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Journal Abstract Search

139 related items for PubMed ID: 2625948

  • 41. [X chromosome dominant hereditary nephritis: characterization by pedigree analysis and simple studies in general practice].
    Wälchli P.
    Praxis (Bern 1994); 1999 Oct 28; 88(44):1811-4. PubMed ID: 10584551
    [Abstract] [Full Text] [Related]

  • 42.
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  • 43. Familial nephropathy and deafness: first observation of a family and close relatives in Switzerland.
    Dubach UC, Minder FC, Antener I.
    Helv Med Acta; 1966 Apr 28; 33(1):36-43. PubMed ID: 5927986
    [No Abstract] [Full Text] [Related]

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  • 46. [Alport's syndrome or hereditary nephropathy with deafness. Further familial study].
    Burguet W, Lefebvre P, Booz G, Delwaide PJ, Van Cauwenberge H.
    J Genet Hum; 1966 Jun 28; 15(1):7-20. PubMed ID: 5963517
    [No Abstract] [Full Text] [Related]

  • 47. [Hereditary nephritis (Alport's syndrome). Clinical, histological, ultrastructural and immunohistological study].
    Imbasciati E, Gaboardi F, Limido D, Tarantino A, Chiccoli C.
    Minerva Nefrol; 1973 Jun 28; 20(3):148-61. PubMed ID: 4586688
    [No Abstract] [Full Text] [Related]

  • 48. Association of familial nephritis without deafness and multiple sclerosis.
    Czeizel AE, Uri-Szabó K.
    Clin Nephrol; 1994 Oct 28; 42(4):277-8. PubMed ID: 7834925
    [No Abstract] [Full Text] [Related]

  • 49. de-novo Alport syndrome: for the diagnosis of inherited glomerulonephritis with neither any family history nor extrarenal manifestation.
    Fukushima T, Nomura S, Kawai S, Osawa G.
    Clin Nephrol; 1997 Aug 28; 48(2):134-5. PubMed ID: 9285155
    [No Abstract] [Full Text] [Related]

  • 50. Hereditary renal disease associated with deafness; Alport's syndrome.
    Van Buchem FS, Beetstra A.
    Proc K Ned Akad Wet C; 1965 Aug 28; 68(5):350-9. PubMed ID: 4221522
    [No Abstract] [Full Text] [Related]

  • 51. [Case of Alport's syndrome in an adult].
    Shishkin AN, Zus' BA, Pevzner AS.
    Ter Arkh; 1985 Aug 28; 57(9):135-6. PubMed ID: 4082039
    [No Abstract] [Full Text] [Related]

  • 52. Autosomal dominant nephritis with renal failure of non-Alport type: clinical and molecular studies.
    Ilan T, Shohat T, Tobar A, Magal N, Yahav M, Halpern GJ, Rechavi G, Shohat M.
    Isr Med Assoc J; 2001 Jul 28; 3(7):488-91. PubMed ID: 11791413
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  • 53. [Alport's syndrome with familial abnormality of the external ear].
    Firek H.
    Przegl Lek; 1984 Jul 28; 41(10):633-5. PubMed ID: 6545706
    [No Abstract] [Full Text] [Related]

  • 54. [Alport's syndrome].
    Kozyr' VI, Pindrikov LL, Dziubko NP.
    Ter Arkh; 1981 Jul 28; 53(6):124-6. PubMed ID: 7281024
    [No Abstract] [Full Text] [Related]

  • 55. [Progressive hereditary nephritis].
    Frederiksen L.
    Ugeskr Laeger; 1987 May 11; 149(20):1314-6. PubMed ID: 3603773
    [No Abstract] [Full Text] [Related]

  • 56. Hereditary nephritis--a family study.
    Malhotra KK, Kathpalia SC, Tandon HD, Kumar R, Dhawan IK, Kapoor BM.
    J Assoc Physicians India; 1976 Aug 11; 24(8):543-7. PubMed ID: 1025137
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  • 58. [Analysis of 223 cases of hereditary deafness].
    Zhuang JM, Wang DX.
    Zhonghua Yi Xue Za Zhi; 1986 Jan 11; 66(1):25-8. PubMed ID: 3091213
    [No Abstract] [Full Text] [Related]

  • 59. [Hereditary hematuric nephropathy].
    Prekop R, Mydlík M, Jurkovic I.
    Cesk Pediatr; 1970 Mar 11; 25(3):125-7. PubMed ID: 5440263
    [No Abstract] [Full Text] [Related]

  • 60. [Auditory lesions in Alport's syndrome (hereditary hematuric nephritis)].
    Babai F, Bettez P.
    Ann Anat Pathol (Paris); 1968 Mar 11; 13(3):289-302. PubMed ID: 5727103
    [No Abstract] [Full Text] [Related]

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