RELN and VLDLR mutations underlie two distinguishable clinico-radiological phenotypes von Valence, S., Garel, C., Barth, M., Toutain, A., Paris, C., Amsallem, D., Barthez, M.-A., Mayer, M., Rodriguez, D., Burglen, L.

Volltext

Mechanisms for variable expressivity of inherited SCN1A mutations causing Dravet syndrome von Depienne, Christel, Trouillard, Oriane, Gourfinkel-An, Isabelle, Saint-Martin, Cécile, Bouteiller, Delphine, Graber, Denis, Barthez-Carpentier, Marie-Anne, Gautier, Agnès, Villeneuve, Nathalie, Dravet, Charlotte, Livet, Marie-Odile, Rivier-Ringenbach, Clothilde, Adam, Claude, Dupont, Sophie, Baulac, Stéphanie, Héron, Delphine, Nabbout, Rima, LeGuern, Eric

Volltext

Retinoic acid therapy in "degenerative-like" neuro-langerhans cell histiocytosis: A prospective pilot study von Idbaih, Ahmed, Donadieu, J., Barthez, M.A., Geissmann, F., Bertrand, Y., Hermine, O., Brugières, L., Genereau, T., Thomas, C., Hoang-Xuan, K.

Volltext

Recurrence of the T666M Calcium Channel CACNA1A Gene Mutation in Familial Hemiplegic Migraine with Progressive Cerebellar Ataxia von Ducros, A., Denier, C., Joutel, A., Vahedi, K., Michel, A., Darcel, F., Madigand, M., Guerouaou, D., Tison, F., Julien, J., Hirsch, E., Chedru, F., Bisgård, C., Lucotte, G., Després, P., Billard, C., Barthez, M.A., Ponsot, G., Bousser, M.G., Tournier-Lasserve, E.

Volltext

The FHM1 Mutation S218L: A Severe Clinical Phenotype? A Case Report and Review of the Literature von Debiais, S, Hommet, C, Bonnaud, I, Barthez, MA, Rimbaux, S, Riant, F, Autret, A

Volltext

Xq27 FRAXA Locus is a Strong Candidate for Dyslexia: Evidence from a Genome-Wide Scan in French Families von Huc-Chabrolle, M., Charon, C., Guilmatre, A., Vourc’h, P., Tripi, G., Barthez, M. A., Sizaret, E., Thepault, R. A., Le Gallic, S., Hager, J., Toutain, A., Raynaud, M., Andres, C., Campion, D., Laumonnier, F., Bonnet-Brilhault, F.

Volltext

ADHD in childhood epilepsy: Clinical determinants of severity and of the response to methylphenidate von Rheims, Sylvain, Herbillon, Vania, Villeneuve, Nathalie, Auvin, Stéphane, Napuri, Silvia, Cances, Claude, Berquin, Patrick, Castelneau, Pierre, Nguyen The Tich, Sylvie, Villega, Frédéric, Isnard, Hervé, Nabbout, Rima, Gaillard, Ségolène, Mercier, Catherine, Kassai, Behrouz, Arzimanoglou, Alexis, Pedespan, Jean‐Michel, Bellescize, Julitta, Keo‐Kosal, Pascale, Panagiotakaki, Eleni, Montavont, Alexandra, Ostrowski‐Coste, Karine, Milh, Mathieu, Chiron, Catherine, Chemaly, Nicole, Bellavoine, Vanina, Barthez, Marie‐Anne

Volltext

Causes-of-death analysis of patients with cardiac resynchronization therapy: an analysis of the CeRtiTuDe cohort study von Marijon, Eloi, Leclercq, Christophe, Narayanan, Kumar, Boveda, Serge, Klug, Didier, Lacaze-Gadonneix, Jonathan, Defaye, Pascal, Jacob, Sophie, Piot, Olivier, Deharo, Jean-Claude, Perier, Marie-Cecile, Mulak, Genevieve, Hermida, Jean-Sylvain, Milliez, Paul, Gras, Daniel, Cesari, Olivier, Hidden-Lucet, Françoise, Anselme, Frederic, Chevalier, Philippe, Maury, Philippe, Sadoul, Nicolas, Bordachar, Pierre, Cazeau, Serge, Chauvin, Michel, Empana, Jean-Philippe, Jouven, Xavier, Daubert, Jean-Claude, Le Heuzey, Jean-Yves

