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Nihon Shinkei Seishin Yakurigaku Zasshi = Japanese Journal of Psychopharmacology|July 30, 2014
[From pathogenesis to treatment of genetic intellectual disabilities: a lesson from Angelman syndrome research]Shinji SaitohNihon Rinsho. Japanese Journal of Clinical Medicine|January 19, 2010
[Care continuity for patients with Prader-Willi syndrome during transition from childhood to adulthood]Shinji SaitohAcute Medicine & Surgery|November 24, 2020
CHARACTERISTICS and considerations in the medical treatment of COVID-19 in childrenKazunori Imai, Asako Matsushima, Shinji SaitohAmerican Journal of Medical Genetics. Part A|June 10, 2006
A new detection method for ATRX gene mutations using a mismatch-specific endonucleaseTakahito Wada, Yoshimitsu Fukushima, Shinji SaitohBrain & Development|December 27, 2005
A novel splicing mutation of the ATRX gene in ATR-X syndromeTakahito Wada, Masae Sakakibara, Yoshimitsu Fukushima, et al.American Journal of Medical Genetics. Part A|August 16, 2005
Non-skewed X-inactivation may cause mental retardation in a female carrier of X-linked alpha-thalassemia/mental retardation syndrome (ATR-X): X-inactivation study of nine female carriers of ATR-XTakahito Wada, Hideo Sugie, Yoshimitsu Fukushima, et al.Biosensors|December 24, 2025
Temporal Changes in Brain Light Scattering and Its Independent Variables Within 2 Days of LifeKennosuke Tsuda, Sachiko Iwata, Shinji Saitoh, et al.Brain & Development|January 9, 2021
Variance in the pathophysiological impact of the hemizygosity of gamma-aminobutyric acid type A receptor subunit genes between Prader-Willi syndrome and Angelman syndromeKiyoshi Egawa, Shinji Saitoh, Naoko Asahina, et al.Eneurologicalsci|December 14, 2020
Short-latency somatosensory-evoked potentials demonstrate cortical dysfunction in patients with Angelman syndromeKiyoshi Egawa, Shinji Saitoh, Naoko Asahina, et al.Pageof 27