Search Results - "Mathijssen, I. M. J."

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  1. 1

    Quality of life in children suffering from headaches: a systematic literature review by Ombashi, S., Tsangaris, E., Heeres, A. G., van Roey, V., Neuteboom, R. F., van Veelen-Vincent, M. L. C., Jansson, K., Mathijssen, I. M. J., Klassen, A. F., Versnel, S. L.

    Published in Journal of headache and pain (18-09-2023)
    “…Background Headaches are the most common complaints among pediatric populations. Determining the cause and appropriate treatment for headaches may be…”
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    Journal Article
  2. 2

    The impact of obstructive sleep apnea on growth in patients with syndromic and complex craniosynostosis: a retrospective study by Yang, S., Mathijssen, I. M. J., Joosten, K. F. M.

    Published in European journal of pediatrics (01-12-2022)
    “…Given the high prevalence of OSA in children with syndromic and complex craniosynostosis (SCC) and the consequences of untreated OSA, it is important to assess…”
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  3. 3

    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.

    Published in Neuroradiology (01-12-2022)
    “…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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  4. 4

    Spring-assisted posterior vault expansion in multisuture craniosynostosis by de Jong, T., van Veelen, M. L. C., Mathijssen, I. M. J.

    Published in Child's nervous system (01-05-2013)
    “…Purpose Patients with Apert and Crouzon syndromes and craniofrontonasal dysplasia need a vault expansion within the first year of life to treat or prevent the…”
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  5. 5

    Obstructive sleep apnoea in Treacher Collins syndrome: prevalence, severity and cause by Plomp, R.G, Bredero-Boelhouwer, H.H, Joosten, K.F.M, Wolvius, E.B, Hoeve, H.L.J, Poublon, R.M.L, Mathijssen, I.M.J

    “…Abstract This cohort study in 35 patients (13 children) evaluates the prevalence, severity and anatomical cause of obstructive sleep apnoea syndrome (OSAS) in…”
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  6. 6

    Obstructive sleep apnea in children with syndromic craniosynostosis: long-term respiratory outcome of midface advancement by Bannink, N, Nout, E, Wolvius, E.B, Hoeve, H.L.J, Joosten, K.F.M, Mathijssen, I.M.J

    “…Abstract Almost 50% of patients with Apert, Crouzon or Pfeiffer syndrome develop obstructive sleep apnea (OSA), mainly due to midface hypoplasia. Midface…”
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  8. 8

    Satisfaction with facial appearance and its determinants in adults with severe congenital facial disfigurement: A case-referent study by Versnel, S.L, Duivenvoorden, H.J, Passchier, J, Mathijssen, I.M.J

    “…Summary Background Patients with severe congenital facial disfigurement have a long track record of operations and hospital visits by the time they are 18…”
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  9. 9

    Advancement of the midface, from conventional Le Fort III osteotomy to Le Fort III distraction: review of the literature by Nout, E, Cesteleyn, L.L.M, van der Wal, K.G.H, van Adrichem, L.N.A, Mathijssen, I.M.J, Wolvius, E.B

    “…Abstract Since its introduction in about 1950, the Le Fort III (LF III) procedure has become a widely accepted treatment for correction of midface hypoplasia…”
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  10. 10

    Brain volume in infants with metopic synostosis: Less white matter volume with an accelerated growth pattern in early life by Gaillard, L., Tjaberinga, M. C., Dremmen, M. H. G., Mathijssen, I. M. J., Vrooman, H. A.

    Published in Journal of anatomy (01-12-2024)
    “…Metopic synostosis patients are at risk for neurodevelopmental disorders despite a negligible risk of intracranial hypertension. To gain insight into the…”
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  11. 11

    Can parents predict obstructive sleep apnea in children with syndromic or complex craniosynostosis? by Bannink, N, Mathijssen, I.M.J, Joosten, K.F.M

    “…Abstract Obstructive sleep apnea (OSA) is a clinical syndrome characterized by snoring, apneas and difficulty in breathing. These symptoms can be rated and a…”
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  12. 12

    Comparison of two surgical protocols for the treatment of unilateral cleft lip and palate: a multidisciplinary systematic review and meta-analysis by van Roey, V.L., Ombashi, S., Pleumeekers, M.M., Mathijssen, I.M.J., Mink van der Molen, A.B., Munill, M., Versnel, S.L.

