These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

136 related items for PubMed ID: 19026701

  • 21. Familial Mediterranean fever is no longer a rare disease in Japan.
    Migita K, Izumi Y, Jiuchi Y, Iwanaga N, Kawahara C, Agematsu K, Yachie A, Masumoto J, Fujikawa K, Yamasaki S, Nakamura T, Ubara Y, Koga T, Nakashima Y, Shimizu T, Umeda M, Nonaka F, Yasunami M, Eguchi K, Yoshiura K, Kawakami A.
    Arthritis Res Ther; 2016 Jul 30; 18():175. PubMed ID: 27473114
    [Abstract] [Full Text] [Related]

  • 22.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 23.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 24. MEFV E148Q polymorphism is associated with Henoch-Schönlein purpura in Chinese children.
    He X, Lu H, Kang S, Luan J, Liu Z, Yin W, Yao H, Ding Y, Li T, Heng CK.
    Pediatr Nephrol; 2010 Oct 30; 25(10):2077-82. PubMed ID: 20602240
    [Abstract] [Full Text] [Related]

  • 25. Genetic variation in the familial Mediterranean fever gene (MEFV) and risk for Crohn's disease and ulcerative colitis.
    Villani AC, Lemire M, Louis E, Silverberg MS, Collette C, Fortin G, Nimmo ER, Renaud Y, Brunet S, Libioulle C, Belaiche J, Bitton A, Gaudet D, Cohen A, Langelier D, Rioux JD, Arnott ID, Wild GE, Rutgeerts P, Satsangi J, Vermeire S, Hudson TJ, Franchimont D.
    PLoS One; 2009 Sep 28; 4(9):e7154. PubMed ID: 19784369
    [Abstract] [Full Text] [Related]

  • 26. Validation of genome-wide associated variants for Kawasaki disease in a Taiwanese case-control sample.
    Chen MR, Chang TY, Chiu NC, Chi H, Yang KD, Chang L, Huang DT, Huang FY, Lien YP, Lin WS, Lin CL, Chang LY, Lee YJ.
    Sci Rep; 2020 Jul 16; 10(1):11756. PubMed ID: 32678208
    [Abstract] [Full Text] [Related]

  • 27.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 28. A study of familial Mediterranean Fever (MEFV) gene mutations in Egyptian children with type 1 diabetes mellitus.
    Anwar GM, Fouad HM, Abd El-Hamid A, Mahmoud F, Musa N, Lotfi H, Salah N.
    Eur J Med Genet; 2015 Jan 16; 58(1):31-4. PubMed ID: 25449140
    [Abstract] [Full Text] [Related]

  • 29. Kawasaki disease and familial mediterranean fever gene mutations, is there any link?
    Salehzadeh F, Mirzarahimi M, Hosseini Asl S, Nematdoust Haghi R.
    Open Access Rheumatol; 2019 Jan 16; 11():127-131. PubMed ID: 31191052
    [Abstract] [Full Text] [Related]

  • 30.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 31.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 32. A polymorphism in the promoter of the CD14 gene (CD14/-159) is associated with the development of coronary artery lesions in patients with Kawasaki disease.
    Nishimura S, Zaitsu M, Hara M, Yokota G, Watanabe M, Ueda Y, Imayoshi M, Ishii E, Tasaki H, Hamasaki Y.
    J Pediatr; 2003 Sep 16; 143(3):357-62. PubMed ID: 14517520
    [Abstract] [Full Text] [Related]

  • 33. MEFV gene mutations in Henoch-Schönlein purpura.
    Altug U, Ensari C, Sayin DB, Ensari A.
    Int J Rheum Dis; 2013 Jun 16; 16(3):347-51. PubMed ID: 23981758
    [Abstract] [Full Text] [Related]

  • 34. Prevalence and significance of MEFV gene mutations in patients with gouty arthritis.
    Karaarslan A, Kobak S, Kaya I, Intepe N, Orman M, Berdelı A.
    Rheumatol Int; 2016 Nov 16; 36(11):1585-1589. PubMed ID: 27587294
    [Abstract] [Full Text] [Related]

  • 35. Association between sequence variations of the Mediterranean fever gene and fibromyalgia syndrome in a cohort of Turkish patients.
    Karakus N, Yigit S, Inanir A, Inanir S, Toprak H, Okan S.
    Clin Chim Acta; 2012 Dec 24; 414():36-40. PubMed ID: 23010357
    [Abstract] [Full Text] [Related]

  • 36.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 37. Association of vascular endothelial growth factor (VEGF) and VEGF receptor gene polymorphisms with coronary artery lesions of Kawasaki disease.
    Kariyazono H, Ohno T, Khajoee V, Ihara K, Kusuhara K, Kinukawa N, Mizuno Y, Hara T.
    Pediatr Res; 2004 Dec 24; 56(6):953-9. PubMed ID: 15470196
    [Abstract] [Full Text] [Related]

  • 38. MEFV gene pathogenic variants: a risk factor for dysmenorrhea in the Turkish population.
    Nacar MC, Yigit S, Ozsoy AZ, Demirturk F, Nursal AF, Karakus N.
    Nucleosides Nucleotides Nucleic Acids; 2024 Dec 24; 43(7):643-654. PubMed ID: 38133485
    [Abstract] [Full Text] [Related]

  • 39. The effect of FcγRIIA and FcγRIIB on coronary artery lesion formation and intravenous immunoglobulin treatment responses in children with Kawasaki disease.
    Chang LS, Lo MH, Li SC, Yang MY, Hsieh KS, Kuo HC.
    Oncotarget; 2017 Jan 10; 8(2):2044-2052. PubMed ID: 27893416
    [Abstract] [Full Text] [Related]

  • 40. Integrin α2 gene polymorphism is a risk factor of coronary artery lesions in Chinese children with Kawasaki disease.
    Yuan J, Jiang Z, Li M, Li W, Gu X, Wang Z, Pi L, Xu Y, Zhou H, Zhang B, Deng Q, Wang Y, Huang P, Zhang L, Gu X.
    Pediatr Rheumatol Online J; 2021 Feb 08; 19(1):12. PubMed ID: 33557870
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 7.