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Journal Abstract Search

454 related items for PubMed ID: 20804103

  • 1. Spectrum of collagen type IV nephropathies: from thin basement membrane nephropathy to Alport syndrome.
    Vizjak A, Ferluga D.
    Srp Arh Celok Lek; 2008 Dec; 136 Suppl 4():323-6. PubMed ID: 20804103
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  • 2. [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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  • 3. Autosomal dominant form of type IV collagen nephropathy exists among patients with hereditary nephritis difficult to diagnose clinicopathologically.
    Imafuku A, Nozu K, Sawa N, Hasegawa E, Hiramatsu R, Kawada M, Hoshino J, Tanaka K, Ishii Y, Takaichi K, Fujii T, Ohashi K, Iijima K, Ubara Y.
    Nephrology (Carlton); 2018 Oct 25; 23(10):940-947. PubMed ID: 28704582
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  • 4. [Alport syndrome: Hereditary nephropathy associated with mutations in genes coding for type IV collagen chains].
    Heidet L, Gubler MC.
    Nephrol Ther; 2016 Dec 25; 12(7):544-551. PubMed ID: 27816395
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  • 5. Quantitative analysis of glomerular type IV collagen alpha3-5 chain expression in children with thin basement membrane disease.
    Ueda T, Nakajima M, Akazawa H, Maruhashi Y, Shimoyama H, Sakagami Y, Takagawa K, Kamitsuji H, Naito I, Sado Y, Yoshioka A.
    Nephron; 2002 Oct 25; 92(2):271-8. PubMed ID: 12218303
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  • 6. Alport syndrome and thin glomerular basement membrane nephropathy: a practical approach to diagnosis.
    Haas M.
    Arch Pathol Lab Med; 2009 Feb 25; 133(2):224-32. PubMed ID: 19195966
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  • 7. A unique evolution of the kidney phenotype in a patient with autosomal recessive Alport syndrome.
    Vischini G, Kapp ME, Wheeler FC, Hopp L, Fogo AB.
    Hum Pathol; 2018 Nov 25; 81():229-234. PubMed ID: 29530752
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  • 8. Frequent COL4 mutations in familial microhematuria accompanied by later-onset Alport nephropathy due to focal segmental glomerulosclerosis.
    Papazachariou L, Papagregoriou G, Hadjipanagi D, Demosthenous P, Voskarides K, Koutsofti C, Stylianou K, Ioannou P, Xydakis D, Tzanakis I, Papadaki A, Kallivretakis N, Nikolakakis N, Perysinaki G, Gale DP, Diamantopoulos A, Goudas P, Goumenos D, Soloukides A, Boletis I, Melexopoulou C, Georgaki E, Frysira E, Komianou F, Grekas D, Paliouras C, Alivanis P, Vergoulas G, Pierides A, Daphnis E, Deltas C.
    Clin Genet; 2017 Nov 25; 92(5):517-527. PubMed ID: 28632965
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  • 10. Alport syndrome. An inherited disorder of renal, ocular, and cochlear basement membranes.
    Kashtan CE.
    Medicine (Baltimore); 1999 Sep 25; 78(5):338-60. PubMed ID: 10499074
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  • 15. Glomerular Basement Membrane Protein Expression and the Diagnosis and Prognosis of Autosomal Dominant Alport Syndrome.
    Akihisa T, Sato M, Wakayama Y, Taneda S, Horita S, Hirose O, Makabe S, Kataoka H, Mori T, Sohara E, Uchida S, Nitta K, Mochizuki T.
    Kidney Med; 2019 Sep 25; 1(6):391-396. PubMed ID: 32734219
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  • 16. Thin glomerular basement membrane disease: clinical significance of a morphological diagnosis--a collaborative study of the Italian Renal Immunopathology Group.
    Frascà GM, Onetti-Muda A, Mari F, Longo I, Scala E, Pescucci C, Roccatello D, Alpa M, Coppo R, Li Volti G, Feriozzi S, Bergesio F, Schena FP, Renieri A, Italian Renal Immunopathology Group.
    Nephrol Dial Transplant; 2005 Mar 25; 20(3):545-51. PubMed ID: 15618242
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  • 17. Familial hematuria due to type IV collagen mutations: Alport syndrome and thin basement membrane nephropathy.
    Kashtan CE.
    Curr Opin Pediatr; 2004 Apr 25; 16(2):177-81. PubMed ID: 15021198
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  • 18. X-linked Alport Syndrome with Type IV Collagen α5 Chain Staining Revealing Normal Expression in the Glomerular Basement Membrane and Negative on Bowman's Capsule and Distal Tubular Basement Membrane: A Case Report.
    Okamoto T, Shima H, Doi T, Nozu K, Inoue T, Tashiro M, Wariishi S, Bando H, Azuma H, Iwasaka N, Ohara T, Okada K, Minakuchi J.
    Tohoku J Exp Med; 2023 Sep 20; 261(1):69-73. PubMed ID: 37495524
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  • 19. Familial hematuric syndromes--Alport syndrome, thin glomerular basement membrane disease and Fechtner/Epstein syndromes.
    Kashtan CE.
    Contrib Nephrol; 2001 Sep 20; (136):79-99. PubMed ID: 11688406
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