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Journal Abstract Search

132 related items for PubMed ID: 24333525

  • 1. An unusual case of familial lymphedema.
    Dean SM, Starr J.
    Ann Vasc Surg; 2014 Jul; 28(5):1314.e1-3. PubMed ID: 24333525
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  • 2. [Atypical symptoms of Fabry's disease: sudden bilateral deafness, lymphoedema and Lown-Ganong-Levine syndrome].
    Undas A, Ryś D, Wegrzyn W, Musiał J.
    Pol Arch Med Wewn; 2002 Nov; 108(5):1085-90. PubMed ID: 12685250
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  • 4. Fabry disease. A case report.
    Kotnik J, Kotnik F, Desnick RJ.
    Acta Dermatovenerol Alp Pannonica Adriat; 2005 Mar; 14(1):15-9. PubMed ID: 15818441
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  • 5. [Clinical courses of two male siblings on hemodialysis for Fabry disease ].
    Itoh K, Tanaka M, Matsushita K, Miyamura N, Nishida K, Araki E, Nonoguchi H, Tomita K.
    Nihon Jinzo Gakkai Shi; 2005 Mar; 47(2):121-7. PubMed ID: 15859134
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  • 6. [Fabry's disease and familial lymphedema. Description of 2 cases].
    Savi M, Neri TM, Asinari G, Pietrini V, Tagliavini F, Migone L.
    Minerva Med; 1980 Oct 13; 71(39):2851-6. PubMed ID: 6776448
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  • 10. Meige disease (familial lymphedema praecox) and cleft palate: report of a family and review of the literature.
    Figueroa AA, Pruzansky S, Rollnick BR.
    Cleft Palate J; 1983 Apr 13; 20(2):151-7. PubMed ID: 6342849
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  • 12. Noonan syndrome in an adult family presenting with chronic lymphedema.
    Miller M, Motulsky AC.
    Am J Med; 1978 Aug 13; 65(2):379-83. PubMed ID: 686024
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  • 13. Late diagnosis of Fabry disease caused by a de novo mutation in a patient with end stage renal disease.
    Pisani A, Daniele A, Di Domenico C, Nigro E, Salvatore F, Riccio E.
    BMC Res Notes; 2015 Nov 24; 8():711. PubMed ID: 26602202
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  • 14. Renal transplantation between siblings with unrecognized Fabry disease.
    Taneda S, Honda K, Nakajima I, Huchinoue S, Oda H.
    Transplant Proc; 2013 Nov 24; 45(1):115-8. PubMed ID: 23375284
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  • 15. [A case of Fabry's disease detected by renal biopsy findings].
    Yamada S, Ito H, Ohashi T, Yasumoto Y, Yamashita W, Harada R, Arima T, Osaki K, Nakashima A, Maeda T.
    Fukuoka Igaku Zasshi; 1990 Aug 24; 81(8):266-70. PubMed ID: 2172129
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  • 16. [A family with a rare disease].
    Capelo J, Soares C, Carragoso A, Ribeiro P, Girão F, Henriques P.
    Acta Med Port; 2010 Aug 24; 23(3):499-504. PubMed ID: 20654270
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  • 18. Congenital lymphedema of the upper extremity. A case report.
    Sim YJ, Seo JH.
    Eur J Phys Rehabil Med; 2008 Mar 24; 44(1):89-91. PubMed ID: 18385633
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  • 19. Point mutation in the alpha-galactosidase A gene of atypical Fabry disease with only nephropathy.
    Sawada K, Mizoguchi K, Hishida A, Kaneko E, Koide Y, Nishimura K, Kimura M.
    Clin Nephrol; 1996 May 24; 45(5):289-94. PubMed ID: 8738659
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