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4. Sinistralité du Club « Cœlio » : analyse d’une expérience pluri-professionnelle Franco-Belge

Author

Auvray, S., Barthes, T., Bellouard, A., Bertrand, D., Bokobsa, B., Burnon, D., Charbit, L., Closset, J., Cossa, J.P., Dabrowski, A., Delaby, J., Deleuze, A., Denet, C., Desfachelles, J.P., Dugue, T., Framery, D., Fromont, G., Hauters, P., Herbiere, P., Johanet, H., Landenne, J., Ledaguenel, P., Lepere, M., Longeville, J.H., Maisonnette, F., Magne, E., Malvaux, P., Marchand, P., Merlier, O., Navez, B., Olagne, E., Piquard, A., Portet, R., Rubay, R., Saint-Marc, O., Schramm, R., Siriser, F., Valverde, A., Vernay, L., Zaranis, C., Delaunay, F., Delaunay, T., Van Vyve, E., and Cardin, J.-L.

Published
2019
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5. Analysis of malpractice claims: The Franco-Belgian “Cœlio Club” experience

Author

Auvray, S., Barthes, T., Bellouard, A., Bertrand, C., Bokobsa, B., Burnon, D., Charbit, L., Closset, J., Cossa, J.P., Dabrowski, A., Delaby, J., Deleuze, A., Denet, C., Desfachelles, J.P., Dugue, T., Framery, D., Fromont, G., Hauters, P., Herbiere, P., Johanet, H., Landenne, J., Ledaguenel, P., Lepere, M., Longeville, J.H., Maisonnette, F., Magne, E., Malvaux, P., Marchand, P., Merlier, O., Navez, B., Olagne, E., Piquard, A., Portet, R., Rubay, R., Saint-Marc, O., Schramm, R., Siriser, F., Valverde, A., Vernay, L., Zaranis, C., Delaunay, F., Delaunay, T., Van Vyve, E., and Cardin, J.-L.

Published
2019
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6. Centralizing surgery for ovarian cancer in a 'non-centralizing' country (Belgium): the UNGO (UCLouvain Network of Gynaecological Oncology) experience.

Author

Luyckx, Mathieu, Jouret, Mathieu, Sawadogo, Kismendsida, Waterkeyn, Marc, Grandjean, Frédéric, Van Gossum, Jean-Paul, Dubois, Nathanael, Malvaux, Vincent, Verreth, Lucie, Grandjean, Pascale, Bruger, Annika Malin, Jadoul, Pascale, Maillard, Charlotte, Gerday, Amandine, Baurain, Jean-François, and Squifflet, Jean-Luc

Published
2024
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17. Analysis of malpractice claims: The Franco-Belgian “Cœlio Club” experience

Author

Delaunay, F., primary, Delaunay, T., additional, Van Vyve, E., additional, Cardin, J.-L., additional, Auvray, S., additional, Barthes, T., additional, Bellouard, A., additional, Bertrand, C., additional, Bokobsa, B., additional, Burnon, D., additional, Charbit, L., additional, Closset, J., additional, Cossa, J.P., additional, Dabrowski, A., additional, Delaby, J., additional, Deleuze, A., additional, Denet, C., additional, Desfachelles, J.P., additional, Dugue, T., additional, Framery, D., additional, Fromont, G., additional, Hauters, P., additional, Herbiere, P., additional, Johanet, H., additional, Landenne, J., additional, Ledaguenel, P., additional, Lepere, M., additional, Longeville, J.H., additional, Maisonnette, F., additional, Magne, E., additional, Malvaux, P., additional, Marchand, P., additional, Merlier, O., additional, Navez, B., additional, Olagne, E., additional, Piquard, A., additional, Portet, R., additional, Rubay, R., additional, Saint-Marc, O., additional, Schramm, R., additional, Siriser, F., additional, Valverde, A., additional, Vernay, L., additional, and Zaranis, C., additional

Published
2019
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18. Sinistralité du Club « Cœlio » : analyse d’une expérience pluri-professionnelle Franco-Belge

