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Page 1
Hypoperfusion in caudate nuclei in patients with brain-lung-thyroid syndrome.
Uematsu M, Haginoya K, Kikuchi A, Nakayama T, Kakisaka Y, Numata Y, Kobayashi T, Hino-Fukuyo N, Fujiwara I, Kure S. Uematsu M, et al. Among authors: nakayama t. J Neurol Sci. 2012 Apr 15;315(1-2):77-81. doi: 10.1016/j.jns.2011.11.025. Epub 2011 Dec 12. J Neurol Sci. 2012. PMID: 22166853
Unique discrepancy between cerebral blood flow and glucose metabolism in hemimegalencephaly.
Uematsu M, Haginoya K, Togashi N, Hino-Fukuyo N, Nakayama T, Kikuchi A, Abe Y, Wakusawa K, Matsumoto Y, Kakisaka Y, Kobayashi T, Hirose M, Yokoyama H, Iinuma K, Iwasaki M, Nakasato N, Kaneta T, Akasaka M, Kamei A, Tsuchiya S. Uematsu M, et al. Among authors: nakayama t. Epilepsy Res. 2010 Dec;92(2-3):201-8. doi: 10.1016/j.eplepsyres.2010.09.010. Epub 2010 Oct 20. Epilepsy Res. 2010. PMID: 20965696
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
The usefulness of subtraction ictal SPECT and ictal near-infrared spectroscopic topography in patients with West syndrome.
Haginoya K, Uematsu M, Munakata M, Kakisaka Y, Kikuchi A, Nakayama T, Hino-Fukuyo N, Tsuburaya R, Kitamura T, Sato-Shirai I, Abe Y, Matsumoto Y, Wakusawa K, Kobayashi T, Ishitobi M, Togashi N, Iwasaki M, Nakasato N, Iinuma K. Haginoya K, et al. Among authors: nakayama t. Brain Dev. 2013 Nov;35(10):887-93. doi: 10.1016/j.braindev.2013.08.011. Epub 2013 Sep 15. Brain Dev. 2013. PMID: 24047572 Review.
Genomic analysis identifies candidate pathogenic variants in 9 of 18 patients with unexplained West syndrome.
Hino-Fukuyo N, Kikuchi A, Arai-Ichinoi N, Niihori T, Sato R, Suzuki T, Kudo H, Sato Y, Nakayama T, Kakisaka Y, Kubota Y, Kobayashi T, Funayama R, Nakayama K, Uematsu M, Aoki Y, Haginoya K, Kure S. Hino-Fukuyo N, et al. Among authors: nakayama t, nakayama k. Hum Genet. 2015 Jun;134(6):649-58. doi: 10.1007/s00439-015-1553-6. Epub 2015 Apr 16. Hum Genet. 2015. PMID: 25877686 Clinical Trial.
A case of 3p deletion syndrome associated with cerebellar hemangioblastoma.
Suzuki-Muromoto S, Hino-Fukuyo N, Haginoya K, Kikuchi A, Sato H, Sato Y, Nakayama T, Kubota Y, Kakisaka Y, Uematsu M, Kumabe T, Kure S. Suzuki-Muromoto S, et al. Among authors: nakayama t. Brain Dev. 2016 Feb;38(2):257-60. doi: 10.1016/j.braindev.2015.07.005. Epub 2015 Sep 11. Brain Dev. 2016. PMID: 26365017
5,351 results