Monogenic cerebral small‐vessel diseases: diagnosis and therapy. Consensus recommendations of the European Academy of Neurology von Mancuso, M., Arnold, M., Bersano, A., Burlina, A., Chabriat, H., Debette, S., Enzinger, C., Federico, A., Filla, A., Finsterer, J., Hunt, D., Lesnik Oberstein, S., Tournier‐Lasserve, E., Markus, H. S.

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CADASIL: yesterday, today, tomorrow von Chabriat, H., Joutel, A., Tournier‐Lasserve, E., Bousser, M. G.

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Prevalence of COL4A1 and COL4A2 mutations in severe fetal multifocal hemorrhagic and/or ischemic cerebral lesions von 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.

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Heritable and non-heritable uncommon causes of stroke von Bersano, A., Kraemer, M., Burlina, A., Mancuso, M., Finsterer, J., Sacco, S., Salvarani, C., Caputi, L., Chabriat, H., Oberstein, S. Lesnik, Federico, A., Lasserve, E. Tournier, Hunt, D., Dichgans, M., Arnold, M., Debette, S., Markus, H. S.

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Rare metabolic disease mimicking COL4A1/COL4A2 fetal brain phenotype von Coste, T., Aloui, C., Petit, F., Moutton, S., Devisme, L., Wells, C. F., Leboucq, N., Verpillat, P., Yvert, M., Rivier, F., Tournier‐Lasserve, E.

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Mutations within the Programmed Cell Death 10 Gene Cause Cerebral Cavernous Malformations von Bergametti, F., Denier, C., Labauge, P., Arnoult, M., Boetto, S., Clanet, M., Coubes, P., Echenne, B., Ibrahim, R., Irthum, B., Jacquet, G., Lonjon, M., Moreau, J.J., Neau, J.P., Parker, F., Tremoulet, M., Tournier-Lasserve, E.

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Frequency and phenotypes of cutaneous vascular malformations in a consecutive series of 417 patients with familial cerebral cavernous malformations von Sirvente, J, Enjolras, O, Wassef, M, Tournier-Lasserve, E, Labauge, P

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Elicited repetitive daily blindness : A new phenotype associated with hemiplegic migraine and SCN1A mutations von VAHEDI, K, DEPIENNE, C, BOUSSER, M.-G, LE FORT, D, RIANT, F, CHAINE, P, TROUILLARD, O, GAUDRIC, A, MORRIS, M. A, LEGUERN, E, TOURNIER-LASSERVE, E

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Fetal intracerebral hemorrhage and cataract: think COL4A1 von Colin, E, Sentilhes, L, Sarfati, A, Mine, M, Guichet, A, Ploton, C, Boussion, F, Delorme, B, Tournier-Lasserve, E, Bonneau, D

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Deep intronic KRIT1 mutation in a family with clinically silent multiple cerebral cavernous malformations von Riant, F., Odent, S., Cecillon, M., Pasquier, L., de Baracé, C., Carney, M.P., Tournier-Lasserve, E.

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Episodic ataxia type 2: unusual aspects in clinical and genetic presentation. Special emphasis in childhood von Bertholon, P, Chabrier, S, Riant, F, Tournier-Lasserve, E, Peyron, R

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The Genetic Basis of Moyamoya Disease von Mertens, R., Graupera, M., Gerhardt, H., Bersano, A., Tournier-Lasserve, E., Mensah, M. A., Mundlos, S., Vajkoczy, P.

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Mutations within the MGC4607 Gene Cause Cerebral Cavernous Malformations von Denier, C., Goutagny, S., Labauge, P., Krivosic, V., Arnoult, M, Cousin, A., Benabid, A.L., Comoy, J., Frerebeau, P., Gilbert, B., Houtteville, J.P., Jan, M., Lapierre, F., Loiseau, H., Menei, P., Mercier, P., Moreau, J.J., Nivelon-Chevallier, A., Parker, F., Redondo, A.M., Scarabin, J.M., Tremoulet, M., Zerah, M., Maciazek, J., Tournier-Lasserve, E.

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ACUTE URINARY RETENTION DUE TO A NOVEL COLLAGEN COL4A1 MUTATION von ROUAUD, T, LABAUGE, P, TOURNIER LASSERVE, E, MINE, M, COUSTANS, M, DEBURGHGRAEVE, V, EDAN, G

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Severe Attacks of Familial Hemiplegic Migraine, Childhood Epilepsy and ATP1A2 Mutation von Lebas, A, Guyant-Maréchal, L, Hannequin, D, Riant, F, Tournier-Lasserve, E, Parain, D

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De novo mutations in ATP1A2 and CACNA1A are frequent in early-onset sporadic hemiplegic migraine von Riant, F, Ducros, A, Ploton, C, Barbance, C, Depienne, C, Tournier-Lasserve, E

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High prevalence of CACNA1A truncations and broader clinical spectrum in episodic ataxia type 2 von DENIER, C, DUCROS, A, GAYOU, A, PERROUTY, B, SOISSON, T, AUTRET, A, WARTER, J. M, VIGHETTO, A, VAN BOGAERT, P, ALAMOWITCH, S, ROULLET, E, TOURNIER-LASSERVE, E, VAHEDI, K, JOUTEL, A, THIERRY, P, RITZ, A, CASTELNOVO, G, DEONNA, T, GERARD, P, DEVOIZE, J. L

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Clinical spectrum of CADASIL: a study of 7 families von Chabriat, H, Vahedi, K, Bousser, M.G, Iba-Zizen, M.T, Joutel, A, Nibbio, A, Nagy, T.G, Tournier Lasserve, E, Krebs, M.O, Julien, J, Ducrocq, X, Levasseur, M, Mas, J.L, Dubois, B, Homeyer, P, Lyon-Caen, O

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CACNA1A gene de novo mutation causing hemiplegic migraine, coma, and cerebellar atrophy von VAHEDI, K, DENIER, C, DUCROS, A, BOUSSON, V, LEVY, C, CHABRIAT, H, HAGUENAU, M, TOURNIER-LASSERVE, E, BOUSSER, M. G

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Leukoencephalopathy with calcifications and cysts (LCC): 5 cases and literature review von Osman, O., Labrune, P., Reiner, P., Sarov, M., Nasser, G., Riant, F., Tournier-lasserve, E., Chabriat, H., Denier, C.

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