Prevalence of COL4A1 and COL4A2 mutations in severe fetal multifocal hemorrhagic and/or ischemic cerebral lesions
Maurice, P., Guilbaud, L., Garel, J., Mine, M., Dugas, A., Friszer, S., Maisonneuve, E., Moutard, M.‐L., Coste, T., Héron, D., Tournier‐Lasserve, E., Garel, C., Jouannic, J.‐M.
Published in Ultrasound in obstetrics & gynecology (01.05.2021)
Published in Ultrasound in obstetrics & gynecology (01.05.2021)
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Using medical exome sequencing to identify the causes of neurodevelopmental disorders: Experience of 2 clinical units and 216 patients
Chérot, E., Keren, B., Dubourg, C., Carré, W., Fradin, M., Lavillaureix, A., Afenjar, A., Burglen, L., Whalen, S., Charles, P., Marey, I., Heide, S., Jacquette, A., Heron, D., Doummar, D., Rodriguez, D., Billette de Villemeur, T., Moutard, M.‐L., Guët, A., Xavier, J., Périsse, D., Cohen, D., Demurger, F., Quélin, C., Depienne, C., Odent, S., Nava, C., David, V., Pasquier, L., Mignot, C.
Published in Clinical genetics (01.03.2018)
Published in Clinical genetics (01.03.2018)
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Feasibility and Added Value of Fetal DTI Tractography in the Evaluation of an Isolated Short Corpus Callosum: Preliminary Results
Millischer, A-E, Grevent, D, Sonigo, P, Bahi-Buisson, N, Desguerre, I, Mahallati, H, Bault, J-P, Quibel, T, Couderc, S, Moutard, M-L, Julien, E, Dangouloff, V, Bessieres, B, Malan, V, Attie, T, Salomon, L-J, Boddaert, N
Published in American journal of neuroradiology : AJNR (01.01.2022)
Published in American journal of neuroradiology : AJNR (01.01.2022)
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Normal EEG in childhood: From neonates to adolescents
Eisermann, M, Kaminska, A, Moutard, M.-L, Soufflet, C, Plouin, P
Published in Neurophysiologie clinique (01.01.2013)
Published in Neurophysiologie clinique (01.01.2013)
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Prenatal unilateral cerebellar hypoplasia in a series of 26 cases: significance and implications for prenatal diagnosis
Massoud, M., Cagneaux, M., Garel, C., Varene, N., Moutard, M.‐L., Billette, T., Benezit, A., Rougeot, C., Jouannic, J.‐M., Massardier, J., Gaucherand, P., Desportes, V., Guibaud, L.
Published in Ultrasound in obstetrics & gynecology (01.10.2014)
Published in Ultrasound in obstetrics & gynecology (01.10.2014)
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Biometry of the Corpus Callosum in Children: MR Imaging Reference Data
GAREL, C, CONT, I, ALBERTI, C, JOSSERAND, E, MOUTARD, M. L, DUCOU LE POINTE, H
Published in American journal of neuroradiology : AJNR (01.09.2011)
Published in American journal of neuroradiology : AJNR (01.09.2011)
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Pediatric outcome of children with the prenatal diagnosis of isolated septal agenesis
Damaj, L., Bruneau, B., Ferry, M., Moutard, M.-L., Garel, C., Odent, S., Adamsbaum, C., Avni, F., Tréguier, C., Lazaro, L.
Published in Prenatal diagnosis (01.12.2010)
Published in Prenatal diagnosis (01.12.2010)
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Xq28 duplication including MECP2 in six unreported affected females: what can we learn for diagnosis and genetic counselling?
El Chehadeh, S., Touraine, R., Prieur, F., Reardon, W., Bienvenu, T., Chantot‐Bastaraud, S., Doco‐Fenzy, M., Landais, E., Philippe, C., Marle, N., Callier, P., Mosca‐Boidron, A.‐L., Mugneret, F., Le Meur, N., Goldenberg, A., Guerrot, A.‐M., Chambon, P., Satre, V., Coutton, C., Jouk, P.‐S., Devillard, F., Dieterich, K., Afenjar, A., Burglen, L., Moutard, M.‐L., Addor, M.‐C., Lebon, S., Martinet, D., Alessandri, J.‐L., Doray, B., Miguet, M., Devys, D., Saugier‐Veber, P., Drunat, S., Aral, B., Kremer, V., Rondeau, S., Tabet, A.‐C., Thevenon, J., Thauvin‐Robinet, C., Perreton, N., Des Portes, V., Faivre, L.
