Maeda J - Search Results

1

Kosaki K, Bird LM, Maeda J, Higuchi M, Jones MC, Matsumoto M. Kosaki K, et al. Among authors: maeda j. Am J Med Genet A. 2004 Jun 15;127A(3):310-2. doi: 10.1002/ajmg.a.30022. Am J Med Genet A. 2004. PMID: 15150786

2

Bronchomalacia associated with pulmonary atresia, ventricular septal defect and major aortopulmonary collateral arteries, and chromosome 22q11.2 deletion.

Yamagishi H, Maeda J, Higuchi M, Katada Y, Yamagishi C, Matsuo N, Kojima Y. Yamagishi H, et al. Among authors: maeda j. Clin Genet. 2002 Sep;62(3):214-9. doi: 10.1034/j.1399-0004.2002.620305.x. Clin Genet. 2002. PMID: 12220436

3

Genitourinary anomaly in congenital varicella syndrome: case report and review.

Fujita H, Yoshii A, Maeda J, Kosaki K, Shishido S, Nakai H, Awazu M. Fujita H, et al. Among authors: maeda j. Pediatr Nephrol. 2004 May;19(5):554-7. doi: 10.1007/s00467-004-1420-5. Epub 2004 Mar 10. Pediatr Nephrol. 2004. PMID: 15015072

4

Mechanisms underlying early development of pulmonary vascular obstructive disease in Down syndrome: An imbalance in biosynthesis of thromboxane A2 and prostacyclin.

Fukushima H, Kosaki K, Sato R, Yagihashi T, Gatayama R, Kodo K, Hayashi T, Nakazawa M, Tsuchihashi T, Maeda J, Kojima Y, Yamagishi H, Takahashi T. Fukushima H, et al. Among authors: maeda j. Am J Med Genet A. 2010 Aug;152A(8):1919-24. doi: 10.1002/ajmg.a.33555. Am J Med Genet A. 2010. PMID: 20583254

5

Severe obstructive sleep apnea in Loeys-Dietz syndrome successfully treated using continuous positive airway pressure.

Takenouchi T, Saito H, Maruoka R, Oishi N, Torii C, Maeda J, Takahashi T, Kosaki K. Takenouchi T, et al. Among authors: maeda j. Am J Med Genet A. 2013 Jul;161A(7):1733-6. doi: 10.1002/ajmg.a.35953. Epub 2013 May 17. Am J Med Genet A. 2013. PMID: 23686861

6

Variable severity of cardiovascular phenotypes in patients with an early-onset form of Marfan syndrome harboring FBN1 mutations in exons 24-32.

Maeda J, Kosaki K, Shiono J, Kouno K, Aeba R, Yamagishi H. Maeda J, et al. Heart Vessels. 2016 Oct;31(10):1717-23. doi: 10.1007/s00380-016-0793-2. Epub 2016 Jan 21. Heart Vessels. 2016. PMID: 26796135 Review.

7

Successful Total Pericardiectomy for Constrictive Pericarditis in the First Series of Japanese Patients With Mulibrey Nanism.

Yasuhara J, Omori S, Maeda J, Nakagawa N, Kamada M, Kosaki K, Aeba R, Yamagishi H. Yasuhara J, et al. Among authors: maeda j. Can J Cardiol. 2018 May;34(5):690.e5-690.e8. doi: 10.1016/j.cjca.2018.02.008. Epub 2018 Feb 13. Can J Cardiol. 2018. PMID: 29731032

8

Phenotypic discordance in monozygotic twins with 22q11.2 deletion.

Yamagishi H, Ishii C, Maeda J, Kojima Y, Matsuoka R, Kimura M, Takao A, Momma K, Matsuo N. Yamagishi H, et al. Among authors: maeda j. Am J Med Genet. 1998 Jul 24;78(4):319-21. Am J Med Genet. 1998. PMID: 9714432

9

Frequent association of 22q11.2 deletion with tetralogy of Fallot.

Maeda J, Yamagishi H, Matsuoka R, Ishihara J, Tokumura M, Fukushima H, Ueda H, Takahashi E, Yoshiba S, Kojima Y. Maeda J, et al. Am J Med Genet. 2000 Jun 5;92(4):269-72. doi: 10.1002/(sici)1096-8628(20000605)92:4<269::aid-ajmg9>3.0.co;2-l. Am J Med Genet. 2000. PMID: 10842294

10

Ventricular septal defect associated with microdeletions of chromosome 22q11.2.

Yamagishi H, Maeda J, Tokumura M, Yoshiba S, Takahashi E, Fukushima H, Yamagishi C, Matsuo N, Kojima Y. Yamagishi H, et al. Among authors: maeda j. Clin Genet. 2000 Dec;58(6):493-6. doi: 10.1034/j.1399-0004.2000.580612.x. Clin Genet. 2000. PMID: 11149621

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