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No to Hattatsu = Brain and Development|March 26, 2016
[The rewards of working with medicine for patients with severe motor and intellectual disabilities]Kiyokuni MiuraNo to Hattatsu = Brain and Development|January 24, 2008
[Various central nervous system involvements in dystrophinopathy: clinical and genetic considerations]Ari Nakamura, Yoshiki Miyazaki, Toshiyuki Kumagai, et al.No to Hattatsu = Brain and Development|February 23, 2012
[Survival analysis for patients with severe motor and intellectual disabilities following tracheotomy]Koichi Maruyama, Hirokazu Kurahashi, Motomasa Suzuki, et al.American Journal of Medical Genetics. Part A|June 4, 2016
Establishing SON in 21q22.11 as a cause a new syndromic form of intellectual disability: Possible contribution to Braddock-Carey syndrome phenotypeToshiki Takenouchi, Kiyokuni Miura, Tomoko Uehara, et al.Epilepsia|April 14, 2010
Frameshift mutations of the ARX gene in familial Ohtahara syndromeMitushiro Kato, Norihisa Koyama, Masayasu Ohta, et al.No to Hattatsu = Brain and Development|July 20, 2005
[Tracheostomy for home-care patients with severe motor and intellectual disabilities]Kiyokuni Miura, Yoshiko Suzuki, Toshiyuki Kumagai, et al.Journal of Pediatric Surgery|September 10, 2005
Variations in aganglionic segment length of the enteric neural plexus in Mowat-Wilson syndromeNaoko Ishihara, Atsuyoshi Shimada, Junji Kato, et al.No to Hattatsu = Brain and Development|January 29, 2005
[Clinical symptoms of the Rett syndrome patients with MECP2 gene abnormalities]Kiyokuni Miura, Toshiyuki Kumagai, Yoshiko Suzuki, et al.Pediatric Research|July 9, 2021
Death review of children receiving medical care at homeJun Natsume, Atsushi Numaguchi, Atsuko Ohno, et al.World Journal of Clinical Cases|June 29, 2023
Reading impairment after neonatal hypoglycemia with parieto-temporo-occipital injury without cortical blindness: A case reportNaoko Kurahashi, Shunsuke Ogaya, Yuki Maki, et al.Pageof 2