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Journal Abstract Search

499 related items for PubMed ID: 21326171

  • 1. Aberrant glycosylation of IgA1 is inherited in both pediatric IgA nephropathy and Henoch-Schönlein purpura nephritis.
    Kiryluk K, Moldoveanu Z, Sanders JT, Eison TM, Suzuki H, Julian BA, Novak J, Gharavi AG, Wyatt RJ.
    Kidney Int; 2011 Jul; 80(1):79-87. PubMed ID: 21326171
    [Abstract] [Full Text] [Related]

  • 2. A cross-sectional analysis of clinicopathologic similarities and differences between Henoch-Schönlein purpura nephritis and IgA nephropathy.
    Sugiyama M, Wada Y, Kanazawa N, Tachibana S, Suzuki T, Matsumoto K, Iyoda M, Honda H, Shibata T.
    PLoS One; 2020 Jul; 15(4):e0232194. PubMed ID: 32324811
    [Abstract] [Full Text] [Related]

  • 3. Clinical significance of serum and mesangial galactose-deficient IgA1 in patients with IgA nephropathy.
    Wada Y, Matsumoto K, Suzuki T, Saito T, Kanazawa N, Tachibana S, Iseri K, Sugiyama M, Iyoda M, Shibata T.
    PLoS One; 2018 Jul; 13(11):e0206865. PubMed ID: 30388165
    [Abstract] [Full Text] [Related]

  • 4. Serum levels of galactose-deficient IgA in children with IgA nephropathy and Henoch-Schönlein purpura.
    Lau KK, Wyatt RJ, Moldoveanu Z, Tomana M, Julian BA, Hogg RJ, Lee JY, Huang WQ, Mestecky J, Novak J.
    Pediatr Nephrol; 2007 Dec; 22(12):2067-72. PubMed ID: 17943324
    [Abstract] [Full Text] [Related]

  • 5. Inherited IgA glycosylation pattern in IgA nephropathy and HSP nephritis: where do we go next?
    Boyd JK, Barratt J.
    Kidney Int; 2011 Jul; 80(1):8-10. PubMed ID: 21673733
    [Abstract] [Full Text] [Related]

  • 6. Aberrant IgA1 Glycosylation in IgA Nephropathy: A Systematic Review.
    Sun Q, Zhang Z, Zhang H, Liu X.
    PLoS One; 2016 Jul; 11(11):e0166700. PubMed ID: 27870872
    [Abstract] [Full Text] [Related]

  • 7. IgA nephropathy and Henoch-Schoenlein purpura nephritis: aberrant glycosylation of IgA1, formation of IgA1-containing immune complexes, and activation of mesangial cells.
    Novak J, Moldoveanu Z, Renfrow MB, Yanagihara T, Suzuki H, Raska M, Hall S, Brown R, Huang WQ, Goepfert A, Kilian M, Poulsen K, Tomana M, Wyatt RJ, Julian BA, Mestecky J.
    Contrib Nephrol; 2007 Jul; 157():134-8. PubMed ID: 17495451
    [Abstract] [Full Text] [Related]

  • 8. Galactose-deficient IgA1 in African Americans with IgA nephropathy: serum levels and heritability.
    Hastings MC, Moldoveanu Z, Julian BA, Novak J, Sanders JT, McGlothan KR, Gharavi AG, Wyatt RJ.
    Clin J Am Soc Nephrol; 2010 Nov; 5(11):2069-74. PubMed ID: 20634323
    [Abstract] [Full Text] [Related]

  • 9. Evaluation of IgA1 O-glycosylation in Henoch-Schönlein Purpura Nephritis Using Mass Spectrometry.
    Nakazawa S, Imamura R, Kawamura M, Kato T, Abe T, Iwatani H, Yamanaka K, Uemura M, Kishikawa H, Nishimura K, Tajiri M, Wada Y, Nonomura N.
    Transplant Proc; 2019 Jun; 51(5):1481-1487. PubMed ID: 31084922
    [Abstract] [Full Text] [Related]

