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

Kentaro Sawano

Showing results (1-10 of 20) with videos related to

Pageof 2
Sort By:
Archives of Disease in Childhood|November 13, 2021
Carotenoderma with hypothyroidismKentaro Sawano, Keisuke Nagasaki
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|October 22, 2020
Letter to the Editor: Testosterone priming increased growth hormone peak levels in the stimulation test and suppressed gonadotropin secretion in three Japanese adolescent boysKentaro Sawano, Keisuke Nagasaki
BMJ Case Reports|April 23, 2022
Asymmetrical Graves' disease in children: potential usefulness of potassium iodide monotherapyKyoko Fukahori, Kentaro Sawano, Hiroshi Yoshida, et al.
Congenital Anomalies|June 22, 2021
Two cases of cytochrome P450 oxidoreductase deficiency with severe scoliosis and surgery requirementTakanori Onuki, Yoshiaki Ohtsu, Shota Hiroshima, et al.
Congenital Anomalies|April 15, 2023
Klinefelter syndrome with penoscrotal transposition and diphallia: A case studyYugo Kawakami, Kentaro Sawano, Nao Shibata, et al.
Congenital Anomalies|September 30, 2021
A Japanese family with a heterozygous novel mutation in the Indian hedgehog gene exhibiting a broad spectrum of clinical features and radiological findingsTakanori Onuki, Nao Shibata, Shota Hiroshima, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|February 27, 2024
Hypocarnitinemia in twins after maternal pivalate-conjugated antibiotic therapyTakuya Fuse, Yuta Aizawa, Hiromi Nyuzuki, et al.
Children (Basel, Switzerland)|August 26, 2023
A Study of Maternal Patients Diagnosed with Inborn Errors of Metabolism Due to Positive Newborn Mass Screening in Their NewbornsTakanori Onuki, Shota Hiroshima, Kentaro Sawano, et al.
Frontiers in Endocrinology|July 3, 2025
<i>De novo</i> retrotransposon insertion into the <i>FGFR1</i> gene in a boy with congenital hypogonadotropic hypogonadism: a case reportKentaro Sawano, Keisuke Nagasaki, Erina Suzuki, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|October 6, 2025
Utility of the FT3-to-FT4 ratio as a screening marker for pediatric Graves' diseaseKazuhiro Shimura, Kentaro Sawano, Keisuke Nagasaki, et al.
Pageof 2

Showing results (1-10 of 20) with videos related to

Sort By:
Pageof 2
Archives of Disease in Childhood|November 13, 2021
Carotenoderma with hypothyroidismKentaro Sawano, Keisuke Nagasaki
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|October 22, 2020
Letter to the Editor: Testosterone priming increased growth hormone peak levels in the stimulation test and suppressed gonadotropin secretion in three Japanese adolescent boysKentaro Sawano, Keisuke Nagasaki
BMJ Case Reports|April 23, 2022
Asymmetrical Graves' disease in children: potential usefulness of potassium iodide monotherapyKyoko Fukahori, Kentaro Sawano, Hiroshi Yoshida, et al.
Congenital Anomalies|June 22, 2021
Two cases of cytochrome P450 oxidoreductase deficiency with severe scoliosis and surgery requirementTakanori Onuki, Yoshiaki Ohtsu, Shota Hiroshima, et al.
Congenital Anomalies|April 15, 2023
Klinefelter syndrome with penoscrotal transposition and diphallia: A case studyYugo Kawakami, Kentaro Sawano, Nao Shibata, et al.
Congenital Anomalies|September 30, 2021
A Japanese family with a heterozygous novel mutation in the Indian hedgehog gene exhibiting a broad spectrum of clinical features and radiological findingsTakanori Onuki, Nao Shibata, Shota Hiroshima, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|February 27, 2024
Hypocarnitinemia in twins after maternal pivalate-conjugated antibiotic therapyTakuya Fuse, Yuta Aizawa, Hiromi Nyuzuki, et al.
Children (Basel, Switzerland)|August 26, 2023
A Study of Maternal Patients Diagnosed with Inborn Errors of Metabolism Due to Positive Newborn Mass Screening in Their NewbornsTakanori Onuki, Shota Hiroshima, Kentaro Sawano, et al.
Frontiers in Endocrinology|July 3, 2025
<i>De novo</i> retrotransposon insertion into the <i>FGFR1</i> gene in a boy with congenital hypogonadotropic hypogonadism: a case reportKentaro Sawano, Keisuke Nagasaki, Erina Suzuki, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|October 6, 2025
Utility of the FT3-to-FT4 ratio as a screening marker for pediatric Graves' diseaseKazuhiro Shimura, Kentaro Sawano, Keisuke Nagasaki, et al.
Pageof 2