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Journal Abstract Search


144 related items for PubMed ID: 10100367

  • 1. Autosomal dominant polycystic kidney disease associated with familial sensorineural deafness.
    Mora C, Navarro JF, García J, Gallego E, Macía M, Méndez ML, Chahin J, Rivero A.
    Scand J Urol Nephrol; 1999 Feb; 33(1):63-5. PubMed ID: 10100367
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  • 2. Familial IgA nephropathy associated with bilateral sensorineural deafness.
    Chahin J, Ortiz A, Mendez L, Gallego E, Garcia-Perez J, Garcia-Castro G, Julian BA, Egido J.
    Am J Kidney Dis; 1992 Jun; 19(6):592-6. PubMed ID: 1595709
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  • 3. Evaluation of colonic diverticular disease in autosomal dominant polycystic kidney disease without end-stage renal disease.
    Sharp CK, Zeligman BE, Johnson AM, Duley I, Gabow PA.
    Am J Kidney Dis; 1999 Nov; 34(5):863-8. PubMed ID: 10561142
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  • 4. 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; 17(3):320-5. PubMed ID: 16970251
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  • 5. Renal prognosis in Alport's and related syndromes: influence of the mode of inheritance.
    Pochet JM, Bobrie G, Landais P, Goldfarb B, Grünfeld JP.
    Nephrol Dial Transplant; 1989 Sep; 4(12):1016-21. PubMed ID: 2517321
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  • 6. Bilineal inheritance of pathogenic PKD1 and PKD2 variants in a Czech family with autosomal dominant polycystic kidney disease - a case report.
    Elisakova V, Merta M, Reiterova J, Baxova A, Kotlas J, Hirschfeldova K, Obeidova L, Tesar V, Stekrova J.
    BMC Nephrol; 2018 Jul 04; 19(1):163. PubMed ID: 29973168
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  • 11. A new syndrome of autosomal recessive nephropathy, deafness, and hyperparathyroidism.
    Edwards BD, Patton MA, Dilly SA, Eastwood JB.
    J Med Genet; 1989 May 04; 26(5):289-93. PubMed ID: 2732989
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  • 12. [ADPKD and intracranial aneurysms: indications for screening, follow-up and clinical management].
    Econimo L, Zeni L, Cortinovis R, Alberici F, Izzi C, Scolari F.
    G Ital Nefrol; 2021 Oct 26; 38(5):. PubMed ID: 34713642
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  • 13. Autosomal dominant polycystic kidney disease: pathophysiology and treatment.
    McCarthy S, McMullen M.
    ANNA J; 1997 Feb 26; 24(1):45-51; quiz 52-3. PubMed ID: 9146123
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  • 14. Cystic fibrosis and the phenotypic expression of autosomal dominant polycystic kidney disease.
    O'Sullivan DA, Torres VE, Gabow PA, Thibodeau SN, King BF, Bergstralh EJ.
    Am J Kidney Dis; 1998 Dec 26; 32(6):976-83. PubMed ID: 9856513
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  • 17. Hereditary thrombocytopenia, deafness, and renal disease.
    Eckstein JD, Filip DJ, Watts JC.
    Ann Intern Med; 1975 May 26; 82(5):639-45. PubMed ID: 1137259
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  • 18. PKD2-Related Autosomal Dominant Polycystic Kidney Disease: Prevalence, Clinical Presentation, Mutation Spectrum, and Prognosis.
    Cornec-Le Gall E, Audrézet MP, Renaudineau E, Hourmant M, Charasse C, Michez E, Frouget T, Vigneau C, Dantal J, Siohan P, Longuet H, Gatault P, Ecotière L, Bridoux F, Mandart L, Hanrotel-Saliou C, Stanescu C, Depraetre P, Gie S, Massad M, Kersalé A, Séret G, Augusto JF, Saliou P, Maestri S, Chen JM, Harris PC, Férec C, Le Meur Y.
    Am J Kidney Dis; 2017 Oct 26; 70(4):476-485. PubMed ID: 28356211
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