Iijima K - Search Results

1

Clinical features in very early-onset demyelinating disease with anti-MOG antibody.

Nishiyama M, Nagase H, Matsumoto M, Tomioka K, Awano H, Tanaka T, Toyoshima D, Fujita K, Maruyama A, Oyazato Y, Saeki K, Shiraishi K, Takada S, Kaneko K, Takahashi T, Nakashima I, Iijima K. Nishiyama M, et al. Among authors: iijima k. Brain Dev. 2017 Oct;39(9):756-762. doi: 10.1016/j.braindev.2017.05.004. Epub 2017 May 24. Brain Dev. 2017. PMID: 28551039

2

Molecular analysis of TSC2/PKD1 contiguous gene deletion syndrome.

Oyazato Y, Iijima K, Emi M, Sekine T, Kamei K, Takanashi J, Nakao H, Namai Y, Nozu K, Matsuo M. Oyazato Y, et al. Among authors: iijima k. Kobe J Med Sci. 2011 Jun 9;57(1):E1-10. Kobe J Med Sci. 2011. PMID: 22169896 Free article.

3

A Japanese child with geleophysic dysplasia caused by a novel mutation of FBN1.

Lee T, Takeshima Y, Okizuka Y, Hamahira K, Kusunoki N, Awano H, Yagi M, Sakai N, Matsuo M, Iijima K. Lee T, et al. Among authors: iijima k. Gene. 2013 Jan 10;512(2):456-9. doi: 10.1016/j.gene.2012.10.060. Epub 2012 Nov 2. Gene. 2013. PMID: 23124041 Clinical Trial.

4

A prostaglandin D2 metabolite is elevated in the urine of Duchenne muscular dystrophy patients and increases further from 8 years old.

Nakagawa T, Takeuchi A, Kakiuchi R, Lee T, Yagi M, Awano H, Iijima K, Takeshima Y, Urade Y, Matsuo M. Nakagawa T, et al. Among authors: iijima k. Clin Chim Acta. 2013 Aug 23;423:10-4. doi: 10.1016/j.cca.2013.03.031. Epub 2013 Apr 19. Clin Chim Acta. 2013. PMID: 23603101

5

Childhood-onset hereditary pancreatitis with mutations in the CT gene and SPINK1 gene.

Awano H, Lee T, Yagi M, Masamune A, Kume K, Takeshima Y, Iijima K. Awano H, et al. Among authors: iijima k. Pediatr Int. 2013 Oct;55(5):646-9. doi: 10.1111/ped.12152. Pediatr Int. 2013. PMID: 24134754

6

Differences in carrier frequency between mothers of Duchenne and Becker muscular dystrophy patients.

Lee T, Takeshima Y, Kusunoki N, Awano H, Yagi M, Matsuo M, Iijima K. Lee T, et al. Among authors: iijima k. J Hum Genet. 2014 Jan;59(1):46-50. doi: 10.1038/jhg.2013.119. Epub 2013 Nov 14. J Hum Genet. 2014. PMID: 24225992 Free PMC article.

7

Genotype-phenotype correlations in alternating hemiplegia of childhood.

Sasaki M, Ishii A, Saito Y, Morisada N, Iijima K, Takada S, Araki A, Tanabe Y, Arai H, Yamashita S, Ohashi T, Oda Y, Ichiseki H, Hirabayashi S, Yasuhara A, Kawawaki H, Kimura S, Shimono M, Narumiya S, Suzuki M, Yoshida T, Oyazato Y, Tsuneishi S, Ozasa S, Yokochi K, Dejima S, Akiyama T, Kishi N, Kira R, Ikeda T, Oguni H, Zhang B, Tsuji S, Hirose S. Sasaki M, et al. Among authors: iijima k. Neurology. 2014 Feb 11;82(6):482-90. doi: 10.1212/WNL.0000000000000102. Epub 2014 Jan 15. Neurology. 2014. PMID: 24431296

8

Dried umbilical cord is a potential material for retrospective diagnosis of intrauterine enterovirus infection.

Morioka I, Matsumoto M, Miwa A, Yokota T, Matsuo K, Koda T, Nagasaka M, Shibata A, Fujita K, Yamane M, Yamada H, Enomoto M, Chikahira M, Iijima K. Morioka I, et al. Among authors: iijima k. J Matern Fetal Neonatal Med. 2014 Nov;27(17):1820-2. doi: 10.3109/14767058.2013.879701. Epub 2014 Feb 3. J Matern Fetal Neonatal Med. 2014. PMID: 24433096

9

[Clinical manifestations of three neonates with family histories of Menkes disease].

Yagi M, Kusunoki N, Lee T, Awano H, Morioka I, Kodama H, Takeshima Y, Iijima K. Yagi M, et al. Among authors: iijima k. No To Hattatsu. 2014 Jan;46(1):26-9. No To Hattatsu. 2014. PMID: 24620427 Japanese.

10

[Clinical manifestations of Menkes disease vary according to patient's genotype and the initiation time of treatment with copper-histidine injections].

Yagi M, Kusunoki N, Lee T, Awano H, Kodama H, Takeshima Y, Iijima K. Yagi M, et al. Among authors: iijima k. No To Hattatsu. 2014 May;46(3):227-8. No To Hattatsu. 2014. PMID: 24902345 Japanese. No abstract available.

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