Shimojima K[au] - Search Results

Year	Number of Results
1979	1
1996	1
1998	1
2002	1
2004	1
2008	3
2009	13
2010	12
2011	15
2012	16
2013	19
2014	17
2015	18
2016	17
2017	19
2018	4
2019	2
2020	1
2022	0

1

A de novo microdeletion involving PAFAH1B (LIS1) related to lissencephaly phenotype.

Shimojima K, Okumura A, Yamamoto T. Shimojima K, et al. Data Brief. 2015 Jul 23;4:488-91. doi: 10.1016/j.dib.2015.07.017. eCollection 2015 Sep. Data Brief. 2015. PMID: 26958590 Free PMC article.

2

Pelizaeus-Merzbacher disease as a chromosomal disorder.

Yamamoto T, Shimojima K. Yamamoto T, et al. Among authors: shimojima k. Congenit Anom (Kyoto). 2013 Mar;53(1):3-8. doi: 10.1111/cga.12005. Congenit Anom (Kyoto). 2013. PMID: 23480352 Review.

3

Clinical impacts of genomic copy number gains at Xq28.

Yamamoto T, Shimojima K, Shimada S, Yokochi K, Yoshitomi S, Yanagihara K, Imai K, Okamoto N. Yamamoto T, et al. Among authors: shimojima k. Hum Genome Var. 2014 Jul 24;1:14001. doi: 10.1038/hgv.2014.1. eCollection 2014. Hum Genome Var. 2014. PMID: 27081496 Free PMC article. Review.

4

Infantile spasms related to a 5q31.2-q31.3 microdeletion including PURA.

Shimojima K, Okamoto N, Ohmura K, Nagase H, Yamamoto T. Shimojima K, et al. Hum Genome Var. 2018 Mar 29;5:18007. doi: 10.1038/hgv.2018.7. eCollection 2018. Hum Genome Var. 2018. PMID: 29619234 Free PMC article.

5

Neurological manifestations of 2q31 microdeletion syndrome.

Okamoto N, Kimura S, Shimojima K, Yamamoto T. Okamoto N, et al. Among authors: shimojima k. Congenit Anom (Kyoto). 2017 Nov;57(6):197-200. doi: 10.1111/cga.12212. Epub 2017 Mar 24. Congenit Anom (Kyoto). 2017. PMID: 28145600

6

Characteristics of 2p15-p16.1 microdeletion syndrome: Review and description of two additional patients.

Shimojima K, Okamoto N, Yamamoto T. Shimojima K, et al. Congenit Anom (Kyoto). 2015 Aug;55(3):125-32. doi: 10.1111/cga.12112. Congenit Anom (Kyoto). 2015. PMID: 25900130 Review.

7

Application of array-based comparative genome hybridization in children with developmental delay or mental retardation.

Liang JS, Shimojima K, Yamamoto T. Liang JS, et al. Among authors: shimojima k. Pediatr Neonatol. 2008 Dec;49(6):213-7. doi: 10.1016/S1875-9572(09)60013-9. Pediatr Neonatol. 2008. PMID: 19166117 Free article. Review.

8

Somatic mosaic deletions involving SCN1A cause Dravet syndrome.

Nakayama T, Ishii A, Yoshida T, Nasu H, Shimojima K, Yamamoto T, Kure S, Hirose S. Nakayama T, et al. Among authors: shimojima k. Am J Med Genet A. 2018 Mar;176(3):657-662. doi: 10.1002/ajmg.a.38596. Epub 2018 Jan 17. Am J Med Genet A. 2018. PMID: 29341473

9

Tatton-Brown-Rahman syndrome due to 2p23 microdeletion.

Okamoto N, Toribe Y, Shimojima K, Yamamoto T. Okamoto N, et al. Among authors: shimojima k. Am J Med Genet A. 2016 May;170A(5):1339-42. doi: 10.1002/ajmg.a.37588. Epub 2016 Feb 11. Am J Med Genet A. 2016. PMID: 26866722

10

Effect of salivary secretion with mouthguard use on seasonal allergic rhinitis symptom improvement.

Tani-Ishii N, Muromachi K, Mutoh N, Suzuki J, Shimojima K, Fujimaki R, Kezuka H, Koba T, Ta K. Tani-Ishii N, et al. Among authors: shimojima k. J Oral Biosci. 2020 Jun;62(2):205-211. doi: 10.1016/j.job.2020.04.003. Epub 2020 May 11. J Oral Biosci. 2020. PMID: 32407887

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

Search Page

Search Results