Taniguchi Y - Search Results

1

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: taniguchi y. 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

2

Congenital Contractural Arachnodactyly without FBN1 or FBN2 Gene Mutations Complicated by Dilated Cardiomyopathy.

Yagi H, Hatano M, Takeda N, Harada S, Suzuki Y, Taniguchi Y, Shintani Y, Morita H, Kanamori N, Aoyama T, Watanabe M, Manabe I, Akazawa H, Kinugawa K, Komuro I. Yagi H, et al. Among authors: taniguchi y. Intern Med. 2015;54(10):1237-41. doi: 10.2169/internalmedicine.54.4280. Epub 2015 May 15. Intern Med. 2015. PMID: 25986263 Free article.

3

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. Among authors: taniguchi y. 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.

4

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: taniguchi y. 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.

5

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: taniguchi y. 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.

6

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: taniguchi y. Circ Genom Precis Med. 2018 Jun;11(6):e002058. doi: 10.1161/CIRCGEN.117.002058. Circ Genom Precis Med. 2018. PMID: 29848614

7

Predictive Physical Manifestations for Progression of Scoliosis in Marfan Syndrome.

Taniguchi Y, Matsubayashi Y, Kato S, Doi T, Takeda N, Yagi H, Inuzuka R, Oshima Y, Tanaka S. Taniguchi Y, et al. Spine (Phila Pa 1976). 2021 Aug 1;46(15):1020-1025. doi: 10.1097/BRS.0000000000003939. Spine (Phila Pa 1976). 2021. PMID: 34228694

8

Clinical Impact of Copy Number Variation on the Genetic Diagnosis of Syndromic Aortopathies.

Takeda N, Inuzuka R, Yagi H, Morita H, Ando M, Yamauchi H, Taniguchi Y, Porto KJ, Kanaya T, Ishiura H, Mitsui J, Tsuji S, Toda T, Ono M, Komuro I. Takeda N, et al. Among authors: taniguchi y. Circ Genom Precis Med. 2021 Aug;14(4):e003458. doi: 10.1161/CIRCGEN.121.003458. Epub 2021 Jul 30. Circ Genom Precis Med. 2021. PMID: 34325513 No abstract available.

9

Impact of pathogenic FBN1 variant types on the development of severe scoliosis in patients with Marfan syndrome.

Taniguchi Y, Takeda N, Inuzuka R, Matsubayashi Y, Kato S, Doi T, Yagi H, Yamauchi H, Ando M, Oshima Y, Tanaka S. Taniguchi Y, et al. J Med Genet. 2023 Jan;60(1):74-80. doi: 10.1136/jmedgenet-2021-108186. Epub 2021 Dec 16. J Med Genet. 2023. PMID: 34916231 Free PMC article.

10

Family with congenital contractural arachnodactyly due to a novel multiexon deletion of the FBN2 gene.

Yagi H, Takiguchi H, Takeda N, Inuzuka R, Taniguchi Y, Porto KJ, Ishiura H, Mitsui J, Morita H, Komuro I. Yagi H, et al. Among authors: taniguchi y. Clin Case Rep. 2022 Feb 9;10(2):e05335. doi: 10.1002/ccr3.5335. eCollection 2022 Feb. Clin Case Rep. 2022. PMID: 35154713 Free PMC article.

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