dr. R.J.B. Sakkers
Assistant Professor - medical
- Department of Orthopaedics
Contact
Research Output (73)
Correlation between ultrasonic and radiographic imaging of developmental dysplasia of the hip
Spaans A. J., Beek F. J.A., Uiterwaal C. S.P.M., Pruijs J. E.H., Sakkers R. J. 1 apr 2019, In: Journal of Children's Orthopaedics. 13 , p. 155-160 6 p.
CT synthesis from MR images for orthopedic applications in the lower arm using a conditional generative adversarial network
Zijlstra F., Willemsen K., Florkow M. C., Sakkers R. J.B., Weinans H. H., Van Der Wal B. C.H., Van Stralen M., Seevinck P. R. 1 jan 2019,
Further delineation of the GDF6 related multiple synostoses syndrome
Terhal Paulien A., Verbeek Nienke E., Knoers Nine, Nievelstein Rutger J.A.J., van den Ouweland Ans, Sakkers Ralph J , Speleman Lucienne, van Haaften Gijs 2018, In: American Journal of Medical Genetics. Part A. 176 , p. 225-229
Amputation and rotationplasty in children with limb deficiencies:current concepts
Sakkers Ralph, van Wijk Iris 1 dec 2016, In: Journal of Children's Orthopaedics. 10 , p. 619-626 8 p.
Aangeboren en verworven aandoeningen aan armen en benen
van Wijk Iris, Sakkers RJB, Plomp A 2015, p. 465-487 23 p.
Skeletdysplasie en arthrogryposis multiplex congenita
van Wijk Iris, Sakkers RJB, Plomp A 2015, p. 489-511
Efficacy and safety of bisphosponate therapy in children with osteogenesis imperfecta: a systematic review
Rijks Ester B G, Bongers B.C., Vlemmix MJG, Boot A.M., van Dijk ATH, Sakkers RJB, van Brussel M 2015, In: Hormone research in pædiatrics. 84 , p. 26-42
Osteogenesis Imperfecta: een multidisciplinaire aangelegenheid in diagnostiek en behandeling
Sakkers RJB, van Wijk I, Bartels B, G Janus 2014, In: Praktische Pediatrie.
Prevalence and development of orthopaedic symptoms in the dutch hurler patient population after haematopoietic stem cell transplantation
Stoop F. J., Kruyt M. C., van der Linden M. H., Sakkers R. J.B., van Hasselt P. M., Castelein R. M.C. 1 jan 2013, 9 , p. 17-29 13 p.
Treatment of hip dysplasia in patients with mucopolysaccharidosis type I after hematopoietic stem cell transplantation: results of an international consensus procedure.
Langereis E.J., Borgo A., Crushell E., Harmatz P.R., van Hasselt P.M., Jones S.A., Kelly P.M., Lampe C., van der Lee J.H., Odent T., Sakkers R.J.B., Scarpa M., Schafroth M.U., Struijs P.A., Valayannopoulos V., White K.K., Wijburg F.A. 2013, In: Orphanet Journal of Rare Diseases. 8 , p. 155 1 p.