Hayashidani M - Search Results

Year	Number of Results
1983	1
1997	1
2005	1
2010	3
2011	1
2013	1
2014	1
2017	1
2025	0

1

Segmental and full paternal isodisomy for chromosome 14 in three patients: narrowing the critical region and implication for the clinical features.

Kagami M, Nishimura G, Okuyama T, Hayashidani M, Takeuchi T, Tanaka S, Ishino F, Kurosawa K, Ogata T. Kagami M, et al. Among authors: hayashidani m. Am J Med Genet A. 2005 Oct 1;138A(2):127-32. doi: 10.1002/ajmg.a.30941. Am J Med Genet A. 2005. PMID: 16152632 Review.

2

Aortic aneurysm and craniosynostosis in a family with Cantu syndrome.

Hiraki Y, Miyatake S, Hayashidani M, Nishimura Y, Matsuura H, Kamada M, Kawagoe T, Yunoki K, Okamoto N, Yofune H, Nakashima M, Tsurusaki Y, Satisu H, Murakami A, Miyake N, Nishimura G, Matsumoto N. Hiraki Y, et al. Among authors: hayashidani m. Am J Med Genet A. 2014 Jan;164A(1):231-6. doi: 10.1002/ajmg.a.36228. Epub 2013 Nov 25. Am J Med Genet A. 2014. PMID: 24352916

3

Zebrafish gene knockdowns imply roles for human YWHAG in infantile spasms and cardiomegaly.

Komoike Y, Fujii K, Nishimura A, Hiraki Y, Hayashidani M, Shimojima K, Nishizawa T, Higashi K, Yasukawa K, Saitsu H, Miyake N, Mizuguchi T, Matsumoto N, Osawa M, Kohno Y, Higashinakagawa T, Yamamoto T. Komoike Y, et al. Among authors: hayashidani m. Genesis. 2010 Apr;48(4):233-43. doi: 10.1002/dvg.20607. Genesis. 2010. PMID: 20146355

4

Palivizumab Prophylaxis in Preterm Infants and Subsequent Recurrent Wheezing. Six-Year Follow-up Study.

Mochizuki H, Kusuda S, Okada K, Yoshihara S, Furuya H, Simões EAF; Scientific Committee for Elucidation of Infantile Asthma. Mochizuki H, et al. Am J Respir Crit Care Med. 2017 Jul 1;196(1):29-38. doi: 10.1164/rccm.201609-1812OC. Am J Respir Crit Care Med. 2017. PMID: 28152315

5

Clinical characteristics of perinatal lethal hypophosphatasia: a report of 6 cases.

Nakamura-Utsunomiya A, Okada S, Hara K, Miyagawa S, Takeda K, Fukuhara R, Nakata Y, Hayashidani M, Tachikawa K, Michigami T, Ozono K, Kobayashi M. Nakamura-Utsunomiya A, et al. Among authors: hayashidani m. Clin Pediatr Endocrinol. 2010 Jan;19(1):7-13. doi: 10.1297/cpe.19.7. Epub 2010 Mar 11. Clin Pediatr Endocrinol. 2010. PMID: 23926372 Free PMC article.

6

A de novo deletion of 20q11.2-q12 in a boy presenting with abnormal hands and feet, retinal dysplasia, and intractable feeding difficulty.

Hiraki Y, Nishimura A, Hayashidani M, Terada Y, Nishimura G, Okamoto N, Nishina S, Tsurusaki Y, Doi H, Saitsu H, Miyake N, Matsumoto N. Hiraki Y, et al. Among authors: hayashidani m. Am J Med Genet A. 2011 Feb;155A(2):409-14. doi: 10.1002/ajmg.a.33818. Epub 2011 Jan 13. Am J Med Genet A. 2011. PMID: 21271663

7

A case of 21q-syndrome with half normal SOD-1 activity.

Yoshimitsu K, Hatano S, Kobayashi Y, Takeoka Y, Hayashidani M, Ueda K, Nomura K, Ohama K, Usui T. Yoshimitsu K, et al. Among authors: hayashidani m. Hum Genet. 1983;64(2):200-2. doi: 10.1007/BF00327128. Hum Genet. 1983. PMID: 6885062

8

Significance of immature platelet fraction and CD41-positive cells at birth in early onset neonatal thrombocytopenia.

Kihara H, Ohno N, Karakawa S, Mizoguchi Y, Fukuhara R, Hayashidani M, Nomura S, Nakamura K, Kobayashi M. Kihara H, et al. Among authors: hayashidani m. Int J Hematol. 2010 Mar;91(2):245-51. doi: 10.1007/s12185-009-0482-3. Int J Hematol. 2010. PMID: 20082160

9

Severe lactic acidosis and neonatal death in Pearson syndrome.

Muraki K, Goto Y, Nishino I, Hayashidani M, Takeuchi S, Horai S, Sakura N, Ueda K. Muraki K, et al. Among authors: hayashidani m. J Inherit Metab Dis. 1997 Mar;20(1):43-8. doi: 10.1023/a:1005305422544. J Inherit Metab Dis. 1997. PMID: 9061566

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