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Signe Sparre Beck-Nielsen

Showing results (1-10 of 39) with videos related to

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Danish Medical Journal|February 2, 2012
Rickets in DenmarkSigne Sparre Beck-Nielsen
Ugeskrift for Laeger|October 29, 2014
[Severe vitamin D deficiency causing hypocalcaemic seizures in an ethnic Danish teenager]Signe Sparre Beck-Nielsen, Niels Thomas Hertel
Clinical Oral Investigations|June 14, 2017
Craniofacial and dental characteristics of patients with vitamin-D-dependent rickets type 1A compared to controls and patients with X-linked hypophosphatemiaHans Gjørup, Signe Sparre Beck-Nielsen, Dorte Haubek
Ugeskrift for Laeger|February 24, 2006
[Vitamin D1alpha-hydroxylase deficiency as the cause of severe rickets in a 1-year-old-old boy]Signe Sparre Beck-Nielsen, Niels Thomas Hertel, Bendt Brock-Jacobsen
Journal of Oral Rehabilitation|October 15, 2020
Oral health-related quality of life in X-linked hypophosphataemia and osteogenesis imperfectaHans Gjørup, Signe Sparre Beck-Nielsen, Jannie Dahl Hald, et al.
Ugeskrift for Laeger|May 21, 2010
[Fibroblast growth factor 23--a phosphate regulating hormone]Signe Sparre Beck-Nielsen, Susanne Møller Pedersen, Moustapha Kassem, et al.
Calcified Tissue International|November 17, 2017
Impact of Conventional Medical Therapy on Bone Mineral Density and Bone Turnover in Adult Patients with X-Linked Hypophosphatemia: A 6-Year Prospective Cohort StudyVikram Vinod Shanbhogue, Stinus Hansen, Niklas Rye Jørgensen, et al.
Calcified Tissue International|February 3, 2019
Elevated Bone Remodeling Markers of CTX and P1NP in Addition to Sclerostin in Patients with X-linked Hypophosphatemia: A Cross-Sectional Controlled StudyStinus Hansen, Vikram V Shanbhogue, Niklas Rye Jørgensen, et al.
JBMR Plus|September 29, 2025
Increased lifelong burden of comorbidities without increased early mortality in hereditary hypophosphatemia: a Danish register studySigne Sparre Beck-Nielsen, Rikke Færgemann Hansen, Ulla Ege Johansen, et al.
Bone|October 3, 2025
A deep intronic PHEX variant in a large Danish family with hereditary hypophosphatemia and a milder skeletal, but more severe dental phenotypeJenny Blechingberg, Kristian Alsbjerg Skipper, Signe Sparre Beck-Nielsen, et al.
Pageof 4

Showing results (1-10 of 39) with videos related to

Sort By:
Pageof 4
Danish Medical Journal|February 2, 2012
Rickets in DenmarkSigne Sparre Beck-Nielsen
Ugeskrift for Laeger|October 29, 2014
[Severe vitamin D deficiency causing hypocalcaemic seizures in an ethnic Danish teenager]Signe Sparre Beck-Nielsen, Niels Thomas Hertel
Clinical Oral Investigations|June 14, 2017
Craniofacial and dental characteristics of patients with vitamin-D-dependent rickets type 1A compared to controls and patients with X-linked hypophosphatemiaHans Gjørup, Signe Sparre Beck-Nielsen, Dorte Haubek
Ugeskrift for Laeger|February 24, 2006
[Vitamin D1alpha-hydroxylase deficiency as the cause of severe rickets in a 1-year-old-old boy]Signe Sparre Beck-Nielsen, Niels Thomas Hertel, Bendt Brock-Jacobsen
Journal of Oral Rehabilitation|October 15, 2020
Oral health-related quality of life in X-linked hypophosphataemia and osteogenesis imperfectaHans Gjørup, Signe Sparre Beck-Nielsen, Jannie Dahl Hald, et al.
Ugeskrift for Laeger|May 21, 2010
[Fibroblast growth factor 23--a phosphate regulating hormone]Signe Sparre Beck-Nielsen, Susanne Møller Pedersen, Moustapha Kassem, et al.
Calcified Tissue International|November 17, 2017
Impact of Conventional Medical Therapy on Bone Mineral Density and Bone Turnover in Adult Patients with X-Linked Hypophosphatemia: A 6-Year Prospective Cohort StudyVikram Vinod Shanbhogue, Stinus Hansen, Niklas Rye Jørgensen, et al.
Calcified Tissue International|February 3, 2019
Elevated Bone Remodeling Markers of CTX and P1NP in Addition to Sclerostin in Patients with X-linked Hypophosphatemia: A Cross-Sectional Controlled StudyStinus Hansen, Vikram V Shanbhogue, Niklas Rye Jørgensen, et al.
JBMR Plus|September 29, 2025
Increased lifelong burden of comorbidities without increased early mortality in hereditary hypophosphatemia: a Danish register studySigne Sparre Beck-Nielsen, Rikke Færgemann Hansen, Ulla Ege Johansen, et al.
Bone|October 3, 2025
A deep intronic PHEX variant in a large Danish family with hereditary hypophosphatemia and a milder skeletal, but more severe dental phenotypeJenny Blechingberg, Kristian Alsbjerg Skipper, Signe Sparre Beck-Nielsen, et al.
Pageof 4