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Toshimi Michigami

Showing results (111-120 of 138) with videos related to

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Endocrine Journal|January 29, 2025
Efficacy of asfotase alfa in a patient with adult-onset hypophosphatasia without obvious bone lesions: a case report with review of literatureSeiji Nishikage, Masaaki Yamamoto, Takahiro Niikura, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|February 8, 2020
Clinical Practice Guidelines for HypophosphatasiaToshimi Michigami, Yasuhisa Ohata, Makoto Fujiwara, et al.
Endocrine Journal|July 3, 2015
Nationwide survey of fibroblast growth factor 23 (FGF23)-related hypophosphatemic diseases in Japan: prevalence, biochemical data and treatmentItsuro Endo, Seiji Fukumoto, Keiichi Ozono, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|August 9, 2013
Clinical characteristics of perinatal lethal hypophosphatasia: a report of 6 casesAkari Nakamura-Utsunomiya, Satoshi Okada, Keiichi Hara, et al.
The Journal of Clinical Endocrinology and Metabolism|March 18, 2011
Circulating levels of soluble alpha-Klotho are markedly elevated in human umbilical cord bloodYasuhisa Ohata, Hitomi Arahori, Noriyuki Namba, et al.
Bone|July 2, 2014
Hypophosphatemic osteomalacia and bone sclerosis caused by a novel homozygous mutation of the FAM20C gene in an elderly man with a mild variant of Raine syndromeShinji Takeyari, Takehisa Yamamoto, Yuka Kinoshita, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|March 5, 2015
Reversible Deterioration in Hypophosphatasia Caused by Renal Failure With Bisphosphonate TreatmentTim Cundy, Toshimi Michigami, Kanako Tachikawa, et al.
Calcified Tissue International|March 13, 2025
Prevalence of Comorbid Hyperparathyroidism and Its Association with Renal Dysfunction in Asian Patients with X-Linked Hypophosphatemic Rickets/OsteomalaciaNobuaki Ito, Hee Gyung Kang, Toshimi Michigami, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|June 1, 2006
Sp1 family of transcription factors regulates the human alpha2 (XI) collagen gene (COL11A2) in Saos-2 osteoblastic cellsTomohiro Goto, Yoshito Matsui, Russell J Fernandes, et al.
Hepatology Research : the Official Journal of the Japan Society of Hepatology|August 30, 2018
CYP7A1 expression in hepatocytes is retained with upregulated fibroblast growth factor 19 in pediatric biliary atresiaYasuhiro Hasegawa, Masanobu Kawai, Kazuhiko Bessho, et al.
Pageof 14

Showing results (111-120 of 138) with videos related to

Sort By:
Pageof 14
Endocrine Journal|January 29, 2025
Efficacy of asfotase alfa in a patient with adult-onset hypophosphatasia without obvious bone lesions: a case report with review of literatureSeiji Nishikage, Masaaki Yamamoto, Takahiro Niikura, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|February 8, 2020
Clinical Practice Guidelines for HypophosphatasiaToshimi Michigami, Yasuhisa Ohata, Makoto Fujiwara, et al.
Endocrine Journal|July 3, 2015
Nationwide survey of fibroblast growth factor 23 (FGF23)-related hypophosphatemic diseases in Japan: prevalence, biochemical data and treatmentItsuro Endo, Seiji Fukumoto, Keiichi Ozono, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|August 9, 2013
Clinical characteristics of perinatal lethal hypophosphatasia: a report of 6 casesAkari Nakamura-Utsunomiya, Satoshi Okada, Keiichi Hara, et al.
The Journal of Clinical Endocrinology and Metabolism|March 18, 2011
Circulating levels of soluble alpha-Klotho are markedly elevated in human umbilical cord bloodYasuhisa Ohata, Hitomi Arahori, Noriyuki Namba, et al.
Bone|July 2, 2014
Hypophosphatemic osteomalacia and bone sclerosis caused by a novel homozygous mutation of the FAM20C gene in an elderly man with a mild variant of Raine syndromeShinji Takeyari, Takehisa Yamamoto, Yuka Kinoshita, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|March 5, 2015
Reversible Deterioration in Hypophosphatasia Caused by Renal Failure With Bisphosphonate TreatmentTim Cundy, Toshimi Michigami, Kanako Tachikawa, et al.
Calcified Tissue International|March 13, 2025
Prevalence of Comorbid Hyperparathyroidism and Its Association with Renal Dysfunction in Asian Patients with X-Linked Hypophosphatemic Rickets/OsteomalaciaNobuaki Ito, Hee Gyung Kang, Toshimi Michigami, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|June 1, 2006
Sp1 family of transcription factors regulates the human alpha2 (XI) collagen gene (COL11A2) in Saos-2 osteoblastic cellsTomohiro Goto, Yoshito Matsui, Russell J Fernandes, et al.
Hepatology Research : the Official Journal of the Japan Society of Hepatology|August 30, 2018
CYP7A1 expression in hepatocytes is retained with upregulated fibroblast growth factor 19 in pediatric biliary atresiaYasuhiro Hasegawa, Masanobu Kawai, Kazuhiko Bessho, et al.
Pageof 14