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

Reiko Horikawa

Showing results (61-70 of 212) with videos related to

Pageof 22
Sort By:
Journal of Human Genetics|November 12, 2010
Androgenetic/biparental mosaicism in a girl with Beckwith-Wiedemann syndrome-like and upd(14)pat-like phenotypesKazuki Yamazawa, Kazuhiko Nakabayashi, Kentaro Matsuoka, et al.
Pediatric Research|January 28, 2006
Cytochrome P450 oxidoreductase deficiency in three patients initially regarded as having 21-hydroxylase deficiency and/or aromatase deficiency: diagnostic value of urine steroid hormone analysisMaki Fukami, Tomonobu Hasegawa, Reiko Horikawa, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|January 7, 2015
Inborn errors of ketone body utilizationTomohiro Hori, Seiji Yamaguchi, Haruo Shinkaku, et al.
Journal of the Endocrine Society|December 15, 2025
Seven-year Safety and Efficacy of Somapacitan in Children With GH Deficiency: Final Results From REAL 3Lars Sävendahl, Tadej Battelino, Michael Højby, et al.
Journal of Hepatology|January 17, 2012
4-Phenylbutyrate modulates ubiquitination of hepatocanalicular MRP2 and reduces serum total bilirubin concentrationHisamitsu Hayashi, Tadahaya Mizuno, Reiko Horikawa, et al.
Endocrine Journal|November 8, 2017
Efficacy and safety of two doses of Norditropin<sup>®</sup> (somatropin) in short stature due to Noonan syndrome: a 2-year randomized, double-blind, multicenter trial in Japanese patientsKeiichi Ozono, Tsutomu Ogata, Reiko Horikawa, et al.
Endocrine Journal|February 6, 2008
A case of malignant pheochromocytoma with Holt-Oram syndromeAi Yoshihara, Akiyo Tanabe, Hiroshi Saito, et al.
Journal of Human Genetics|March 7, 2008
Identification and characterization of cryptic SHOX intragenic deletions in three Japanese patients with Léri-Weill dyschondrosteosisMaki Fukami, Sumito Dateki, Fumiko Kato, et al.
Molecular Genetics and Metabolism|May 22, 2010
A novel mutation (c.951C>T) in an exonic splicing enhancer results in exon 10 skipping in the human mitochondrial acetoacetyl-CoA thiolase geneToshiyuki Fukao, Reiko Horikawa, Yasuhiro Naiki, et al.
Public Health Nutrition|August 5, 2020
Association between dietary intake and serum biomarkers of long-chain PUFA in Japanese preschool childrenEmiko Ando, Naho Morisaki, Keiko Asakura, et al.
Pageof 22

Showing results (61-70 of 212) with videos related to

Sort By:
Pageof 22
Journal of Human Genetics|November 12, 2010
Androgenetic/biparental mosaicism in a girl with Beckwith-Wiedemann syndrome-like and upd(14)pat-like phenotypesKazuki Yamazawa, Kazuhiko Nakabayashi, Kentaro Matsuoka, et al.
Pediatric Research|January 28, 2006
Cytochrome P450 oxidoreductase deficiency in three patients initially regarded as having 21-hydroxylase deficiency and/or aromatase deficiency: diagnostic value of urine steroid hormone analysisMaki Fukami, Tomonobu Hasegawa, Reiko Horikawa, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|January 7, 2015
Inborn errors of ketone body utilizationTomohiro Hori, Seiji Yamaguchi, Haruo Shinkaku, et al.
Journal of the Endocrine Society|December 15, 2025
Seven-year Safety and Efficacy of Somapacitan in Children With GH Deficiency: Final Results From REAL 3Lars Sävendahl, Tadej Battelino, Michael Højby, et al.
Journal of Hepatology|January 17, 2012
4-Phenylbutyrate modulates ubiquitination of hepatocanalicular MRP2 and reduces serum total bilirubin concentrationHisamitsu Hayashi, Tadahaya Mizuno, Reiko Horikawa, et al.
Endocrine Journal|November 8, 2017
Efficacy and safety of two doses of Norditropin<sup>®</sup> (somatropin) in short stature due to Noonan syndrome: a 2-year randomized, double-blind, multicenter trial in Japanese patientsKeiichi Ozono, Tsutomu Ogata, Reiko Horikawa, et al.
Endocrine Journal|February 6, 2008
A case of malignant pheochromocytoma with Holt-Oram syndromeAi Yoshihara, Akiyo Tanabe, Hiroshi Saito, et al.
Journal of Human Genetics|March 7, 2008
Identification and characterization of cryptic SHOX intragenic deletions in three Japanese patients with Léri-Weill dyschondrosteosisMaki Fukami, Sumito Dateki, Fumiko Kato, et al.
Molecular Genetics and Metabolism|May 22, 2010
A novel mutation (c.951C>T) in an exonic splicing enhancer results in exon 10 skipping in the human mitochondrial acetoacetyl-CoA thiolase geneToshiyuki Fukao, Reiko Horikawa, Yasuhiro Naiki, et al.
Public Health Nutrition|August 5, 2020
Association between dietary intake and serum biomarkers of long-chain PUFA in Japanese preschool childrenEmiko Ando, Naho Morisaki, Keiko Asakura, et al.
Pageof 22