Nakayama T - Search Results

1

[A patient with an early diagnosis of PCDH19-related epilepsy].

Hoshina M, Higurashi N, Abe Y, Mishima H, Hosoya M, Nakayama T, Hirose S. Hoshina M, et al. Among authors: nakayama t. No To Hattatsu. 2015 Jul;47(4):305-9. No To Hattatsu. 2015. PMID: 26353454 Japanese.

2

Efficacy of long term weekly ACTH therapy for intractable epilepsy.

Inui T, Kobayashi T, Kobayashi S, Sato R, Endo W, Kikuchi A, Nakayama T, Uematsu M, Takayanagi M, Kato M, Saitsu H, Matsumoto N, Kure S, Haginoya K. Inui T, et al. Among authors: nakayama t. Brain Dev. 2015 Apr;37(4):449-54. doi: 10.1016/j.braindev.2014.07.004. Epub 2014 Aug 20. Brain Dev. 2015. PMID: 25149137

3

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. 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

4

Dramatic response after functional hemispherectomy in a patient with epileptic encephalopathy carrying a de novo COL4A1 mutation.

Hino-Fukuyo N, Kikuchi A, Iwasaki M, Sato Y, Kubota Y, Kobayashi T, Nakayama T, Haginoya K, Arai-Ichinoi N, Niihori T, Sato R, Suzuki T, Kudo H, Funayama R, Nakayama K, Aoki Y, Kure S. Hino-Fukuyo N, et al. Among authors: nakayama t, nakayama k. Brain Dev. 2017 Apr;39(4):337-340. doi: 10.1016/j.braindev.2016.11.006. Brain Dev. 2017. PMID: 27916450

5

Novel missense mutation in CLN8 in late infantile neuronal ceroid lipofuscinosis: The first report of a CLN8 mutation in Japan.

Katata Y, Uematsu M, Sato H, Suzuki S, Nakayama T, Kubota Y, Kobayashi T, Hino-Fukuyo N, Saitsu H, Kure S. Katata Y, et al. Among authors: nakayama t. Brain Dev. 2016 Mar;38(3):341-5. doi: 10.1016/j.braindev.2015.09.008. Epub 2015 Oct 9. Brain Dev. 2016. PMID: 26443629

6

[Corpus callosotomy for children with intractable generalized epilepsy: factors for long-term seizure remission].

Iwasaki M, Uematsu M, Nakayama T, Fukuyo N, Haginoya K, Jin K, Osawa S, Nakazato N, Tominaga T. Iwasaki M, et al. Among authors: nakayama t. No To Hattatsu. 2013 May;45(3):195-8. No To Hattatsu. 2013. PMID: 23785833 Japanese. No abstract available.

7

Acute encephalitis with refractory, repetitive partial seizures: Pathological findings and a new therapeutic approach using tacrolimus.

Sato Y, Numata-Uematsu Y, Uematsu M, Kikuchi A, Nakayama T, Kakisaka Y, Kobayashi T, Hino-Fukuyo N, Suzuki H, Takahashi Y, Saito Y, Tanuma N, Hayashi M, Iwasaki M, Haginoya K, Kure S. Sato Y, et al. Among authors: nakayama t. Brain Dev. 2016 Sep;38(8):772-6. doi: 10.1016/j.braindev.2016.02.006. Epub 2016 Feb 20. Brain Dev. 2016. PMID: 26906012

8

Early replacement therapy in a first Japanese case with autosomal recessive guanosine triphosphate cyclohydrolase I deficiency with a novel point mutation.

Sato H, Uematsu M, Endo W, Nakayama T, Kobayashi T, Hino-Fukuyo N, Sakamoto O, Shintaku H, Kure S. Sato H, et al. Among authors: nakayama t. Brain Dev. 2014 Mar;36(3):268-71. doi: 10.1016/j.braindev.2013.04.003. Epub 2013 May 6. Brain Dev. 2014. PMID: 23660475

9

RBPJ is disrupted in a case of proximal 4p deletion syndrome with epilepsy.

Nakayama T, Saitsu H, Endo W, Kikuchi A, Uematsu M, Haginoya K, Hino-fukuyo N, Kobayashi T, Iwasaki M, Tominaga T, Kure S, Matsumoto N. Nakayama T, et al. Brain Dev. 2014 Jun;36(6):532-6. doi: 10.1016/j.braindev.2013.07.009. Epub 2013 Aug 16. Brain Dev. 2014. PMID: 23958593

10

[A 3-year-old boy showing an episode of epileptic status provoked by high fever].

Nakayama T. Nakayama T. No To Hattatsu. 2014 Nov;46(6):411-2. No To Hattatsu. 2014. PMID: 25558582 Japanese. No abstract available.

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