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Satoshi Narumi

Showing results (11-20 of 183) with videos related to

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Acta Paediatrica (Oslo, Norway : 1992)|December 5, 2024
Impact of COVID-19 on paediatric care in Japan: Analysis of national health insurance claims dataTakuma Ohnishi, Mari Kinoshita, Satoshi Narumi
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|February 10, 2023
A case of syndromic congenital hypothyroidism with a 15.2 Mb interstitial deletion on 2q12.3q14.2 involving <i>PAX8</i>Megumi Iwahashi-Odano, Miyuki Kitamura, Satoshi Narumi
American Journal of Human Biology : the Official Journal of the Human Biology Council|April 25, 2025
Reference Values of Arm Span and Arm Span to Height Ratio of Japanese Population in Childhood and Adolescence: Comparison With Dutch and Turkish PopulationYasuhiro Hirano, Mikako Inokuchi, Satoshi Narumi, et al.
Hormone Research in Paediatrics|January 19, 2025
Recovery from Atrophic Autoimmune Thyroiditis in a Child: Thyroid Stimulation-Blocking Antibody as a Prognostic MarkerChieko Kusano, Naoaki Hori, Tomonobu Hasegawa, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|November 6, 2018
Methylome analysis of thyroid ectopy shows no disease-specific DNA methylation signatureSatoshi Narumi, Keiko Matsubara, Tomohiro Ishii, et al.
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.
Frontiers in Oncology|July 2, 2025
Epigenetic modifications and their roles in pediatric brain tumor formation: emerging insights from chromatin dysregulationKento Kawata, Owen S Chapman, Satoshi Narumi, et al.
Human Genome Variation|April 28, 2017
Syndromic disorder of sex development due to a novel hemizygous mutation in the carboxyl-terminal domain of <i>ATRX</i>Masaki Takagi, Hiroko Yagi, Ryuji Fukuzawa, 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.
Pageof 19

Showing results (11-20 of 183) with videos related to

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Pageof 19
Acta Paediatrica (Oslo, Norway : 1992)|December 5, 2024
Impact of COVID-19 on paediatric care in Japan: Analysis of national health insurance claims dataTakuma Ohnishi, Mari Kinoshita, Satoshi Narumi
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|February 10, 2023
A case of syndromic congenital hypothyroidism with a 15.2 Mb interstitial deletion on 2q12.3q14.2 involving <i>PAX8</i>Megumi Iwahashi-Odano, Miyuki Kitamura, Satoshi Narumi
American Journal of Human Biology : the Official Journal of the Human Biology Council|April 25, 2025
Reference Values of Arm Span and Arm Span to Height Ratio of Japanese Population in Childhood and Adolescence: Comparison With Dutch and Turkish PopulationYasuhiro Hirano, Mikako Inokuchi, Satoshi Narumi, et al.
Hormone Research in Paediatrics|January 19, 2025
Recovery from Atrophic Autoimmune Thyroiditis in a Child: Thyroid Stimulation-Blocking Antibody as a Prognostic MarkerChieko Kusano, Naoaki Hori, Tomonobu Hasegawa, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|November 6, 2018
Methylome analysis of thyroid ectopy shows no disease-specific DNA methylation signatureSatoshi Narumi, Keiko Matsubara, Tomohiro Ishii, et al.
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.
Frontiers in Oncology|July 2, 2025
Epigenetic modifications and their roles in pediatric brain tumor formation: emerging insights from chromatin dysregulationKento Kawata, Owen S Chapman, Satoshi Narumi, et al.
Human Genome Variation|April 28, 2017
Syndromic disorder of sex development due to a novel hemizygous mutation in the carboxyl-terminal domain of <i>ATRX</i>Masaki Takagi, Hiroko Yagi, Ryuji Fukuzawa, 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.
Pageof 19