Search Results - "De Wever, Ivo"

Atypical neurofibromas in neurofibromatosis type 1 are premalignant tumors by Beert, Eline, Brems, Hilde, Daniëls, Bruno, De Wever, Ivo, Van Calenbergh, Frank, Schoenaers, Joseph, Debiec-Rychter, Maria, Gevaert, Olivier, De Raedt, Thomas, Van Den Bruel, Annick, de Ravel, Thomy, Cichowski, Karen, Kluwe, Lan, Mautner, Victor, Sciot, Raf, Legius, Eric

“…Benign peripheral nerve sheath tumors (PNSTs) are a characteristic feature of neurofibromatosis type I (NF1) patients. NF1 individuals have an 8–13% lifetime…”
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Molecular pathogenesis of multiple gastrointestinal stromal tumors in NF1 patients by Maertens, Ophélia, Prenen, Hans, Debiec-Rychter, Maria, Wozniak, Agnieszka, Sciot, Raf, Pauwels, Patrick, De Wever, Ivo, Vermeesch, Joris R., de Raedt, Thomas, De Paepe, Anne, Speleman, Frank, van Oosterom, Allan, Messiaen, Ludwine, Legius, Eric

“…Gastrointestinal stromal tumors (GISTs) are the most common mesenchymal tumors of the gastrointestinal tract. KIT and PDGFRA activating mutations are the…”
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Intensity modulated radiation-therapy for preoperative posterior abdominal wall irradiation of retroperitoneal liposarcomas by Bossi, Alberto, M.D, De Wever, Ivo, M.D., Ph.D, Van Limbergen, Erik, M.D., Ph.D, Vanstraelen, Bianca

“…Purpose: Preoperative external-beam radiation therapy (preop RT) in the management of Retroperitoneal Liposarcomas (RPLS) typically involves the delivery of…”
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Biallelic inactivation of NF1 in a sporadic plexiform neurofibroma by Beert, Eline, Brems, Hilde, Renard, Marleen, Ferreiro, Julio Finalet, Melotte, Cindy, Thoelen, Reinhilde, De Wever, Ivo, Sciot, Raf, Legius, Eric, Debiec-Rychter, Maria

“…Plexiform neurofibromas are a major cause of morbidity in individuals with neurofibromatosis type 1 (NF1). Sporadically, these tumors appear as an isolated…”
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Intestinal Neurofibromatosis Is a Subtype of Familial GIST and Results From a Dominant Activating Mutation in PDGFRA by de Raedt, Thomas, Cools, Jan, Debiec–Rychter, Maria, Brems, Hilde, Mentens, Nicole, Sciot, Raf, Himpens, Jacques, de Wever, Ivo, Schöffski, Patrick, Marynen, Peter, Legius, Eric

“…Background & Aims: Intestinal neurofibromatosis (Online Mendelian inheritance in Man database number 162220) is an alternate form of neurofibromatosis…”
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Cytogenetic, Clinical, and Morphologic Correlations in 78 Cases of Fibromatosis: A Report from the CHAMP Study Group by De Wever, Ivo, Cin, Paola Dal, Fletcher, Christopher D M, Mandahl, Nils, Mertens, Fredrik, Mitelman, Felix, Rosai, Juan, Rydholm, Anders, Sciot, Raf, Tallini, Giovanni, Van Den Berghe, Herman, Vanni, Roberta, Willén, Helena

“…Whether fibromatoses are neoplastic or reactive lesions has long been controversial and the relationship, if any, between the superficial and deep forms…”
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HMGA proteins in malignant peripheral nerve sheath tumor and synovial sarcoma: preferential expression of HMGA2 in malignant peripheral nerve sheath tumor by Hui, Pei, Li, Ning, Johnson, Chaline, De Wever, Ivo, Sciot, Raf, Manfioletti, Guidalberto, Tallini, Giovanni

“…Histological separation of synovial sarcomas from malignant peripheral nerve sheath tumors can be difficult and available immunohistochemical markers sometimes…”
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Langerhans cell histiocytosis of the cervical spine: a single institution experience in four patients by Tan, Grace, Samson, Ignace, Wever, Ivo De, Goffin, Jan, Demaerel, Philippe, Van Gool, Stefaan W

“…When Langerhans cell histiocytosis (LCH) occurs at critical sites, such as in the cervical spine, there is a substantial risk for morbidity. Therefore, reports…”
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Cytogenetic characterization of tenosynovial giant cell tumors (nodular tenosynovitis) by DAL CIN, P, SCIOT, R, SAMSON, I, DE SMET, L, DE WEVER, I, VAN DAMME, B, VAN DEN BERGHE, H

“…Chromosome investigation in six localized forms of tenosynovial giant cell tumors, also known as modular tenosynovitis, revealed an identical translocation…”
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Pelvic Exenteration: Surgical Aspects and Analysis of Early and Late Morbidity in a Series of 106 Patients by De Wever, Ivo

