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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: numata o. 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: numata o. Pediatr Int. 1999 Jun;41(3):285-91. doi: 10.1046/j.1442-200x.1999.01071.x. Pediatr Int. 1999. PMID: 10365580
Infant case with a malignant form of Brugada syndrome.
Suzuki H, Torigoe K, Numata O, Yazaki S. Suzuki H, et al. Among authors: numata o. J Cardiovasc Electrophysiol. 2000 Nov;11(11):1277-80. doi: 10.1046/j.1540-8167.2000.01277.x. J Cardiovasc Electrophysiol. 2000. PMID: 11083249
Effect of weight loss on body fat distribution in obese children.
Torigoe K, Numata O, Matsunaga M, Tanaka Y, Imai C, Yamazaki H. Torigoe K, et al. Among authors: numata o. Acta Paediatr Jpn. 1997 Feb;39(1):28-33. doi: 10.1111/j.1442-200x.1997.tb03551.x. Acta Paediatr Jpn. 1997. PMID: 9124049
Mitochondrial trifunctional protein deficiency in a lethal neonate.
Yamazaki H, Torigoe K, Numata O, Haniu H, Uchiyama A, Ogawa Y, Kaneko U, Imamura M, Hasegawa S. Yamazaki H, et al. Among authors: numata o. Pediatr Int. 2004 Apr;46(2):178-80. doi: 10.1046/j.1442-200x.2004.01861.x. Pediatr Int. 2004. PMID: 15056246 No abstract available.
120 results