Generic scale-space process for handwriting documents analysis by Joutel, G., Eglin, V., Emptoz, H.

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Curvelets Based Queries for CBIR Application in Handwriting Collections by Joutel, G., Eglin, V., Bres, S., Emptoz, H.

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Consensus statement for diagnosis of subcortical small vessel disease by Korczyn, Amos D, O], [A.

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Specification of CNS macrophage subsets occurs postnatally in defined niches by Masuda, Takahiro, Amann, Lukas, Monaco, Gianni, Sankowski, Roman, Staszewski, Ori, Krueger, Martin, Del Gaudio, Francesca, He, Liqun, Paterson, Neil, Nent, Elisa, Fernández-Klett, Francisco, Yamasaki, Ayato, Frosch, Maximilian, Fliegauf, Maximilian, Bosch, Lance Fredrick Pahutan, Ulupinar, Hatice, Hagemeyer, Nora, Schreiner, Dietmar, Dorrier, Cayce, Tsuda, Makoto, Grothe, Claudia, Joutel, Anne, Daneman, Richard, Betsholtz, Christer, Lendahl, Urban, Knobeloch, Klaus-Peter, Lämmermann, Tim, Priller, Josef, Kierdorf, Katrin, Prinz, Marco

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Author Correction: Specification of CNS macrophage subsets occurs postnatally in defined niches by Masuda, Takahiro, Amann, Lukas, Monaco, Gianni, Sankowski, Roman, Staszewski, Ori, Krueger, Martin, Del Gaudio, Francesca, He, Liqun, Paterson, Neil, Nent, Elisa, Fernández-Klett, Francisco, Yamasaki, Ayato, Frosch, Maximilian, Fliegauf, Maximilian, Bosch, Lance Fredrick Pahutan, Ulupinar, Hatice, Hagemeyer, Nora, Schreiner, Dietmar, Dorrier, Cayce, Tsuda, Makoto, Grothe, Claudia, Joutel, Anne, Daneman, Richard, Betsholtz, Christer, Lendahl, Urban, Knobeloch, Klaus-Peter, Lämmermann, Tim, Priller, Josef, Kierdorf, Katrin, Prinz, Marco

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Strong clustering and stereotyped nature of Notch3 mutations in CADASIL patients by Joutel, Anne, Vahedi, Katayoun, Corpechot, Christophe, Troesch, Alain, Chabriat, Hugues, Vayssière, Céline, Cruaud, Corinne, Maciazek, Jacqueline, Weissenbach, Jean, Bousser, Marie-Germaine, Bach, Jean-François, Tournier-Lasserve, Elisabeth

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Specification of CNS macrophage subsets occurs postnatally in defined niches (vol 604, pg 740, 2022) by Masuda, T, Amann, L, Monaco, G, Sankowski, R, Staszewski, O, Krueger, M, Del, Gaudio F, He, L, Paterson, N, Nent, E

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Clinical spectrum of CADASIL: a study of 7 families by 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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Skin biopsy immunostaining with a Notch3 monoclonal antibody for CADASIL diagnosis by Joutel, Anne, Favrole, Pascal, Labauge, Pierre, Chabriat, Hugues, Lescoat, Christelle, Andreux, Frédéric, Domenga, Valérie, Cécillon, Michaelle, Vahedi, Katayoun, Ducros, Anne, Cave-Riant, Florence, Bousser, Marie Germaine, Tournier-Lasserve, Elisabeth

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A novel hereditary small vessel disease of the brain by Verreault, Steve, Joutel, Anne, Riant, Florence, Neves, Georgina, Rui Silva, Mario, Maciazek, Jacqueline, Tournier-Lasserve, Elizabeth, Bousser, Marie-Germaine, Chabriat, Hugues

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De novo mutation in the Notch3 gene causing CADASIL by Joutel, Anne, Dodick, David D., Parisi, Joseph E., Cecillon, Michaelle, Tournier-Lasserve, Elisabeth, Germaine Bousser, Marie