“…Introduction : The aim of this study was to report the surgical results in a series of pelvic exenterations, its peroperative difficulties, postoperative…”
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Prenatal assessment and management of sacrococcygeal teratoma by Gucciardo, Leonardo, Uyttebroek, Anne, De Wever, Ivo, Renard, Marleen, Claus, Filip, Devlieger, Roland, Lewi, Liesbeth, De Catte, Luc, Deprest, Jan

“…Sacrococcygeal teratoma (SCT) is one of the most common tumors in newborns with a birth prevalence of up to 1 in 21 700 births. Routine fetal anomaly screening…”
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Pelvic Exenteration: Surgical Aspects and Analysis of Early and Late Morbidity in a Series of 106 Patients by De Wever, Ivo

“…The aim of this study was to report the surgical results in a series of pelvic exenterations, its peroperative difficulties, postoperative complications,…”
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Gastrointestinal stromal tumours (GISTs) negative for KIT (CD117 antigen) immunoreactivity by Debiec-Rychter, Maria, Wasag, Bartosz, Stul, Michel, De Wever, Ivo, Van Oosterom, Allan, Hagemeijer, Anne, Sciot, Raf

“…Gastrointestinal stromal tumours (GISTs) are currently defined as mesenchymal tumours of the gastrointestinal tract that express KIT receptor tyrosine kinase…”
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Correlation between Clinicopathological Features and Karyotype in Spindle Cell Sarcomas by Fletcher, Christopher D.M., Dal Cin, Paola, de Wever, Ivo, Mandahl, Nils, Mertens, Fredrik, Mitelman, Felix, Rosai, Juan, Rydholm, Anders, Sciot, Raf, Tallini, Giovanni, van den Berghe, Herman, Vanni, Roberta, Willén, Helena

“…Soft-tissue tumors have proved to be a fruitful area for the identification of reproducible cytogenetic aberrations, especially among pediatric round-cell…”
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Multifocal kaposiform haemangioendothelioma by DERAEDT, Karen, VANDER POORTEN, Vincent, VAN GEET, Chris, RENARD, Marleen, DE WEVER, Ivo, SCIOT, Raf

“…Kaposiform haemangioendothelioma (KHE) is a rare, locally aggressive vascular spindle cell proliferation, with resemblance to Kaposi's sarcoma. This tumour…”
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Trabectedin (ET-743): evaluation of its use in advanced soft-tissue sarcoma by Schöffski, Patrick, Wolter, Pascal, Clement, Paul, Sciot, Raf, De Wever, Ivo, Wozniak, Agnieszka, Stefan, Cristiana, Dumez, Herlinde

“…Trabectedin (ET-743; Yondelis) is a novel DNA-binding agent, originally derived from the marine tunicate, Ecteinascidia turbinata, and now produced…”
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ZIC1 gene expression is controlled by DNA and histone methylation in mesenchymal proliferations by Pourebrahim, Rasoul, Van Dam, Kim, Bauters, Marijke, De Wever, Ivo, Sciot, Raf, Cassiman, Jean-Jacques, Tejpar, Sabine

“…RNA and protein analysis revealed the consistent upregulation of the neural transcription factors ZIC1 and ZIC4 in desmoid tumors and other fibroproliferative…”
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Administration of 24-h intravenous infusions of trabectedin in ambulatory patients with mesenchymal tumors via disposable elastomeric pumps: an effective and patient-friendly palliative treatment option by Schöffski, Patrick, Cerbone, Linda, Wolter, Pascal, De Wever, Ivo, Samson, Ignace, Dumez, Herlinde, Clement, Paul, Wildiers, Hans, Stas, Marguerite

“…Patients with progressive mesenchymal tumours after standard chemotherapy have poor outcome. Trabectedin is approved in Europe as 24-h intravenous (i.v.)…”
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Correlation between clinicopathological features and karyotype in 100 cartilaginous and chordoid tumours. A report from the Chromosomes and Morphology (CHAMP) Collaborative Study Group by Tallini, Giovanni, Dorfman, Howard, Brys, Peter, Dal Cin, Paola, De Wever, Ivo, Fletcher, Christopher D. M., Jonson, Kjell, Mandahl, Nils, Mertens, Fredrik, Mitelman, Felix, Rosai, Juan, Rydholm, Anders, Samson, Ignace, Sciot, Raf, Van den Berghe, Herman, Vanni, Roberta, Willén, Helena

“…The evaluation of chondroid lesions requires full integration of clinical, radiographic, and pathological data; tumour typing is often a challenge for the…”
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Lipoblastoma in a 23-year-old male: distinction from atypical lipomatous tumor using cytogenetic and fluorescence in-situ hybridization analysis by SCIOT, Raf, DE WEVER, Ivo, DEBIEC-RYCHTER, Maria

“…Lipoblastoma is a rare benign tumor that occurs primarily in infancy and early childhood. We present the rare presentation of a 12 cm sized intramuscular…”
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