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Perinatal hypophosphatasia caused by uniparental isodisomy.
Watanabe A, Satoh S, Fujita A, Naing BT, Orimo H, Shimada T. Watanabe A, et al. Among authors: fujita a. Bone. 2014 Mar;60:93-7. doi: 10.1016/j.bone.2013.12.009. Epub 2013 Dec 12. Bone. 2014. PMID: 24334170
Therapy-related Secondary Malignancy After Treatment of Childhood Malignancy: Cases from a Single Center.
Ueda T, Migita M, Itabashi T, Tanabe Y, Uchimura R, Gocho Y, Yamanishi M, Kobayashi F, Yoshino M, Fujita A, Yamanishi S, Kaizu K, Hayakawa J, Asano T, Maeda M, Itoh Y. Ueda T, et al. Among authors: fujita a. J Nippon Med Sch. 2019 Sep 3;86(4):207-214. doi: 10.1272/jnms.JNMS.2018_86-401. Epub 2019 Apr 26. J Nippon Med Sch. 2019. PMID: 31061250 Free article.
Recurrent de novo MAPK8IP3 variants cause neurological phenotypes.
Iwasawa S, Yanagi K, Kikuchi A, Kobayashi Y, Haginoya K, Matsumoto H, Kurosawa K, Ochiai M, Sakai Y, Fujita A, Miyake N, Niihori T, Shirota M, Funayama R, Nonoyama S, Ohga S, Kawame H, Nakayama K, Aoki Y, Matsumoto N, Kaname T, Matsubara Y, Shoji W, Kure S. Iwasawa S, et al. Among authors: fujita a. Ann Neurol. 2019 Jun;85(6):927-933. doi: 10.1002/ana.25481. Epub 2019 Apr 25. Ann Neurol. 2019. PMID: 30945334
1,440 results