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163 related items for PubMed ID: 28049649

  • 1. 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; 28(2):431-438. PubMed ID: 28049649
    [Abstract] [Full Text] [Related]

  • 2. 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; 36(11):2623-2628. PubMed ID: 28963698
    [Abstract] [Full Text] [Related]

  • 3. 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
    [Abstract] [Full Text] [Related]

  • 4. 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
    [Abstract] [Full Text] [Related]

  • 5. 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 08; 272(1):36-44. PubMed ID: 21988333
    [Abstract] [Full Text] [Related]

  • 6. 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
    [Abstract] [Full Text] [Related]

  • 7. Lysozyme amyloidosis-a report on a large German cohort and the characterisation of a novel amyloidogenic lysozyme gene variant.
    Anker S, Hinderhofer K, Baur J, Haupt C, Röcken C, Beimler J, Zeier M, Weiler M, Wühl E, Kimmich C, Schönland S, Hegenbart U.
    Amyloid; 2022 Dec 08; 29(4):245-254. PubMed ID: 35533055
    [Abstract] [Full Text] [Related]

  • 8. A novel lysozyme mutation Phe57Ile associated with hereditary renal amyloidosis.
    Yazaki M, Farrell SA, Benson MD.
    Kidney Int; 2003 May 08; 63(5):1652-7. PubMed ID: 12675840
    [Abstract] [Full Text] [Related]

  • 9. 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 08; 14(11):2639-44. PubMed ID: 10534505
    [Abstract] [Full Text] [Related]

  • 10. 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
    [Abstract] [Full Text] [Related]

  • 11. Hereditary systemic amyloidosis associated with a new apolipoprotein AII stop codon mutation Stop78Arg.
    Yazaki M, Liepnieks JJ, Barats MS, Cohen AH, Benson MD.
    Kidney Int; 2003 Jul 08; 64(1):11-6. PubMed ID: 12787390
    [Abstract] [Full Text] [Related]

  • 12. 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 08; 61(3):907-12. PubMed ID: 11849445
    [Abstract] [Full Text] [Related]

  • 13. Clinical and pathologic characteristics of hereditary apolipoprotein A-I amyloidosis in Ireland.
    Traynor CA, Tighe D, O'Brien FJ, Leavey SF, Dorman AM, Denton MD, Magee C, Conlon PJ.
    Nephrology (Carlton); 2013 Aug 08; 18(8):549-54. PubMed ID: 23730806
    [Abstract] [Full Text] [Related]

  • 14. Renal apolipoprotein A-I amyloidosis: a rare and usually ignored cause of hereditary tubulointerstitial nephritis.
    Gregorini G, Izzi C, Obici L, Tardanico R, Röcken C, Viola BF, Capistrano M, Donadei S, Biasi L, Scalvini T, Merlini G, Scolari F.
    J Am Soc Nephrol; 2005 Dec 08; 16(12):3680-6. PubMed ID: 16221867
    [Abstract] [Full Text] [Related]

  • 15. Novel Type of Renal Amyloidosis Derived from Apolipoprotein-CII.
    Nasr SH, Dasari S, Hasadsri L, Theis JD, Vrana JA, Gertz MA, Muppa P, Zimmermann MT, Grogg KL, Dispenzieri A, Sethi S, Highsmith WE, Merlini G, Leung N, Kurtin PJ.
    J Am Soc Nephrol; 2017 Feb 08; 28(2):439-445. PubMed ID: 27297947
    [Abstract] [Full Text] [Related]

  • 16. Simulations of human lysozyme: probing the conformations triggering amyloidosis.
    Moraitakis G, Goodfellow JM.
    Biophys J; 2003 Apr 08; 84(4):2149-58. PubMed ID: 12668424
    [Abstract] [Full Text] [Related]

  • 17. A new genetic variant of hereditary apolipoprotein A-I amyloidosis: a case-report followed by discussion of diagnostic challenges and therapeutic options.
    Moutafi M, Ziogas DC, Michopoulos S, Bagratuni T, Vasileiou V, Verga L, Merlini G, Palladini G, Matsouka C, Dimopoulos MA, Kastritis E.
    BMC Med Genet; 2019 Jan 21; 20(1):23. PubMed ID: 30665372
    [Abstract] [Full Text] [Related]

  • 18. Combined pulmonary involvement in hereditary lysozyme amyloidosis with associated pulmonary sarcoidosis: a case report.
    McCarthy C, Deegan AP, Garvey JF, McDonnell TJ.
    Sarcoidosis Vasc Diffuse Lung Dis; 2013 Dec 17; 30(4):321-4. PubMed ID: 24351625
    [Abstract] [Full Text] [Related]

  • 19. [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 17; 40(5):323-329. PubMed ID: 30244842
    [Abstract] [Full Text] [Related]

  • 20. Complex p.T88N/W130R mutation in the lysozyme gene leading to hereditary lysozyme amyloidosis with biopsy-proven cardiac involvement.
    Sperry BW, Dispenzieri A, Ikram A, Grogan M, Theis JD, Leung N, Highsmith WE, Maleszewski JJ, Hanna M.
    Amyloid; 2017 Mar 17; 24(1):60-61. PubMed ID: 28330375
    [No Abstract] [Full Text] [Related]

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