    “…There is still no unanimous agreement on the optimal surgical protocol(s) for the treatment of unilateral cleft lip and palate (UCLP), and a huge variety of…”
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  13. 13

    Craniofacial morphology and growth in Muenke syndrome, Saethre-Chotzen syndrome, and TCF12-related craniosynostosis by Choi, T. M., Lijten, O. W., Mathijssen, I. M. J., Wolvius, E. B., Ongkosuwito, E. M.

    Published in Clinical oral investigations (01-03-2022)
    “…Objectives To determine whether the midface of patients with Muenke syndrome, Saethre-Chotzen syndrome, or TCF12- related craniosynostosis is hypoplastic…”
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  14. 14

    Anxiety and depression in adolescents with a visible difference: A systematic review and meta-analysis by van Dalen, M., Dierckx, B., Pasmans, S.G.M.A., Aendekerk, E.W.C., Mathijssen, I.M.J., Koudstaal, M.J., Timman, R., Williamson, H., Hillegers, M.H.J., Utens, E.M.W.J., Okkerse, J.M.E.

    Published in Body image (01-06-2020)
    “…•A meta-analysis was executed with 11 articles to assess depression and anxiety.•Adolescents with a visible difference experience more anxiety than unaffected…”
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  15. 15

    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.

    Published in European journal of paediatric neurology (01-01-2023)
    “…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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  16. 16

    Acceptability and feasibility of an online psychosocial intervention for Dutch adolescents with a visible difference: A mixed-methods study by van Dalen, M., Pasmans, S.G.M.A., Aendekerk, E.W.C., Mathijssen, I.M.J., Koudstaal, M.J., Williamson, H., Hillegers, M.H.J., Utens, E.M.W.J., Okkerse, J.M.E.

    Published in Body image (01-06-2022)
    “…Adolescents with a visible difference can experience difficult social situations, (e.g., people staring or making unwanted comments) and are at risk for mental…”
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  17. 17

    Cervical Spinal Cord Compression and Sleep-Disordered Breathing in Syndromic Craniosynostosis by den Ottelander, B K, de Goederen, R, de Planque, C A, Baart, S J, van Veelen, M L C, Corel, L J A, Joosten, K F M, Mathijssen, I M J, Dremmen, M H G

    Published in American journal of neuroradiology : AJNR (01-01-2021)
    “…Cerebellar tonsillar herniation arises frequently in syndromic craniosynostosis and causes central and obstructive apneas in other diseases through spinal cord…”
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  18. 18

    Functional outcomes in patients with facial dysostosis and severe upper airway obstruction by van der Plas, P.P.J.M., Yang, S., Streppel, M., Pullens, B., Versnel, S.L., Koudstaal, M.J., Wolvius, E.B., Mathijssen, I.M.J., Joosten, K.F.M.

    “…An increased risk of upper airway obstruction (UAO) is seen in up to 95% of patients with facial dysostosis. Secondary to respiratory problems are feeding…”
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  19. 19

    Obstructive sleep apnoea in craniofacial microsomia: analysis of 755 patients by Caron, C.J.J.M, Pluijmers, B.I, Maas, B.D.P.J, Klazen, Y.P, Katz, E.S, Abel, F, van der Schroeff, M.P, Mathijssen, I.M.J, Dunaway, D.J, Mills, C, Gill, D.S, Bulstrode, N, Padwa, B.L, Wolvius, E.B, Joosten, K.F.M, Koudstaal, M.J

    “…Abstract A retrospective cohort study was set up to analyse the prevalence and treatment of obstructive sleep apnoea (OSA) in relation to the severity of the…”
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  20. 20

    Phenotypes of craniofrontonasal syndrome in patients with a pathogenic mutation in EFNB1 by van den Elzen, M E P, Twigg, S R F, Goos, J A C, Hoogeboom, A J M, van den Ouweland, A M W, Wilkie, A O M, Mathijssen, I M J

    Published in European journal of human genetics : EJHG (01-08-2014)
    “…Craniofrontonasal syndrome (CFNS) is an X-linked developmental malformation, caused by mutations in the EFNB1 gene, which have only been described since 2004…”
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