Awashima T - Search Results

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Epileptic phenotype of FGFR3-related bilateral medial temporal lobe dysgenesis.

Okazaki T, Saito Y, Ueda R, Awashima T, Nishimura Y, Yuasa I, Shinohara Y, Adachi K, Sasaki M, Nanba E, Maegaki Y. Okazaki T, et al. Among authors: awashima t. Brain Dev. 2017 Jan;39(1):67-71. doi: 10.1016/j.braindev.2016.07.004. Epub 2016 Jul 30. Brain Dev. 2017. PMID: 27485793

Duchenne muscular dystrophy in a female with compound heterozygous contiguous exon deletions.

Takeshita E, Minami N, Minami K, Suzuki M, Awashima T, Ishiyama A, Komaki H, Nishino I, Sasaki M. Takeshita E, et al. Among authors: awashima t. Neuromuscul Disord. 2017 Jun;27(6):569-573. doi: 10.1016/j.nmd.2017.03.011. Epub 2017 Apr 3. Neuromuscul Disord. 2017. PMID: 28434908

[Electroencephalographic characteristics in patients with febrile status epilepticus].

Ryujin F, Awashima T, Nishikura N, Yoshioka S, Takano T, Takeuchi Y. Ryujin F, et al. Among authors: awashima t. No To Hattatsu. 2015 Jan;47(1):14-6. No To Hattatsu. 2015. PMID: 25803905 Japanese.

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