  • 10. Serum levels of alpha-smooth muscle actin and c-Met as biomarkers of the degree of severity of Henoch-Schonlein purpura nephritis.
    Zhang L, Han C, Sun C, Meng H, Ye F, Na S, Chen F, Zhang D, Jin X.
    Transl Res; 2013 Jan; 161(1):26-36. PubMed ID: 23041443
    [Abstract] [Full Text] [Related]

  • 11. [Value of galactose-deficient IgA1 in the early diagnosis of Henoch-Schönlein purpura nephritis in children].
    Kang ZJ, Liu B, Li ZH, Duan CR, Wu TH, Xun M, Zhang Y, Ding YF, Fu RQ.
    Zhongguo Dang Dai Er Ke Za Zhi; 2019 Feb; 21(2):172-175. PubMed ID: 30782282
    [Abstract] [Full Text] [Related]

  • 12. Abnormal IgA glycosylation in Henoch-Schönlein purpura restricted to patients with clinical nephritis.
    Allen AC, Willis FR, Beattie TJ, Feehally J.
    Nephrol Dial Transplant; 1998 Apr; 13(4):930-4. PubMed ID: 9568852
    [Abstract] [Full Text] [Related]

  • 13. Plasma galactose-deficient immunoglobulin A1 and loss of kidney function in patients with immunoglobulin A vasculitis nephritis.
    Zhang X, Xie X, Shi S, Liu L, Lv J, Zhang H.
    Nephrol Dial Transplant; 2020 Dec 04; 35(12):2117-2123. PubMed ID: 31377786
    [Abstract] [Full Text] [Related]

  • 14. Pathogenesis of Henoch-Schönlein purpura nephritis.
    Lau KK, Suzuki H, Novak J, Wyatt RJ.
    Pediatr Nephrol; 2010 Jan 04; 25(1):19-26. PubMed ID: 19526254
    [Abstract] [Full Text] [Related]

  • 15. Aberrant IgA1 glycosylation is inherited in familial and sporadic IgA nephropathy.
    Gharavi AG, Moldoveanu Z, Wyatt RJ, Barker CV, Woodford SY, Lifton RP, Mestecky J, Novak J, Julian BA.
    J Am Soc Nephrol; 2008 May 04; 19(5):1008-14. PubMed ID: 18272841
    [Abstract] [Full Text] [Related]

  • 16. Serum levels of galactose-deficient IgA1 in Chinese children with IgA nephropathy, IgA vasculitis with nephritis, and IgA vasculitis.
    Tang M, Zhang X, Li X, Lei L, Zhang H, Ling C, Ni J, Lv J, Liu X, Chen X.
    Clin Exp Nephrol; 2021 Jan 04; 25(1):37-43. PubMed ID: 32935202
    [Abstract] [Full Text] [Related]

  • 17. Associations of left renal vein entrapment with IgA nephropathy and Henoch-Schönlein purpura nephritis.
    Wang F, Zhu H, Bao S, Qi H, Xu L, Liu X, Zhai C, Yang X, Wang R.
    Ren Fail; 2022 Dec 04; 44(1):1519-1527. PubMed ID: 36069515
    [Abstract] [Full Text] [Related]

  • 18. Clinical Significance of Serum Galactose-Deficient IgA1 Level in Children with IgA Nephropathy.
    Irabu H, Shimizu M, Kaneko S, Inoue N, Mizuta M, Ohta K, Yachie A.
    J Immunol Res; 2020 Dec 04; 2020():4284379. PubMed ID: 32537466
    [Abstract] [Full Text] [Related]

  • 19. Interleukin-1 receptor antagonist allele: is it a genetic link between Henoch-Schönlein nephritis and IgA nephropathy?
    Liu ZH, Cheng ZH, Yu YS, Tang Z, Li LS.
    Kidney Int; 1997 Jun 04; 51(6):1938-42. PubMed ID: 9186886
    [Abstract] [Full Text] [Related]

  • 20. Immunostaining of galactose-deficient IgA1 by KM55 is not specific for immunoglobulin A nephropathy.
    Zhao L, Peng L, Yang D, Chen S, Lan Z, Zhu X, Yuan S, Chen G, Liu Y, Liu H.
    Clin Immunol; 2020 Aug 04; 217():108483. PubMed ID: 32479989
    [Abstract] [Full Text] [Related]

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