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Noriyuki Namba

Showing results (51-60 of 103) with videos related to

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Biomedical Research (Tokyo, Japan)|April 21, 2020
Low-vacuum scanning electron microscopy may allow early diagnosis of human renal transplant antibody-mediated rejectionHiroki Yokoyama, Shinichi Okada, Yuko Yamada, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|May 29, 2008
Lrp6 hypomorphic mutation affects bone mass through bone resorption in mice and impairs interaction with MesdTakuo Kubota, Toshimi Michigami, Naoko Sakaguchi, et al.
Advances in Therapy|January 31, 2023
Self-Administration of Burosumab in Children and Adults with X-Linked Hypophosphataemia in Two Open-Label, Single-Arm Clinical StudiesTakuo Kubota, Noriyuki Namba, Hiroyuki Tanaka, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|May 24, 2016
Three novel mutations of the MCT8 (SLC16A2) gene: individual and temporal variations of endocrinological and radiological featuresErina Ono, Masamichi Ariga, Sakiko Oshima, et al.
Development, Growth & Differentiation|June 16, 2021
Photoperiod-independent testicular development in the model newt Pleurodeles waltlMitsuki Kyakuno, Rei Nakamori, Ichiro Tazawa, et al.
CEN Case Reports|October 28, 2023
Familial focal segmental glomerulosclerosis with Alport-like glomerular basement changes caused by paired box protein 2 gene variantYuko Yamada, Hiroki Yokoyama, Ryo Kinoshita, et al.
Endocrine Journal|October 5, 2025
Distribution of blood pressure and its positive association with body mass index standard deviation score in pediatric patients with X-linked hypophosphatemia: a sub-group analysis from the SUNFLOWER observational studyKaori Fujiwara, Daijiro Kabata, Ryota Kawai, et al.
Bone|April 9, 2008
Clinical usefulness of measurement of fibroblast growth factor 23 (FGF23) in hypophosphatemic patients: proposal of diagnostic criteria using FGF23 measurementItsuro Endo, Seiji Fukumoto, Keiichi Ozono, et al.
European Journal of Pediatrics|January 7, 2014
Two Japanese familial cases of Caffey disease with and without the common COL1A1 mutation and normal bone density, and review of the literatureTaichi Kitaoka, Yoko Miyoshi, Noriyuki Namba, et al.
Hormone Research in Paediatrics|March 1, 2014
Serum fibroblast growth factor 23 is a useful marker to distinguish vitamin D-deficient rickets from hypophosphatemic ricketsTakuo Kubota, Taichi Kitaoka, Kohji Miura, et al.
Pageof 11

Showing results (51-60 of 103) with videos related to

Sort By:
Pageof 11
Biomedical Research (Tokyo, Japan)|April 21, 2020
Low-vacuum scanning electron microscopy may allow early diagnosis of human renal transplant antibody-mediated rejectionHiroki Yokoyama, Shinichi Okada, Yuko Yamada, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|May 29, 2008
Lrp6 hypomorphic mutation affects bone mass through bone resorption in mice and impairs interaction with MesdTakuo Kubota, Toshimi Michigami, Naoko Sakaguchi, et al.
Advances in Therapy|January 31, 2023
Self-Administration of Burosumab in Children and Adults with X-Linked Hypophosphataemia in Two Open-Label, Single-Arm Clinical StudiesTakuo Kubota, Noriyuki Namba, Hiroyuki Tanaka, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|May 24, 2016
Three novel mutations of the MCT8 (SLC16A2) gene: individual and temporal variations of endocrinological and radiological featuresErina Ono, Masamichi Ariga, Sakiko Oshima, et al.
Development, Growth & Differentiation|June 16, 2021
Photoperiod-independent testicular development in the model newt Pleurodeles waltlMitsuki Kyakuno, Rei Nakamori, Ichiro Tazawa, et al.
CEN Case Reports|October 28, 2023
Familial focal segmental glomerulosclerosis with Alport-like glomerular basement changes caused by paired box protein 2 gene variantYuko Yamada, Hiroki Yokoyama, Ryo Kinoshita, et al.
Endocrine Journal|October 5, 2025
Distribution of blood pressure and its positive association with body mass index standard deviation score in pediatric patients with X-linked hypophosphatemia: a sub-group analysis from the SUNFLOWER observational studyKaori Fujiwara, Daijiro Kabata, Ryota Kawai, et al.
Bone|April 9, 2008
Clinical usefulness of measurement of fibroblast growth factor 23 (FGF23) in hypophosphatemic patients: proposal of diagnostic criteria using FGF23 measurementItsuro Endo, Seiji Fukumoto, Keiichi Ozono, et al.
European Journal of Pediatrics|January 7, 2014
Two Japanese familial cases of Caffey disease with and without the common COL1A1 mutation and normal bone density, and review of the literatureTaichi Kitaoka, Yoko Miyoshi, Noriyuki Namba, et al.
Hormone Research in Paediatrics|March 1, 2014
Serum fibroblast growth factor 23 is a useful marker to distinguish vitamin D-deficient rickets from hypophosphatemic ricketsTakuo Kubota, Taichi Kitaoka, Kohji Miura, et al.
Pageof 11