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Journal Abstract Search


131 related items for PubMed ID: 2739828

  • 21. The Transition from Thin Basement Membranes to Typical Alport Syndrome Morphology in Children.
    Baek H, Lee SI, Park T, Cho M.
    Fetal Pediatr Pathol; 2016; 35(6):369-375. PubMed ID: 27410722
    [Abstract] [Full Text] [Related]

  • 22. Familial hematuric syndromes--Alport syndrome, thin glomerular basement membrane disease and Fechtner/Epstein syndromes.
    Kashtan CE.
    Contrib Nephrol; 2001; (136):79-99. PubMed ID: 11688406
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  • 25. Establishing the diagnosis of benign familial hematuria. The importance of examining the urine sediment of family members.
    Blumenthal SS, Fritsche C, Lemann J.
    JAMA; 1988 Apr 15; 259(15):2263-6. PubMed ID: 3352118
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  • 26. Alport's syndrome. A report of 58 cases and a review of the literature.
    Gubler M, Levy M, Broyer M, Naizot C, Gonzales G, Perrin D, Habib R.
    Am J Med; 1981 Mar 15; 70(3):493-505. PubMed ID: 7211891
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  • 27. [Significance of family studies and kidney biopsies in children with renal hematuria].
    Pistor K, Bachmann H, Rumpelt HJ, Olbing H.
    Monatsschr Kinderheilkd; 1985 May 15; 133(5):269-73. PubMed ID: 4010678
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  • 28. [Collagen type IV nephropathy: from thin basement membrane nephropathy to Alport syndrome].
    Endreffy E, Ondrik Z, Kemény E, Vas Z, Maróti Z, Lencse G, Bereczki C, Haszon I, Túri S, Iványi B.
    Orv Hetil; 2005 Dec 25; 146(52):2647-53. PubMed ID: 16468607
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  • 29. Making the diagnosis of Alport's syndrome.
    Pirson Y.
    Kidney Int; 1999 Aug 25; 56(2):760-75. PubMed ID: 10432421
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  • 30. Alport syndrome and benign familial hematuria (thin basement membrane disease) in two brothers of a family with hematuria.
    Takemura T, Yanagida H, Yagi K, Moriwaki K, Okada M.
    Clin Nephrol; 2003 Sep 25; 60(3):195-200. PubMed ID: 14524583
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  • 32. Autosomal dominant Alport's syndrome: study of a large Tunisian family.
    Kharrat M, Makni S, Makni K, Kammoun K, Charfeddine K, Azaeiz H, Jarraya F, Ben Hmida M, Gubler MC, Ayadi H, Hachicha J.
    Saudi J Kidney Dis Transpl; 2006 Sep 25; 17(3):320-5. PubMed ID: 16970251
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  • 33. Childhood thin GBM disease: review of 22 children with family studies and long-term follow-up.
    Carasi C, Van't Hoff WG, Rees L, Risdon RA, Trompeter RS, Dillon MJ.
    Pediatr Nephrol; 2005 Aug 25; 20(8):1098-105. PubMed ID: 15940548
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  • 35. COL4A4 mutation in thin basement membrane disease previously described in Alport syndrome.
    Buzza M, Wang YY, Dagher H, Babon JJ, Cotton RG, Powell H, Dowling J, Savige J.
    Kidney Int; 2001 Aug 25; 60(2):480-3. PubMed ID: 11473630
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  • 36. Segregation of hematuria in thin basement membrane disease with haplotypes at the loci for Alport syndrome.
    Buzza M, Wilson D, Savige J.
    Kidney Int; 2001 May 25; 59(5):1670-6. PubMed ID: 11318937
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  • 37. Alport's syndrome. Emphasizing electron microscopic studies of the glomerulus.
    Spear GS, Slusser RJ.
    Am J Pathol; 1972 Nov 25; 69(2):213-24. PubMed ID: 4343992
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  • 38. Association of thin basement membrane nephropathy with hypercalciuria, hyperuricosuria and nephrolithiasis.
    Praga M, Martínez MA, Andrés A, Alegre R, Vara J, Morales E, Herrero JC, Novo O, Rodicio JL.
    Kidney Int; 1998 Sep 25; 54(3):915-20. PubMed ID: 9734616
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  • 40. Genetic, clinical, and morphologic heterogeneity in Alport's syndrome.
    Gubler MC, Antignac C, Deschênes G, Knebelmann B, Hors-Cayla MC, Grünfeld JP, Broyer M, Habib R.
    Adv Nephrol Necker Hosp; 1993 Sep 25; 22():15-35. PubMed ID: 8427057
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