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Brain & Development|November 12, 2013
Anti-NMDAR autoimmune encephalitisKazushi Miya, Yukitoshi Takahashi, Hisashi MoriBrain & Development|July 7, 2020
Learning difficulties in Japanese schoolchildren with focal epilepsyMitsuaki Miyazaki, Tomomi Tanaka, Yuichi Adachi, et al.Clinical Nephrology|August 3, 2017
MODY3, renal cysts, and Dandy-Walker variants with a microdeletion spanning the HNF1A geneHiro Matsukura, Mariko Nagamori, Kazushi Miya, et al.International Journal of Clinical and Experimental Pathology|July 18, 2014
An autopsy case of infantile-onset vanishing white matter disease related to an EIF2B2 mutation (V85E) in a hemizygous regionYukiko Hata, Koshi Kinoshita, Kazushi Miya, et al.Seminars in Thoracic and Cardiovascular Surgery|November 8, 2019
Toddler Neurodevelopmental Outcomes Are Associated With School-Age IQ in Children With Single Ventricle PhysiologyAkiko Hiraiwa, Keijiro Ibuki, Tomomi Tanaka, et al.Brain & Development|February 16, 2013
Cortical contribution to scalp EEG gamma rhythms associated with epileptic spasmsKatsuhiro Kobayashi, Kazushi Miya, Tomoyuki Akiyama, et al.American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|February 26, 2004
IgA nephropathy associated with X-linked thrombocytopeniaHiro Matsukura, Hirokazu Kanegane, Kazushi Miya, et al.American Journal of Medical Genetics. Part A|June 9, 2012
An unmasked mutation of EIF2B2 due to submicroscopic deletion of 14q24.3 in a patient with vanishing white matter diseaseShino Shimada, Kazushi Miya, Nozomi Oda, et al.The Journal of Comparative Neurology|August 14, 2008
Serine racemase is predominantly localized in neurons in mouse brainKazushi Miya, Ran Inoue, Yoshimi Takata, et al.Gene|July 10, 2012
A de novo interstitial deletion of 8p11.2 including ANK1 identified in a patient with spherocytosis, psychomotor developmental delay, and distinctive facial featuresKazushi Miya, Keiko Shimojima, Midori Sugawara, et al.Pageof 2