Noriaki Harada - Search Results

Year	Number of Results
2002	3
2003	1
2004	6
2005	5
2006	2
2007	4
2008	1
2009	1
2010	2
2011	3
2012	1
2014	2
2015	3
2016	1
2017	2
2018	3
2019	1
2020	4
2021	1
2022	2
2024	0

1

Novel COL2A1 variants in Japanese patients with spondyloepiphyseal dysplasia congenita.

Akahira-Azuma M, Enomoto Y, Nakamura N, Yokoi T, Minatogawa M, Harada N, Tsurusaki Y, Kurosawa K. Akahira-Azuma M, et al. Among authors: harada n. Hum Genome Var. 2022 May 17;9(1):16. doi: 10.1038/s41439-022-00193-x. Hum Genome Var. 2022. PMID: 35581182 Free PMC article.

2

Divergent variant patterns among 19 patients with Rubinstein-Taybi syndrome uncovered by comprehensive genetic analysis including whole genome sequencing.

Enomoto Y, Yokoi T, Tsurusaki Y, Murakami H, Tominaga M, Minatogawa M, Abe-Hatano C, Kuroda Y, Ohashi I, Ida K, Shiiya S, Kumaki T, Naruto T, Mitsui J, Harada N, Kido Y, Kurosawa K. Enomoto Y, et al. Among authors: harada n. Clin Genet. 2022 Mar;101(3):335-345. doi: 10.1111/cge.14103. Epub 2022 Jan 4. Clin Genet. 2022. PMID: 34958122

3

A novel method for isolating lymphatic endothelial cells from lymphatic malformations and detecting PIK3CA somatic mutation in these isolated cells.

Usui H, Tsurusaki Y, Shimbo H, Saitsu H, Harada N, Kitagawa N, Mochizuki K, Masuda M, Kurosawa K, Shinkai M. Usui H, et al. Among authors: harada n. Surg Today. 2021 Mar;51(3):439-446. doi: 10.1007/s00595-020-02122-3. Epub 2020 Sep 2. Surg Today. 2021. PMID: 32876734

4

Update of the genotype and phenotype of KMT2D and KDM6A by genetic screening of 100 patients with clinically suspected Kabuki syndrome.

Murakami H, Tsurusaki Y, Enomoto K, Kuroda Y, Yokoi T, Furuya N, Yoshihashi H, Minatogawa M, Abe-Hatano C, Ohashi I, Nishimura N, Kumaki T, Enomoto Y, Naruto T, Iwasaki F, Harada N, Ishikawa A, Kawame H, Sameshima K, Yamaguchi Y, Kobayashi M, Tominaga M, Ishikiriyama S, Tanaka T, Suzumura H, Ninomiya S, Kondo A, Kaname T, Kosaki K, Masuno M, Kuroki Y, Kurosawa K. Murakami H, et al. Among authors: harada n. Am J Med Genet A. 2020 Oct;182(10):2333-2344. doi: 10.1002/ajmg.a.61793. Epub 2020 Aug 17. Am J Med Genet A. 2020. PMID: 32803813

5

Acute Effects of Whole-Body Vibration on Peripheral Blood Flow, Vibrotactile Perception and Balance in Older Adults.

Mahbub MH, Hase R, Yamaguchi N, Hiroshige K, Harada N, Bhuiyan ANH, Tanabe T. Mahbub MH, et al. Among authors: harada n. Int J Environ Res Public Health. 2020 Feb 7;17(3):1069. doi: 10.3390/ijerph17031069. Int J Environ Res Public Health. 2020. PMID: 32046205 Free PMC article. Clinical Trial.

6

An efficient genetic test flow for multiple congenital anomalies and intellectual disability.

Yokoi T, Enomoto Y, Tsurusaki Y, Harada N, Saito T, Nagai JI, Naruto T, Kurosawa K. Yokoi T, et al. Among authors: harada n. Pediatr Int. 2020 May;62(5):556-561. doi: 10.1111/ped.14159. Pediatr Int. 2020. PMID: 31955471

7

A systematic review of studies investigating the effects of controlled whole-body vibration intervention on peripheral circulation.

Mahbub MH, Hiroshige K, Yamaguchi N, Hase R, Harada N, Tanabe T. Mahbub MH, et al. Among authors: harada n. Clin Physiol Funct Imaging. 2019 Nov;39(6):363-377. doi: 10.1111/cpf.12589. Epub 2019 Jul 29. Clin Physiol Funct Imaging. 2019. PMID: 31278826

8

Novel SYNGAP1 variant in a patient with intellectual disability and distinctive dysmorphisms.

Kimura Y, Akahira-Azuma M, Harada N, Enomoto Y, Tsurusaki Y, Kurosawa K. Kimura Y, et al. Among authors: harada n. Congenit Anom (Kyoto). 2018 Nov;58(6):188-190. doi: 10.1111/cga.12273. Epub 2018 Feb 13. Congenit Anom (Kyoto). 2018. PMID: 29381230 Review.

9

Clinical Evaluation of the Immunochromatographic System Using Silver Amplification for the Rapid Detection of Mycoplasma pneumoniae.

Namkoong H, Yamazaki M, Ishizaki M, Endo I, Harada N, Aramaki M, Tanaka Y, Kaburagi S, Ichikawa M, Ohata T, Sakaguchi S, Saito F, Nakao A, Yuki H, Mitamura K. Namkoong H, et al. Among authors: harada n. Sci Rep. 2018 Jan 23;8(1):1430. doi: 10.1038/s41598-018-19734-y. Sci Rep. 2018. PMID: 29362380 Free PMC article.

10

Novel AMER1 frameshift mutation in a girl with osteopathia striata with cranial sclerosis.

Enomoto Y, Tsurusaki Y, Harada N, Aida N, Kurosawa K. Enomoto Y, et al. Among authors: harada n. Congenit Anom (Kyoto). 2018 Jul;58(4):145-146. doi: 10.1111/cga.12258. Epub 2017 Nov 16. Congenit Anom (Kyoto). 2018. PMID: 28990699 No abstract available.

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