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Journal Abstract Search

175 related items for PubMed ID: 25217048

  • 1. A new family with hereditary lysozyme amyloidosis with gastritis and inflammatory bowel disease as prevailing symptoms.
    Jean E, Ebbo M, Valleix S, Benarous L, Heyries L, Grados A, Bernit E, Grateau G, Papo T, Granel B, Daniel L, Harlé JR, Schleinitz N.
    BMC Gastroenterol; 2014 Sep 13; 14():159. PubMed ID: 25217048
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  • 7. Hereditary Lysozyme Amyloidosis Variant p.Leu102Ser Associates with Unique Phenotype.
    Nasr SH, Dasari S, Mills JR, Theis JD, Zimmermann MT, Fonseca R, Vrana JA, Lester SJ, McLaughlin BM, Gillespie R, Highsmith WE, Lee JJ, Dispenzieri A, Kurtin PJ.
    J Am Soc Nephrol; 2017 Feb 13; 28(2):431-438. PubMed ID: 28049649
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  • 10. A family with gastrointestinal amyloidosis associated with variant lysozyme.
    Granel B, Serratrice J, Valleix S, Grateau G, Droz D, Lafon J, Sault MC, Chaudier B, Disdier P, Laugier R, Delpech M, Weiller PJ.
    Gastroenterology; 2002 Oct 13; 123(4):1346-9. PubMed ID: 12360495
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  • 14. Lysozyme amyloidosis: report of 4 cases and a review of the literature.
    Granel B, Valleix S, Serratrice J, Chérin P, Texeira A, Disdier P, Weiller PJ, Grateau G.
    Medicine (Baltimore); 2006 Jan 13; 85(1):66-73. PubMed ID: 16523055
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  • 15. [Hereditary and non-hereditary cutaneous amyloidoses].
    Schreml S, Schroeder J, Eder F, Szeimies RM, Landthaler M, Babilas P.
    Pathologe; 2009 May 13; 30(3):197-204. PubMed ID: 19319536
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  • 18. Human lysozyme gene mutations cause hereditary systemic amyloidosis.
    Pepys MB, Hawkins PN, Booth DR, Vigushin DM, Tennent GA, Soutar AK, Totty N, Nguyen O, Blake CC, Terry CJ.
    Nature; 1993 Apr 08; 362(6420):553-7. PubMed ID: 8464497
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  • 20. A severe autosomal-dominant periodic inflammatory disorder with renal AA amyloidosis and colchicine resistance associated to the MEFV H478Y variant in a Spanish kindred: an unusual familial Mediterranean fever phenotype or another MEFV-associated periodic inflammatory disorder?
    Aldea A, Campistol JM, Arostegui JI, Rius J, Maso M, Vives J, Yagüe J.
    Am J Med Genet A; 2004 Jan 01; 124A(1):67-73. PubMed ID: 14679589
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