Ariga T - Search Results

1

Clinical and laboratory features of fatal rapidly progressive interstitial lung disease associated with juvenile dermatomyositis.

Kobayashi N, Takezaki S, Kobayashi I, Iwata N, Mori M, Nagai K, Nakano N, Miyoshi M, Kinjo N, Murata T, Masunaga K, Umebayashi H, Imagawa T, Agematsu K, Sato S, Kuwana M, Yamada M, Takei S, Yokota S, Koike K, Ariga T. Kobayashi N, et al. Among authors: ariga t. Rheumatology (Oxford). 2015 May;54(5):784-91. doi: 10.1093/rheumatology/keu385. Epub 2014 Oct 6. Rheumatology (Oxford). 2015. PMID: 25288783

2

Epitope mapping of anti-alpha-fodrin autoantibody in juvenile Sjögren's syndrome: difference in major epitopes between primary and secondary cases.

Shiari R, Kobayashi I, Toita N, Hatano N, Kawamura N, Okano M, Hayashi Y, Kobayashi K, Ariga T. Shiari R, et al. Among authors: ariga t. J Rheumatol. 2006 Jul;33(7):1395-400. J Rheumatol. 2006. PMID: 16821274

3

Epstein-Barr virus-associated B-cell lymphoma in a patient with DNA ligase IV (LIG4) syndrome.

Toita N, Hatano N, Ono S, Yamada M, Kobayashi R, Kobayashi I, Kawamura N, Okano M, Satoh A, Nakagawa A, Ohshima K, Shindoh M, Takami T, Kobayashi K, Ariga T. Toita N, et al. Among authors: ariga t. Am J Med Genet A. 2007 Apr 1;143A(7):742-5. doi: 10.1002/ajmg.a.31644. Am J Med Genet A. 2007. PMID: 17345618

4

Molecular explanation for the contradiction between systemic Th17 defect and localized bacterial infection in hyper-IgE syndrome.

Minegishi Y, Saito M, Nagasawa M, Takada H, Hara T, Tsuchiya S, Agematsu K, Yamada M, Kawamura N, Ariga T, Tsuge I, Karasuyama H. Minegishi Y, et al. Among authors: ariga t. J Exp Med. 2009 Jun 8;206(6):1291-301. doi: 10.1084/jem.20082767. Epub 2009 Jun 1. J Exp Med. 2009. PMID: 19487419 Free PMC article.

5

Identification of severe combined immunodeficiency by T-cell receptor excision circles quantification using neonatal guthrie cards.

Morinishi Y, Imai K, Nakagawa N, Sato H, Horiuchi K, Ohtsuka Y, Kaneda Y, Taga T, Hisakawa H, Miyaji R, Endo M, Oh-Ishi T, Kamachi Y, Akahane K, Kobayashi C, Tsuchida M, Morio T, Sasahara Y, Kumaki S, Ishigaki K, Yoshida M, Urabe T, Kobayashi N, Okimoto Y, Reichenbach J, Hashii Y, Tsuji Y, Kogawa K, Yamaguchi S, Kanegane H, Miyawaki T, Yamada M, Ariga T, Nonoyama S. Morinishi Y, et al. Among authors: ariga t. J Pediatr. 2009 Dec;155(6):829-33. doi: 10.1016/j.jpeds.2009.05.026. Epub 2009 Jul 22. J Pediatr. 2009. PMID: 19628217 Clinical Trial.

6

X-linked agammaglobulinemia in a 10-year-old boy with a novel non-invariant splice-site mutation in Btk gene.

Maekawa K, Yamada M, Okura Y, Sato Y, Yamada Y, Kawamura N, Ariga T. Maekawa K, et al. Among authors: ariga t. Blood Cells Mol Dis. 2010 Apr 15;44(4):300-4. doi: 10.1016/j.bcmd.2010.01.004. Epub 2010 Feb 1. Blood Cells Mol Dis. 2010. PMID: 20122858

7

Determination of the deletion breakpoints in two patients with contiguous gene syndrome encompassing CYBB gene.

Yamada M, Arai T, Oishi T, Hatano N, Kobayashi I, Kubota M, Suzuki N, Yoda M, Kawamura N, Ariga T. Yamada M, et al. Among authors: ariga t. Eur J Med Genet. 2010 Nov-Dec;53(6):383-8. doi: 10.1016/j.ejmg.2010.08.003. Epub 2010 Sep 21. Eur J Med Genet. 2010. PMID: 20813210

8

Anti-melanoma differentiation-associated gene 5 antibody is a diagnostic and predictive marker for interstitial lung diseases associated with juvenile dermatomyositis.

Kobayashi I, Okura Y, Yamada M, Kawamura N, Kuwana M, Ariga T. Kobayashi I, et al. Among authors: ariga t. J Pediatr. 2011 Apr;158(4):675-7. doi: 10.1016/j.jpeds.2010.11.033. Epub 2011 Jan 13. J Pediatr. 2011. PMID: 21232756

9

Defective IL-10 signaling in hyper-IgE syndrome results in impaired generation of tolerogenic dendritic cells and induced regulatory T cells.

Saito M, Nagasawa M, Takada H, Hara T, Tsuchiya S, Agematsu K, Yamada M, Kawamura N, Ariga T, Tsuge I, Nonoyama S, Karasuyama H, Minegishi Y. Saito M, et al. Among authors: ariga t. J Exp Med. 2011 Feb 14;208(2):235-49. doi: 10.1084/jem.20100799. Epub 2011 Feb 7. J Exp Med. 2011. PMID: 21300911 Free PMC article.

10

Novel compound heterozygous mutations in the C3 gene: hereditary C3 deficiency.

Okura Y, Yamada M, Takezaki S, Nawate M, Takahashi Y, Kida M, Kawamura N, Ariga T. Okura Y, et al. Among authors: ariga t. Pediatr Int. 2011 Apr;53(2):e16-9. doi: 10.1111/j.1442-200X.2010.03259.x. Pediatr Int. 2011. PMID: 21501302 No abstract available.

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