Zobrazeno 1 - 9
of 9
pro vyhledávání: '"B. F. M. Rijken"'
Autor:
C. A. de Planque, J. M. G. Florisson, R. C. Tasker, B. F. M. Rijken, M. L. C. van Veelen, I. M. J. Mathijssen, M. H. Lequin, M. H. G. Dremmen
Publikováno v:
Neuroradiology, 64(12), 2391-2398. Springer-Verlag
Purpose In 7 to 15-year-old operated syndromic craniosynostosis patients, we have shown the presence of microstructural anomalies in brain white matter by using DTI. To learn more about the cause of these anomalies, the aim of the study is to determi
Autor:
Johan de Rooi, Maarten H. Lequin, Wiro J. Niessen, Marie-Lise Charlotte van Veelen-Vincent, Fedde van der Lijn, Yoo Young Hoogendam, Irene M. J. Mathijssen, B. F. M. Rijken
Publikováno v:
Journal of Cranio-Maxillofacial Surgery, 43(6), 813-819. Churchill Livingstone
Objective: Patients with craniosynostosis syndromes are at risk of increased intracranial pressure (ICP) and Chiari I malformation (CMI), caused by a combination of restricted skull growth, venous hypertension, obstructive sleep apnea (OSA), and an o
Autor:
B. F. M. Rijken, Marie-Lise C. van Veelen, Johan de Rooi, Irene M.J. Mathijssen, Maarten H. Lequin
Publikováno v:
Plastic and Reconstructive Surgery, 132(6), 993E-1000E. Lippincott Williams & Wilkins
textabstractBACKGROUND: Cranial sutures and synchondroses tend to close prematurely in patients with Crouzon syndrome. This influences their skull vault and skull base development and may involve in common disturbances such as increased intracranial
Autor:
Bart Spruijt, Koen F. M. Joosten, Irene M. J. Mathijssen, Maarten H. Lequin, Sjoukje E Loudon, B. F. M. Rijken, Marie-Lise C. van Veelen, Bianca K. den Ottelander
Publikováno v:
Plastic and Reconstructive Surgery, 137(1), 112E-121E. Lippincott Williams & Wilkins
Background: Children with Apert and Crouzon-Pfeiffer syndromes are at risk of intracranial hypertension. Until 2005, when the authors switched to occipital expansion, their institution's preferred treatment was fronto-orbital advancement. However, it
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f36c5c0b946c1c37aeeebe1b7eab8c8
https://pure.eur.nl/en/publications/4679a371-ed5f-4ce6-957b-77299e46fa49
https://pure.eur.nl/en/publications/4679a371-ed5f-4ce6-957b-77299e46fa49
Autor:
Froukje Zandstra, Jornt R. De Gruijl, Sebastiaan K. E. Koekkoek, Joel Shapiro, Barry Van Der Ende, Laurens W. J. Bosman, Tom J. H. Ruigrok, Cullen B. Owens, Chris I. De Zeeuw, Jan-Willem Potters, B. F. M. Rijken
Publikováno v:
The Journal of Physiology. 588:3757-3783
The cerebellar cortex is crucial for sensorimotor integration. Sensorimotor inputs converge on cerebellar Purkinje cells via two afferent pathways: the climbing fibre pathway triggering complex spikes, and the mossy fibre–parallel fibre pathway, mo
Autor:
Maarten H. Lequin, Irene M.J. Mathijssen, Y. Lucas, K. A. G. M. van Montfort, Alexander Leemans, B. F. M. Rijken
Publikováno v:
American Journal of Neuroradiology, 36(8), 1558. American Society of Neuroradiology
American Journal of Neuroradiology, 36(8), 1558-1564. American Society of Neuroradiology
AJNR Am J Neuroradiol
American Journal of Neuroradiology, 36(8), 1558-1564. American Society of Neuroradiology
AJNR Am J Neuroradiol
BACKGROUND AND PURPOSE: Patients with craniosynostosis syndromes caused by mutations in FGFR-2, FGFR-3, and TWIST1 genes are characterized by having prematurely fused skull sutures and skull base synchondroses, which result in a skull deformity and a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a5106ed6e55e782d5e54afe7159423c2
https://dspace.library.uu.nl/handle/1874/331766
https://dspace.library.uu.nl/handle/1874/331766
Autor:
Irene M. J. Mathijssen, Marie-Lise C. van Veelen, Maarten H. Lequin, Bianca K. den Ottelander, B. F. M. Rijken
Publikováno v:
Neurosurgical Focus, 38(5). American Association of Neurological Surgeons
OBJECT Patients with syndromic and complex craniosynostosis are characterized by the premature fusion of one or more cranial sutures. These patients are at risk for developing elevated intracranial pressure (ICP). There are several factors known to c
Autor:
Eppo B. Wolvius, H. H. Bredero-Boelhouwer, B. F. M. Rijken, Maarten H. Lequin, Koen F. M. Joosten, Bart Spruijt, M. L. C. van Veelen-Vincent, Bas Pullens, Irene M.J. Mathijssen
Publikováno v:
Childs Nervous System, 31(3), 481-486. Springer-Verlag
Apert syndrome is a rare syndrome characterized by a consistent phenotype including bilateral coronal suture synostosis with an enlarged anterior fontanel, midface hypoplasia, and complex symmetric syndactyly of hands and feet. We present a boy with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f414488a473d02374454e9f354a84c18
https://pure.eur.nl/en/publications/813d1919-e978-4848-8744-e96d5f6799ed
https://pure.eur.nl/en/publications/813d1919-e978-4848-8744-e96d5f6799ed
Publikováno v:
Childs Nervous System, 28(1), 137-140. Springer-Verlag
Child's Nervous System
Child's Nervous System
Purpose Brain abnormalities in patients with syndromic craniosynostosis can either be a direct result of the genetic defect or develop secondary to compression due to craniosynostosis, raised ICP or hydrocephalus. Today it is unknown whether children
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e88264d665d514cc7126ffa3387c1311
https://pure.eur.nl/en/publications/dccb06cf-8185-4456-ad7d-2b1d6eb4645c
https://pure.eur.nl/en/publications/dccb06cf-8185-4456-ad7d-2b1d6eb4645c