Lentilles quadrupolaires magnétiques constituant le dispositif de focalisation du faisceau de mésons $\mu$ du CERN

por Braunersreuther, Eberhard, Chabaud, Vincent, Delorme, C, Morpurgo, Mario
Publicado 1961

Abnormal lateralization of fine motor actions in Tourette syndrome persists into adulthood

por Martino, D., Delorme, C., Pelosin, E., Hartmann, A., Worbe, Y., Avanzino, L.
Publicado 2017

Realisation de chambres a etincelles en toile metallique transparente

por Banaigs, J, Duflo, J, Goldzahl, L, Mouëllic, B, Delorme, C, Kiessler, R, Michaelis, E G
Publicado 1964

A high-intensity $mu$-Meson beam from the 600-MeV CERN Synchrocyclotron

por Citron A, Delorme, C, Farley, FJM, Goldzahl, L, Heintze, J, Michaelis, EG, Morpurgo,M, Overas, H
Publicado 1960

An investigation of $\pi^-$ contamination in $\mu^-$ beams

por Citron, A, Delorme, C, Fries, D E C, Heintze, J, Michaelis, E G, Øverås, H, Shtcherbakov, Yu
Publicado 1962

Encéphalopathies liées au COVID-19 : apport de la TEP-FDG cérébrale dans une série de 4 cas

por Delorme, C., Paccoud, O., Kas, A., Hesters, A., Bombois, S., Maatoug, R., Navarro, V., Bruneteau, G., Demeret, S., Pourcher, V.
Publicado 2020

Scattering of $\mu$ mesons by carbon

por Citron, A, Delorme, C, Fries, D E C, Goldzahl, L, Heintze, J, Michaelis, E G, Richard, C, Øverås, H
Publicado 1962

Manifestations neurologiques associées à l’infection SARS-CoV-2 : le registre français NeuroCOVID

por Meppiel, E., Peiffer-Smadja, N., Maury, A., Delorme, C., Landré, S., Petitgars, P., Sellal, F., Wang, A., Tattevin, P., de Broucker, T.
Publicado 2020

Faisceau intense de mesons $\mu ^-$ de grande purete

por Citron, A, Delorme, C, Farley, Francis J M, Goldzahl, L, Heintze, J, Michaelis, E G, Morpurgo, Mario, Øverås, H, Shtcherbakov, Yu
Publicado 1961

Olfactory and gustatory dysfunctions in COVID-19 outpatients: A prospective cohort study

por Cousyn, L., Sellem, B., Palich, R., Bendetowicz, D., Agher, R., Delorme, C., Tubiana, R., Valantin, M.-A., Seang, S., Schneider, L., Fayçal, A., Dudoit, Y., Abdi, B., Ndoadoumgue, A., Assoumou, L., Katlama, C.
Publicado 2021

Evaluation of patients’ needs to design and assess a patient education program in cancer pain

por Prevost, V, Delorme, C, Heutte, N, Leconte, A, Bechet, C, Licaj, I, Bignon, R, Bisson, C, Cauchin, S, Gicquère, M, Grach, MC, Guillaumé, C, Le Garrec, J, Ropartz, MC, Roux, N, Sep Hieng, V, Le Chevalier, A, Clarisse, B
Publicado 2019

A novel microdeletion syndrome at 3q13.31 characterised by developmental delay, postnatal overgrowth, hypoplastic male genitals, and characteristic facial features

por Molin, A-M, Andrieux, J, Koolen, D A, Malan, V, Carella, M, Colleaux, L, Cormier-Daire, V, David, A, de Leeuw, N, Delobel, B, Duban-Bedu, B, Fischetto, R, Flinter, F, Kjaergaard, S, Kok, F, Krepischi, A C, Le Caignec, C, Ogilvie, C Mackie, Maia, S, Mathieu-Dramard, M, Munnich, A, Palumbo, O, Papadia, F, Pfundt, R, Reardon, W, Receveur, A, Rio, M, Ronsbro Darling, L, Rosenberg, C, Sá, J, Vallee, L, Vincent-Delorme, C, Zelante, L, Bondeson, M-L, Annerén, G
Publicado 2011

