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Mari Satoh

Showing results (11-20 of 31) with videos related to

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Journal of Pediatric Endocrinology & Metabolism : JPEM|February 8, 2012
A 3-year-old girl with Graves' disease with hypoglycemia following transient adrenal hyporesponsivenessMari Satoh, Keiko Aso, Satoshi Ikehara, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|August 9, 2013
Genetic analysis in children with transient thyroid dysfunction or subclinical hypothyroidism detected on neonatal screeningMari Satoh, Keiko Aso, Sayaka Ogikubo, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|May 3, 2014
Prediction of pubertal growth at start of estrogen replacement therapy in turner syndromeToshiaki Tanaka, Reiko Horikawa, Yasuhiro Naiki, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|August 5, 2022
Congenital hypogonadotropic hypogonadism complicated by neuroblastomaYukiko Ueta, Keiko Aso, Youichi Haga, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|March 5, 2013
Congenital hypothyroidism caused by a novel mutation of the dual oxidase 2 (DUOX2) geneAtsuko Yoshizawa-Ogasawara, Sayaka Ogikubo, Mari Satoh, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|May 1, 2015
Hypothyroidism caused by the combination of two heterozygous mutations: one in the TSH receptor gene the other in the DUOX2 geneMari Satoh, Keiko Aso, Sayaka Ogikubo, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|November 14, 2015
Transient congenital hypothyroidism caused by compound heterozygous mutations affecting the NADPH-oxidase domain of DUOX2Atsuko Yoshizawa-Ogasawara, Kiyomi Abe, Sayaka Ogikubo, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|May 3, 2014
Third-generation Aromatase Inhibitor Improved Adult Height in a Japanese Boy with TestotoxicosisAtsuko Yoshizawa-Ogasawara, Noriyuki Katsumata, Reiko Horikawa, et al.
Internal Medicine (Tokyo, Japan)|December 16, 2021
A Gas-forming Liver Abscess with Massive Bleeding into the Abscess Cavity Due to a Ruptured Inferior Phrenic ArteryMari Satoh, Takayuki Kogure, Akinobu Koiwai, et al.
Frontiers in Endocrinology|April 14, 2023
Pubertal induction in Turner syndrome without gonadal function: A possibility of earlier, lower-dose estrogen therapyYukihiro Hasegawa, Tomonobu Hasegawa, Mari Satoh, et al.
Pageof 4

Showing results (11-20 of 31) with videos related to

Sort By:
Pageof 4
Journal of Pediatric Endocrinology & Metabolism : JPEM|February 8, 2012
A 3-year-old girl with Graves' disease with hypoglycemia following transient adrenal hyporesponsivenessMari Satoh, Keiko Aso, Satoshi Ikehara, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|August 9, 2013
Genetic analysis in children with transient thyroid dysfunction or subclinical hypothyroidism detected on neonatal screeningMari Satoh, Keiko Aso, Sayaka Ogikubo, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|May 3, 2014
Prediction of pubertal growth at start of estrogen replacement therapy in turner syndromeToshiaki Tanaka, Reiko Horikawa, Yasuhiro Naiki, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|August 5, 2022
Congenital hypogonadotropic hypogonadism complicated by neuroblastomaYukiko Ueta, Keiko Aso, Youichi Haga, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|March 5, 2013
Congenital hypothyroidism caused by a novel mutation of the dual oxidase 2 (DUOX2) geneAtsuko Yoshizawa-Ogasawara, Sayaka Ogikubo, Mari Satoh, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|May 1, 2015
Hypothyroidism caused by the combination of two heterozygous mutations: one in the TSH receptor gene the other in the DUOX2 geneMari Satoh, Keiko Aso, Sayaka Ogikubo, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|November 14, 2015
Transient congenital hypothyroidism caused by compound heterozygous mutations affecting the NADPH-oxidase domain of DUOX2Atsuko Yoshizawa-Ogasawara, Kiyomi Abe, Sayaka Ogikubo, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|May 3, 2014
Third-generation Aromatase Inhibitor Improved Adult Height in a Japanese Boy with TestotoxicosisAtsuko Yoshizawa-Ogasawara, Noriyuki Katsumata, Reiko Horikawa, et al.
Internal Medicine (Tokyo, Japan)|December 16, 2021
A Gas-forming Liver Abscess with Massive Bleeding into the Abscess Cavity Due to a Ruptured Inferior Phrenic ArteryMari Satoh, Takayuki Kogure, Akinobu Koiwai, et al.
Frontiers in Endocrinology|April 14, 2023
Pubertal induction in Turner syndrome without gonadal function: A possibility of earlier, lower-dose estrogen therapyYukihiro Hasegawa, Tomonobu Hasegawa, Mari Satoh, et al.
Pageof 4