Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Text availability
Article attribute
Article type
Publication date

Search Results

109 results
Filters applied: . Clear all Results are displayed in a computed author sort order. Results by year timeline is unavailable
Page 1
[A girl with dyslexia suspected to have Irlen syndrome, completely relieved by wearing tinted lenses].
Kusano Y, Awaya T, Saito K, Yoshida T, Ide M, Kato T, Heike T, Kato T. Kusano Y, et al. Among authors: awaya t. No To Hattatsu. 2015 Nov;47(6):445-8. No To Hattatsu. 2015. PMID: 26717646 Japanese.
Genetic abnormalities in a large cohort of Coffin-Siris syndrome patients.
Sekiguchi F, Tsurusaki Y, Okamoto N, Teik KW, Mizuno S, Suzumura H, Isidor B, Ong WP, Haniffa M, White SM, Matsuo M, Saito K, Phadke S, Kosho T, Yap P, Goyal M, Clarke LA, Sachdev R, McGillivray G, Leventer RJ, Patel C, Yamagata T, Osaka H, Hisaeda Y, Ohashi H, Shimizu K, Nagasaki K, Hamada J, Dateki S, Sato T, Chinen Y, Awaya T, Kato T, Iwanaga K, Kawai M, Matsuoka T, Shimoji Y, Tan TY, Kapoor S, Gregersen N, Rossi M, Marie-Laure M, McGregor L, Oishi K, Mehta L, Gillies G, Lockhart PJ, Pope K, Shukla A, Girisha KM, Abdel-Salam GMH, Mowat D, Coman D, Kim OH, Cordier MP, Gibson K, Milunsky J, Liebelt J, Cox H, El Chehadeh S, Toutain A, Saida K, Aoi H, Minase G, Tsuchida N, Iwama K, Uchiyama Y, Suzuki T, Hamanaka K, Azuma Y, Fujita A, Imagawa E, Koshimizu E, Takata A, Mitsuhashi S, Miyatake S, Mizuguchi T, Miyake N, Matsumoto N. Sekiguchi F, et al. Among authors: awaya t. J Hum Genet. 2019 Dec;64(12):1173-1186. doi: 10.1038/s10038-019-0667-4. Epub 2019 Sep 17. J Hum Genet. 2019. PMID: 31530938
An epigenetic biomarker for adult high-functioning autism spectrum disorder.
Kimura R, Nakata M, Funabiki Y, Suzuki S, Awaya T, Murai T, Hagiwara M. Kimura R, et al. Among authors: awaya t. Sci Rep. 2019 Sep 20;9(1):13662. doi: 10.1038/s41598-019-50250-9. Sci Rep. 2019. PMID: 31541176 Free PMC article.
Long-term weekly ACTH therapy for relapsed West syndrome in tuberous sclerosis complex: A case report.
Nakata M, Kato T, Ide M, Saito K, Yoshida T, Awaya T, Shibata M, Heike T. Nakata M, et al. Among authors: awaya t. Brain Dev. 2016 Apr;38(4):431-4. doi: 10.1016/j.braindev.2015.10.004. Epub 2015 Oct 21. Brain Dev. 2016. PMID: 26482603
Dysregulation of the oxytocin receptor gene in Williams syndrome.
Kimura R, Tomiwa K, Inoue R, Suzuki S, Nakata M, Awaya T, Kato T, Okazaki S, Heike T, Hagiwara M. Kimura R, et al. Among authors: awaya t. Psychoneuroendocrinology. 2020 May;115:104631. doi: 10.1016/j.psyneuen.2020.104631. Epub 2020 Feb 20. Psychoneuroendocrinology. 2020. PMID: 32114409 Free article.
Integrated DNA methylation analysis reveals a potential role for ANKRD30B in Williams syndrome.
Kimura R, Lardenoije R, Tomiwa K, Funabiki Y, Nakata M, Suzuki S, Awaya T, Kato T, Okazaki S, Murai T, Heike T, Rutten BPF, Hagiwara M. Kimura R, et al. Among authors: awaya t. Neuropsychopharmacology. 2020 Sep;45(10):1627-1636. doi: 10.1038/s41386-020-0675-2. Epub 2020 Apr 18. Neuropsychopharmacology. 2020. PMID: 32303053 Free PMC article.
[Progressive cerebral white matter abnormalities with emaciation and short stature].
Awaya T. Awaya T. No To Hattatsu. 2007 Sep;39(5):333-4. No To Hattatsu. 2007. PMID: 17879605 Japanese. No abstract available.
A combination therapy of whole lung lavage and GM-CSF inhalation in pulmonary alveolar proteinosis.
Yamamoto H, Yamaguchi E, Agata H, Kandatsu N, Komatsu T, Kawai S, Baba K, Awaya T, Nishikomori R, Tsurusawa M, Nakata K. Yamamoto H, et al. Among authors: awaya t. Pediatr Pulmonol. 2008 Aug;43(8):828-30. doi: 10.1002/ppul.20856. Pediatr Pulmonol. 2008. PMID: 18618617
Brain atrophy caused by vitamin B12-deficient anemia in an infant.
Kamei M, Ito Y, Ando N, Awaya T, Yamada T, Nakagawa M, Yamaguchi A, Ohuchi M, Yazaki M, Togari H. Kamei M, et al. Among authors: awaya t. J Pediatr Hematol Oncol. 2011 Oct;33(7):556-8. doi: 10.1097/MPH.0b013e31821e5290. J Pediatr Hematol Oncol. 2011. PMID: 21941150
MRI gadolinium enhancement precedes neuroradiological findings in acute necrotizing encephalopathy.
Yoshida T, Tamura T, Nagai Y, Ueda H, Awaya T, Shibata M, Kato T, Heike T. Yoshida T, et al. Among authors: awaya t. Brain Dev. 2013 Nov;35(10):921-4. doi: 10.1016/j.braindev.2012.11.011. Epub 2012 Dec 20. Brain Dev. 2013. PMID: 23265619
109 results
Jump to page
Feedback