Search Results - "F Van Calenbergh"

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    Neurodevelopmental outcome of children with spina bifida aperta repaired prenatally vs postnatally: systematic review and meta‐analysis by Inversetti, A., Van der Veeken, L., Thompson, D., Jansen, K., Van Calenbergh, F., Joyeux, L., Bosteels, J., Deprest, J.

    Published in Ultrasound in obstetrics & gynecology (01-03-2019)
    “…ABSTRACT Objective To assess the neurodevelopmental outcome of children with spina bifida aperta (SBA) treated prenatally as compared to those treated…”
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    Journal Article
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    Patient empowerment improves follow‐up data collection after fetal surgery for spina bifida: institutional audit by Vergote, S., Van der Stock, J., Kunpalin, Y., Bredaki, E., Maes, H., Banh, S., De Catte, L., Devlieger, R., Lewi, L., Devroe, S., Spencer, R., David, A., De Vloo, P., Van Calenbergh, F., Deprest, J. A.

    Published in Ultrasound in obstetrics & gynecology (01-10-2023)
    “…ABSTRACT Objectives To define and grade fetal and maternal adverse events following fetal surgery for spina bifida and to report on the impact of engaging…”
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    Syndrome of the Trephined presenting as Foix-Chavany-Marie syndrome by Demaerel, R., Klein, S., Van Calenbergh, F.

    Published in Clinical neurology and neurosurgery (01-09-2020)
    “…•Patients with syndrome of the Trephined can present with the Foix-Chavany-Marie syndrome due to focal opercular compression.•Local compression on opercular…”
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    Outcome of 12 antenatally diagnosed fetal arachnoid cysts: Case series and review of the literature by De Keersmaecker, B, Ramaekers, P, Claus, F, Witters, I, Ortibus, E, Naulaers, G, Van Calenbergh, F, De Catte, L

    Published in European journal of paediatric neurology (01-03-2015)
    “…Abstract Objectives To investigate the natural history, associated abnormalities and outcome of 12 fetuses with arachnoid cyst diagnosed antenatally by…”
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    Journal Article
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    Surgery and adjuvant dendritic cell-based tumour vaccination for patients with relapsed malignant glioma, a feasibility study by RUTKOWSKI, S, DE VLEESCHOUWER, S, SÖRENSEN, N, OPITZ, A, VAN GOOL, S. W, KAEMPGEN, E, WOLFF, J. E. A, KÜHL, J, DEMAEREL, P, WARMUTH-METZ, M, FLAMEN, P, VAN CALENBERGH, F, PLETS, C

    Published in British journal of cancer (01-11-2004)
    “…Patients with relapsed malignant glioma have a poor prognosis. We developed a strategy of vaccination using autologous mature dendritic cells loaded with…”
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    Pulmonary metastasis of a meningioma presenting as a solitary pulmonary nodule: 2 case reports by Leemans, J., Van Calenbergh, F., Sciot, R., Debiec-Rychter, M., Decaluwe, H., Nackaerts, K.

    Published in Acta clinica belgica (English ed. Online) (03-03-2016)
    “…Distant metastases of meningioma are rare, especially in grade 1 meningiomas. In a recent literature review, only 115 cases were found. In almost all published…”
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    Posterior fossa decompression for Chiari malformation type I: clinical and radiological presentation, outcome and complications in a retrospective series of 105 procedures by De Vlieger, J., Dejaegher, J., Van Calenbergh, F.

    Published in Acta neurologica Belgica (01-06-2019)
    “…Objective Determining clinical and radiological characteristics, complication rates and outcome for patients undergoing posterior fossa decompression (PFD) and…”
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    Journal Article
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    Reliability of MR Imaging-Based Posterior Fossa and Brain Stem Measurements in Open Spinal Dysraphism in the Era of Fetal Surgery by Aertsen, M, Verduyckt, J, De Keyzer, F, Vercauteren, T, Van Calenbergh, F, De Catte, L, Dymarkowski, S, Demaerel, P, Deprest, J

    Published in American journal of neuroradiology : AJNR (01-01-2019)
    “…Fetal MR imaging is part of the comprehensive prenatal assessment of fetuses with open spinal dysraphism. We aimed to assess the reliability of brain stem and…”
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    A clinical comparison of non-traumatic acute subdural haematomas either related to coagulopathy or of arterial origin without coagulopathy by Depreitere, B, Van Calenbergh, F, van Loon, J

    Published in Acta neurochirurgica (01-07-2003)
    “…Non-traumatic acute subdural haematomas enable study of the morbidity and mortality due to the haematoma without the effect of trauma. Whereas it is known that…”
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    Neurodevelopmental Outcome of Children With Spina Bifida Aperta Repaired Prenatally vs Postnatally: Systematic Review and Meta-analysis by Inversetti, A, Van der Veeken, L, Thompson, D, Jansen, K, Van Calenbergh, F, Joyeux, L, Bosteels, J, Deprest, J

    Published in Obstetrical & gynecological survey (01-08-2019)
    “…(Abstracted from Ultrasound Obstet Gynecol 2019;53:293–301)Spina bifida aperta is characterized by a congenital defect in the vertebral arches, with protrusion…”
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    Journal Article
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    Defining pseudoprogression in glioblastoma multiforme by Van Mieghem, E., Wozniak, A., Geussens, Y., Menten, J., De Vleeschouwer, S., Van Calenbergh, F., Sciot, R., Van Gool, S., Bechter, O. E., Demaerel, P., Wilms, G., Clement, P. M.

    Published in European journal of neurology (01-10-2013)
    “…Background and purpose Pseudoprogression is a frequent phenomenon observed since the introduction of postoperative therapy with radiotherapy and temozolomide…”
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    Risk Analysis of Thrombo-Embolic and Recurrent Bleeding Events in the Management Of Intracranial Haemorrhage Due to Oral Anticoagulation by Vleeschouwer, S. De, Calenbergh, F. Van, Loon, J. van, Nuttin, B., Coffin, J., Plets, C.

    Published in Acta chirurgica belgica (2005)
    “…Purposes : Intracranial haemorrhage (ICH) is a rare but potentially devastating complication of oral anticoagulants (OAC). This raises the difficult clinical…”
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    Craniopharyngioma with malignant transformation: A case report by E, Janssens, PJ, Verhelst, Vleeschouwer S, De, Calenbergh F, Van, E, Hauben, C, Politis, M, Bila

    Published in Oral and maxillofacial surgery cases (01-09-2020)
    “…Craniopharyngiomas are usually slow growing, benign epithelial tumors, arising from cell remnants of Rathke's pouch with its ultimate site of origin being the…”
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    P16.07 BEVACIZUMAB AS PALLIATIVE TREATMENT OF FAMILIAL SCHWANNOMATOSIS by Clement, P. M., Blockmans, D., Bechter, O. E., Van Calenbergh, F., Legius, E.

    Published in Neuro-oncology (Charlottesville, Va.) (01-09-2014)
    “…Familial schwannomatosis is a rare genetic disorder characterized by multiple schwannomas and chronic pain. There are, except for the schwannomas, no…”
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