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Bone Reports
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January 11, 2019
Brown tumor diagnosed three years after parathyroidectomy in a patient with nail-patella syndrome: A case report
Naoya Toriu, Toshiharu Ueno, Hiroki Mizuno, et al.
Bone Reports
|
January 11, 2019
Ectopic expression of Klotho in fibroblast growth factor 23 (FGF23)-producing tumors that cause tumor-induced rickets/osteomalacia (TIO)
Yuka Kinoshita, Yuichi Takashi, Nobuaki Ito, et al.
Bone Reports
|
June 19, 2023
Antipsychotic medication use in association with quantitative heel ultrasound (QUS)
Behnaz Azimi Manavi, Mohammadreza Mohebbi, Amanda L Stuart, et al.
Bone Reports
|
May 30, 2023
Mazabraud's syndrome: A case report supported by molecular studies and review of the literature
Ludvík Kašpar, Jan Balko, Martina Strnadová, et al.
Bone Reports
|
June 9, 2023
Changes in BMD T-score from pre-to post-treatment with biosimilar teriparatide: A single-arm, multi-center study
Mohsen G Soroush, Maryam Kheirandish, Soosan Soroosh
Bone Reports
|
May 6, 2026
Prior treatment, not vitamin D, predicts romosozumab response in 314 osteoporosis patients: A retrospective cohort study
Ryo Nakano, Ayumi Ichisawa, Kenya Saruta, et al.
Bone Reports
|
March 9, 2026
Transferrin-dependent uptake and distribution of iron in osteoclast-like cells
Silvia Dolder, Romina Cabra, Jonas Zaugg, et al.
Bone Reports
|
April 6, 2017
Primary human osteoblasts with reduced alkaline phosphatase and matrix mineralization baseline capacity are responsive to extremely low frequency pulsed electromagnetic field exposure - Clinical implication possible
Sabrina Ehnert, Karsten Falldorf, Anne-Kristin Fentz, et al.
Bone Reports
|
January 13, 2022
Radiological evaluation of pseudofracture after the administration of asfotase alfa in an adult with benign prenatal hypophosphatasia: A case report
Hajime Kato, Naoko Hidaka, Minae Koga, et al.
Bone Reports
|
October 27, 2018
Skeletal disease in a father and daughter with a novel monoallelic WNT1 mutation
Kathleen Ang, Elizabeth Sanchez Rangel, Qianying Yuan, et al.
Page
of 81
Search research articles
Search
Showing results (111-120 of 802) with videos related to
Sort By:
Page
of 81
Bone Reports
|
January 11, 2019
Brown tumor diagnosed three years after parathyroidectomy in a patient with nail-patella syndrome: A case report
Naoya Toriu, Toshiharu Ueno, Hiroki Mizuno, et al.
Bone Reports
|
January 11, 2019
Ectopic expression of Klotho in fibroblast growth factor 23 (FGF23)-producing tumors that cause tumor-induced rickets/osteomalacia (TIO)
Yuka Kinoshita, Yuichi Takashi, Nobuaki Ito, et al.
Bone Reports
|
June 19, 2023
Antipsychotic medication use in association with quantitative heel ultrasound (QUS)
Behnaz Azimi Manavi, Mohammadreza Mohebbi, Amanda L Stuart, et al.
Bone Reports
|
May 30, 2023
Mazabraud's syndrome: A case report supported by molecular studies and review of the literature
Ludvík Kašpar, Jan Balko, Martina Strnadová, et al.
Bone Reports
|
June 9, 2023
Changes in BMD T-score from pre-to post-treatment with biosimilar teriparatide: A single-arm, multi-center study
Mohsen G Soroush, Maryam Kheirandish, Soosan Soroosh
Bone Reports
|
May 6, 2026
Prior treatment, not vitamin D, predicts romosozumab response in 314 osteoporosis patients: A retrospective cohort study
Ryo Nakano, Ayumi Ichisawa, Kenya Saruta, et al.
Bone Reports
|
March 9, 2026
Transferrin-dependent uptake and distribution of iron in osteoclast-like cells
Silvia Dolder, Romina Cabra, Jonas Zaugg, et al.
Bone Reports
|
April 6, 2017
Primary human osteoblasts with reduced alkaline phosphatase and matrix mineralization baseline capacity are responsive to extremely low frequency pulsed electromagnetic field exposure - Clinical implication possible
Sabrina Ehnert, Karsten Falldorf, Anne-Kristin Fentz, et al.
Bone Reports
|
January 13, 2022
Radiological evaluation of pseudofracture after the administration of asfotase alfa in an adult with benign prenatal hypophosphatasia: A case report
Hajime Kato, Naoko Hidaka, Minae Koga, et al.
Bone Reports
|
October 27, 2018
Skeletal disease in a father and daughter with a novel monoallelic WNT1 mutation
Kathleen Ang, Elizabeth Sanchez Rangel, Qianying Yuan, et al.
Page
of 81