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Nihon Rinsho. Japanese Journal of Clinical Medicine
|
March 19, 2005
[Muscular dystrophy]
Eri Kondo, Kayoko Saito, Makiko Osawa
Congenital Anomalies
|
June 22, 2018
Long-term natural history of an adult patient with distal 22q11.2 deletion from low copy repeat-D to E
Mari Matsuo, Toshiyuki Yamamoto, Kayoko Saito
Nihon Rinsho. Japanese Journal of Clinical Medicine
|
June 11, 2009
[Gene mutation and genetic counseling]
Mari Matsuo, Mari Urano, Kayoko Saito
Brain & Development
|
December 23, 2025
Reply to "Comment on 'Survival motor neuron protein is the optimal biomarker for evaluating the risdiplam treatment'"
Tamaki Kato, Noriko Otsuki, Mamoru Yokomura, et al.
Cell and Tissue Research
|
February 29, 2012
Human first-trimester chorionic villi have a myogenic potential
Reiko Arakawa, Ryoko Aoki, Masayuki Arakawa, et al.
Frontiers in Pediatrics
|
July 25, 2022
Factors Surrounding the Healthcare Transition From Pediatric to Adult Care in 5p- Syndrome: A Survey Among Healthcare Professionals
Yuko Ishizaki, Mari Matsuo, Kayoko Saito, et al.
Brain & Development
|
November 18, 2019
Analysis of spinal muscular atrophy-like patients by targeted resequencing
Shinichi Hosokawa, Yuji Kubo, Reiko Arakawa, et al.
Pediatric Neurology
|
October 22, 2013
Corticosteroid therapy for duchenne muscular dystrophy: improvement of psychomotor function
Yuko Sato, Akemi Yamauchi, Mari Urano, et al.
Brain & Development
|
July 8, 2010
New insights into the pathogenesis of spinal muscular atrophy
Yasushi Ito, Noriyuki Shibata, Kayoko Saito, et al.
Pediatric Neurology
|
April 16, 2008
Three patients with severe bilateral frontoparietal polymicrogyria
Tomohiro Nakayama, Hirokazu Oguni, Makoto Funatsuka, et al.
Page
of 16
Search research articles
Search
Showing results (11-20 of 152) with videos related to
Sort By:
Page
of 16
Nihon Rinsho. Japanese Journal of Clinical Medicine
|
March 19, 2005
[Muscular dystrophy]
Eri Kondo, Kayoko Saito, Makiko Osawa
Congenital Anomalies
|
June 22, 2018
Long-term natural history of an adult patient with distal 22q11.2 deletion from low copy repeat-D to E
Mari Matsuo, Toshiyuki Yamamoto, Kayoko Saito
Nihon Rinsho. Japanese Journal of Clinical Medicine
|
June 11, 2009
[Gene mutation and genetic counseling]
Mari Matsuo, Mari Urano, Kayoko Saito
Brain & Development
|
December 23, 2025
Reply to "Comment on 'Survival motor neuron protein is the optimal biomarker for evaluating the risdiplam treatment'"
Tamaki Kato, Noriko Otsuki, Mamoru Yokomura, et al.
Cell and Tissue Research
|
February 29, 2012
Human first-trimester chorionic villi have a myogenic potential
Reiko Arakawa, Ryoko Aoki, Masayuki Arakawa, et al.
Frontiers in Pediatrics
|
July 25, 2022
Factors Surrounding the Healthcare Transition From Pediatric to Adult Care in 5p- Syndrome: A Survey Among Healthcare Professionals
Yuko Ishizaki, Mari Matsuo, Kayoko Saito, et al.
Brain & Development
|
November 18, 2019
Analysis of spinal muscular atrophy-like patients by targeted resequencing
Shinichi Hosokawa, Yuji Kubo, Reiko Arakawa, et al.
Pediatric Neurology
|
October 22, 2013
Corticosteroid therapy for duchenne muscular dystrophy: improvement of psychomotor function
Yuko Sato, Akemi Yamauchi, Mari Urano, et al.
Brain & Development
|
July 8, 2010
New insights into the pathogenesis of spinal muscular atrophy
Yasushi Ito, Noriyuki Shibata, Kayoko Saito, et al.
Pediatric Neurology
|
April 16, 2008
Three patients with severe bilateral frontoparietal polymicrogyria
Tomohiro Nakayama, Hirokazu Oguni, Makoto Funatsuka, et al.
Page
of 16