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Journal Abstract Search

111 related items for PubMed ID: 1583644

  • 41. [Autosomal dominant polycystic kidney disease: detection of a new mutation in the PKD1 gene].
    Iglesias DM, Manrique M, Arrizurieta EE, Kornblihtt AR, Herrera M, Martín RS, Bernath VA.
    Medicina (B Aires); 1999; 59(2):133-7. PubMed ID: 10413889
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  • 42. Analysis of polycystic kidney disease with two new microsatellite markers.
    Bozza A, Stefani S, De Paoli Vitali E, Perini L, del Senno L.
    Boll Soc Ital Biol Sper; 1994 Apr; 70(4):129-33. PubMed ID: 8086157
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  • 43. [Autosomal dominant polycystic kidney and genetic markers of chromosome 16].
    Ferec C, Bourbigot B, Simon P, Whebe B, Treguer H, Hervé JP, Saleun JP, Cledes J.
    Nephrologie; 1990 Apr; 11(2):79-82. PubMed ID: 1975432
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  • 44. PKD1 and PKD2 mutations in Slovenian families with autosomal dominant polycystic kidney disease.
    Vouk K, Strmecki L, Stekrova J, Reiterova J, Bidovec M, Hudler P, Kenig A, Jereb S, Zupanic-Pajnic I, Balazic J, Haarpaintner G, Leskovar B, Adamlje A, Skoflic A, Dovc R, Hojs R, Komel R.
    BMC Med Genet; 2006 Jan 23; 7():6. PubMed ID: 16430766
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  • 45. [Molecular diagnosis of adult dominant polycystic kidney disease in the Canary Islands].
    Torres MJ, Rodríguez Pérez JC, Hernández Socorro CR, Anabitarte A, Caballero A, Vázquez C, Fernández-Burriel M, Pérez Borges P, Palop L.
    Nefrologia; 2006 Jan 23; 26(6):666-72. PubMed ID: 17227243
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  • 46. Genetic linkage analysis of autosomal dominant polycystic kidney disease in a Turkish family.
    Sungur C, Alikaşifoglu M, Breuning MH, Peters DJ.
    Nephron; 1995 Jan 23; 70(3):388. PubMed ID: 7477639
    [No Abstract] [Full Text] [Related]

  • 47. DNA microsatellite analysis of families with autosomal dominant polycystic kidney disease types 1 and 2: evaluation of clinical heterogeneity between both forms of the disease.
    Coto E, Sanz de Castro S, Aguado S, Alvarez J, Arias M, Menéndez MJ, López-Larrea C.
    J Med Genet; 1995 Jun 23; 32(6):442-5. PubMed ID: 7666395
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  • 49. Phenotypic variability in PKD1: the family as a starting point.
    Guay-Woodford LM.
    Kidney Int; 1999 Jul 23; 56(1):344-6. PubMed ID: 10411712
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  • 53. Loss of heterozygosity in renal and hepatic epithelial cystic cells from ADPKD1 patients.
    Badenas C, Torra R, Pérez-Oller L, Mallolas J, Talbot-Wright R, Torregrosa V, Darnell A.
    Eur J Hum Genet; 2000 Jul 23; 8(7):487-92. PubMed ID: 10909847
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  • 54. Confirmation of a gene locus for medullary cystic kidney disease (MCKD2) on chromosome 16p12.
    Hateboer N, Gumbs C, Teare MD, Coles GA, Griffiths D, Ravine D, Futreal PA, Rahman N.
    Kidney Int; 2001 Oct 23; 60(4):1233-9. PubMed ID: 11576337
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  • 55. Genetic and clinical studies in autosomal dominant polycystic kidney disease type 1 (ADPKD1).
    Coto E, Aguado S, Alvarez J, Menéndez Díaz MJ, López-Larrea C.
    J Med Genet; 1992 Apr 23; 29(4):243-6. PubMed ID: 1583643
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  • 57. Chromosome 4 localization of a second gene for autosomal dominant polycystic kidney disease.
    Peters DJ, Spruit L, Saris JJ, Ravine D, Sandkuijl LA, Fossdal R, Boersma J, van Eijk R, Nørby S, Constantinou-Deltas CD.
    Nat Genet; 1993 Dec 23; 5(4):359-62. PubMed ID: 8298643
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  • 58. Type identification of autosomal dominant polycystic kidney disease by analysis of fluorescent short tandem repeat markers.
    Lin WD, Wu JY, Tsai FJ, Gau MT, Lee CC.
    J Formos Med Assoc; 2002 Aug 23; 101(8):567-71. PubMed ID: 12440087
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  • 59. Cosegregation of bipolar disorder and autosomal-dominant medullary cystic kidney disease in a large family.
    Kimmel RJ, Kovacs I, Vrabel C, Wood B, Schalling M, Kelsoe JR.
    Am J Psychiatry; 2005 Oct 23; 162(10):1972-4. PubMed ID: 16199849
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  • 60. The Han:SPRD rat is not a genetic model of human autosomal dominant polycystic kidney disease type 1.
    Nauta J, Goedbloed MA, Luider TM, Hoogeveen AT, van den Ouweland AM, Halley DJ.
    Lab Anim; 1997 Jul 23; 31(3):241-7. PubMed ID: 9230505
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