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Heterotopic pancreas in the esophagus diagnosed by EUS-guided FNA.
Goto J, Ohashi S, Okamura S, Urano F, Hosoi T, Ishikawa H, Segawa K, Hirooka Y, Ohmiya N, Itoh A, Hashimoto S, Niwa Y, Goto H. Goto J, et al. Among authors: goto h. Gastrointest Endosc. 2005 Nov;62(5):812-4. doi: 10.1016/j.gie.2005.04.031. Gastrointest Endosc. 2005. PMID: 16246709 No abstract available.
Evaluating Japanese patients with the Marfan syndrome using high-throughput microarray-based mutational analysis of fibrillin-1 gene.
Ogawa N, Imai Y, Takahashi Y, Nawata K, Hara K, Nishimura H, Kato M, Takeda N, Kohro T, Morita H, Taketani T, Morota T, Yamazaki T, Goto J, Tsuji S, Takamoto S, Nagai R, Hirata Y. Ogawa N, et al. Among authors: goto j. Am J Cardiol. 2011 Dec 15;108(12):1801-7. doi: 10.1016/j.amjcard.2011.07.053. Epub 2011 Sep 10. Am J Cardiol. 2011. PMID: 21907952
Total deletion and a missense mutation of ITPR1 in Japanese SCA15 families.
Hara K, Shiga A, Nozaki H, Mitsui J, Takahashi Y, Ishiguro H, Yomono H, Kurisaki H, Goto J, Ikeuchi T, Tsuji S, Nishizawa M, Onodera O. Hara K, et al. Among authors: goto j. Neurology. 2008 Aug 19;71(8):547-51. doi: 10.1212/01.wnl.0000311277.71046.a0. Epub 2008 Jun 25. Neurology. 2008. PMID: 18579805
Identification of novel SNPs of ABCD1, ABCD2, ABCD3, and ABCD4 genes in patients with X-linked adrenoleukodystrophy (ALD) based on comprehensive resequencing and association studies with ALD phenotypes.
Matsukawa T, Asheuer M, Takahashi Y, Goto J, Suzuki Y, Shimozawa N, Takano H, Onodera O, Nishizawa M, Aubourg P, Tsuji S. Matsukawa T, et al. Among authors: goto j. Neurogenetics. 2011 Feb;12(1):41-50. doi: 10.1007/s10048-010-0253-6. Epub 2010 Jul 27. Neurogenetics. 2011. PMID: 20661612 Free PMC article.
727 results