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PUBMED FOR HANDHELDS

Journal Abstract Search


66 related items for PubMed ID: 6809680

  • 1. Diffuse mesangial sclerosis and ocular abnormalities in two siblings.
    Barakat AY, Khoury LA, Allam CK, Najjar SS.
    Int J Pediatr Nephrol; 1982 Mar; 3(1):33-5. PubMed ID: 6809680
    [No Abstract] [Full Text] [Related]

  • 2. [Familial infantile nephrotic syndrome with ocular abnormalities].
    Glastre C, Cochat P, Colon S, Bouvier R, Cottin X, Giffon D, Wright C, Dijoud F, David L.
    Pediatrie; 1989 Mar; 44(7):555-8. PubMed ID: 2812971
    [Abstract] [Full Text] [Related]

  • 3. Familial infantile nephrotic syndrome with ocular abnormalities.
    Glastre C, Cochat P, Bouvier R, Colon S, Cottin X, Giffon D, Wright C, Dijoud F, David L.
    Pediatr Nephrol; 1990 Jul; 4(4):340-2. PubMed ID: 2206901
    [Abstract] [Full Text] [Related]

  • 4. [Role of asymmetry of eye structure in the etiology of squint and persistent amblyopia].
    Wodowozow A.
    Klin Oczna; 1969 Jul; 39(6):843-7. PubMed ID: 4983111
    [No Abstract] [Full Text] [Related]

  • 5. Infantile nephrotic syndrome with diffuse mesangial sclerosis: a disturbance of glomerular basement membrane development?
    Rumpelt HJ, Bachmann HJ.
    Clin Nephrol; 1980 Mar; 13(3):146-50. PubMed ID: 7379364
    [Abstract] [Full Text] [Related]

  • 6. Mesangial deposits of IgM in patients with the nephrotic syndrome.
    Mampaso F, Gonzalo A, Teruel J, Losada M, Gallego N, Ortuno J, Bellas C.
    Clin Nephrol; 1981 Nov; 16(5):230-4. PubMed ID: 7030545
    [Abstract] [Full Text] [Related]

  • 7. [Prognosis of nephrosis].
    Habib R, Kleinknecht C, Gubler MC, Levy M, Guillot M, Gagnadoux MF, Broyer M.
    Bol Med Hosp Infant Mex; 1981 Nov; 38(3):447-55. PubMed ID: 7271976
    [Abstract] [Full Text] [Related]

  • 8. 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
    [Abstract] [Full Text] [Related]

  • 9. Familial early-onset nephrotic syndrome: diffuse mesangial sclerosis. Clinico-pathological study of a kindred.
    Mendelsohn HB, Krauss M, Berant M, Lichtig C.
    Acta Paediatr Scand; 1982 Sep; 71(5):753-8. PubMed ID: 7180443
    [Abstract] [Full Text] [Related]

  • 10. Diffuse mesangial sclerosis: a congenital glomerulopathy with nephrotic syndrome.
    Habib R, Gubler MC, Antignac C, Gagnadoux MF.
    Adv Nephrol Necker Hosp; 1993 Sep; 22():43-57. PubMed ID: 8381254
    [No Abstract] [Full Text] [Related]

  • 11. [Demonstration of mesangial IgA deposits in kidney biopsies of pediatric patients: comparison with the clinical picture].
    Kern BE, di Rocco D, Lütschg J, Lüthy C, Zimmermann A, Gerber HA, Oetliker OH, Bianchetti MG.
    Praxis (Bern 1994); 1995 Oct 10; 84(41):1158-64. PubMed ID: 7481326
    [Abstract] [Full Text] [Related]

  • 12. [Idiopathic nephrotic syndrome with minimal glomerular lesions or with diffuse mesangial proliferation. Comparison of 2 groups of children].
    Giani M, Ripanti G, Stucchi C, Bettinelli A, Bertoletti A, Claris Appiani A, Ghio L, Gaboardi F, Edefonti A.
    Minerva Nefrol; 1980 Oct 10; 27(4):539-42. PubMed ID: 7254677
    [No Abstract] [Full Text] [Related]

  • 13. [Bilateral colobomatous pit of the optical papilla associated with macular degenerative manifestations. Study of 3 cases in the same family].
    Secchi AG.
    Minerva Oftalmol; 1967 Oct 10; 9(6):213-8. PubMed ID: 4979415
    [No Abstract] [Full Text] [Related]

  • 14. A novel mutation of laminin β2 (LAMB2) in two siblings with renal failure.
    Falix FA, Bennebroek CA, van der Zwaag B, Lapid-Gortzak R, Florquin S, Oosterveld MJ.
    Eur J Pediatr; 2017 Apr 10; 176(4):515-519. PubMed ID: 28188379
    [Abstract] [Full Text] [Related]

  • 15. [Central maculopathy and colobomatous papillary fossete. Case report].
    Rubichi E.
    Ann Ottalmol Clin Ocul; 1970 May 10; 96(5):241-51. PubMed ID: 4998567
    [No Abstract] [Full Text] [Related]

  • 16. Ocular findings in lissencephaly.
    Nabi NU, Mezer E, Blaser SI, Levin AA, Buncic JR.
    J AAPOS; 2003 Jun 10; 7(3):178-84. PubMed ID: 12825057
    [Abstract] [Full Text] [Related]

  • 17. Significance of mesangial IgM deposition in "minimal change" nephrotic syndrome.
    Vilches AR, Turner DR, Cameron JS, Ogg CS, Chantler C, Williams DG.
    Lab Invest; 1982 Jan 10; 46(1):10-5. PubMed ID: 7054586
    [Abstract] [Full Text] [Related]

  • 18. [Heterozygotic mutation in NPHS2 gene as a cause of familial steroid resistant nephrotic syndrome in two siblings--case report].
    Drozdz D, Pietrzyk JA, Wierzchowska-Słowiaczek E, Sancewicz-Pach K, Antignac C, Miezyński W.
    Przegl Lek; 2006 Jan 10; 63 Suppl 3():85-6. PubMed ID: 16898497
    [Abstract] [Full Text] [Related]

  • 19. A syndrome comprising childhood-onset glomerular kidney disease and ocular abnormalities with progressive loss of vision is caused by mutated LAMB2.
    Matejas V, Al-Gazali L, Amirlak I, Zenker M.
    Nephrol Dial Transplant; 2006 Nov 10; 21(11):3283-6. PubMed ID: 16921188
    [Abstract] [Full Text] [Related]

  • 20. [Primary nephrotic syndrome. Follow-up of 202 pediatric patients].
    Caletti MG, Gallo G, Zumino D, Díaz MA, Vitacco M.
    Bol Med Hosp Infant Mex; 1981 Nov 10; 38(3):457-72. PubMed ID: 7271977
    [Abstract] [Full Text] [Related]


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