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7,914 results
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Intermediate form between alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism.
Sasaki M, Ishii A, Saito Y, Hirose S. Sasaki M, et al. Among authors: saito y. Mov Disord. 2014 Jan;29(1):153-4. doi: 10.1002/mds.25659. Epub 2013 Sep 30. Mov Disord. 2014. PMID: 24123283 No abstract available.
Hyperkinetic movement disorder in a child treated by globus pallidus stimulation.
Sato K, Nakagawa E, Saito Y, Komaki H, Sakuma H, Sugai K, Sasaki M, Kaido T, Nakama H, Otsuki T. Sato K, et al. Among authors: saito y. Brain Dev. 2009 Jun;31(6):452-5. doi: 10.1016/j.braindev.2008.08.003. Epub 2008 Sep 17. Brain Dev. 2009. PMID: 18801630
Postnatal evolution of cortical malformation in the "non-affected" hemisphere of hemimegalencephaly.
Kometani H, Sugai K, Saito Y, Nakagawa E, Sakuma H, Komaki H, Sasaki M, Adachi Y, Kaneko Y, Otsuki T, Hamano S. Kometani H, et al. Among authors: saito y. Brain Dev. 2010 May;32(5):412-6. doi: 10.1016/j.braindev.2009.03.003. Epub 2009 Apr 2. Brain Dev. 2010. PMID: 19345027
Hemiconvulsion-hemiplegia syndrome in a patient with severe myoclonic epilepsy in infancy.
Sakakibara T, Nakagawa E, Saito Y, Sakuma H, Komaki H, Sugai K, Sasaki M, Kurahashi H, Hirose S. Sakakibara T, et al. Among authors: saito y. Epilepsia. 2009 Sep;50(9):2158-62. doi: 10.1111/j.1528-1167.2009.02175.x. Epub 2009 Jun 26. Epilepsia. 2009. PMID: 19563349
Electrophysiological evidence of cerebral dysfunction in childhood opsoclonus-myoclonus syndrome.
Sakuma H, Shimizu Y, Saito Y, Sugai K, Inagaki M, Kaga M, Sasaki M. Sakuma H, et al. Among authors: saito y. Mov Disord. 2010 May 15;25(7):940-5. doi: 10.1002/mds.23084. Mov Disord. 2010. PMID: 20461811
Evolution of hemiplegic attacks and epileptic seizures in alternating hemiplegia of childhood.
Saito Y, Inui T, Sakakibara T, Sugai K, Sakuma H, Sasaki M. Saito Y, et al. Epilepsy Res. 2010 Aug;90(3):248-58. doi: 10.1016/j.eplepsyres.2010.05.013. Epub 2010 Jun 26. Epilepsy Res. 2010. PMID: 20580529
Polymicrogyria and infantile spasms in a patient with 1p36 deletion syndrome.
Saito Y, Kubota M, Kurosawa K, Ichihashi I, Kaneko Y, Hattori A, Komaki H, Nakagawa E, Sugai K, Sasaki M. Saito Y, et al. Brain Dev. 2011 May;33(5):437-41. doi: 10.1016/j.braindev.2010.07.004. Epub 2010 Aug 13. Brain Dev. 2011. PMID: 20708863
CD4+ CD25(high) regulatory T cell in childhood ocular myasthenia gravis.
Sakuma H, Katayama A, Saito Y, Komaki H, Nakagawa E, Sugai K, Sasaki M. Sakuma H, et al. Among authors: saito y. Brain Dev. 2011 May;33(5):442-4. doi: 10.1016/j.braindev.2010.08.002. Epub 2010 Aug 24. Brain Dev. 2011. PMID: 20797828
Concurrence of multiple types of eyelid synkinesia in a patient with congenital anomalies.
Ishiyama A, Saito Y, Sugai K, Sasaki M, Yamazaki H, Kohama M. Ishiyama A, et al. Among authors: saito y. Brain Dev. 2012 Feb;34(2):140-2. doi: 10.1016/j.braindev.2011.02.007. Epub 2011 Mar 23. Brain Dev. 2012. PMID: 21435806
Profiles of blood biomarkers in alternating hemiplegia of childhood--increased MMP-9 and decreased substance P indicates its pathophysiology.
Inui T, Saito Y, Sakuma H, Hatakeyama H, Goto Y, Arai H, Sasaki M. Inui T, et al. Among authors: saito y. Brain Dev. 2012 Mar;34(3):196-200. doi: 10.1016/j.braindev.2011.04.008. Epub 2011 May 7. Brain Dev. 2012. PMID: 21550738
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