Volltext

Clinical profile of patients with ATP1A3 mutations in Alternating Hemiplegia of Childhood-a study of 155 patients von Panagiotakaki, Eleni, De Grandis, Elisa, Stagnaro, Michela, Heinzen, Erin L, Fons, Carmen, Sisodiya, Sanjay, de Vries, Boukje, Goubau, Christophe, Weckhuysen, Sarah, Kemlink, David, Scheffer, Ingrid, Lesca, Gaëtan, Rabilloud, Muriel, Klich, Amna, Ramirez-Camacho, Alia, Ulate-Campos, Adriana, Campistol, Jaume, Giannotta, Melania, Moutard, Marie-Laure, Doummar, Diane, Hubsch-Bonneaud, Cecile, Jaffer, Fatima, Cross, Helen, Gurrieri, Fiorella, Tiziano, Danilo, Nevsimalova, Sona, Nicole, Sophie, Neville, Brian, van den Maagdenberg, Arn M J M, Mikati, Mohamad, Goldstein, David B, Vavassori, Rosaria, Arzimanoglou, Alexis

Volltext

New insights into genotype―phenotype correlations for the doublecortin-related lissencephaly spectrum von BAHI-BUISSON, Nadia, SOUVILLE, Isabelle, LOUIS LEGER, Pierre, ELIE, Caroline, BODDAERT, Nathalie, BELDJORD, Cherif, CHELLY, Jamel, FRANCIS, Fiona, EUROPEAN CONSORTIUM, Sbh-Lis, FOURNIOL, Franck J, TOUSSAINT, Aurelie, MOORES, Carolyn A, HOUDUSSE, Anne, YVES LEMAITRE, Jean, POIRIER, Karine, KHALAF-NAZZAL, Reham, HULLY, Marie

Volltext

La formation des doctorants à l'information scientifique et technique von Boudry, Christophe, Caillet, Christelle, Chuiton, Céline, Denecker, Claire, Dornier, Carole, Durand-Barthez, Manuel, Fructus, Isabelle, Grossmann, Francis, Guerreiro, Romain, Lachapelle, Frédérique Flamerie de, Lainé-Cruzel, Sylvie, Lefebvre, Muriel, L’Hostis, Dominique, Malingre, Marie-Laure, Ogier, Nicole, Pierrot, Raluca, Roland-Guill, Michel, Schöpfel, Joachim, Serres, Alexandre, Sorel, Nelly, Speck, Kristin, Torras i Calvo, Maria-Carme, Volland-Nail, Patricia

Volltext

Étude comparative des cytopénies auto-immunes isolées ou dans le cadre d’un syndrome d’Evans au cours du lupus : à propos de 95 observations von Fabre-Barthez, A., Barba, T., Reynaud, Q., Durieu, I., Baudet, A., Perard, L., Hot, A., Sève, P.

Volltext

Psychocognitive and psychiatric disorders associated with developmental dyslexia: A clinical and scientific issue von Huc-Chabrolle, M, Barthez, M-A, Tripi, G, Barthélémy, C, Bonnet-Brilhault, F

Volltext

Langerhans Cell Histiocytosis and the Central Nervous System in Childhood: Evolution and Prognostic Factors. Results of a Collaborative Study von Barthez, Marie-Anne, Araujo, Elizabeth, Donadieu, Jean

Volltext

Sleep EEG and Developmental Dysphasia: Lack of a Consistent Relationship with Paroxysmal EEG Activity During Sleep von Duvelleroy-Hommet, C., Billard, C., Lucas, B., Gillet, P., Barthez, M. A., Santini, J. J., Degiovanni, E., Henry, F., De Toffol, B., Autret, A.

Volltext

Clinically Observed Chickenpox and the Risk of Childhood-onset Multiple Sclerosis von Mikaeloff, Yann, Caridade, Guillaume, Suissa, Samy, Tardieu, Marc

Volltext

VNIR and SWIR spectra of terrestrial feldspathic rocks and powders (sample NR1 as an example) von Barthez, Marie

Volltext bestellen

National Observatory on the Therapeutic Management in Ambulatory Care Patients Aged 65 and Over, with Type 2 Diabetes, Chronic Pain or Atrial Fibrillation von Becquemont, Laurent, Benattar-Zibi, Linda, Bertin, Philippe, Berrut, Gilles, Corruble, Emmanuelle, Danchin, Nicolas, Delespierre, Tiba, Derumeaux, Geneviève, Falissard, Bruno, Forette, Francoise, Hanon, Olivier, Pasquier, Florence, Pinget, Michel, Ourabah, Rissane, Piedvache, Céline

Volltext

Study of unilateral hemisphere performance in children with developmental dysphasia von Duvelleroy-Hommet, C., Gillet, P., Billard, C., Loisel, M.L., Barthez, M.A., Santini, J.J., Autret, A.

Volltext

Effectiveness of early beta interferon on the first attack after confirmed multiple sclerosis: A comparative cohort study von Mikaeloff, Yann, Caridade, Guillaume, Tardieu, Marc, Suissa, Samy

Volltext