Yamanaka M - Search Results

1

Paternal uniparental disomy 14 and related disorders: placental gene expression analyses and histological examinations.

Kagami M, Matsuoka K, Nagai T, Yamanaka M, Kurosawa K, Suzumori N, Sekita Y, Miyado M, Matsubara K, Fuke T, Kato F, Fukami M, Ogata T. Kagami M, et al. Among authors: yamanaka m. Epigenetics. 2012 Oct;7(10):1142-50. doi: 10.4161/epi.21937. Epub 2012 Aug 23. Epigenetics. 2012. PMID: 22917972 Free PMC article.

2

Prenatal findings of paternal uniparental disomy 14: report of four patients.

Yamanaka M, Ishikawa H, Saito K, Maruyama Y, Ozawa K, Shibasaki J, Nishimura G, Kurosawa K. Yamanaka M, et al. Am J Med Genet A. 2010 Mar;152A(3):789-91. doi: 10.1002/ajmg.a.33247. Am J Med Genet A. 2010. PMID: 20186803 No abstract available.

3

Paternal UPD14 is responsible for a distinctive malformation complex.

Kurosawa K, Sasaki H, Sato Y, Yamanaka M, Shimizu M, Ito Y, Okuyama T, Matsuo M, Imaizumi K, Kuroki Y, Nishimura G. Kurosawa K, et al. Among authors: yamanaka m. Am J Med Genet. 2002 Jul 1;110(3):268-72. doi: 10.1002/ajmg.10404. Am J Med Genet. 2002. PMID: 12116236

4

Sirenomelia with a de novo balanced translocation 46,X,t(X;16)(p11.23;p12.3).

Kurosawa K, Tanoshima-Takei M, Yamamoto T, Ishikawa H, Masuno M, Tanaka Y, Yamanaka M. Kurosawa K, et al. Among authors: yamanaka m. Congenit Anom (Kyoto). 2012 Jun;52(2):106-10. doi: 10.1111/j.1741-4520.2011.00326.x. Congenit Anom (Kyoto). 2012. PMID: 22639997

5

Hepatoblastoma in an infant with paternal uniparental disomy 14.

Horii M, Horiuchi H, Momoeda M, Nakagawa M, Hirata M, Kusakawa I, Yamanaka M. Horii M, et al. Among authors: yamanaka m. Congenit Anom (Kyoto). 2012 Dec;52(4):219-20. doi: 10.1111/j.1741-4520.2012.00364.x. Congenit Anom (Kyoto). 2012. PMID: 23181499

6

Origin and mechanisms of formation of fetus-in-fetu: two cases with genotype and methylation analyses.

Miura S, Miura K, Yamamoto T, Yamanaka M, Saito K, Hirabuki T, Kurosawa K, Harada N, Ishizaki-Yamasaki Y, Matsumoto N, Hirahara F, Yoshiura K, Masuzaki H, Niikawa N. Miura S, et al. Among authors: yamanaka m. Am J Med Genet A. 2006 Aug 15;140(16):1737-43. doi: 10.1002/ajmg.a.31362. Am J Med Genet A. 2006. PMID: 16835914

7

Fetal outcome of trisomy 18 diagnosed after 22 weeks of gestation: Experience of 123 cases at a single perinatal center.

Nagase H, Ishikawa H, Toyoshima K, Itani Y, Furuya N, Kurosawa K, Hirahara F, Yamanaka M. Nagase H, et al. Among authors: yamanaka m. Congenit Anom (Kyoto). 2016 Jan;56(1):35-40. doi: 10.1111/cga.12118. Congenit Anom (Kyoto). 2016. PMID: 26104883

8

A large interstitial deletion of 17p13.1p11.2 involving the Smith-Magenis chromosome region in a girl with multiple congenital anomalies.

Yamamoto T, Ueda H, Kawataki M, Yamanaka M, Asou T, Kondoh Y, Harada N, Matsumoto N, Kurosawa K. Yamamoto T, et al. Among authors: yamanaka m. Am J Med Genet A. 2006 Jan 1;140(1):88-91. doi: 10.1002/ajmg.a.31055. Am J Med Genet A. 2006. PMID: 16333830

9

Prenatal management of the fetus with lethal malformation: from a study of oligohydramnios sequence.

Nagase H, Ishikawa H, Nishikawa T, Kurosawa K, Itani Y, Yamanaka M. Nagase H, et al. Among authors: yamanaka m. Fetal Pediatr Pathol. 2011;30(3):145-9. doi: 10.3109/15513815.2010.547552. Epub 2011 Feb 28. Fetal Pediatr Pathol. 2011. PMID: 21355684

10

Congenital omphalocele and polyhydramnios: a study of 52 cases.

Ozawa K, Ishikawa H, Maruyama Y, Nagata T, Nagase H, Itani Y, Kurosawa K, Yamanaka M. Ozawa K, et al. Among authors: yamanaka m. Fetal Diagn Ther. 2011;30(3):184-8. doi: 10.1159/000327542. Epub 2011 Jun 25. Fetal Diagn Ther. 2011. PMID: 21709401

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