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Mari Urano

Showing results (1-10 of 11) with videos related to

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Nihon Rinsho. Japanese Journal of Clinical Medicine|June 11, 2009
[Gene mutation and genetic counseling]Mari Matsuo, Mari Urano, Kayoko Saito
Pediatric Neurology|October 22, 2013
Corticosteroid therapy for duchenne muscular dystrophy: improvement of psychomotor functionYuko Sato, Akemi Yamauchi, Mari Urano, et al.
Journal of Human Genetics|July 1, 2016
Target resequencing of neuromuscular disease-related genes using next-generation sequencing for patients with undiagnosed early-onset neuromuscular disordersYuri Kitamura, Eri Kondo, Mari Urano, et al.
Brain & Development|June 12, 2017
Relationships between long-term observations of motor milestones and genotype analysis results in childhood-onset Japanese spinal muscular atrophy patientsKaori Kaneko, Reiko Arakawa, Mari Urano, et al.
Japanese Journal of Ophthalmology|December 31, 2010
A case of Fukuyama congenital muscular dystrophy associated with negative electroretinogramsHiroyuki Kondo, Kayoko Saito, Mari Urano, et al.
Brain & Development|August 28, 2021
Epidemiological investigation of spinal muscular atrophy in JapanMayuri Ito, Akemi Yamauchi, Mari Urano, et al.
Journal of Genetic Counseling|November 11, 2016
Genetic Counseling for Couples Seeking Noninvasive Prenatal Testing in Japan: Experiences of Pregnant Women and their PartnersMotoko Watanabe, Mari Matsuo, Masaki Ogawa, et al.
Muscle & Nerve|January 3, 2013
Charcot-Marie-Tooth disease type 4C in Japan: report of a caseMasahiro Iguchi, Akihiro Hashiguchi, Eiichi Ito, et al.
Orphanet Journal of Rare Diseases|February 28, 2025
Analysis of SMN protein in umbilical cord blood and postnatal peripheral blood of neonates with SMA: a rationale for prompt treatment initiation to prevent SMA developmentNoriko Otsuki, Tamaki Kato, Mamoru Yokomura, et al.
Journal of the American College of Cardiology|July 15, 2017
Progressive Atrial Conduction Defects Associated With Bone Malformation Caused by a Connexin-45 MutationAkiko Seki, Taisuke Ishikawa, Xavier Daumy, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Nihon Rinsho. Japanese Journal of Clinical Medicine|June 11, 2009
[Gene mutation and genetic counseling]Mari Matsuo, Mari Urano, Kayoko Saito
Pediatric Neurology|October 22, 2013
Corticosteroid therapy for duchenne muscular dystrophy: improvement of psychomotor functionYuko Sato, Akemi Yamauchi, Mari Urano, et al.
Journal of Human Genetics|July 1, 2016
Target resequencing of neuromuscular disease-related genes using next-generation sequencing for patients with undiagnosed early-onset neuromuscular disordersYuri Kitamura, Eri Kondo, Mari Urano, et al.
Brain & Development|June 12, 2017
Relationships between long-term observations of motor milestones and genotype analysis results in childhood-onset Japanese spinal muscular atrophy patientsKaori Kaneko, Reiko Arakawa, Mari Urano, et al.
Japanese Journal of Ophthalmology|December 31, 2010
A case of Fukuyama congenital muscular dystrophy associated with negative electroretinogramsHiroyuki Kondo, Kayoko Saito, Mari Urano, et al.
Brain & Development|August 28, 2021
Epidemiological investigation of spinal muscular atrophy in JapanMayuri Ito, Akemi Yamauchi, Mari Urano, et al.
Journal of Genetic Counseling|November 11, 2016
Genetic Counseling for Couples Seeking Noninvasive Prenatal Testing in Japan: Experiences of Pregnant Women and their PartnersMotoko Watanabe, Mari Matsuo, Masaki Ogawa, et al.
Muscle & Nerve|January 3, 2013
Charcot-Marie-Tooth disease type 4C in Japan: report of a caseMasahiro Iguchi, Akihiro Hashiguchi, Eiichi Ito, et al.
Orphanet Journal of Rare Diseases|February 28, 2025
Analysis of SMN protein in umbilical cord blood and postnatal peripheral blood of neonates with SMA: a rationale for prompt treatment initiation to prevent SMA developmentNoriko Otsuki, Tamaki Kato, Mamoru Yokomura, et al.
Journal of the American College of Cardiology|July 15, 2017
Progressive Atrial Conduction Defects Associated With Bone Malformation Caused by a Connexin-45 MutationAkiko Seki, Taisuke Ishikawa, Xavier Daumy, et al.
Pageof 2