Ichikawa K - Search Results

1

Phenotype of GABA-transaminase deficiency.

Koenig MK, Hodgeman R, Riviello JJ, Chung W, Bain J, Chiriboga CA, Ichikawa K, Osaka H, Tsuji M, Gibson KM, Bonnen PE, Pearl PL. Koenig MK, et al. Among authors: ichikawa k. Neurology. 2017 May 16;88(20):1919-1924. doi: 10.1212/WNL.0000000000003936. Epub 2017 Apr 14. Neurology. 2017. PMID: 28411234 Free PMC article. Review.

2

Serial Magnetic Resonance Imaging and ¹H-Magnetic Resonance Spectroscopy in GABA Transaminase Deficiency: A Case Report.

Ichikawa K, Tsuji M, Tsuyusaki Y, Tomiyasu M, Aida N, Goto T. Ichikawa K, et al. JIMD Rep. 2019;43:7-12. doi: 10.1007/8904_2018_95. Epub 2018 Feb 25. JIMD Rep. 2019. PMID: 29478219 Free PMC article.

3

Epilepsy in Christianson syndrome: Two cases of Lennox-Gastaut syndrome and a review of literature.

Ikeda A, Yamamoto A, Ichikawa K, Tsuyusaki Y, Tsuji M, Iai M, Enomoto Y, Murakami H, Kurosawa K, Miyatake S, Matsumoto N, Goto T. Ikeda A, et al. Among authors: ichikawa k. Epilepsy Behav Rep. 2019 Dec 5;13:100349. doi: 10.1016/j.ebr.2019.100349. eCollection 2020. Epilepsy Behav Rep. 2019. PMID: 31879735 Free PMC article.

4

Rasmussen syndrome combined with IgA deficiency and membranous nephropathy.

Ichikawa K, Takeshita S, Ito S, Nezu A. Ichikawa K, et al. Pediatr Neurol. 2009 Jun;40(6):468-70. doi: 10.1016/j.pediatrneurol.2008.12.008. Pediatr Neurol. 2009. PMID: 19433284

5

Cyclosporine for acute encephalopathy with biphasic seizures and late reduced diffusion.

Watanabe Y, Motoi H, Oyama Y, Ichikawa K, Takeshita S, Mori M, Nezu A, Yokota S. Watanabe Y, et al. Among authors: ichikawa k. Pediatr Int. 2014 Aug;56(4):577-82. doi: 10.1111/ped.12288. Epub 2014 May 28. Pediatr Int. 2014. PMID: 24418041

6

Seventeen-year long-term survival of a case of neonatal nonketotic hyperglycinemia.

Ichikawa K, Inami Y, Kaneko K. Ichikawa K, et al. Pediatr Int. 2020 Sep;62(9):1111-1113. doi: 10.1111/ped.14254. Epub 2020 Aug 5. Pediatr Int. 2020. PMID: 32754929 No abstract available.

7

Novel mutations in SH3TC2 in a young Japanese girl with Charcot-Marie-Tooth disease type 4C.

Ichikawa K, Numasawa K, Takeshita S, Hashiguchi A, Takashima H. Ichikawa K, et al. Pediatr Int. 2016 Nov;58(11):1252-1254. doi: 10.1111/ped.13152. Pediatr Int. 2016. PMID: 27882734

8

Late-onset Leigh syndrome with m.9176T>C mutation in the mitochondrial ATPase 6 gene.

Ichikawa K, Tsuyusaki Y, Shimbo H, Goto T. Ichikawa K, et al. Pediatr Int. 2019 Oct;61(10):1055-1056. doi: 10.1111/ped.13991. Epub 2019 Oct 18. Pediatr Int. 2019. PMID: 31625254 No abstract available.

9

Fulminant form of acute disseminated encephalomyelitis in a child treated with mild hypothermia.

Ichikawa K, Motoi H, Oyama Y, Watanabe Y, Takeshita S. Ichikawa K, et al. Pediatr Int. 2013 Dec;55(6):e149-51. doi: 10.1111/ped.12180. Pediatr Int. 2013. PMID: 24330300

10

Reply to the letter: "Is the variant m.9176T>C in MT-ATP6 truly responsibly for Leigh syndrome?".

Ichikawa K. Ichikawa K. Pediatr Int. 2021 Feb;63(2):240. doi: 10.1111/ped.14519. Pediatr Int. 2021. PMID: 33629425 No abstract available.

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