Author

Delaunay, F., primary, Delaunay, T., additional, Van Vyve, E., additional, Cardin, J.-L., additional, Auvray, S., additional, Barthes, T., additional, Bellouard, A., additional, Bertrand, D., additional, Bokobsa, B., additional, Burnon, D., additional, Charbit, L., additional, Closset, J., additional, Cossa, J.P., additional, Dabrowski, A., additional, Delaby, J., additional, Deleuze, A., additional, Denet, C., additional, Desfachelles, J.P., additional, Dugue, T., additional, Framery, D., additional, Fromont, G., additional, Hauters, P., additional, Herbiere, P., additional, Johanet, H., additional, Landenne, J., additional, Ledaguenel, P., additional, Lepere, M., additional, Longeville, J.H., additional, Maisonnette, F., additional, Magne, E., additional, Malvaux, P., additional, Marchand, P., additional, Merlier, O., additional, Navez, B., additional, Olagne, E., additional, Piquard, A., additional, Portet, R., additional, Rubay, R., additional, Saint-Marc, O., additional, Schramm, R., additional, Siriser, F., additional, Valverde, A., additional, Vernay, L., additional, and Zaranis, C., additional

Published
2019
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23. Risk factors of perioperative morbimortality after laparoscopic sleeve gastrectomy: a club coelio multicenter study

Author

Tulelli, B., primary, Loi, P., additional, van Vyve, E., additional, Johanet, H., additional, Fromont, G., additional, Dabrowski, A., additional, Piquart, A., additional, Delaunay, T., additional, Ledaguenel, P., additional, Navez, B., additional, Maisonnette, F., additional, Lepere, M., additional, Dugué, T., additional, Demoor, V., additional, Bokobza, B., additional, Staudt, Jp., additional, Hauters, P., additional, Malvaux, P., additional, and Closset, J., additional

Published
2017
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24. Prevention of vaccine-matched and mismatched influenza in children aged 6–35 months: a multinational randomised trial across five influenza seasons

Author

Claeys, Carine, Zaman, Khalequ, Dbaibo, Ghassan, Li, Ping, Izu, Allen, Kosalaraksa, Pope, Rivera, Luis, Acosta, Beatriz, Arroba Basanta, Maria Luisa, Aziz, Asma, Cabanero, Miguel Angel, Chandrashekaran, Vijayalakshmi, Corsaro, Bartholomew, Cousin, Luis, Diaz, Adolfo, Diez-Domingo, Javier, Dinleyici, Ener Cagri, Faust, Saul N, Friel, Damien, Garcia-Sicilia, Jose, Gomez-Go, Grace D, Antoinette Gonzales, Maria Liza, Hughes, Stephen M, Jackowska, Teresa, Kant, Shashi, Lucero, Marilla, Malvaux, Ludovic, Mares Bermudez, Josep, Martinon-Torres, Federico, Miranda, Mariano, Montellano, May, Peix Sambola, Maria Amor, Prymula, Roman, Puthanakit, Thanyawee, Ruzkova, Renata, Sadowska-Krawczenko, Iwona, Salamanca de la Cueva, Ignacio, Sokal, Etienne, Soni, Jyoti, Szymanski, Henryk, Ulied, Angels, Schuind, Anne, Jain, Varsha K, Innis, Bruce L, Acostas, Beatriz, Amanullah, Arshad, Ariza, Miguel, Arroba Basanta, Maria Luisa, Aziz, Asma, Bautista, Milagros, Bavdekar, Ashish, Bodalia, Bhavesh, Bravo, Lulu C, Brzostek, Jerzy, Cabanero, Miguel Angel, Caldwell, Ian, Carmona, Alfonso, Chandrashekaran, Vijayalakshmi, Claeys, Carine, Corsaro, Bartholomew, Cousin, Luis, Danier, Jasur, Dbaibo, Ghassan, Diaz Cirujano, Ana Isabel, Diaz, Adolfo, Diez-Domingo, Javier, Dinleyici, Ener Cagri, Docx, Martine, Drazan, Daniel, Faust, Saul N, Galaj, Andrzej, Garcia Rodriguez, Fermin, Garcia-Sicilia, Jose, Gonzales, Maria Liza Antoinette, Gomez-Go, Grace D, Gooding, Trevor, Hacimustafaoglu, Mustafa, Heath, Paul, Heaton, Paul, Hughes, Stephen M, Innis, Bruce L, Izu, Allen, Jackowska, Teresa, Jain, Varsha K, Kant, Shashi, Kosalaraksa, Pope, Lalwani, Sanjay, Langlands, Jennifer, Li, Ping, Logghe, Karl, Lucero, Marilla, Malvaux, Ludovic, Mantyka, Jolanta, Mares Bermudez, Josep, Martinon-Torres, Federico, McNally, Damien, Miszczak-Kowalska, Edyta, Montellano, May, Peix Sambola, Maria Amor, Prymula, Roman, Puthanakit, Thanyawee, Rivera, Luis, Royal, Simon, Ruzkova, Renata, Sablan, Benjamin, Sadowska-Krawczenko, Iwona, Salamanca de la Cueva, Ignacio, Schuind, Anne, Snape, Matthew, Soni, Jyoti, Tomlinson, Richard, Ulied, Angels, Verghote, Marc, Vertruyen, Andre, Wheeler, Marie, and Zaman, Khalequ

