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Recurrent p.N767S mutation in the ATP2A2 gene in a Japanese family with haemorrhagic Darier disease clinically mimicking epidermolysis bullosa simplex with mottled pigmentation.
Hamada T, Yasumoto S, Karashima T, Ishii N, Shimada H, Kawano Y, Imayama S, McGrath JA, Hashimoto T. Hamada T, et al. Among authors: kawano y. Br J Dermatol. 2007 Sep;157(3):605-8. doi: 10.1111/j.1365-2133.2007.08086.x. Epub 2007 Jul 16. Br J Dermatol. 2007. PMID: 17635506 No abstract available.
Apoptosis in perforated cornea of a patient with graft-versus-host disease.
Yoshida A, Kawano Y, Kato K, Yoshida S, Yoshikawa H, Muta T, Eto T, Gondo H, Shibuya T, Ishibashi T, Yamana T. Yoshida A, et al. Among authors: kawano y. Can J Ophthalmol. 2006 Aug;41(4):472-5. doi: 10.1016/s0008-4182(06)80010-4. Can J Ophthalmol. 2006. PMID: 16883364
p53AIP1 expression can be a prognostic marker in non-small cell lung cancer.
Yamashita SI, Masuda Y, Yoshida N, Matsuzaki H, Kurizaki T, Haga Y, Ikei S, Miyawaki M, Kawano Y, Chujyo M, Kawahara K. Yamashita SI, et al. Among authors: kawano y. Clin Oncol (R Coll Radiol). 2008 Mar;20(2):148-51. doi: 10.1016/j.clon.2007.08.006. Epub 2007 Sep 12. Clin Oncol (R Coll Radiol). 2008. PMID: 17851056
Infantile onset myasthenia gravis with MuSK antibodies.
Murai H, Noda T, Himeno E, Kawano Y, Ohyagi Y, Shiraishi H, Motomura M, Kira J. Murai H, et al. Among authors: kawano y. Neurology. 2006 Jul 11;67(1):174. doi: 10.1212/01.wnl.0000223835.51268.12. Neurology. 2006. PMID: 16832105 No abstract available.
2,368 results