Monogenic cerebral small‐vessel diseases: diagnosis and therapy. Consensus recommendations of the European Academy of Neurology
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.
Published in European journal of neurology (01.06.2020)
Published in European journal of neurology (01.06.2020)
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CADASIL: yesterday, today, tomorrow
Chabriat, H., Joutel, A., Tournier‐Lasserve, E., Bousser, M. G.
Published in European journal of neurology (01.08.2020)
Published in European journal of neurology (01.08.2020)
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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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Heritable and non-heritable uncommon causes of stroke
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.
Published in Journal of neurology (01.08.2021)
Published in Journal of neurology (01.08.2021)
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Rare metabolic disease mimicking COL4A1/COL4A2 fetal brain phenotype
Coste, T., Aloui, C., Petit, F., Moutton, S., Devisme, L., Wells, C. F., Leboucq, N., Verpillat, P., Yvert, M., Rivier, F., Tournier‐Lasserve, E.
Published in Ultrasound in obstetrics & gynecology (01.12.2022)
Published in Ultrasound in obstetrics & gynecology (01.12.2022)
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Mutations within the Programmed Cell Death 10 Gene Cause Cerebral Cavernous Malformations
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.
Published in American journal of human genetics (01.01.2005)
Published in American journal of human genetics (01.01.2005)
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Frequency and phenotypes of cutaneous vascular malformations in a consecutive series of 417 patients with familial cerebral cavernous malformations
Sirvente, J, Enjolras, O, Wassef, M, Tournier-Lasserve, E, Labauge, P
Published in Journal of the European Academy of Dermatology and Venereology (01.09.2009)
Published in Journal of the European Academy of Dermatology and Venereology (01.09.2009)
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Elicited repetitive daily blindness: a new phenotype associated with hemiplegic migraine and SCN1A mutations
Vahedi, K, Depienne, C, Le Fort, D, Riant, F, Chaine, P, Trouillard, O, Gaudric, A, Morris, M A, Leguern, E, Tournier-Lasserve, E, Bousser, M-G
Published in Neurology (31.03.2009)
Published in Neurology (31.03.2009)
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Fetal intracerebral hemorrhage and cataract: think COL4A1
Colin, E, Sentilhes, L, Sarfati, A, Mine, M, Guichet, A, Ploton, C, Boussion, F, Delorme, B, Tournier-Lasserve, E, Bonneau, D
Published in Journal of perinatology (01.01.2014)
Published in Journal of perinatology (01.01.2014)
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Deep intronic KRIT1 mutation in a family with clinically silent multiple cerebral cavernous malformations
Riant, F., Odent, S., Cecillon, M., Pasquier, L., de Baracé, C., Carney, M.P., Tournier-Lasserve, E.
Published in Clinical genetics (01.12.2014)
Published in Clinical genetics (01.12.2014)
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Journal Article
Mutations within the MGC4607 Gene Cause Cerebral Cavernous Malformations
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.
Published in American journal of human genetics (01.02.2004)
Published in American journal of human genetics (01.02.2004)
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Journal Article
Acute urinary retention due to a novel collagen COL4A1 mutation
Rouaud, T, Labauge, P, Tournier Lasserve, E, Mine, M, Coustans, M, Deburghgraeve, V, Edan, G
Published in Neurology (24.08.2010)
Published in Neurology (24.08.2010)
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Journal Article
Severe Attacks of Familial Hemiplegic Migraine, Childhood Epilepsy and ATP1A2 Mutation
Lebas, A, Guyant-Maréchal, L, Hannequin, D, Riant, F, Tournier-Lasserve, E, Parain, D
Published in Cephalalgia (01.07.2008)
Published in Cephalalgia (01.07.2008)
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The Genetic Basis of Moyamoya Disease
Mertens, R., Graupera, M., Gerhardt, H., Bersano, A., Tournier-Lasserve, E., Mensah, M. A., Mundlos, S., Vajkoczy, P.
Published in Translational stroke research (01.02.2022)
Published in Translational stroke research (01.02.2022)
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High prevalence of CACNA1A truncations and broader clinical spectrum in episodic ataxia type 2
Denier, C, Ducros, A, Vahedi, K, Joutel, A, Thierry, P, Ritz, A, Castelnovo, G, Deonna, T, Gérard, P, Devoize, J L, Gayou, A, Perrouty, B, Soisson, T, Autret, A, Warter, J M, Vighetto, A, Van Bogaert, P, Alamowitch, S, Roullet, E, Tournier-Lasserve, E
Published in Neurology (10.06.1999)
Published in Neurology (10.06.1999)
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CACNA1A gene de novo mutation causing hemiplegic migraine, coma, and cerebellar atrophy
Vahedi, K, Denier, C, Ducros, A, Bousson, V, Levy, C, Chabriat, H, Haguenau, M, Tournier-Lasserve, E, Bousser, M G
Published in Neurology (10.10.2000)
Published in Neurology (10.10.2000)
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Journal Article
Clinical spectrum of CADASIL: a study of 7 families
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
Published in The Lancet (British edition) (07.10.1995)
Published in The Lancet (British edition) (07.10.1995)
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Journal Article
De novo mutations in ATP1A2 and CACNA1A are frequent in early-onset sporadic hemiplegic migraine
Riant, F, Ducros, A, Ploton, C, Barbance, C, Depienne, C, Tournier-Lasserve, E
Published in Neurology (14.09.2010)
Published in Neurology (14.09.2010)
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Hemorrhagic stroke associated with the Iowa amyloid precursor protein mutation
Greenberg, S M, Shin, Y, Grabowski, T J, Cooper, G E, Rebeck, G W, Iglesias, S, Chapon, F, Tournier-Lasserve, E, Baron, J-C
Published in Neurology (25.03.2003)
Published in Neurology (25.03.2003)
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