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Journal Abstract Search

126 related items for PubMed ID: 12360495

  • 1. 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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  • 3. Hereditary renal amyloidosis caused by a new variant lysozyme W64R in a French family.
    Valleix S, Drunat S, Philit JB, Adoue D, Piette JC, Droz D, MacGregor B, Canet D, Delpech M, Grateau G.
    Kidney Int; 2002 Mar; 61(3):907-12. PubMed ID: 11849445
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  • 5. 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. 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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  • 9. 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. A new lysozyme tyr54asn mutation causing amyloidosis in a family of Swedish ancestry with gastrointestinal symptoms.
    Girnius S, Skinner M, Spencer B, Prokaeva T, Bartholomew C, O'Hara C, Seldin DC, Connors LH.
    Amyloid; 2012 Dec 08; 19(4):182-5. PubMed ID: 22978355
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  • 15. Vitreous amyloidosis with autonomic neuropathy of the digestive tract associated with a novel transthyretin p.Gly87Arg variant in a Bangladeshi patient: a case report.
    Terrier B, Colombat M, Beugnet C, Quéant A, London J, Daudin JB, Le Jeunne C, Mouthon L, Monnet D, Cauquil C, Lacroix C, Adams D, Brézin A, Valleix S.
    J Med Case Rep; 2017 Aug 13; 11(1):222. PubMed ID: 28802308
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  • 17. A novel variant of transthyretin, 59Thr-->Lys, associated with autosomal dominant cardiac amyloidosis in an Italian family.
    Booth DR, Tan SY, Hawkins PN, Pepys MB, Frustaci A.
    Circulation; 1995 Feb 15; 91(4):962-7. PubMed ID: 7850982
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  • 18. [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 15; 40(5):323-329. PubMed ID: 30244842
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  • 19. The analysis of gastrointestinal amyloidosis in 78 patients with chronic renal failure.
    Bilezikçi B, Demirhan B, Haberal AN, Boyacioglu S, Güngen Y.
    Amyloid; 2000 Dec 15; 7(4):278-83. PubMed ID: 11132097
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  • 20. Clinical recognition of Al type amyloidosis of the luminal gastrointestinal tract.
    James DG, Zuckerman GR, Sayuk GS, Wang HL, Prakash C.
    Clin Gastroenterol Hepatol; 2007 May 15; 5(5):582-8. PubMed ID: 17428737
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