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Page 1
Cover Image, Volume 176A, Number 1, January 2018.
Ikenoue S, Miyakoshi K, Ishii T, Sato Y, Otani T, Akiba Y, Kasuga Y, Ochiai D, Matsumoto T, Ichihashi Y, Matsuzaki Y, Tachikawa K, Michigami T, Nishimura G, Ikeda K, Hasegawa T, Tanaka M. Ikenoue S, et al. Among authors: matsuzaki y. Am J Med Genet A. 2018 Jan;176(1):i. doi: 10.1002/ajmg.a.38585. Am J Med Genet A. 2018. PMID: 29232060
Discordant fetal phenotype of hypophosphatasia in two siblings.
Ikenoue S, Miyakoshi K, Ishii T, Sato Y, Otani T, Akiba Y, Kasuga Y, Ochiai D, Matsumoto T, Ichihashi Y, Matsuzaki Y, Tachikawa K, Michigami T, Nishimura G, Ikeda K, Hasegawa T, Tanaka M. Ikenoue S, et al. Among authors: matsuzaki y. Am J Med Genet A. 2018 Jan;176(1):171-174. doi: 10.1002/ajmg.a.38531. Epub 2017 Nov 21. Am J Med Genet A. 2018. PMID: 29160033
Local reactions after BCG vaccination in Japan.
Ikeda K, Matsuzaki Y. Ikeda K, et al. Among authors: matsuzaki y. Pediatr Neonatol. 2021 Jan;62(1):115-116. doi: 10.1016/j.pedneo.2020.10.011. Epub 2020 Nov 3. Pediatr Neonatol. 2021. PMID: 33191135 Free article. No abstract available.
Tubular dysfunction in extremely low birth weight survivors.
Matsumura K, Matsuzaki Y, Hida M, Ikeda K, Awazu M. Matsumura K, et al. Among authors: matsuzaki y. Clin Exp Nephrol. 2019 Mar;23(3):395-401. doi: 10.1007/s10157-018-1645-4. Epub 2018 Sep 20. Clin Exp Nephrol. 2019. PMID: 30238383
[No title available]
[No authors listed] [No authors listed] PMID: 33349628
A neonatal case of HDR syndrome and a vascular ring with a novel GATA3 mutation.
Kusakawa M, Sato T, Hosoda A, Araki E, Matsuzaki Y, Yamashita Y, Ishihara J, Inagaki Y, Uchida N, Ishii T, Hasegawa T. Kusakawa M, et al. Among authors: matsuzaki y. Hum Genome Var. 2019 Dec 23;6:55. doi: 10.1038/s41439-019-0087-1. eCollection 2019. Hum Genome Var. 2019. PMID: 31885872 Free PMC article.
1,022 results