X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes

por Hu, H, Haas, S A, Chelly, J, Van Esch, H, Raynaud, M, de Brouwer, A P M, Weinert, S, Froyen, G, Frints, S G M, Laumonnier, F, Zemojtel, T, Love, M I, Richard, H, Emde, A-K, Bienek, M, Jensen, C, Hambrock, M, Fischer, U, Langnick, C, Feldkamp, M, Wissink-Lindhout, W, Lebrun, N, Castelnau, L, Rucci, J, Montjean, R, Dorseuil, O, Billuart, P, Stuhlmann, T, Shaw, M, Corbett, M A, Gardner, A, Willis-Owen, S, Tan, C, Friend, K L, Belet, S, van Roozendaal, K E P, Jimenez-Pocquet, M, Moizard, M-P, Ronce, N, Sun, R, O'Keeffe, S, Chenna, R, van Bömmel, A, Göke, J, Hackett, A, Field, M, Christie, L, Boyle, J, Haan, E, Nelson, J, Turner, G, Baynam, G, Gillessen-Kaesbach, G, Müller, U, Steinberger, D, Budny, B, Badura-Stronka, M, Latos-Bieleńska, A, Ousager, L B, Wieacker, P, Rodríguez Criado, G, Bondeson, M-L, Annerén, G, Dufke, A, Cohen, M, Van Maldergem, L, Vincent-Delorme, C, Echenne, B, Simon-Bouy, B, Kleefstra, T, Willemsen, M, Fryns, J-P, Devriendt, K, Ullmann, R, Vingron, M, Wrogemann, K, Wienker, T F, Tzschach, A, van Bokhoven, H, Gecz, J, Jentsch, T J, Chen, W, Ropers, H-H, Kalscheuer, V M
Publicado 2016

A novel highly-penetrant form of obesity due to microdeletions on chromosome 16p11.2

por Walters, R. G., Jacquemont, S., Valsesia, A., de Smith, A. J., Martinet, D., Andersson, J., Falchi, M., Chen, F., Andrieux, J., Lobbens, S., Delobel, B., Stutzmann, F., Moustafa, J. S. El-Sayed, Chèvre, J.-C., Lecoeur, C., Vatin, V., Bouquillon, S., Buxton, J. L., Boute, O., Holder-Espinasse, M., Cuisset, J.-M., Lemaitre, M.-P., Ambresin, A.-E., Brioshi, A., Gaillard, M., Giusti, V., Fellmann, F., Ferrarini, A., Hadjikhani, N., Campion, D., Guilmatre, A., Goldenberg, A., Calmels, N., Mandel, J.-L., Le Caignec, C., David, A., Isidor, B., Cordier, M.-P., Dupuis-Girod, S., Labalme, A., Sanlaville, D., Béri-Deixheimer, M., Jonveaux, P., Leheup, B., Õunap, K., Bochukova, E. G., Henning, E., Keogh, J., Ellis, R. J., MacDermot, K. D., Vincent-Delorme, C., Plessis, G., Touraine, R., Philippe, A., Malan, V., Mathieu-Dramard, M., Chiesa, J., Blaumeiser, B., Kooy, R. F., Caiazzo, R., Pigeyre, M., Balkau, B., Sladek, R., Bergmann, S., Mooser, V., Waterworth, D., Reymond, A., Vollenweider, P., Waeber, G., Kurg, A., Palta, P., Esko, T., Metspalu, A., Nelis, M., Elliott, P., Hartikainen, A.-L., McCarthy, M. I., Peltonen, L., Carlsson, L., Jacobson, P., Sjöström, L., Huang, N., Hurles, M. E., O’Rahilly, S., Farooqi, I. S., Männik, K., Jarvelin, M.-R., Pattou, F., Meyre, D., Walley, A. J., Coin, L. J. M., Blakemore, A. I. F., Froguel, P., Beckmann, J. S.
Publicado 2010