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Journal Abstract Search

447 related items for PubMed ID: 19195966

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  • 2. 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; 23(10):940-947. PubMed ID: 28704582
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  • 3. Thin basement membrane nephropathy.
    Savige J, Rana K, Tonna S, Buzza M, Dagher H, Wang YY.
    Kidney Int; 2003 Oct; 64(4):1169-78. PubMed ID: 12969134
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  • 4. Alport syndrome and thin basement membrane nephropathy.
    Thorner PS.
    Nephron Clin Pract; 2007 Oct; 106(2):c82-8. PubMed ID: 17570934
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  • 6. Temporal retinal thinning and the diagnosis of Alport syndrome and Thin basement membrane nephropathy.
    Chen Y, Colville D, Ierino F, Symons A, Savige J.
    Ophthalmic Genet; 2018 Apr; 39(2):208-214. PubMed ID: 29172845
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  • 10. [Alport syndrome: Hereditary nephropathy associated with mutations in genes coding for type IV collagen chains].
    Heidet L, Gubler MC.
    Nephrol Ther; 2016 Dec; 12(7):544-551. PubMed ID: 27816395
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  • 11. 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; 92(5):517-527. PubMed ID: 28632965
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  • 12. 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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  • 15. Chronic renal failure and shortened lifespan in COL4A3+/- mice: an animal model for thin basement membrane nephropathy.
    Beirowski B, Weber M, Gross O.
    J Am Soc Nephrol; 2006 Jul; 17(7):1986-94. PubMed ID: 16775036
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  • 16. Genetic, Clinical, and Pathologic Backgrounds of Patients with Autosomal Dominant Alport Syndrome.
    Kamiyoshi N, Nozu K, Fu XJ, Morisada N, Nozu Y, Ye MJ, Imafuku A, Miura K, Yamamura T, Minamikawa S, Shono A, Ninchoji T, Morioka I, Nakanishi K, Yoshikawa N, Kaito H, Iijima K.
    Clin J Am Soc Nephrol; 2016 Aug 08; 11(8):1441-1449. PubMed ID: 27281700
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  • 17. Three Novel Heterozygous COL4A4 Mutations Result in Three Different Collagen Type IV Kidney Disease Phenotypes.
    Li A, Gao EZ, Cui YX, Liu JH, Lv X, Wei XX, Xia XY, Gao CL, Liu FX, Xia ZK, Asan, Liu ZH, Li XJ.
    Cytogenet Genome Res; 2018 Aug 08; 154(1):30-36. PubMed ID: 29669314
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  • 19. How to resolve confusion in the clinical setting for the diagnosis of heterozygous COL4A3 or COL4A4 gene variants? Discussion and suggestions from nephrologists.
    Imafuku A, Nozu K, Sawa N, Nakanishi K, Ubara Y.
    Clin Exp Nephrol; 2020 Aug 08; 24(8):651-656. PubMed ID: 32232700
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