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Journal Abstract Search

226 related items for PubMed ID: 22074998

  • 1. HLA-DRB1 allele frequencies and C4 copy number variation in Finnish sarcoidosis patients and associations with disease prognosis.
    Wennerström A, Pietinalho A, Vauhkonen H, Lahtela L, Palikhe A, Hedman J, Purokivi M, Varkki E, Seppänen M, Lokki ML, Selroos O, Finnish Sarcoidosis Study Group.
    Hum Immunol; 2012 Jan; 73(1):93-100. PubMed ID: 22074998
    [Abstract] [Full Text] [Related]

  • 2. Genetically determined partial complement C4 deficiency states are not independent risk factors for SLE in UK and Spanish populations.
    Boteva L, Morris DL, Cortés-Hernández J, Martin J, Vyse TJ, Fernando MM.
    Am J Hum Genet; 2012 Mar 09; 90(3):445-56. PubMed ID: 22387014
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  • 4. HLA-DRB1* alleles and symptoms associated with Heerfordt's syndrome in sarcoidosis.
    Darlington P, Tallstedt L, Padyukov L, Kockum I, Cederlund K, Eklund A, Grunewald J.
    Eur Respir J; 2011 Nov 09; 38(5):1151-7. PubMed ID: 21565911
    [Abstract] [Full Text] [Related]

  • 5. HLA serological and class II genotyping in sarcoidosis patients in Japan.
    Ishihara M, Ishida T, Inoko H, Ando H, Naruse T, Nose Y, Ohno S.
    Jpn J Ophthalmol; 1996 Nov 09; 40(1):86-94. PubMed ID: 8739505
    [Abstract] [Full Text] [Related]

  • 6. Severe pulmonary sarcoidosis is strongly associated with the haplotype HLA-DQB1*0602-DRB1*150101.
    Voorter CE, Drent M, van den Berg-Loonen EM.
    Hum Immunol; 2005 Jul 09; 66(7):826-35. PubMed ID: 16112030
    [Abstract] [Full Text] [Related]

  • 7. Relation of HLA-A, -B, -DRB1 alleles and haplotypes in patients with acute leukemia: a case control study.
    Uçar F, Sönmez M, Erkut N, Balcı M, Yücel B, Yılmaz M, Erduran E, Ovalı E.
    Arch Med Res; 2011 May 09; 42(4):305-10. PubMed ID: 21820609
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  • 8. Pediatric and adult forms of type I autoimmune hepatitis in Argentina: evidence for differential genetic predisposition.
    Pando M, Larriba J, Fernandez GC, Fainboim H, Ciocca M, Ramonet M, Badia I, Daruich J, Findor J, Tanno H, Cañero-Velasco C, Fainboim L.
    Hepatology; 1999 Dec 09; 30(6):1374-80. PubMed ID: 10573514
    [Abstract] [Full Text] [Related]

  • 9. Complete deficiencies of complement C4A and C4B including 2-bp insertion in codon 1213 are genetic risk factors of systemic lupus erythematosus in Thai populations.
    Ittiprasert W, Kantachuvesiri S, Pavasuthipaisit K, Verasertniyom O, Chaomthum L, Totemchokchyakarn K, Kitiyanant Y.
    J Autoimmun; 2005 Aug 09; 25(1):77-84. PubMed ID: 15998580
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  • 11. Copy number variations of complement component C4 are associated with Behçet's disease but not with ankylosing spondylitis associated with acute anterior uveitis.
    Hou S, Qi J, Liao D, Zhang Q, Fang J, Zhou Y, Liu Y, Bai L, Zhang M, Kijlstra A, Yang P.
    Arthritis Rheum; 2013 Nov 09; 65(11):2963-70. PubMed ID: 23918728
    [Abstract] [Full Text] [Related]

  • 12. HLA in a cohort of Brazilian patients with sarcoidosis.
    da Costa CH, Silva VL, Fabricio-Silva GM, Usnayo M, Rufino R, Porto LC.
    Hum Immunol; 2013 Oct 09; 74(10):1326-32. PubMed ID: 23911360
    [Abstract] [Full Text] [Related]