Abstract

Despite the importance of vaccinating children younger than 5 years, few studies evaluating vaccine prevention of influenza have been reported in this age group. We evaluated efficacy of an inactivated quadrivalent influenza vaccine (IIV4) in children aged 6–35 months.

Published
2018
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32. Autosomal dominant transmission of congenital thyroid hypoplasia due to loss-of-function mutation of PAX8

Author

Vilain C, Rydlewski C, Duprez L, Heinrichs C, Marc Abramowicz, Malvaux P, Renneboog B, Parma J, Costagliola S, and Vassart G

Subjects
Adult, Base Sequence, Molecular Sequence Data, Thyroid Gland, Infant, Nuclear Proteins, Thyroid Diseases, DNA-Binding Proteins, PAX8 Transcription Factor, Hypothyroidism, Mutation, Congenital Hypothyroidism, Trans-Activators, Humans, Paired Box Transcription Factors, Female, Amino Acid Sequence, Genes, Dominant
Abstract

Congenital hypothyroidism (CH) is a relatively frequent and potentially severe disease. It is classically subdivided into: 1) thyroid dysgenesis (TD), a defect in the organogenesis of the gland leading to hypoplastic, ectopic, or absent thyroid gland; or 2) thyroid dyshormonogenesis, a defect in one of the biochemical mechanisms responsible for thyroid hormone synthesis. Most cases of TD are sporadic, although familial occurrences have occasionally been described. Recently, several genes have been implicated in a small proportion of TD, but, in the majority of the cases, the etiology remains unknown. PAX8 is a transcription factor involved in thyroid development. So far, three loss-of-function mutations of PAX8 have been described, two in sporadic cases and one in familial thyroid hypoplasia. Here, we describe a novel mutation of PAX8 causing autosomal dominant transmission of CH with thyroid hypoplasia. The mutation consists of the substitution of a tyrosine for cysteine 57 in the paired domain of PAX8. When tested in cotransfection experiments with a thyroid peroxidasse promoter construct, the mutant allele was unable to exert its normal transactivation effect on transcription. Our results give further evidence that, contrary to the situation in knockout mice, haplo-insufficiency of PAX8 is a cause of CH in humans.

