Maruyama K - Search Results

1

Distinctive facies, macrocephaly, and developmental delay are signs of a PTEN mutation in childhood.

Kato K, Mizuno S, Inaba M, Fukumura S, Kurahashi N, Maruyama K, Ieda D, Ohashi K, Hori I, Negishi Y, Hattori A, Saitoh S. Kato K, et al. Among authors: maruyama k. Brain Dev. 2018 Sep;40(8):678-684. doi: 10.1016/j.braindev.2018.04.008. Epub 2018 May 8. Brain Dev. 2018. PMID: 29752200

2

Cardio-facio-cutaneous syndrome and moyamoya syndrome.

Ishiguro Y, Kubota T, Takenaka J, Maruyama K, Okumura A, Negoro T, Watanabe K. Ishiguro Y, et al. Among authors: maruyama k. Brain Dev. 2002 Jun;24(4):245-9. doi: 10.1016/s0387-7604(02)00014-1. Brain Dev. 2002. PMID: 12015168

3

Single photon emission computed tomography and serial MRI in preterm infants with kernicterus.

Okumura A, Hayakawa F, Maruyama K, Kubota T, Kato K, Watanabe K. Okumura A, et al. Among authors: maruyama k. Brain Dev. 2006 Jul;28(6):348-52. doi: 10.1016/j.braindev.2005.11.004. Epub 2006 Feb 14. Brain Dev. 2006. PMID: 16481141

4

Antiepileptic treatment against clustered seizures in benign partial epilepsy in infancy.

Okumura A, Kato T, Hayakawa F, Maruyama K, Kubota T, Natsume J, Negoro T, Watanabe K. Okumura A, et al. Among authors: maruyama k. Brain Dev. 2006 Oct;28(9):582-5. doi: 10.1016/j.braindev.2006.04.003. Epub 2006 May 30. Brain Dev. 2006. PMID: 16730937

5

Clinical and radiological features of Japanese patients with a severe phenotype due to CASK mutations.

Takanashi J, Okamoto N, Yamamoto Y, Hayashi S, Arai H, Takahashi Y, Maruyama K, Mizuno S, Shimakawa S, Ono H, Oyanagi R, Kubo S, Barkovich AJ, Inazawa J. Takanashi J, et al. Among authors: maruyama k. Am J Med Genet A. 2012 Dec;158A(12):3112-8. doi: 10.1002/ajmg.a.35640. Epub 2012 Nov 19. Am J Med Genet A. 2012. PMID: 23165780

6

Thalamic lesions in acute encephalopathy with biphasic seizures and late reduced diffusion.

Kurahashi N, Tsuji T, Kato T, Ogaya S, Umemura A, Yamada K, Kurahashi H, Maruyama K, Takeuchi T, Kubota T, Saitoh S, Natsume J, Okumura A. Kurahashi N, et al. Among authors: maruyama k. Pediatr Neurol. 2014 Nov;51(5):701-5. doi: 10.1016/j.pediatrneurol.2014.07.013. Epub 2014 Jul 16. Pediatr Neurol. 2014. PMID: 25193414

7

[Two pediatric cases of chronic progressive subdural hematoma with brain atrophy following acute encephalitis/encephalopathy requiring surgical hematoma removal].

Yamada K, Kurahashi H, Ogaya S, Kurahashi N, Umemura A, Kawamura Y, Kato M, Maruyama K, Nagasaka M. Yamada K, et al. Among authors: maruyama k. No To Hattatsu. 2016 Jan;48(1):49-51. No To Hattatsu. 2016. PMID: 27012112 Japanese. No abstract available.

8

The effects of co-medications on lamotrigine clearance in Japanese children with epilepsy.

Takeuchi T, Natsume J, Kidokoro H, Ishihara N, Yamamoto H, Azuma Y, Ito Y, Kurahashi N, Tsuji T, Suzuki M, Itomi K, Yamada K, Kurahashi H, Abe S, Okumura A, Maruyama K, Negoro T, Watanabe K, Kojima S. Takeuchi T, et al. Among authors: maruyama k. Brain Dev. 2016 Sep;38(8):723-30. doi: 10.1016/j.braindev.2016.03.004. Epub 2016 Mar 28. Brain Dev. 2016. PMID: 27033151

9

Arts syndrome with a novel missense mutation in the PRPS1 gene: A case report.

Maruyama K, Ogaya S, Kurahashi N, Umemura A, Yamada K, Hashiguchi A, Takashima H, Torres RJ, Aso K. Maruyama K, et al. Brain Dev. 2016 Nov;38(10):954-958. doi: 10.1016/j.braindev.2016.05.003. Epub 2016 May 30. Brain Dev. 2016. PMID: 27256512

10

Characteristics of epilepsy in patients with Kabuki syndrome with KMT2D mutations.

Kurahashi N, Miyake N, Mizuno S, Koshimizu E, Kurahashi H, Yamada K, Natsume J, Aoki Y, Nakamura M, Taniai H, Maki Y, Abe-Hatano C, Matsumoto N, Maruyama K. Kurahashi N, et al. Among authors: maruyama k. Brain Dev. 2017 Sep;39(8):672-677. doi: 10.1016/j.braindev.2017.03.025. Epub 2017 Apr 9. Brain Dev. 2017. PMID: 28404210

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