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Autosomal dominant leukoencephalopathy and subcortical ischemic stroke : a clinicopathological study by BAUDRIMONT, M, DUBAS, F, JOUTEL, A, TOURNIER-LASSERVE, E, BOUSSER, M.-G

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Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia by Joutel, Anne, Corpechot, Christophe, Ducros, Anne, Vahedi, Katayoun, Chabriat, Hugues, Mouton, Philippe, Alamowitch, Sonia, Domenga, Valérie, Cécillion, Michaelle, Maréchal, Emmanuelle, Maciazek, Jacqueline, Vayssière, Céline, Cruaud, Corinne, Cabanis, Emmanuel-Alain, Ruchoux, Marie Madeleine, Weissenbach, Jean, Bach, Jean François, Bousser, Marie Germaine, Tournier-Lasserve, Elisabeth

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Recurrence of the T666M Calcium Channel CACNA1A Gene Mutation in Familial Hemiplegic Migraine with Progressive Cerebellar Ataxia by 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.

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Notch3 Mutations in Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL), a Mendelian Condition Causing Stroke and Vascular Dementia by JOUTEL, ANNE, CORPECHOT, CHRISTOPHE, DUCROS, ANNE, VAHEDI, KATAYOUN, CHABRIAT, HUGUES, MOUTON, PHILIPPE, ALAMOWITCH, SONIA, DOMENGA, VALÉRIE, CÉCILLION, MICHAELLE, MARÉCHAL, EMMANUELLE, MACIAZEK, JACQUELINE, VAYSSIÈRE, CÉLINE, CRUAUD, CORINNE, CABANIS, EMMANUEL-ALAIN, RUCHOUX, MARIE MADELEINE, WEISSENBACH, JEAN, BACH, JEAN FRANÇOIS, BOUSSER, MARIE GERMAINE, TOURNIER-LASSERVE, ELISABETH

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Brain stem MRI signal abnormalities in CADASIL by CHABRIAT, H, MRISSA, R, LEVY, C, VAHEDI, K, TAILLIA, H, IBA-ZIZEN, M. T, JOUTEL, A, TOURNIER-LASSERVE, E, BOUSSER, M.-G

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Genetic heterogeneity of familial hemiplegic migraine by JOUTEL, A, DUCROS, A, MAZIACEK, J, WEISSENBACH, J, BOUSSER, M. G, TOURNIER-LASSERVE, E, VAHEDI, K, LABAUGE, P, DELRIEU, O, PINSARD, N, MANCINI, J, PONSOT, G, GOUTTIERE, F, GASTAUT, J. L

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Reference center for rare vascular diseases of the eye and brain by Chabriat, H

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Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, genetic homogeneity, and mapping of the locus within a 2-cM interval by DUCROS, A, NAGY, T, GOAS, J. Y, LYON-CAEN, O, DUBOIS, B, DUCROCQ, X, SALSA, F, RAGNO, M, BURKHARD, P, BASSETTI, C, HUTCHINSON, M, VERIN, M, ALAMOWITCH, S, VIADER, F, CHAPON, F, LEVASSEUR, M, MAS, J. L, DELRIEU, O, MACIAZEK, J, PRIEUR, M, MOHRENWEISER, H, BACH, J. F, BOUSSER, M. G, NIBBIO, A, TOURNIER-LASSERVE, E, JOUTEL, A, VAHEDI, K, CHABRIAT, H, IBA-ZIZEN, M. T, JULIEN, J, DAVOUS, P

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A Human Homolog of Bacterial Acetolactate Synthase Genes Maps within the CADASIL Critical Region by Joutel, A., Ducros, A., Alamowitch, S., Cruaud, C., Domenga, V., Maréchal, E., Vahedi, K., Chabriat, H., Bousser, M.G., Tournier-Lasserve, E.

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