300 results on '"Rauch, A."'
Search Results
2. Arthrogryposis multiplex congenita: dental and maxillofacial phenotype — A scoping review
3. Accelerated mineralization kinetics in children with osteogenesis imperfecta type 1
4. Cortical bone material / compositional properties in growing children and young adults aged 1.5–23 years, as a function of gender, age, metabolic activity, and growth spurt
5. Assessment of longitudinal bone growth in osteogenesis imperfecta using metacarpophalangeal pattern profiles
6. Bone densities and bone geometry in children and adolescents with arthrogryposis
7. Missing and unerupted teeth in osteogenesis imperfecta
8. Muscle transcriptome in mouse models of osteogenesis imperfecta
9. Osteogenesis imperfecta tooth level phenotype analysis: Cross-sectional study
10. Multisite longitudinal calibration of HR-pQCT scanners and precision in osteogenesis imperfecta
11. Effects of treatment with a bone-targeted prostaglandin E2 receptor 4 agonist C3 (Mes-1007) in a mouse model of severe osteogenesis imperfecta
12. TNF-α modulation via Etanercept restores bone regeneration of atrophic non-unions
13. Musculoskeletal phenotype in two unrelated individuals with a recurrent nonsense variant in SGMS2
14. Arthrogryposis multiplex congenita: dental and maxillofacial phenotype — A scoping review
15. X-linked hypophosphatemia caused by a deep intronic variant in PHEX identified by PCR-based RNA analysis of urine-derived cells
16. Novel ActRIIB ligand trap increases muscle mass and improves bone geometry in a mouse model of severe osteogenesis imperfecta
17. Mendelian bone fragility disorders
18. Five-year efficacy and safety of asfotase alfa therapy for adults and adolescents with hypophosphatasia
19. Novel WNT1 mutations in children with osteogenesis imperfecta: Clinical and functional characterization
20. Crispr-Cas9 engineered osteogenesis imperfecta type V leads to severe skeletal deformities and perinatal lethality in mice
21. Increased bone matrix mineralization in treatment-naïve children with inflammatory bowel disease
22. Scoliosis in osteogenesis imperfecta caused by COL1A1/COL1A2 mutations — genotype–phenotype correlations and effect of bisphosphonate treatment
23. Effect of high-dose vitamin D supplementation on bone density in youth with osteogenesis imperfecta: A randomized controlled trial
24. Bone matrix hypermineralization in prolyl-3 hydroxylase 1 deficient mice
25. Behavioral signs of pain and functional impairment in a mouse model of osteogenesis imperfecta
26. The functional muscle–bone unit in patients with osteogenesis imperfecta type I
27. The effect of SERPINF1 in-frame mutations in osteogenesis imperfecta type VI
28. Unique micro- and nano-scale mineralization pattern of human osteogenesis imperfecta type VI bone
29. Craniofacial and dental phenotype of two girls with osteogenesis imperfecta due to mutations in CRTAP
30. Pediatric reference Raman data for material characteristics of iliac trabecular bone
31. Skeletal characteristics associated with homozygous and heterozygous WNT1 mutations
32. Accelerated mineralization kinetics in children with osteogenesis imperfecta type 1
33. Dominant osteogenesis imperfecta with low bone turnover caused by a heterozygous SP7 variant
34. Effect of sclerostin antibody treatment in a mouse model of severe osteogenesis imperfecta
35. Mineral particle size in children with osteogenesis imperfecta type I is not increased independently of specific collagen mutations
36. Cortical bone material / compositional properties in growing children and young adults aged 1.5-23 years, as a function of gender, age, metabolic activity, and growth spurt
37. CRTAP deficiency leads to abnormally high bone matrix mineralization in a murine model and in children with osteogenesis imperfecta type VII
38. Bone densities and bone geometry in children and adolescents with arthrogryposis
39. Higher BMC and areal BMD in children and grandchildren of individuals with hip or knee replacement
40. Mendelian bone fragility disorders
41. Five-year efficacy and safety of asfotase alfa therapy for adults and adolescents with hypophosphatasia
42. Normative data on mineralization density distribution in iliac bone biopsies of children, adolescents and young adults
43. Osteogenesis imperfecta tooth level phenotype analysis: Cross-sectional study
44. International Society for Clinical Densitometry 2007 Adult and Pediatric Official Positions
45. Sex-specific developmental changes in muscle size and bone geometry at the femoral shaft
46. TNF-α modulation via Etanercept restores bone regeneration of atrophic non-unions
47. Novel WNT1 mutations in children with osteogenesis imperfecta: Clinical and functional characterization
48. Musculoskeletal phenotype in two unrelated individuals with a recurrent nonsense variant in SGMS2
49. Long-bone changes after pamidronate discontinuation in children and adolescents with osteogenesis imperfecta
50. Osteogenesis imperfecta type VI in childhood and adolescence: Effects of cyclical intravenous pamidronate treatment
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