Published
2001

37. Autosomal dominant transmission of congenital thyroid hypoplasia due to loss-of-function mutation of PAX8.

Author

Vilain, Catheline, Rydlewski, C., Duprez, Laurence, Heinrichs, Claudine, Abramowicz, Marc, Malvaux, P, Renneboog, Benoît, Parma, Jasmine, Costagliola, Sabine, Vassart, Gilbert, Vilain, Catheline, Rydlewski, C., Duprez, Laurence, Heinrichs, Claudine, Abramowicz, Marc, Malvaux, P, Renneboog, Benoît, Parma, Jasmine, Costagliola, Sabine, and Vassart, Gilbert

Abstract

Congenital hypothyroidism (CH) is a relatively frequent and potentially severe disease. It is classically subdivided into: 1) thyroid dysgenesis (TD), a defect in the organogenesis of the gland leading to hypoplastic, ectopic, or absent thyroid gland; or 2) thyroid dyshormonogenesis, a defect in one of the biochemical mechanisms responsible for thyroid hormone synthesis. Most cases of TD are sporadic, although familial occurrences have occasionally been described. Recently, several genes have been implicated in a small proportion of TD, but, in the majority of the cases, the etiology remains unknown. PAX8 is a transcription factor involved in thyroid development. So far, three loss-of-function mutations of PAX8 have been described, two in sporadic cases and one in familial thyroid hypoplasia. Here, we describe a novel mutation of PAX8 causing autosomal dominant transmission of CH with thyroid hypoplasia. The mutation consists of the substitution of a tyrosine for cysteine 57 in the paired domain of PAX8. When tested in cotransfection experiments with a thyroid peroxidasse promoter construct, the mutant allele was unable to exert its normal transactivation effect on transcription. Our results give further evidence that, contrary to the situation in knockout mice, haplo-insufficiency of PAX8 is a cause of CH in humans., Case Reports, Journal Article, Research Support, Non-U.S. Gov't, SCOPUS: ar.j, info:eu-repo/semantics/published

Published
2001

42. Final Height in Children with Idiopathic Growth Hormone Deficiency Treated with Recombinant Human Growth Hormone: The Belgian Experience

Author

Thomas, M., primary, Massa, G., additional, Bourguignon, J.-P., additional, Craen, M., additional, de Schepper, J., additional, de Zegher, F., additional, Dooms, L., additional, Du Caju, M., additional, François, I., additional, Heinrichs, C., additional, Malvaux, P., additional, Rooman, R., additional, Thiry-Counson, G., additional, Vandeweghe, M., additional, and Maes, M., additional

Published
2001
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43. Variations in pituitary-gonadal suppression during intranasal buserelin and intramuscular depot-triptorelin therapy for central precocious puberty. Belgian Study Group for Pediatric Endocrinology.

Author

UCL - MD/GYPE - Département de gynécologie, d'obstétrique et de pédiatrie, Heinrichs, C, Craen, M, Vanderschueren-Lodeweyckx, M, Malvaux, P., Fawe, L, Bourguignon, J P, UCL - MD/GYPE - Département de gynécologie, d'obstétrique et de pédiatrie, Heinrichs, C, Craen, M, Vanderschueren-Lodeweyckx, M, Malvaux, P., Fawe, L, and Bourguignon, J P

Abstract

This study evaluated pubertal development, growth and pituitary-gonadal suppression in 21 patients with central precocious puberty treated with buserelin intranasally and switched after a mean of 2.1 yr to depot-triptorelin given im for 1 year. Arrest or regression of puberty was observed in 12 patients while progression of puberty during therapy was seen in 9 patients (6 on buserelin, 2 on triptorelin and 1 on both therapies). The increment in serum LH and FSH concentrations after sc injection of short-acting triptorelin was greater on buserelin than on triptorelin therapy, particularly in patients with evidence of progression of puberty. Height velocity during therapy showed a reduction which paralleled the decelerating phase of the normal pubertal growth spurt. The rate of bone maturation during therapy was inversely related to pretreatment bone age. Predicted final height showed marked individual variations which were inversely related to predicted adult height before therapy. These data indicate that differences in the nature and route of administration of Gn-RH agonist therapy for central precocious puberty can be of importance for inhibition of pituitary gonadotropin secretion and development of secondary sex characteristics. Height velocity and bone maturation are age-related and the change in predicted adult height depends on pretreatment level.

Published
1994

44. La pathologie thyroïdienne

Author

UCL - (SLuc) Service d'endocrinologie et de nutrition, Malvaux, P., UCL - (SLuc) Service d'endocrinologie et de nutrition, and Malvaux, P.

Published
1994

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