French guidelines for the diagnosis and management of Tourette syndrome von Hartmann, A., Ansquer, S., Brefel-Courbon, C., Burbaud, P., Castrioto, A., Czernecki, V., Damier, P., Deniau, E., Drapier, S., Jalenques, I., Marechal, O., Priou, T., Spodenkiewicz, M., Thobois, S., Roubertie, A., Witjas, T., Anheim, M.

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Deciphering the natural history of SCA7 in children von Bah, M. G., Rodriguez, D., Cazeneuve, C., Mochel, F., Devos, D., Suppiej, A., Roubertie, A., Meunier, I., Gitiaux, C., Curie, A., Klapczynski, F., Allani‐Essid, N., Carneiro, M., Van Minkelen, R., Kievit, A., Fluss, J., Leheup, B., Ratbi, L., Héron, D., Gras, D., Do Cao, J., Pichard, S., Strubi‐Villaume, I., Audo, I., Lesca, G., Charles, P., Dubois, F., Comet‐Didierjean, P., Capri, Y., Barondiot, C., Barathon, M., Ewenczyk, C., Durr, A., Mignot, C.

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Mutational spectrum of CDKL5 in early-onset encephalopathies: a study of a large collection of French patients and review of the literature von Nemos, C, Lambert, L, Giuliano, F, Doray, B, Roubertie, A, Goldenberg, A, Delobel, B, Layet, V, N'guyen, MA, Saunier, A, Verneau, F, Jonveaux, P, Philippe, C

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Dermatological and genetic data in tuberous sclerosis: A prospective single-center study of 38 patients von Secco, L.-P., Coubes, C., Meyer, P., Chenine, L., Roubertie, A., Malinge, M.-C., Bessis, D.

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Treatment for dystonia in childhood von Roubertie, A., Mariani, L. L., Fernandez-Alvarez, E., Doummar, D., Roze, E.

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Bilateral facial nerve palsy associated with Epstein-Barr virus infection in a 3-year-old boy von Grassin, M, Rolland, A, Leboucq, N, Roubertie, A, Rivier, F, Meyer, P

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Refinement of cortical dysgeneses spectrum associated with TUBA1A mutations von Bahi-Buisson, N, Poirier, K, Boddaert, N, Saillour, Y, Castelnau, L, Philip, N, Buyse, G, Villard, L, Joriot, S, Marret, S, Bourgeois, M, Van Esch, H, Lagae, L, Amiel, J, Hertz-Pannier, L, Roubertie, A, Rivier, F, Pinard, J M, Beldjord, C, Chelly, J

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Absence of antibodies to glutamate receptor type 3 (GluR3) in Rasmussen encephalitis von WATSON, R, JIANG, Y, HART, Y, PALACE, J, BEESON, D, VINCENT, A, LANG, B, BERMUDEZ, I, HOULIHAN, L, CLOVER, L, MCKNIGHT, K, CROSS, J. H, HART, I. K, ROUBERTIE, A, VALMIER, J

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Benign paroxysmal tonic upgaze, benign paroxysmal torticollis, episodic ataxia and CACNA1A mutation in a family von Roubertie, A., Echenne, B., Leydet, J., Soete, S., Krams, B., Rivier, F., Riant, F., Tournier-Lasserve, E.

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A two part, multi-centre, multiple dose study of Erythrocyte Encapsulated Thymidine Phosphorylase (EETP) in patients with Mitochondrial Neurogastrointestinal Encephalomyopathy (MNG... von Nirmalananthan, N, Levene, M, Filosto, M, Klopstock, T, Kornblum, C, Mandel, H, Rahman, S, Roubertie, A, Scarpelli, M, Bax, B.E

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Chronic Diarrhea in l-Amino Acid Decarboxylase (AADC) Deficiency: A Prominent Clinical Finding Among a Series of Ten French Patients von Spitz, M. A., Nguyen, M. A., Roche, S., Heron, B., Milh, M., de Lonlay, P., Lion-François, L., Testard, H., Napuri, S., Barth, M., Fournier-Favre, S., Christa, L., Vianey-Saban, C., Corne, C., Roubertie, A.

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Partial acute transverse myelitis is a predictor of multiple sclerosis in children von Meyer, P, Leboucq, N, Molinari, N, Roubertie, A, Carneiro, M, Walther-Louvier, U, Cuntz-Shadfar, D, Leydet, J, Cheminal, R, Cambonie, G, Echenne, B, Rondouin, G, Deiva, K, Mikaeloff, Y, Rivier, F

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The genetic pathophysiology of dominant optic atrophy von Lenaers, G., Charif, M., Amati‐Bonneau, P., Chao de la Barca, J., Procaccio, V., Gerber, S., Kaplan, J., Roubertie, A., Meunier, I., Reynier, P., Rozet, J.M., Hamel, C., Bonneau, D.

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Unexpected neurological sequelae following propofol anesthesia in infants: Three case reports von Meyer, P, Langlois, C, Soëte, S, Leydet, J, Echenne, B, Rivier, F, Bonafé, A, Roubertie, A

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Infantile systemic hyalinosis von Meyer, P, Tournier, C, Bessis, D, Rolland, A, Carme, E, Roubertie, A, Ribrault, A, Hajj-Verkindere, E, Lebre, A.S, Rivier, F

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Pediatric cerebral venous thrombosis: Description and prognosis according to the physiopathological mechanism in a population of 40 cases von Durand, S, Meyer, P, Leboucq, N, Langlois, C, Carneiro, M, Roubertie, A, Walther-Louvier, U, Cuntz, D, Leydet, J, Plan, O, Combes, C, Cambonie, G, Rivier, F

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Anti-tumor necrosis factor alpha therapy, Adalimumab, in Rasmussen's encephalitis von Villeneuve, N, Lagarde, S, Lepine, A, Laguitton, V, Bulteau, C, Roubertie, A, Barthez, M.A, Trommsdorff, V, Lefranc, J, Des Portes, V, Quartier, P, Wehbi, S, McGonigal, A, Bartolomei, F, Milh, M

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Systematic Analysis of Brain MRI Findings in Adaptor Protein Complex 4–Associated Hereditary Spastic Paraplegia von Ebrahimi-Fakhari, Darius, Alecu, Julian E., Ziegler, Marvin, Geisel, Gregory, Jordan, Catherine, D'Amore, Angelica, Yeh, Rebecca C., Akula, Shyam K., Saffari, Afshin, Prabhu, Sanjay P., Sahin, Mustafa, Yang, Edward

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Update on the treatment of childhood movement disorders: Focus on dystonia von Roubertie, A, Echenne, B

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α7-Acetylcholine receptor antibodies in two patients with Rasmussen encephalitis von WATSON, R, JEPSON, J. E. C, BEESON, D, VINCENT, A, LANG, B, BERMUDEZ, I, ALEXANDER, S, HART, Y, MCKNIGHT, K, ROUBERTIE, A, FECTO, F, VALMIER, J, SATTELLE, D. B

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