Dowa Y - Search Results

1

Acute encephalopathy with biphasic seizures and late reduced diffusion; posterior frontal hyperperfusion before late seizures revealed by arterial spin labeling: A case report.

Morita K, Shiihara T, Suzuki E, Shimizu Y, Dowa Y, Watanabe M. Morita K, et al. Among authors: dowa y. Brain Dev. 2021 Jun;43(6):714-718. doi: 10.1016/j.braindev.2021.02.001. Epub 2021 Mar 2. Brain Dev. 2021. PMID: 33663993

2

A case of mumps-related acute encephalopathy with biphasic seizures and late reduced diffusion.

Hazama K, Shiihara T, Tsukagoshi H, Hasegawa S, Dowa Y, Watanabe M. Hazama K, et al. Among authors: dowa y. Brain Dev. 2017 Oct;39(9):808-810. doi: 10.1016/j.braindev.2017.04.012. Epub 2017 May 10. Brain Dev. 2017. PMID: 28501474

3

Rhinovirus-associated acute encephalitis/encephalopathy and cerebellitis.

Hazama K, Shiihara T, Tsukagoshi H, Matsushige T, Dowa Y, Watanabe M. Hazama K, et al. Among authors: dowa y. Brain Dev. 2019 Jun;41(6):551-554. doi: 10.1016/j.braindev.2019.02.014. Epub 2019 Mar 6. Brain Dev. 2019. PMID: 30850156

4

Multiple cerebral cysts are another possible feature of Jacobsen syndrome.

Dowa Y, Shiihara T. Dowa Y, et al. Brain Dev. 2020 Sep;42(8):626. doi: 10.1016/j.braindev.2020.06.019. Epub 2020 Jul 17. Brain Dev. 2020. PMID: 32684377 No abstract available.

5

A case of pyridoxine-dependent epilepsy with novel ALDH7A1 mutations.

Dowa Y, Shiihara T, Akiyama T, Hasegawa K, Inoue F, Watanabe M. Dowa Y, et al. Oxf Med Case Reports. 2020 May 6;2020(3):omaa008. doi: 10.1093/omcr/omaa008. eCollection 2020 Mar. Oxf Med Case Reports. 2020. PMID: 32395249 Free PMC article.

6

Sweet Potato Was Not So Sweet: Undetected Foreign-body Aspiration in a Healthy Child Leading to Acute Bronchial Asthma.

Dowa Y, Yamada Y, Kato M, Matsumoto N, Kama Y, Shiihara T. Dowa Y, et al. Tokai J Exp Clin Med. 2019 Apr 20;44(1):1-4. Tokai J Exp Clin Med. 2019. PMID: 30963521 Free article.

7

Pyridoxal in the Cerebrospinal Fluid May Be a Better Indicator of Vitamin B6-dependent Epilepsy Than Pyridoxal 5'-Phosphate.

Akiyama T, Hyodo Y, Hasegawa K, Oboshi T, Imai K, Ishihara N, Dowa Y, Koike T, Yamamoto T, Shibasaki J, Shimbo H, Fukuyama T, Takano K, Shiraku H, Takeshita S, Okanishi T, Baba S, Kubota M, Hamano SI, Kobayashi K. Akiyama T, et al. Among authors: dowa y. Pediatr Neurol. 2020 Dec;113:33-41. doi: 10.1016/j.pediatrneurol.2020.08.020. Epub 2020 Sep 2. Pediatr Neurol. 2020. PMID: 32980745 Free article.

8

Two siblings with 11qter deletion syndrome that had been rescued in their mother by uniparental disomy.

Kawai M, Tsutsumi M, Suzuki F, Sameshima K, Dowa Y, Kyoya T, Inagaki H, Kurahashi H. Kawai M, et al. Among authors: dowa y. Eur J Med Genet. 2019 Mar;62(3):224-228. doi: 10.1016/j.ejmg.2018.07.018. Epub 2018 Jul 18. Eur J Med Genet. 2019. PMID: 30031150

9

Congenital neuroblastoma in a patient with partial trisomy of 2p.

Dowa Y, Yamamoto T, Abe Y, Kobayashi M, Hoshino R, Tanaka K, Aida N, Take H, Kato K, Tanaka Y, Ariyama J, Harada N, Matsumoto N, Kurosawa K. Dowa Y, et al. J Pediatr Hematol Oncol. 2006 Jun;28(6):379-82. doi: 10.1097/00043426-200606000-00011. J Pediatr Hematol Oncol. 2006. PMID: 16794507

10

Tetralogy of Fallot associated with pulmonary atresia and major aortopulmonary collateral arteries in a patient with interstitial deletion of 16q21-q22.1.

Yamamoto T, Dowa Y, Ueda H, Kawataki M, Asou T, Sasaki Y, Harada N, Matsumoto N, Matsuoka R, Kurosawa K. Yamamoto T, et al. Among authors: dowa y. Am J Med Genet A. 2008 Jun 15;146A(12):1575-80. doi: 10.1002/ajmg.a.32204. Am J Med Genet A. 2008. PMID: 18470894

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