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Journal Abstract Search

135 related items for PubMed ID: 10994174

  • 1.
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  • 2. Genetic linkage of autosomal-dominant Alport syndrome with leukocyte inclusions and macrothrombocytopenia (Fechtner syndrome) to chromosome 22q11-13.
    Toren A, Amariglio N, Rozenfeld-Granot G, Simon AJ, Brok-Simoni F, Pras E, Rechavi G.
    Am J Hum Genet; 1999 Dec; 65(6):1711-7. PubMed ID: 10577925
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  • 3. [Alport's syndrome: hereditary nephropathy with hematuria and deafness].
    Giger C, Guignard JP, Pelet B, Campiche M, Krstic R.
    Rev Med Suisse Romande; 1988 Apr; 108(4):349-55. PubMed ID: 3387770
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  • 4. Alport's syndrome: can carriers be identified by audiometry?
    Sirimanna KS, France E, Stephens SD.
    Clin Otolaryngol Allied Sci; 1995 Apr; 20(2):158-63. PubMed ID: 7634524
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  • 7. 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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  • 9. Fechtner syndrome: report of a third family and literature review.
    Rocca B, Laghi F, Zini G, Maggiano N, Landolfi R.
    Br J Haematol; 1993 Oct; 85(2):423-6. PubMed ID: 8280620
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  • 12. [Pedigree analysis of two families with Alport's syndrome].
    Wässer S, Theile H, Schöne D, Lemme B.
    Padiatr Grenzgeb; 1980 Oct; 19(3):167-71. PubMed ID: 7454376
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  • 13. [Hereditary nephritis with bearing loss of the receiver type (Alport's syndrome) with a description of 2 cases].
    Zhelev N, Astrug A, Konstantinova B, Henov D.
    Vutr Boles; 1974 Oct; 13(6):137-44. PubMed ID: 4467473
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  • 14. [Fechtner syndrome, a nonmuscle myosin heavy chain 9 gene mutation related disease: a case report and literature review].
    Hu R, Hao JH, Yang HL, Zhu Y, Li SY, Zhao J, Lin FR, Niu ZY.
    Zhonghua Xue Ye Xue Za Zhi; 2011 Feb; 32(2):103-6. PubMed ID: 21429376
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  • 15. [Chronic hereditary nephritis with hearing loss (Alport's syndrome)].
    Zientalska-Rumińska E, Stankiewicz-Szymczak W, Moszyński B.
    Otolaryngol Pol; 1989 Feb; 43(5-6):401-8. PubMed ID: 2640496
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  • 17. Fechtner syndrome: physiologic analysis of macrothrombocytopenia.
    McBane RD, Elliott MA, White JG, Charlesworth JE, Costopoulos MG, Owen WG, Nichols WL.
    Blood Coagul Fibrinolysis; 2000 Apr; 11(3):243-7. PubMed ID: 10870804
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  • 19. Hereditary nephropathy with nerve deafness (Alport's syndrome).
    Ferguson AC, Rance CP.
    Am J Dis Child; 1972 Jul; 124(1):84-8. PubMed ID: 5033754
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  • 20. [Chronic hereditary nephropathy with deafness and ocular lesions].
    Hauser J.
    Schweiz Med Wochenschr; 1974 May 18; 104(20):724-8. PubMed ID: 4829630
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