  • 13. A large-scale association study identified multiple HLA-DRB1 alleles associated with ACPA-negative rheumatoid arthritis in Japanese subjects.
    Terao C, Ohmura K, Kochi Y, Ikari K, Maruya E, Katayama M, Shimada K, Murasawa A, Honjo S, Takasugi K, Matsuo K, Tajima K, Suzuki A, Yamamoto K, Momohara S, Yamanaka H, Yamada R, Saji H, Matsuda F, Mimori T.
    Ann Rheum Dis; 2011 Dec 09; 70(12):2134-9. PubMed ID: 21873689
    [Abstract] [Full Text] [Related]

  • 14. Effects of Complement C4 Gene Copy Number Variations, Size Dichotomy, and C4A Deficiency on Genetic Risk and Clinical Presentation of Systemic Lupus Erythematosus in East Asian Populations.
    Chen JY, Wu YL, Mok MY, Wu YJ, Lintner KE, Wang CM, Chung EK, Yang Y, Zhou B, Wang H, Yu D, Alhomosh A, Jones K, Spencer CH, Nagaraja HN, Lau YL, Lau CS, Yu CY.
    Arthritis Rheumatol; 2016 Jun 09; 68(6):1442-1453. PubMed ID: 26814708
    [Abstract] [Full Text] [Related]

  • 15. HLA associations and Löfgren's syndrome.
    Grunewald J.
    Expert Rev Clin Immunol; 2012 Jan 09; 8(1):55-62. PubMed ID: 22149340
    [Abstract] [Full Text] [Related]

  • 16. Genetic association of HLA-DQB1 and HLA-DRB1 polymorphisms with alopecia areata in the Italian population.
    Megiorni F, Pizzuti A, Mora B, Rizzuti A, Garelli V, Maxia C, Carlesimo M, Fotruna MC, Delle Chiaie R, Cavaggioni G, Rossi A.
    Br J Dermatol; 2011 Oct 09; 165(4):823-7. PubMed ID: 21692766
    [Abstract] [Full Text] [Related]

  • 17. HLA-Cw*1202-B*5201-DRB1*1502 haplotype increases risk for ulcerative colitis but reduces risk for Crohn's disease.
    Okada Y, Yamazaki K, Umeno J, Takahashi A, Kumasaka N, Ashikawa K, Aoi T, Takazoe M, Matsui T, Hirano A, Matsumoto T, Kamatani N, Nakamura Y, Yamamoto K, Kubo M.
    Gastroenterology; 2011 Sep 09; 141(3):864-871.e1-5. PubMed ID: 21699788
    [Abstract] [Full Text] [Related]

  • 18. Gene copy-number variations (CNVs) of complement C4 and C4A deficiency in genetic risk and pathogenesis of juvenile dermatomyositis.
    Lintner KE, Patwardhan A, Rider LG, Abdul-Aziz R, Wu YL, Lundström E, Padyukov L, Zhou B, Alhomosh A, Newsom D, White P, Jones KB, O'Hanlon TP, Miller FW, Spencer CH, Yu CY.
    Ann Rheum Dis; 2016 Sep 09; 75(9):1599-606. PubMed ID: 26493816
    [Abstract] [Full Text] [Related]

  • 19. Association of tumour necrosis factor-alpha, lymphotoxin-alpha and HLA-DRB1 gene polymorphisms with Löfgren's syndrome in Czech patients with sarcoidosis.
    Mrazek F, Holla LI, Hutyrova B, Znojil V, Vasku A, Kolek V, Welsh KI, Vacha J, du Bois RM, Petrek M.
    Tissue Antigens; 2005 Feb 09; 65(2):163-71. PubMed ID: 15713215
    [Abstract] [Full Text] [Related]

  • 20. HLA and susceptibility to juvenile idiopathic arthritis: a study of affected sibpairs in an isolated Finnish population.
    Säilä H, Pitkäniemi J, Tuomilehto J, Savolainen A, Alakulppi N, Tuomilehto-Wolf E, Leirisalo-Repo M, Aho K.
    J Rheumatol; 2004 Nov 09; 31(11):2281-5. PubMed ID: 15517645
    [Abstract] [Full Text] [Related]

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