Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Satoshi Okada

Showing results (261-270 of 408) with videos related to

Pageof 41
Sort By:
Plos One|March 9, 2013
A novel homozygous p.R1105X mutation of the AP4E1 gene in twins with hereditary spastic paraplegia and mycobacterial diseaseXiao-Fei Kong, Aziz Bousfiha, Abdelfettah Rouissi, et al.
International Journal of Neonatal Screening|July 21, 2021
Pilot Study on Neonatal Screening for Methylmalonic Acidemia Caused by Defects in the Adenosylcobalamin Synthesis Pathway and Homocystinuria Caused by Defects in Homocysteine RemethylationReiko Kagawa, Go Tajima, Takako Maeda, et al.
Hormone Research in Paediatrics|February 19, 2018
Incidence and Characteristics of Adrenal Crisis in Children Younger than 7 Years with 21-Hydroxylase Deficiency: A Nationwide Survey in JapanTomohiro Ishii, Masanori Adachi, Kei Takasawa, et al.
Langmuir : the ACS Journal of Surfaces and Colloids|April 18, 2019
Liquid Marbles in Nature: Craft of Aphids for SurvivalMoe Kasahara, Shin-Ichi Akimoto, Takahiko Hariyama, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|August 28, 2023
Age-specific incidence of joint disease in paediatric patients with haemophilia: A single-centre real-world outcome based on consecutive US examinationYoko Mizoguchi, Chihiro Tani, Mika Aizawa, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|October 14, 2017
Clinical characteristics of septo-optic dysplasia accompanied by congenital central hypothyroidism in JapanKeisuke Nagasaki, Takuo Kubota, Hironori Kobayashi, et al.
The Journal of Allergy and Clinical Immunology|April 17, 2020
APRIL-dependent lifelong plasmacyte maintenance and immunoglobulin production in humansTzu-Wen Yeh, Tsubasa Okano, Takuya Naruto, et al.
Journal of Pediatric Gastroenterology and Nutrition|August 1, 2020
Ruxolitinib Response in an Infant With Very-early-onset Inflammatory Bowel Disease and Gain-of-function STAT1 MutationKaren P Acker, Rachel Borlack, Alina Iuga, et al.
Molecular Genetics and Metabolism|March 8, 2016
Significance of ACADM mutations identified through newborn screening of MCAD deficiency in JapanKeiichi Hara, Go Tajima, Satoshi Okada, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|April 22, 2020
A nationwide questionnaire survey targeting Japanese pediatric endocrinologists regarding transitional care in childhood, adolescent, and young adult cancer survivorsYoko Miyoshi, Tohru Yorifuji, Chikako Shimizu, et al.
Pageof 41

Showing results (261-270 of 408) with videos related to

Sort By:
Pageof 41
Plos One|March 9, 2013
A novel homozygous p.R1105X mutation of the AP4E1 gene in twins with hereditary spastic paraplegia and mycobacterial diseaseXiao-Fei Kong, Aziz Bousfiha, Abdelfettah Rouissi, et al.
International Journal of Neonatal Screening|July 21, 2021
Pilot Study on Neonatal Screening for Methylmalonic Acidemia Caused by Defects in the Adenosylcobalamin Synthesis Pathway and Homocystinuria Caused by Defects in Homocysteine RemethylationReiko Kagawa, Go Tajima, Takako Maeda, et al.
Hormone Research in Paediatrics|February 19, 2018
Incidence and Characteristics of Adrenal Crisis in Children Younger than 7 Years with 21-Hydroxylase Deficiency: A Nationwide Survey in JapanTomohiro Ishii, Masanori Adachi, Kei Takasawa, et al.
Langmuir : the ACS Journal of Surfaces and Colloids|April 18, 2019
Liquid Marbles in Nature: Craft of Aphids for SurvivalMoe Kasahara, Shin-Ichi Akimoto, Takahiko Hariyama, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|August 28, 2023
Age-specific incidence of joint disease in paediatric patients with haemophilia: A single-centre real-world outcome based on consecutive US examinationYoko Mizoguchi, Chihiro Tani, Mika Aizawa, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|October 14, 2017
Clinical characteristics of septo-optic dysplasia accompanied by congenital central hypothyroidism in JapanKeisuke Nagasaki, Takuo Kubota, Hironori Kobayashi, et al.
The Journal of Allergy and Clinical Immunology|April 17, 2020
APRIL-dependent lifelong plasmacyte maintenance and immunoglobulin production in humansTzu-Wen Yeh, Tsubasa Okano, Takuya Naruto, et al.
Journal of Pediatric Gastroenterology and Nutrition|August 1, 2020
Ruxolitinib Response in an Infant With Very-early-onset Inflammatory Bowel Disease and Gain-of-function STAT1 MutationKaren P Acker, Rachel Borlack, Alina Iuga, et al.
Molecular Genetics and Metabolism|March 8, 2016
Significance of ACADM mutations identified through newborn screening of MCAD deficiency in JapanKeiichi Hara, Go Tajima, Satoshi Okada, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|April 22, 2020
A nationwide questionnaire survey targeting Japanese pediatric endocrinologists regarding transitional care in childhood, adolescent, and young adult cancer survivorsYoko Miyoshi, Tohru Yorifuji, Chikako Shimizu, et al.
Pageof 41