aoun B; Caldas Afonso A; Szymanik-Grzelak H; Lipska BS; Schnaidt S; Schaefer F;
    Clin J Am Soc Nephrol; 2015 Apr; 10(4):592-600. PubMed ID: 25635037
    [TBL] [Abstract][Full Text] [Related]  

  • 42. [Multicenter study on present status of diagnosis and treatment of steroid-resistant nephrotic syndrome in children].
    Subspecialty Group Of Nephrology, The Society Of Pediatrics Chinese Medical Association
    Zhonghua Er Ke Za Zhi; 2014 Jul; 52(7):483-7. PubMed ID: 25224050
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Glomerular tip lesion: a distinct entity within the minimal change disease/focal segmental glomerulosclerosis spectrum.
    Stokes MB; Markowitz GS; Lin J; Valeri AM; D'Agati VD
    Kidney Int; 2004 May; 65(5):1690-702. PubMed ID: 15086908
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Recurrence of nephrotic syndrome following kidney transplantation is associated with initial native kidney biopsy findings.
    Pelletier JH; Kumar KR; Engen R; Bensimhon A; Varner JD; Rheault MN; Srivastava T; Straatmann C; Silva C; Davis TK; Wenderfer SE; Gibson K; Selewski D; Barcia J; Weng P; Licht C; Jawa N; Kallash M; Foreman JW; Wigfall DR; Chua AN; Chambers E; Hornik CP; Brewer ED; Nagaraj SK; Greenbaum LA; Gbadegesin RA
    Pediatr Nephrol; 2018 Oct; 33(10):1773-1780. PubMed ID: 29982878
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Inverted formin 2-related Charcot-Marie-Tooth disease: extension of the mutational spectrum and pathological findings in Schwann cells and axons.
    Roos A; Weis J; Korinthenberg R; Fehrenbach H; Häusler M; Züchner S; Mache C; Hubmann H; Auer-Grumbach M; Senderek J
    J Peripher Nerv Syst; 2015 Mar; 20(1):52-9. PubMed ID: 25676889
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Dysregulation of podocyte phenotype in idiopathic collapsing glomerulopathy and HIV-associated nephropathy.
    Yang Y; Gubler MC; Beaufils H
    Nephron; 2002 Jul; 91(3):416-23. PubMed ID: 12119471
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Histopathological diagnosis and outcome of paediatric nephrotic syndrome.
    Ejaz I; Khan HI; Javaid BK; Rasool G; Bhatti MT
    J Coll Physicians Surg Pak; 2004 Apr; 14(4):229-33. PubMed ID: 15228828
    [TBL] [Abstract][Full Text] [Related]  

  • 48. A clinicopathological comparison between IgA nephropathy and Henoch-Schönlein purpura nephritis in children: use of the Oxford classification.
    Li X; Tang M; Yao X; Zhang N; Fan J; Zhou N; Sun Q; Chen Z; Meng Q; Lei L; Zhang H; Ling C; Hua L; Chen X; Liu X
    Clin Exp Nephrol; 2019 Dec; 23(12):1382-1390. PubMed ID: 31468231
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Immunohistochemical distribution of endothelin in biopsies of pediatric nephrotic syndrome.
    Murer L; Zacchello G; Basso G; Scarpa A; Montini G; Chiozza ML; Zacchello F
    Am J Nephrol; 1994; 14(3):157-61. PubMed ID: 7977473
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Cell-cycle regulatory proteins in the podocyte in collapsing glomerulopathy in children.
    Srivastava T; Garola RE; Singh HK
    Kidney Int; 2006 Aug; 70(3):529-35. PubMed ID: 16775597
    [TBL] [Abstract][Full Text] [Related]  

  • 51. [Nephrotic syndrom with focal and segmental glomerulosclerosis in Dakar: epidemiological and clinicopathological characteristics (about 134 cases)].
    Niang A; Dial C; Ka EF; Lèye A; Pouye A; Ka MM; Mbengue M; Droz D; Diouf B
    Dakar Med; 2008; 53(1):45-51. PubMed ID: 19102117
    [TBL] [Abstract][Full Text] [Related]  

  • 52. C1q nephropathy: a variant of focal segmental glomerulosclerosis.
    Markowitz GS; Schwimmer JA; Stokes MB; Nasr S; Seigle RL; Valeri AM; D'Agati VD
    Kidney Int; 2003 Oct; 64(4):1232-40. PubMed ID: 12969141
    [TBL] [Abstract][Full Text] [Related]  

  • 53. A quantitative analysis of the glomeruli in focal segmental glomerulosclerosis.
    Suzuki J; Yoshikawa N; Nakamura H
    Pediatr Nephrol; 1994 Aug; 8(4):416-9. PubMed ID: 7947029
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Novel mutations in the inverted formin 2 gene of Chinese families contribute to focal segmental glomerulosclerosis.
    Xie J; Hao X; Azeloglu EU; Ren H; Wang Z; Ma J; Liu J; Ma X; Wang W; Pan X; Zhang W; Zhong F; Li Y; Meng G; Kiryluk K; He JC; Gharavi AG; Chen N
    Kidney Int; 2015 Sep; 88(3):593-604. PubMed ID: 26039629
    [TBL] [Abstract][Full Text] [Related]  

  • 55. A novel INF2 mutation in a Korean family with autosomal dominant intermediate Charcot-Marie-Tooth disease and focal segmental glomerulosclerosis.
    Park HJ; Kim HJ; Hong YB; Nam SH; Chung KW; Choi BO
    J Peripher Nerv Syst; 2014 Jun; 19(2):175-9. PubMed ID: 24750328
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Urinary peptide profiling to differentiate between minimal change disease and focal segmental glomerulosclerosis.
    Pérez V; Ibernón M; López D; Pastor MC; Navarro M; Navarro-Muñoz M; Bonet J; Romero R
    PLoS One; 2014; 9(1):e87731. PubMed ID: 24498182
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Low birthweight and premature birth are risk factors for podocytopenia and focal segmental glomerulosclerosis.
    Ikezumi Y; Suzuki T; Karasawa T; Yamada T; Hasegawa H; Nishimura H; Uchiyama M
    Am J Nephrol; 2013; 38(2):149-57. PubMed ID: 23920104
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Glomerular parietal epithelial expression of CD44 in minimal change nephrotic syndrome and primary focal segmental glomerulosclerosis: A clinico-pathological study.
    Paul EN; Satish S; Kelur KK; Shetty MS
    Indian J Pathol Microbiol; 2023; 66(3):526-532. PubMed ID: 37530333
    [TBL] [Abstract][Full Text] [Related]  

  • 59. [Minimal change disease and focal segmental glomerulosclerosis].
    Müller-Deile J; Schenk H; Schiffer M
    Internist (Berl); 2019 May; 60(5):450-457. PubMed ID: 30887070
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Ectopic expression of CLDN2 in podocytes is associated with childhood onset nephrotic syndrome.
    Kanno S; Kume Y; Maeda R; Ono A; Suyama K; Kawasaki Y; Hosoya M
    Pediatr Res; 2019 Oct; 86(4):485-491. PubMed ID: 31086291
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 31.