Published in Clinical genetics (01.04.2017)
Published in Clinical genetics (01.04.2017)
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Fetal intracerebral hemorrhage and COL4A1 mutation: promise and uncertainty
Garel, C., Rosenblatt, J., Moutard, M. L., Heron, D., Gelot, A., Gonzales, M., Miné, E., Jouannic, J. M.
Published in Ultrasound in obstetrics & gynecology (01.02.2013)
Published in Ultrasound in obstetrics & gynecology (01.02.2013)
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Periventricular nodular heterotopia on prenatal ultrasound and magnetic resonance imaging
Blondiaux, E., Sileo, C., Nahama‐Allouche, C., Moutard, M. L., Gelot, A., Jouannic, J. M., Ducou le Pointe, H., Garel, C.
Published in Ultrasound in obstetrics & gynecology (01.08.2013)
Published in Ultrasound in obstetrics & gynecology (01.08.2013)
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Doublecortin Is the Major Gene Causing X-Linked Subcortical Laminar Heterotopia (SCLH)
des Portes, Vincent, Francis, Fiona, Pinard, Jean-Marc, Desguerre, Isabelle, Moutard, Marie-Laure, Snoeck, Irina, Meiners, Linda C., Capron, François, Cusmai, Raffaella, Ricci, Stefano, Motte, Jacques, Echenne, Bernard, Ponsot, Gérard, Dulac, Olivier, Chelly, Jamel, Beldjord, Cherif
Published in Human molecular genetics (01.07.1998)
Published in Human molecular genetics (01.07.1998)
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Agitation and changes of Bispectral Index and electroencephalographic-derived variables during sevoflurane induction in children: clonidine premedication reduces agitation compared with midazolam
Constant, I, Leport, Y, Richard, P, Moutard, M-L, Murat, I
Published in British journal of anaesthesia : BJA (01.04.2004)
Published in British journal of anaesthesia : BJA (01.04.2004)
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Prenatal Diagnosis of 18q-Syndrome: A Case of Fetal Mosaicism with a Normal Karyotype in Chorionic Villi
Anselem, O., Bazin, A., Mechler, C., Blin, G., Garel, C., Aboura, A., Moutard, M.-L., Mandelbrot, L.
Published in Fetal diagnosis and therapy (01.10.2010)
Published in Fetal diagnosis and therapy (01.10.2010)
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A second locus for Aicardi-Goutières syndrome at chromosome 13q14–21
Ali, M, Highet, L J, Lacombe, D, Goizet, C, King, M D, Tacke, U, van der Knaap, M S, Lagae, L, Rittey, C, Brunner, H G, van Bokhoven, H, Hamel, B, Oade, Y A, Sanchis, A, Desguerre, I, Cau, D, Mathieu, N, Moutard, M L, Lebon, P, Kumar, D, Jackson, A P, Crow, Y J
Published in Journal of medical genetics (01.05.2006)
Published in Journal of medical genetics (01.05.2006)
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Changes in electroencephalogram and autonomic cardiovascular activity during induction of anesthesia with Sevoflurane compared with halothane in Children
CONSTANT, I, DUBOIS, M.-C, PIAT, V, MOUTARD, M.-L, MCCUE, M, MURAT, I
Published in Anesthesiology (Philadelphia) (01.12.1999)
Published in Anesthesiology (Philadelphia) (01.12.1999)
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Infantile spasms with basal ganglia MRI hypersignal may reveal mitochondrial disorder due to T8993G MT DNA mutation
Desguerre, I, Pinton, F, Nabbout, R, Moutard, M L, N'Guyen, S, Marsac, C, Ponsot, G, Dulac, O
Published in Neuropediatrics (01.10.2003)
Published in Neuropediatrics (01.10.2003)
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Five new TTF1/NKX2.1 mutations in brain–lung–thyroid syndrome: rescue by PAX8 synergism in one case
Carré, Aurore, Szinnai, Gabor, Castanet, Mireille, Sura-Trueba, Sylvia, Tron, Elodie, Broutin-L’Hermite, Isabelle, Barat, Pascal, Goizet, Cyril, Lacombe, Didier, Moutard, Marie-Laure, Raybaud, Christine, Raynaud-Ravni, Catherine, Romana, Serge, Ythier, Hubert, Léger, Juliane, Polak, Michel
Published in Human molecular genetics (15.06.2009)
Published in Human molecular genetics (15.06.2009)
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Prenatal features of isolated subependymal pseudocysts associated with adverse pregnancy outcome
Esteban, H., Blondiaux, E., Audureau, E., Sileo, C., Moutard, M. L., Gelot, A., Jouannic, J. M., Ducou le Pointe, H., Garel, C.
Published in Ultrasound in obstetrics & gynecology (01.12.2015)
Published in Ultrasound in obstetrics & gynecology (01.12.2015)
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