Search Results - "Rijken, B F M"

A diffusion tensor imaging analysis of white matter microstructures in non-operated craniosynostosis patients by de Planque, C. A., Florisson, J. M. G., Tasker, R. C., Rijken, B. F. M., van Veelen, M. L. C., Mathijssen, I. M. J., Lequin, M. H., Dremmen, M. H. G.

“…Purpose In 7 to 15-year-old operated syndromic craniosynostosis patients, we have shown the presence of microstructural anomalies in brain white matter by…”
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Sphenoid dysplasia in patients with neurofibromatosis type 1: Clinical features and imaging findings including cerebrospinal fluid alterations by Rijken, B.F.M., van Veelen-Vincent, M.L.C., Mathijssen, I.M.J.

“…Neurofibromatosis Type 1 (NF-1) is a genetic disorder that occurs in 1:2500–3000 live births and may involve multiple organs. An uncommon but well-known…”
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Diffusion Tensor Imaging and Fiber Tractography in Children with Craniosynostosis Syndromes by Rijken, B F M, Leemans, A, Lucas, Y, van Montfort, K, Mathijssen, I M J, Lequin, M H

“…Patients with craniosynostosis syndromes caused by mutations in FGFR-2, FGFR-3, and TWIST1 genes are characterized by having prematurely fused skull sutures…”
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Neurological deficits are present in syndromic craniosynostosis patients with and without tonsillar herniation by Doerga, P.N., Rijken, B.F.M., Bredero-Boelhouwer, H., Joosten, K.F.M., Neuteboom, R.F., Tasker, R.C., Dremmen, M.H.G., Lequin, M.H., van Veelen, M.L.C., Mathijssen, I.M.J.

“…Children with syndromic craniosynostosis (sCS) have a higher incidence of cerebellar tonsillar herniation (TH) than the general population. In the general…”
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Brain and ventricular volume in patients with syndromic and complex craniosynostosis by de Jong, T., Rijken, B. F. M., Lequin, M. H., van Veelen, M. L. C., Mathijssen, I. M. J.

“…Purpose Brain abnormalities in patients with syndromic craniosynostosis can either be a direct result of the genetic defect or develop secondary to compression…”
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Atypical presentation of a newborn with Apert syndrome by Spruijt, B., Rijken, B. F. M., Joosten, K. F. M., Bredero-Boelhouwer, H. H., Pullens, B., Lequin, M. H., Wolvius, E. B., van Veelen-Vincent, M. L. C., Mathijssen, I. M. J.

“…Introduction Apert syndrome is a rare syndrome characterized by a consistent phenotype including bilateral coronal suture synostosis with an enlarged anterior…”
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