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Journal Abstract Search

169 related items for PubMed ID: 16523055

  • 1. 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; 85(1):66-73. PubMed ID: 16523055
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  • 2. Hereditary renal amyloidosis associated with variant lysozyme in a large English family.
    Gillmore JD, Booth DR, Madhoo S, Pepys MB, Hawkins PN.
    Nephrol Dial Transplant; 1999 Nov; 14(11):2639-44. PubMed ID: 10534505
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  • 3. 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; 123(4):1346-9. PubMed ID: 12360495
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  • 4. Hereditary systemic amyloidosis with renal involvement.
    Hawkins PN.
    J Nephrol; 2003 Oct; 16(3):443-8. PubMed ID: 12832750
    [Abstract] [Full Text] [Related]

  • 5. [Lysozyme amyloidosis].
    Scafi M, Valleix S, Benyamine A, Jean E, Harlé JR, Rossi P, Daniel L, Schleinitz N, Granel B.
    Rev Med Interne; 2019 May; 40(5):323-329. PubMed ID: 30244842
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  • 6. Hereditary lysozyme amyloidosis -- phenotypic heterogeneity and the role of solid organ transplantation.
    Sattianayagam PT, Gibbs SD, Rowczenio D, Pinney JH, Wechalekar AD, Gilbertson JA, Hawkins PN, Lachmann HJ, Gillmore JD.
    J Intern Med; 2012 Jul; 272(1):36-44. PubMed ID: 21988333
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  • 7. 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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  • 10. Hereditary renal amyloidosis with a variant lysozyme p.Trp82Arg in a Chinese family: case report and literature review.
    Li Z, Xu H, Liu D, Li D, Liu G, Wang SX.
    BMC Nephrol; 2019 Aug 08; 20(1):310. PubMed ID: 31395023
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  • 13. Hereditary lysozyme amyloidosis with sicca syndrome, digestive, arterial, and tracheobronchial involvement: case-based review.
    Benyamine A, Bernard-Guervilly F, Tummino C, Macagno N, Daniel L, Valleix S, Granel B.
    Clin Rheumatol; 2017 Nov 08; 36(11):2623-2628. PubMed ID: 28963698
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  • 14. ALys amyloidosis caused by compound heterozygosity in exon 2 (Thr70Asn) and exon 4 (Trp112Arg) of the lysozyme gene.
    Röcken C, Becker K, Fändrich M, Schroeckh V, Stix B, Rath T, Kähne T, Dierkes J, Roessner A, Albert FW.
    Hum Mutat; 2006 Jan 08; 27(1):119-20. PubMed ID: 16329101
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  • 15. Misdiagnosis of hereditary amyloidosis as AL (primary) amyloidosis.
    Lachmann HJ, Booth DR, Booth SE, Bybee A, Gilbertson JA, Gillmore JD, Pepys MB, Hawkins PN.
    N Engl J Med; 2002 Jun 06; 346(23):1786-91. PubMed ID: 12050338
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  • 18. Amyloidosis of the gastrointestinal tract: a 13-year, single-center, referral experience.
    Cowan AJ, Skinner M, Seldin DC, Berk JL, Lichtenstein DR, O'Hara CJ, Doros G, Sanchorawala V.
    Haematologica; 2013 Jan 06; 98(1):141-6. PubMed ID: 22733017
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  • 19. The clinical and biochemical spectrum of hereditary amyloidosis.
    Varga J, Wohlgethan JR.
    Semin Arthritis Rheum; 1988 Aug 06; 18(1):14-28. PubMed ID: 2847318
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