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

Naoko Amano

Showing results (1-10 of 49) with videos related to

Pageof 5
Sort By:
The Journal of Clinical Endocrinology and Metabolism|April 9, 2024
Response to Letter to the Editor From Janot et al: "Single-Exon Deletions of ZNRF3 Exon 2 Cause Congenital Adrenal Hypoplasia"Naoko Amano, Satoshi Narumi, Tomohiro Ishii, et al.
Urology|March 31, 2010
The effect of intramuscular testosterone enanthate treatment on stretched penile length in prepubertal boys with hypospadiasTomohiro Ishii, Mie Hayashi, Ayuko Suwanai, et al.
Current Opinion in Pediatrics|June 4, 2024
Biochemical monitoring of 21-hydroxylase deficiency: a clinical utility of overnight fasting urine pregnanetriolYukihiro Hasegawa, Tomoyo Itonaga, Tomohiro Ishii, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|May 3, 2014
A novel mutation of androgen receptor gene in complete androgen insensitivity syndromeSatoshi Narumi, Naoko Amano, Rumi Hachiya, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|July 23, 2020
A novel <i>NPR2</i> mutation (p.Arg388Gln) in a patient with acromesomelic dysplasia, type MaroteauxNaoko Amano, Hiroshi Kitoh, Satoshi Narumi, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|January 8, 2025
Current understanding and perspectives on growth and long-acting GH therapy in JapanYukihiro Hasegawa, Kento Ikegawa, Marie Mitani-Konno, et al.
CEN Case Reports|May 17, 2017
Transient Fanconi syndrome in two preterm infants with hydronephrosis and urinary tract infectionTakahiro Tominaga, Takeshi Sato, Yosuke Ichihashi, et al.
Clinical Epigenetics|June 9, 2025
Multi-locus methylation analyses reveal GNAS methylation defects in three patients with the Beckwith-Wiedemann syndrome phenotype and no molecular defects in the 11p15.5 imprinted regionTatsuki Urakawa, Yuri Kanamaru, Naoko Amano, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|May 3, 2014
Growth failure in an infant with congenital nephrogenic diabetes insipidus during sodium restrictionGoro Sasaki, Tomohiro Ishii, Naoko Amano, et al.
Endocrine Journal|June 11, 2019
Effects of pre- and post-pubertal dihydrotestosterone treatment on penile length in 5α-reductase type 2 deficiencyGoro Sasaki, Tomohiro Ishii, Naoaki Hori, et al.
Pageof 5

Showing results (1-10 of 49) with videos related to

Sort By:
Pageof 5
The Journal of Clinical Endocrinology and Metabolism|April 9, 2024
Response to Letter to the Editor From Janot et al: "Single-Exon Deletions of ZNRF3 Exon 2 Cause Congenital Adrenal Hypoplasia"Naoko Amano, Satoshi Narumi, Tomohiro Ishii, et al.
Urology|March 31, 2010
The effect of intramuscular testosterone enanthate treatment on stretched penile length in prepubertal boys with hypospadiasTomohiro Ishii, Mie Hayashi, Ayuko Suwanai, et al.
Current Opinion in Pediatrics|June 4, 2024
Biochemical monitoring of 21-hydroxylase deficiency: a clinical utility of overnight fasting urine pregnanetriolYukihiro Hasegawa, Tomoyo Itonaga, Tomohiro Ishii, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|May 3, 2014
A novel mutation of androgen receptor gene in complete androgen insensitivity syndromeSatoshi Narumi, Naoko Amano, Rumi Hachiya, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|July 23, 2020
A novel <i>NPR2</i> mutation (p.Arg388Gln) in a patient with acromesomelic dysplasia, type MaroteauxNaoko Amano, Hiroshi Kitoh, Satoshi Narumi, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|January 8, 2025
Current understanding and perspectives on growth and long-acting GH therapy in JapanYukihiro Hasegawa, Kento Ikegawa, Marie Mitani-Konno, et al.
CEN Case Reports|May 17, 2017
Transient Fanconi syndrome in two preterm infants with hydronephrosis and urinary tract infectionTakahiro Tominaga, Takeshi Sato, Yosuke Ichihashi, et al.
Clinical Epigenetics|June 9, 2025
Multi-locus methylation analyses reveal GNAS methylation defects in three patients with the Beckwith-Wiedemann syndrome phenotype and no molecular defects in the 11p15.5 imprinted regionTatsuki Urakawa, Yuri Kanamaru, Naoko Amano, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|May 3, 2014
Growth failure in an infant with congenital nephrogenic diabetes insipidus during sodium restrictionGoro Sasaki, Tomohiro Ishii, Naoko Amano, et al.
Endocrine Journal|June 11, 2019
Effects of pre- and post-pubertal dihydrotestosterone treatment on penile length in 5α-reductase type 2 deficiencyGoro Sasaki, Tomohiro Ishii, Naoaki Hori, et al.
Pageof 5