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PUBMED FOR HANDHELDS

Journal Abstract Search


116 related items for PubMed ID: 7397031

  • 1. [Congenital nephrotic syndrome of Finnish type (report of a case)].
    Vargas Rosendo R, Rivero López JE, Alemán Velázquez P.
    Bol Med Hosp Infant Mex; 1980; 37(3):549-58. PubMed ID: 7397031
    [Abstract] [Full Text] [Related]

  • 2. [The Finnish-type congenital nephrotic syndrome. Comments on 2 cases].
    Sabău I, Potencz E.
    Rev Pediatr Obstet Ginecol Pediatr; 1989; 38(1):79-86. PubMed ID: 2505364
    [Abstract] [Full Text] [Related]

  • 3. Two cases of congenital nephrotic syndrome.
    Iitaka K, Motoyama O, Hojo M, Iwanami N, Koshino H, Nakamura S, Moriya S.
    Clin Exp Nephrol; 2004 Jun; 8(2):146-9. PubMed ID: 15235932
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  • 4. Congenital nephrotic syndrome of Finnish type and other types of early familial nephrotic syndromes.
    Norio R.
    Birth Defects Orig Artic Ser; 1974 Jun; 10(4):69-72. PubMed ID: 4470912
    [Abstract] [Full Text] [Related]

  • 5. Proteinuria in congenital nephrotic syndrome of the Finnish type.
    Huttunen NP, Vehaskari M, Viikari M, Laipio ML.
    Clin Nephrol; 1980 Jan; 13(1):12-9. PubMed ID: 6988118
    [Abstract] [Full Text] [Related]

  • 6. Histopathologic variability of the congenital nephrotic syndrome.
    Martul EV, Cuesta MG, Churg I.
    Clin Nephrol; 1987 Oct; 28(4):161-8. PubMed ID: 3319307
    [Abstract] [Full Text] [Related]

  • 7. Congenital nephrotic syndrome of the Finnish type: report of one case.
    Lin JH, Tsau YK, Tsai WS, Chen CH.
    Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi; 1997 Oct; 38(6):481-3. PubMed ID: 9473823
    [Abstract] [Full Text] [Related]

  • 8. [Congenital nephrotic syndrome associated with congenital toxoplasmosis].
    Roussel B, Pinon JM, Birembaut P, Rullier J, Pennaforte F.
    Arch Fr Pediatr; 1987 Nov; 44(9):795-7. PubMed ID: 3328575
    [Abstract] [Full Text] [Related]

  • 9. Congenital nephrotic syndrome masquerading as respiratory illness.
    Aslam M, DeGrazia M, Hossain T.
    Am J Perinatol; 2008 Oct; 25(9):601-4. PubMed ID: 18841537
    [Abstract] [Full Text] [Related]

  • 10. [Finnish-type nephrotic syndrome: report of the fourth case in Italy and review of the literature].
    Costantino G, Barresi G, Mammì F, Costantino D, Tuccari G.
    Pediatr Med Chir; 1982 Oct; 4(5):551-4. PubMed ID: 6927356
    [Abstract] [Full Text] [Related]

  • 11. [Congenital nephrotic syndrome of the Finnish type: description of a case].
    Lato M, Bucciarelli E, Losito A.
    Lav Ist Anat Istol Patol Univ Studi Perugia; 1978 Oct; 38(2):41-50. PubMed ID: 739805
    [No Abstract] [Full Text] [Related]

  • 12. Podocytes are firmly attached to glomerular basement membrane in kidneys with heavy proteinuria.
    Lahdenkari AT, Lounatmaa K, Patrakka J, Holmberg C, Wartiovaara J, Kestilä M, Koskimies O, Jalanko H.
    J Am Soc Nephrol; 2004 Oct; 15(10):2611-8. PubMed ID: 15466265
    [Abstract] [Full Text] [Related]

  • 13. Congenital nephrotic syndrome of Finnish type.
    Mittal BV, Kandoth PW, Kamath J, Lahiri K, Sane SY.
    Indian J Pathol Microbiol; 1988 Oct; 31(4):326-9. PubMed ID: 3229807
    [No Abstract] [Full Text] [Related]

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  • 15. 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
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  • 18. Noncollagenous matrix components of glomeruli in congenital nephrotic syndrome of the Finnish type: evidence of abnormal splitting of nidogen?
    Ljungberg P, Haltia A, Kuusela P, Jalanko H, Holmberg C, Holthöfer H.
    Exp Nephrol; 1996 Apr; 4(5):286-94. PubMed ID: 8931984
    [Abstract] [Full Text] [Related]

  • 19. [Congenital and infantile nephrotic syndrome].
    Niaudet P.
    Nephrol Ther; 2005 Mar; 1(1):63-70. PubMed ID: 16895669
    [Abstract] [Full Text] [Related]

  • 20. Mutation spectrum in the nephrin gene (NPHS1) in congenital nephrotic syndrome.
    Beltcheva O, Martin P, Lenkkeri U, Tryggvason K.
    Hum Mutat; 2001 May; 17(5):368-73. PubMed ID: 11317351
    [Abstract] [Full Text] [Related]


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