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Hidenori Haruna

Showing results (1-10 of 26) with videos related to

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Journal of Pediatric Endocrinology & Metabolism : JPEM|November 16, 2019
Gallstone formation due to rapid weight loss through hyperthyroidismSatoshi Nakano, Mitsuyoshi Suzuki, Hidenori Haruna, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|August 9, 2013
Prolonged Intracranial Hypertension after Recombinant Growth Hormone Therapy due to Impaired CSF AbsorptionKaoru Obinata, Ayako Kamata, Keiji Kinoshita, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|June 7, 2008
Changes in the presence of urine Helicobacter pylori antibody in Japanese children in three different age groupsYukiko Naito, Toshiaki Shimizu, Hidenori Haruna, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|February 19, 2008
Expression of COX-1, COX-2, and PPAR-gamma in the gastric mucosa of children with Helicobacter pylori infectionHidenori Haruna, Toshiaki Shimizu, Yoshikazu Ohtsuka, et al.
International Journal of Pediatrics|May 11, 2010
Assessment of Growth Disturbance in Japanese Children with IBDTetsuo Shono, Mayuko Kato, Yo Aoyagi, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|May 8, 2009
Studies of anti-inflammatory effects of Rooibos tea in ratsHaruna Baba, Yoshikazu Ohtsuka, Hidenori Haruna, et al.
The Tohoku Journal of Experimental Medicine|May 29, 2015
Phenotypic Variability and Newly Identified Mutations of the IVD Gene in Japanese Patients with Isovaleric AcidemiaOsamu Sakamoto, Natsuko Arai-Ichinoi, Hiroshi Mitsubuchi, et al.
Clinical Endocrinology|October 26, 2012
A report of two novel NR5A1 mutation families: possible clinical phenotype of psychiatric symptoms of anxiety and/or depressionAyuko S Suwanai, Tomohiro Ishii, Hidenori Haruna, et al.
Clinical Endocrinology|September 22, 2011
Isolated growth hormone deficiency in two siblings because of paternal mosaicism for a mutation in the GH1 geneMayuko Tsubahara, Yoshitaka Hayashi, Shin-ichi Niijima, et al.
Pediatric Surgery International|December 18, 2008
Immunological investigation of the hepatic tissue from infants with biliary atresiaHaruna Baba, Yoshikazu Ohtsuka, Tohru Fujii, et al.
Pageof 3

Showing results (1-10 of 26) with videos related to

Sort By:
Pageof 3
Journal of Pediatric Endocrinology & Metabolism : JPEM|November 16, 2019
Gallstone formation due to rapid weight loss through hyperthyroidismSatoshi Nakano, Mitsuyoshi Suzuki, Hidenori Haruna, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|August 9, 2013
Prolonged Intracranial Hypertension after Recombinant Growth Hormone Therapy due to Impaired CSF AbsorptionKaoru Obinata, Ayako Kamata, Keiji Kinoshita, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|June 7, 2008
Changes in the presence of urine Helicobacter pylori antibody in Japanese children in three different age groupsYukiko Naito, Toshiaki Shimizu, Hidenori Haruna, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|February 19, 2008
Expression of COX-1, COX-2, and PPAR-gamma in the gastric mucosa of children with Helicobacter pylori infectionHidenori Haruna, Toshiaki Shimizu, Yoshikazu Ohtsuka, et al.
International Journal of Pediatrics|May 11, 2010
Assessment of Growth Disturbance in Japanese Children with IBDTetsuo Shono, Mayuko Kato, Yo Aoyagi, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|May 8, 2009
Studies of anti-inflammatory effects of Rooibos tea in ratsHaruna Baba, Yoshikazu Ohtsuka, Hidenori Haruna, et al.
The Tohoku Journal of Experimental Medicine|May 29, 2015
Phenotypic Variability and Newly Identified Mutations of the IVD Gene in Japanese Patients with Isovaleric AcidemiaOsamu Sakamoto, Natsuko Arai-Ichinoi, Hiroshi Mitsubuchi, et al.
Clinical Endocrinology|October 26, 2012
A report of two novel NR5A1 mutation families: possible clinical phenotype of psychiatric symptoms of anxiety and/or depressionAyuko S Suwanai, Tomohiro Ishii, Hidenori Haruna, et al.
Clinical Endocrinology|September 22, 2011
Isolated growth hormone deficiency in two siblings because of paternal mosaicism for a mutation in the GH1 geneMayuko Tsubahara, Yoshitaka Hayashi, Shin-ichi Niijima, et al.
Pediatric Surgery International|December 18, 2008
Immunological investigation of the hepatic tissue from infants with biliary atresiaHaruna Baba, Yoshikazu Ohtsuka, Tohru Fujii, et al.
Pageof 3