Kubota K - Search Results

1

Acute encephalopathy in children with tuberous sclerosis complex.

Numoto S, Kurahashi H, Sato A, Kubota M, Shiihara T, Okanishi T, Tanaka R, Kuki I, Fukuyama T, Kashiwagi M, Ikeno M, Kubota K, Akasaka M, Mimaki M, Okumura A. Numoto S, et al. Among authors: kubota m, kubota k. Orphanet J Rare Dis. 2021 Jan 6;16(1):5. doi: 10.1186/s13023-020-01646-8. Orphanet J Rare Dis. 2021. PMID: 33407677 Free PMC article.

2

Brain magnetic resonance imaging findings and auditory brainstem response in a child with spastic paraplegia 2 due to a PLP1 splice site mutation.

Kubota K, Saito Y, Ohba C, Saitsu H, Fukuyama T, Ishiyama A, Saito T, Komaki H, Nakagawa E, Sugai K, Sasaki M, Matsumoto N. Kubota K, et al. Brain Dev. 2015 Jan;37(1):158-62. doi: 10.1016/j.braindev.2014.03.001. Epub 2014 Mar 28. Brain Dev. 2015. PMID: 24685771

3

Effect of levodopa on pathological gait in Dravet syndrome: A randomized crossover trial using three-dimensional gait analysis.

Suzuki T, Natsume J, Ito Y, Ito T, Noritake K, Kinoshita F, Fukasawa T, Tsuji T, Itomi K, Kurahashi H, Kubota K, Okanishi T, Saitoh S, Sugiura H, Watanabe H, Takahashi Y, Kidokoro H. Suzuki T, et al. Among authors: kubota k. Epilepsia. 2024 May;65(5):1304-1313. doi: 10.1111/epi.17888. Epub 2024 Mar 12. Epilepsia. 2024. PMID: 38469885 Clinical Trial.

4

Immunoglobulin A vasculitis complicated with posterior reversible encephalopathy syndrome and reversible cerebral vasoconstriction syndrome.

Ninomiya H, Kubota K, Kimura T, Kawamoto N, Fukao T. Ninomiya H, et al. Among authors: kubota k. Pediatr Int. 2019 Aug;61(8):836-838. doi: 10.1111/ped.13947. Epub 2019 Aug 26. Pediatr Int. 2019. PMID: 31449351 Review. No abstract available.

5

Facial palsy as an unusual presenting symptom associated with acute myeloid leukemia.

Kubota K, Ozeki M, Hori T, Kanda K, Funato M, Asano T, Fukao T, Kondo N. Kubota K, et al. Pediatr Int. 2014 Aug;56(4):e37-40. doi: 10.1111/ped.12384. Pediatr Int. 2014. PMID: 25252069

6

POLR3A variants in striatal involvement without diffuse hypomyelination.

Hiraide T, Kubota K, Kono Y, Watanabe S, Matsubayashi T, Nakashima M, Kaname T, Fukao T, Shimozawa N, Ogata T, Saitsu H. Hiraide T, et al. Among authors: kubota k. Brain Dev. 2020 Apr;42(4):363-368. doi: 10.1016/j.braindev.2019.12.012. Epub 2020 Jan 10. Brain Dev. 2020. PMID: 31932101

7

Congenital inner ear malformations without sensorineural hearing loss in children.

Ozeki M, Kato Z, Sasai H, Kubota K, Funato M, Orii K, Kaneko H, Fukao T, Kondo N. Ozeki M, et al. Among authors: kubota k. Int J Pediatr Otorhinolaryngol. 2009 Oct;73(10):1484-7. doi: 10.1016/j.ijporl.2009.07.013. Epub 2009 Aug 19. Int J Pediatr Otorhinolaryngol. 2009. PMID: 19695719 Review.

8

Levetiracetam-Associated Decrease in Pitch Perception.

Kubota K, Shikano H, Fujii H, Nakashima Y, Fukao T. Kubota K, et al. Am J Ther. 2019 Jul/Aug;26(4):e527-e528. doi: 10.1097/MJT.0000000000000754. Am J Ther. 2019. PMID: 31169560 No abstract available.

9

Novel variants of ABCC9 in Japanese children with Cantú syndrome.

Kubota K, Yamamoto T, Miyatake S, Matsumoto N, Fukao T. Kubota K, et al. Pediatr Int. 2020 Mar;62(3):410-412. doi: 10.1111/ped.14098. Epub 2020 Mar 21. Pediatr Int. 2020. PMID: 32198910 No abstract available.

10

Two novel cases of biallelic SMPD4 variants with brain structural abnormalities.

Aoki S, Watanabe K, Kato M, Konishi Y, Kubota K, Kobayashi E, Nakashima M, Saitsu H. Aoki S, et al. Among authors: kubota k. Neurogenetics. 2024 Jan;25(1):3-11. doi: 10.1007/s10048-023-00737-5. Epub 2023 Oct 26. Neurogenetics. 2024. PMID: 37882972 Review.

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