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Ikuma Fujiwara

Showing results (1-10 of 74) with videos related to

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Nihon Rinsho. Japanese Journal of Clinical Medicine|July 5, 2006
[Vitamin D-dependent rickets type I, II]Ikuma Fujiwara
The Journal of Pediatrics|June 24, 2008
Ultrasound appearance of thyroid tissue in hypothyroid infantsEishin Ogawa, Kanako Kojima-Ishii, Ikuma Fujiwara
Metabolism: Clinical and Experimental|October 2, 2009
Novel CYP17A1 mutation in a Japanese patient with combined 17alpha-hydroxylase/17,20-lyase deficiencyNoriyuki Katsumata, Eishin Ogawa, Ikuma Fujiwara, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|September 2, 2003
Subacute thyroiditis in children: patient report and review of the literatureEishin Ogawa, Yuriko Katsushima, Ikuma Fujiwara, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|April 5, 2021
Emergent treatment using glucose/insulin infusing for ketoacidosis in T2 deficiencyTomohiro Nakagawa, Kaoru Kuroda, Ikuma Fujiwara, et al.
Journal of Bone and Mineral Metabolism|May 22, 2017
Responsiveness to pamidronate treatment is not related to the genotype of type I collagen in patients with osteogenesis imperfectaJunko Kanno, Akiko Saito-Hakoda, Shigeo Kure, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|March 26, 2003
Hypophosphatemia in juvenile patients with systemic lupus erythematosusIkuma Fujiwara, Eishin Ogawa, Yoshiaki Kondo, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|March 7, 2003
Abnormal regulation of renal 25-hydroxyvitamin D-1alpha-hydroxylase activity in X-linked hypophosphatemia: a translational or post-translational defectIkuma Fujiwara, Rolands Aravindan, Ron L Horst, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|August 9, 2013
Nateglinide is Effective for Diabetes Mellitus with Reactive Hypoglycemia in a Child with a Compound Heterozygous ABCC8 MutationAkiko Saito-Hakoda, Tohru Yorifuji, Junko Kanno, et al.
No Shinkei Geka. Neurological Surgery|June 14, 2006
[Precocious puberty caused by hCG-producing germinoma involving the bilateral basal ganglia and cerebral white matter without 1ypical radiologic findings: case report]Shinichiro Sugiyama, Toshihiro Kumabe, Masaki Mino, et al.
Pageof 8

Showing results (1-10 of 74) with videos related to

Sort By:
Pageof 8
Nihon Rinsho. Japanese Journal of Clinical Medicine|July 5, 2006
[Vitamin D-dependent rickets type I, II]Ikuma Fujiwara
The Journal of Pediatrics|June 24, 2008
Ultrasound appearance of thyroid tissue in hypothyroid infantsEishin Ogawa, Kanako Kojima-Ishii, Ikuma Fujiwara
Metabolism: Clinical and Experimental|October 2, 2009
Novel CYP17A1 mutation in a Japanese patient with combined 17alpha-hydroxylase/17,20-lyase deficiencyNoriyuki Katsumata, Eishin Ogawa, Ikuma Fujiwara, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|September 2, 2003
Subacute thyroiditis in children: patient report and review of the literatureEishin Ogawa, Yuriko Katsushima, Ikuma Fujiwara, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|April 5, 2021
Emergent treatment using glucose/insulin infusing for ketoacidosis in T2 deficiencyTomohiro Nakagawa, Kaoru Kuroda, Ikuma Fujiwara, et al.
Journal of Bone and Mineral Metabolism|May 22, 2017
Responsiveness to pamidronate treatment is not related to the genotype of type I collagen in patients with osteogenesis imperfectaJunko Kanno, Akiko Saito-Hakoda, Shigeo Kure, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|March 26, 2003
Hypophosphatemia in juvenile patients with systemic lupus erythematosusIkuma Fujiwara, Eishin Ogawa, Yoshiaki Kondo, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|March 7, 2003
Abnormal regulation of renal 25-hydroxyvitamin D-1alpha-hydroxylase activity in X-linked hypophosphatemia: a translational or post-translational defectIkuma Fujiwara, Rolands Aravindan, Ron L Horst, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|August 9, 2013
Nateglinide is Effective for Diabetes Mellitus with Reactive Hypoglycemia in a Child with a Compound Heterozygous ABCC8 MutationAkiko Saito-Hakoda, Tohru Yorifuji, Junko Kanno, et al.
No Shinkei Geka. Neurological Surgery|June 14, 2006
[Precocious puberty caused by hCG-producing germinoma involving the bilateral basal ganglia and cerebral white matter without 1ypical radiologic findings: case report]Shinichiro Sugiyama, Toshihiro Kumabe, Masaki Mino, et al.
Pageof 8