Mirko Rehberg
Overview
Explore the profile of Mirko Rehberg including associated specialties, affiliations and a list of published articles.
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29
Citations
195
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Recent Articles
1.
Stasek S, Zaucke F, Hoyer-Kuhn H, Etich J, Reincke S, Arndt I, et al.
J Pediatr Endocrinol Metab
. 2024 Dec;
38(1):1-15.
PMID: 39670712
The formation of functional bone requires a delicate interplay between osteogenesis and osteolysis. Disturbances in this subtle balance result in an increased risk for fractures. Besides its mechanical function, bone...
2.
Klein M, Obermaier M, Mutze H, Wilden S, Rehberg M, Schlingmann K, et al.
Pediatr Nephrol
. 2024 Jun;
39(11):3221-3231.
PMID: 38914781
Background: X-linked hypophosphatemia (XLH) is a rare inherited phosphate-wasting disorder associated with bone and dental complications. Health-related quality of life (HRQoL) is reduced in XLH patients on conventional treatment with...
3.
Sagar R, Astrom E, Chitty L, Crowe B, David A, DeVile C, et al.
BMJ Open
. 2024 Jun;
14(6):e079767.
PMID: 38834319
Introduction: Severe osteogenesis imperfecta (OI) is a debilitating disease with no cure or sufficiently effective treatment. Mesenchymal stem cells (MSCs) have good safety profile, show promising effects and can form...
4.
Etich J, Semler O, Stevenson N, Stephan A, Besio R, Garibaldi N, et al.
EMBO Mol Med
. 2023 Jun;
15(7):e17528.
PMID: 37292039
Osteogenesis imperfecta (OI) is a hereditary skeletal disorder primarily affecting collagen type I structure and function, causing bone fragility and occasionally versatile extraskeletal symptoms. This study expands the spectrum of...
5.
Ewert A, Rehberg M, Schlingmann K, Hiort O, John-Kroegel U, Metzing O, et al.
J Clin Endocrinol Metab
. 2023 Apr;
108(10):e998-e1006.
PMID: 37097907
Context: Burosumab has been approved for the treatment of children and adults with X-linked hypophosphatemia (XLH). Real-world data and evidence for its efficacy in adolescents are lacking. Objective: To assess...
6.
Maghnie M, Semler O, Guillen-Navarro E, Selicorni A, Heath K, Haeusler G, et al.
Orphanet J Rare Dis
. 2023 Mar;
18(1):56.
PMID: 36922864
Background: Achondroplasia, caused by a pathogenic variant in the fibroblast growth factor receptor 3 gene, is the most common skeletal dysplasia. The Lifetime Impact of Achondroplasia Study in Europe (LIAISE;...
7.
Schwanitz von Keitz P, Kleimeier D, Lutter C, Rehberg M, Mittelmeier W, Kasch R, et al.
Heliyon
. 2022 Dec;
8(12):e11942.
PMID: 36478850
Background: With an incidence of 2-4% in all newborns, developmental dysplasia of the hip, DDH, represents the most frequent congenital disorder of the skeletal system in Germany. The therapy options...
8.
Reiter U, Eckert A, Dunstheimer D, Pozza S, Lullwitz C, Golembowski S, et al.
Pediatr Diabetes
. 2022 Jan;
23(3):362-369.
PMID: 35064955
Objective: To study diabetic cataract in type 1 diabetes in a large pediatric cohort. Methods: The 92,633 patients aged 0.5-21 years from German/Austrian multicenter diabetes registry (DPV) were analyzed. The...
9.
Schafmeyer L, Linden T, Sill H, Rehberg M, Schoenau E, Duran I
J Clin Densitom
. 2021 Aug;
25(1):73-80.
PMID: 34456143
Localized neurological diseases such as spina bifida are often accompanied by normal upper limb and spinal bone mineral density (BMD), whereas regional BMD of the lower limbs may be decreased....
10.
Martakis K, Stark C, Rehberg M, Jackels M, Schoenau E, Duran I
J Pediatr Endocrinol Metab
. 2021 Jul;
34(10):1273-1282.
PMID: 34271602
Objectives: Obesity has often been associated with high low-density-lipoprotein cholesterol (LDL-C) and triglyceride plasma concentrations, known risk factors for diabetes mellitus and cardiovascular disease. Study objective was to evaluate the...