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American Journal of Medical Genetics. Part A|March 13, 2012
Recessive RYR1 mutations in a patient with severe congenital nemaline myopathy with ophthalomoplegia identified through massively parallel sequencingEri Kondo, Takafumi Nishimura, Tomoki Kosho, et al.Acta Oto-Laryngologica|March 8, 2018
A rational approach to identifying newborns with hearing loss caused by congenital cytomegalovirus infection by dried blood spot screeningHideaki Moteki, Yuichi Isaka, Yuji Inaba, et al.Pediatrics and Neonatology|April 28, 2023
Factors associated with the development of epilepsy in very low birth weight infantsToshimichi Fukao, Fumikazu Sano, Atsushi Nemoto, et al.Journal of Leukocyte Biology|September 10, 2003
STI571 inhibits growth and adhesion of human mast cells in cultureKouichi Takeuchi, Kenichi Koike, Takehiko Kamijo, et al.Brain & Development|September 27, 2021
Successful treatment of congenital myasthenic syndrome caused by a novel compound heterozygous variant in RAPSNMaki Saito, Masashi Ogasawara, Yuji Inaba, et al.Brain & Development|December 3, 2013
A case of Bardet-Biedl syndrome complicated with intracranial hypertension in a Japanese childKen Saida, Yuji Inaba, Makito Hirano, et al.Scientific Reports|September 26, 2025
Automated differentiation of acute encephalopathy with biphasic seizures and late reduced diffusion and prolonged febrile seizures in acute phaseMasayoshi Oguri, Tohru Okanishi, Ichiro Kuki, et al.American Journal of Medical Genetics. Part A|April 4, 2019
PIEZO2 deficiency is a recognizable arthrogryposis syndrome: A new case and literature reviewTomomi Yamaguchi, Kyoko Takano, Yuji Inaba, et al.Evidence-Based Complementary and Alternative Medicine : Ecam|August 5, 2014
Traditional Japanese medicine daikenchuto improves functional constipation in poststroke patientsTakehiro Numata, Shin Takayama, Muneshige Tobita, et al.Spine|March 25, 2017
Rigid Occipitocervical Instrumented Fusion for Atlantoaxial Instability in an 18-Month-Old Toddler With Brachytelephalangic Chondrodysplasia Punctata: A Case ReportHiroki Oba, Jun Takahashi, Kyoko Takano, et al.Pageof 10