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Complete paternal uniparental isodisomy for chromosome 1 revealed by mutation analyses of the TRKA (NTRK1) gene encoding a receptor tyrosine kinase for nerve growth factor in a patient with congenital insensitivity to pain with anhidrosis.
Miura Y, Hiura M, Torigoe K, Numata O, Kuwahara A, Matsunaga M, Hasegawa S, Boku N, Ino H, Mardy S, Endo F, Matsuda I, Indo Y. Miura Y, et al. Among authors: ino h. Hum Genet. 2000 Sep;107(3):205-9. doi: 10.1007/s004390000369. Hum Genet. 2000. PMID: 11071380 Free article.
Contingent negative variation in children with anorexia nervosa.
Torigoe K, Numata O, Sato T, Imai C, Takeuchi K, Yamazaki H, Hotta H, Boku N, Yazaki S, Sudo S, Kuwabara A, Hasegawa S, Hiura M, Ino H. Torigoe K, et al. Among authors: ino h. Pediatr Int. 1999 Jun;41(3):285-91. doi: 10.1046/j.1442-200x.1999.01071.x. Pediatr Int. 1999. PMID: 10365580
Neurotological studies upon intoxication by organic mercury compounds.
Mizukoshi K, Nagaba M, Ohno Y, Ishikawa K, Aoyagi M, Watanabe Y, Kato I, Ino H. Mizukoshi K, et al. Among authors: ino h. ORL J Otorhinolaryngol Relat Spec. 1975;37(2):74-87. doi: 10.1159/000275209. ORL J Otorhinolaryngol Relat Spec. 1975. PMID: 1168884
Normal predictive function in smooth pursuit.
Ohashi N, Watanabe Y, Mizukoshi K, Ino H. Ohashi N, et al. Among authors: ino h. Adv Otorhinolaryngol. 1988;41:118-21. doi: 10.1159/000416043. Adv Otorhinolaryngol. 1988. PMID: 3213694 No abstract available.
Diagnostic value of DP phenomenon in the nystagmic reaction.
Koike Y, Mizukoshi K, Wada A, Haba A, Takahashi T, Takashima M, Ino H. Koike Y, et al. Among authors: ino h. Acta Otolaryngol. 1967 Aug;64(2):166-73. doi: 10.3109/00016486709139103. Acta Otolaryngol. 1967. PMID: 6055798 No abstract available.
306 results