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Signe Sparre Beck-Nielsen

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Recent Articles
11.
Brandi M, Ariceta G, Beck-Nielsen S, Boot A, Briot K, Collantes C, et al.
Ther Adv Chronic Dis . 2022 Sep; 13:20406223221117471. PMID: 36082134
Background: X-linked hypophosphataemia (XLH) is a rare, inherited, phosphate-wasting disorder that elevates fibroblast growth factor 23 (FGF23), causing renal phosphate-wasting and impaired active vitamin D (1,25(OH)D) synthesis. Disease characteristics include...
12.
Gjorup H, Beck-Nielsen S, Hald J, Haubek D
J Oral Rehabil . 2020 Oct; 48(2):160-168. PMID: 33058298
X-linked hypophosphataemia (XLH) and osteogenesis imperfecta (OI) are rare congenital disorders characterised by skeletal dysplasia. The two disorders may include dental anomalies potentially affecting individual well-being. The aims of study...
13.
Jorgensen C, Poulsen V, Sandahl M, Underbjerg L, Kristensen S, Piec I, et al.
Int J Endocrinol Metab . 2020 Jan; 17(4):e91454. PMID: 31903094
Background: Standard treatment of hypophosphatemic rickets (HR) is oral phosphate tablets plus vitamin D. Due to the rapid absorption of phosphate tablets, frequent daily doses are necessary, which is cumbersome...
14.
Beck-Nielsen S, Mughal Z, Haffner D, Nilsson O, Levtchenko E, Ariceta G, et al.
Orphanet J Rare Dis . 2019 Feb; 14(1):58. PMID: 30808384
Background: X-linked hypophosphatemia (XLH) is an inherited disease of phosphate metabolism in which inactivating mutations of the Phosphate Regulating Endopeptidase Homolog, X-Linked (PHEX) gene lead to local and systemic effects...
15.
Hansen S, Shanbhogue V, Jorgensen N, Beck-Nielsen S
Calcif Tissue Int . 2019 Feb; 104(6):591-598. PMID: 30710161
Aspects of bone remodeling have only been scarcely studied in X-linked hypophosphatemia (XLH). In this cross-sectional controlled study, we assessed biochemical indices of bone remodeling and sclerostin in 27 adult...
16.
Jolving L, Nielsen J, Kesmodel U, Nielsen R, Norgard B, Beck-Nielsen S
Clin Epidemiol . 2018 Oct; 10:1381-1390. PMID: 30310330
Objective: Maternal thyroid disease (TD) during pregnancy is associated with adverse birth outcomes, but little is known on its long-term outcomes. We aimed to examine if children born to mothers...
17.
Christensen M, Beck-Nielsen S, Dalgard C, Larsen S, Lykkedegn S, Kyhl H, et al.
PLoS One . 2018 Jun; 13(6):e0198724. PMID: 29889866
Background And Aim: Long standing vitamin D deficiency in children causes rickets with growth impairment. We investigated whether sub-ischial leg length (SLL) is shorter, and cephalo-caudal length:length (CCL:L) ratio and...
18.
Shanbhogue V, Hansen S, Jorgensen N, Beck-Nielsen S
Calcif Tissue Int . 2017 Nov; 102(3):321-328. PMID: 29143140
X-linked hypophosphatemia (XLH) is a rare, inheritable disorder manifesting as rickets in children and osteomalacia in adults. While conventional medical treatment with oral phosphate and alfacalcidol is recommended in childhood,...
19.
Gjorup H, Beck-Nielsen S, Haubek D
Clin Oral Investig . 2017 Jun; 22(2):745-755. PMID: 28608052
Material And Methods: Ten patients with VDDR1A were identified. The reference group for the comparison of cephalometric findings was 49 adults without chronic disease. The reference group for the comparison...
20.
Lykkedegn S, Beck-Nielsen S, Sorensen G, Andersen L, Fruekilde P, Nielsen J, et al.
Clin Nutr . 2016 Nov; 36(6):1621-1627. PMID: 27817876
Background & Aims: Hypovitaminosis D, defined as serum 25-hydroxyvitamin D (s-25(OH)D) <50 nmol/L, is frequent in pregnant women and neonates worldwide and has been associated with both low birth weight...