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Misayo Matsuyama

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Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|February 1, 2024
A novel variant of <i>IGSF1</i> in siblings with congenital central hypothyroidism whose diagnosis was prompted by school health checkupsYoshiko Yamamura, Maki Fukami, Misayo Matsuyama, et al.
Japanese Journal of Radiology|April 17, 2021
3D fat-suppressed T1-weighted volume isotropic turbo spin-echo acquisition (VISTA) imaging for the evaluation of the ectopic posterior pituitary glandMinako Azuma, Yoshihito Kadota, Misayo Matsuyama, et al.
JMA Journal|November 12, 2025
Interference of Intravenous Acetaminophen with Continuous Glucose Monitoring SystemMisayo Matsuyama, Satoru Meiri, Hirotake Sawada, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|August 5, 2022
Goiter in a 6-year-old patient with novel thyroglobulin gene variant (Gly145Glu) causing intracellular thyroglobulin transport disorder: Correlation between goiter size and the free T3 to free T4 ratioMisayo Matsuyama, Hirotake Sawada, Shinobu Inoue, et al.
Human Genome Variation|September 11, 2023
Novel splice site variant of TMEM38B in osteogenesis imperfecta type XIVYoshihiko Kodama, Satoru Meiri, Tomoko Asada, et al.
JIMD Reports|February 11, 2015
Infantile Cases of Sitosterolaemia with Novel Mutations in the ABCG5 Gene: Extreme Hypercholesterolaemia is Exacerbated by BreastfeedingHayato Tada, Masa-Aki Kawashiri, Mutsuko Takata, et al.
Medicine|September 11, 2024
An autopsy case of an adult woman with Rapid-Onset Obesity with Hypoventilation, Hypothalamic, Autonomic Dysregulation, and Neuroendocrine Tumors (ROHHAD(NET)) syndrome developing nonalcoholic steatohepatitis and hepatocellular carcinoma: A case reportSatoru Hasuike, Yoshinori Ozono, Keisuke Uchida, et al.
Plos One|December 18, 2018
Familial episodic limb pain in kindreds with novel Nav1.9 mutationsRisako Kabata, Hiroko Okuda, Atsuko Noguchi, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|February 1, 2024
A novel variant of <i>IGSF1</i> in siblings with congenital central hypothyroidism whose diagnosis was prompted by school health checkupsYoshiko Yamamura, Maki Fukami, Misayo Matsuyama, et al.
Japanese Journal of Radiology|April 17, 2021
3D fat-suppressed T1-weighted volume isotropic turbo spin-echo acquisition (VISTA) imaging for the evaluation of the ectopic posterior pituitary glandMinako Azuma, Yoshihito Kadota, Misayo Matsuyama, et al.
JMA Journal|November 12, 2025
Interference of Intravenous Acetaminophen with Continuous Glucose Monitoring SystemMisayo Matsuyama, Satoru Meiri, Hirotake Sawada, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|August 5, 2022
Goiter in a 6-year-old patient with novel thyroglobulin gene variant (Gly145Glu) causing intracellular thyroglobulin transport disorder: Correlation between goiter size and the free T3 to free T4 ratioMisayo Matsuyama, Hirotake Sawada, Shinobu Inoue, et al.
Human Genome Variation|September 11, 2023
Novel splice site variant of TMEM38B in osteogenesis imperfecta type XIVYoshihiko Kodama, Satoru Meiri, Tomoko Asada, et al.
JIMD Reports|February 11, 2015
Infantile Cases of Sitosterolaemia with Novel Mutations in the ABCG5 Gene: Extreme Hypercholesterolaemia is Exacerbated by BreastfeedingHayato Tada, Masa-Aki Kawashiri, Mutsuko Takata, et al.
Medicine|September 11, 2024
An autopsy case of an adult woman with Rapid-Onset Obesity with Hypoventilation, Hypothalamic, Autonomic Dysregulation, and Neuroendocrine Tumors (ROHHAD(NET)) syndrome developing nonalcoholic steatohepatitis and hepatocellular carcinoma: A case reportSatoru Hasuike, Yoshinori Ozono, Keisuke Uchida, et al.
Plos One|December 18, 2018
Familial episodic limb pain in kindreds with novel Nav1.9 mutationsRisako Kabata, Hiroko Okuda, Atsuko Noguchi, et al.
Pageof 1