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Brain & Development|June 29, 2007
Seizure-genotype relationship in Fukuyama-type congenital muscular dystrophyMieko Yoshioka, Yoshihisa Higuchi, Tatsuya Fujii, et al.Brain & Development|May 28, 2003
Leigh syndrome associated with West syndromeMasahiro Tsuji, Shigekazu Kuroki, Haruko Maeda, et al.Brain & Development|January 18, 2006
A case of congenital neuromuscular disease with uniform type 1 fibersHaruko Maeda Sakamoto, Mieko Yoshioka, Masahiro Tsuji, et al.Brain & Development|December 24, 2017
Novel BICD2 mutation in a Japanese family with autosomal dominant lower extremity-predominant spinal muscular atrophy-2Mieko Yoshioka, Naoya Morisada, Daisaku Toyoshima, et al.Annals of Neurology|February 26, 2003
A new mutation of the fukutin gene in a non-Japanese patientFatma Silan, Mieko Yoshioka, Kazuhiro Kobayashi, et al.Journal of Autism and Developmental Disorders|November 30, 2017
Congenital Cytomegalovirus Infection in Children with Autism Spectrum Disorder: Systematic Review and Meta-AnalysisKaori Maeyama, Kazumi Tomioka, Hiroaki Nagase, et al.Journal of Autism and Developmental Disorders|March 17, 2021
Genetic Analysis of UGT1A1 Polymorphisms Using Preserved Dried Umbilical Cord for Assessing the Potential of Neonatal Jaundice as a Risk Factor for Autism Spectrum Disorder in ChildrenTomoko Horinouchi, Kaori Maeyama, Masashi Nagai, et al.Brain & Development|January 26, 2005
Multi-institutional study on the correlation between chromosomal abnormalities and epilepsyTomohiro Kumada, Masatoshi Ito, Tomoko Miyajima, et al.Pageof 2