Fujita D - Search Results

1

Peripartum type B aortic dissection in patients with Marfan syndrome who underwent aortic root replacement: a case series study.

Sayama S, Takeda N, Iriyama T, Inuzuka R, Maemura S, Fujita D, Yamauchi H, Nawata K, Bougaki M, Hyodo H, Shitara R, Nakayama T, Komatsu A, Nagamatsu T, Osuga Y, Fujii T. Sayama S, et al. Among authors: fujita d. BJOG. 2018 Mar;125(4):487-493. doi: 10.1111/1471-0528.14635. Epub 2017 May 2. BJOG. 2018. PMID: 28294527

2

Pathophysiology and Japanese clinical characteristics in Marfan syndrome.

Fujita D, Takeda N, Imai Y, Inuzuka R, Komuro I, Hirata Y. Fujita D, et al. Pediatr Int. 2014 Aug;56(4):484-91. doi: 10.1111/ped.12423. Pediatr Int. 2014. PMID: 24931486 Review.

3

Authors' reply re: Peripartum type B aortic dissection in patients with Marfan syndrome who underwent aortic root replacement: a case series study.

Sayama S, Takeda N, Iriyama T, Inuzuka R, Maemura S, Fujita D, Yamauchi H, Nawata K, Bougaki M, Hyodo H, Shitara R, Nakayama T, Komatsu A, Nagamatsu T, Osuga Y, Fujii T. Sayama S, et al. Among authors: fujita d. BJOG. 2018 Mar;125(4):502-503. doi: 10.1111/1471-0528.14778. Epub 2017 Aug 10. BJOG. 2018. PMID: 28799184 No abstract available.

4

Pathophysiology and Management of Cardiovascular Manifestations in Marfan and Loeys-Dietz Syndromes.

Takeda N, Yagi H, Hara H, Fujiwara T, Fujita D, Nawata K, Inuzuka R, Taniguchi Y, Harada M, Toko H, Akazawa H, Komuro I. Takeda N, et al. Among authors: fujita d. Int Heart J. 2016 May 25;57(3):271-7. doi: 10.1536/ihj.16-094. Epub 2016 May 13. Int Heart J. 2016. PMID: 27181042 Free article. Review.

5

Impact of Pathogenic FBN1 Variant Types on the Progression of Aortic Disease in Patients With Marfan Syndrome.

Takeda N, Inuzuka R, Maemura S, Morita H, Nawata K, Fujita D, Taniguchi Y, Yamauchi H, Yagi H, Kato M, Nishimura H, Hirata Y, Ikeda Y, Kumagai H, Amiya E, Hara H, Fujiwara T, Akazawa H, Suzuki JI, Imai Y, Nagai R, Takamoto S, Hirata Y, Ono M, Komuro I. Takeda N, et al. Among authors: fujita d. Circ Genom Precis Med. 2018 Jun;11(6):e002058. doi: 10.1161/CIRCGEN.117.002058. Circ Genom Precis Med. 2018. PMID: 29848614

6

A deletion mutation in myosin heavy chain 11 causing familial thoracic aortic dissection in two Japanese pedigrees.

Imai Y, Morita H, Takeda N, Miya F, Hyodo H, Fujita D, Tajima T, Tsunoda T, Nagai R, Kubo M, Komuro I. Imai Y, et al. Among authors: fujita d. Int J Cardiol. 2015 Sep 15;195:290-2. doi: 10.1016/j.ijcard.2015.05.178. Epub 2015 Jun 3. Int J Cardiol. 2015. PMID: 26056961 No abstract available.

7

A novel mutation of TGFBR2 causing Loeys-Dietz syndrome complicated with pregnancy-related fatal cervical arterial dissections.

Fujita D, Takeda N, Morita H, Kato M, Nishimura H, Inuzuka R, Taniguchi Y, Nawata K, Hyodo H, Imai Y, Hirata Y, Komuro I. Fujita D, et al. Int J Cardiol. 2015 Dec 15;201:288-90. doi: 10.1016/j.ijcard.2015.07.109. Epub 2015 Aug 8. Int J Cardiol. 2015. PMID: 26301661 No abstract available.

8

A deleterious MYH11 mutation causing familial thoracic aortic dissection.

Takeda N, Morita H, Fujita D, Inuzuka R, Taniguchi Y, Nawata K, Komuro I. Takeda N, et al. Among authors: fujita d. Hum Genome Var. 2015 Aug 6;2:15028. doi: 10.1038/hgv.2015.28. eCollection 2015. Hum Genome Var. 2015. PMID: 27081537 Free PMC article.

9

Impairment of flow-mediated dilation correlates with aortic dilation in patients with Marfan syndrome.

Takata M, Amiya E, Watanabe M, Omori K, Imai Y, Fujita D, Nishimura H, Kato M, Morota T, Nawata K, Ozeki A, Watanabe A, Kawarasaki S, Hosoya Y, Nakao T, Maemura K, Nagai R, Hirata Y, Komuro I. Takata M, et al. Among authors: fujita d. Heart Vessels. 2014 Jul;29(4):478-85. doi: 10.1007/s00380-013-0393-3. Epub 2013 Jul 14. Heart Vessels. 2014. PMID: 23852405

10

Congenital contractural arachnodactyly complicated with aortic dilatation and dissection: Case report and review of literature.

Takeda N, Morita H, Fujita D, Inuzuka R, Taniguchi Y, Imai Y, Hirata Y, Komuro I. Takeda N, et al. Among authors: fujita d. Am J Med Genet A. 2015 Oct;167A(10):2382-7. doi: 10.1002/ajmg.a.37162. Epub 2015 May 14. Am J Med Genet A. 2015. PMID: 25975422

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