Peripheral nerve entrapments.

von Namerow, N S, Campion, D S, Bluestone, R, Cracchiolo, A
Veröffentlicht 1977

Mechanism of action of reserpine in producing gastric haemorrhage and erosion in the mouse

von Blackman, J. G., Campion, D. S., Fastier, F. N.
Veröffentlicht 1959

Ataxic variant of Alzheimer's disease caused by Pro117Ala PSEN1 mutation

von Anheim, M, Hannequin, D, Boulay, C, Martin, C, Campion, D, Tranchant, C
Veröffentlicht 2007

Spastic paraparesis and atypical dementia caused by PSEN1 mutation (P264L), responsible for Alzheimer's disease

von Jacquemont, M, Campion, D, Hahn, V, Tallaksen, C, Frebourg, T, Brice, A, Durr, A
Veröffentlicht 2002

APP locus duplication in a Finnish family with dementia and intracerebral haemorrhage

von Rovelet‐Lecrux, A, Frebourg, T, Tuominen, H, Majamaa, K, Campion, D, Remes, A M
Veröffentlicht 2007

Unusual phenotypic alteration of β amyloid precursor protein (βAPP) maturation by a new Val-715 → Met βAPP-770 mutation responsible for probable early-onset Alzheimer’s disease...

von Ancolio, K., Dumanchin, C., Barelli, H., Warter, J. M., Brice, A., Campion, D., Frébourg, T., Checler, F.
Veröffentlicht 1999

Molecular diagnosis of autosomal dominant early onset Alzheimer's disease: an update

von Raux, G, Guyant-Marechal, L, Martin, C, Bou, J, Penet, C, Brice, A, Hannequin, D, Frebourg, T, Campion, D
Veröffentlicht 2005

The severe form of type I hyperprolinaemia results from homozygous inactivation of the PRODH gene

von Jacquet, H, Berthelot, J, Bonnemains, C, Simard, G, Saugier-Veber, P, Raux, G, Campion, D, Bonneau, D, Frebourg, T
Veröffentlicht 2003

Homozygosity at the dopamine D3 receptor locus is not associated with schizophrenia.

von Laurent, C, Savoye, C, Samolyk, D, Meloni, R, Mallet, J, Campion, D, Martinez, M, D'Amato, T, Bastard, C, Dollfus, S
Veröffentlicht 1994

De novo presenilin 1 mutations are rare in clinically sporadic, early onset Alzheimer's disease cases. French Alzheimer's Disease Study Group.

von Dumanchin, C, Brice, A, Campion, D, Hannequin, D, Martin, C, Moreau, V, Agid, Y, Martinez, M, Clerget-Darpoux, F, Frebourg, T
Veröffentlicht 1998

Absence of the amyloid precursor protein gene mutation (APP717: Val->Ile) in 85 cases of early onset Alzheimer's disease.

von Brice, A, Boch, A L, Stevanin, G, Khati, C, Dubois, B, Agid, Y, Campion, D, Clerget, F, Mallet, J, Bellis, M
Veröffentlicht 1993

No founder effect in three novel Alzheimer's disease families with APP 717 Val-->Ile mutation. Clerget-darpoux. French Alzheimer's Disease Study Group.

von Campion, D, Brice, A, Hannequin, D, Charbonnier, F, Dubois, B, Martin, C, Michon, A, Penet, C, Bellis, M, Calenda, A, Martinez, M, Agid, Y, Clerget-Darpoux, F, Frebourg, T
Veröffentlicht 1996

No effect of the α1-antichymotrypsin A allele in Alzheimer's disease

von Didierjean, O, Martinez, M, Campion, D, Hannequin, D, Dubois, B, Martin, C, Puel, M, Anterion, C, Pasquier, F, Moreau, O, Babron, M, Penet, C, Agid, Y, Clerget-Darpoux, F, Frebourg, T, Brice, A
Veröffentlicht 1997

Early-onset autosomal dominant Alzheimer disease: prevalence, genetic heterogeneity, and mutation spectrum.

von Campion, D, Dumanchin, C, Hannequin, D, Dubois, B, Belliard, S, Puel, M, Thomas-Anterion, C, Michon, A, Martin, C, Charbonnier, F, Raux, G, Camuzat, A, Penet, C, Mesnage, V, Martinez, M, Clerget-Darpoux, F, Brice, A, Frebourg, T
Veröffentlicht 1999

Apolipoprotein E and Alzheimer disease: genotype-specific risks by age and sex.

von Bickeböller, H, Campion, D, Brice, A, Amouyel, P, Hannequin, D, Didierjean, O, Penet, C, Martin, C, Pérez-Tur, J, Michon, A, Dubois, B, Ledoze, F, Thomas-Anterion, C, Pasquier, F, Puel, M, Demonet, J F, Moreaud, O, Babron, M C, Meulien, D, Guez, D, Chartier-Harlin, M C, Frebourg, T, Agid, Y, Martinez, M, Clerget-Darpoux, F
Veröffentlicht 1997

Increased expression of BIN1 mediates Alzheimer genetic risk by modulating tau pathology

von Chapuis, J, Hansmannel, F, Gistelinck, M, Mounier, A, Van Cauwenberghe, C, Kolen, K V, Geller, F, Sottejeau, Y, Harold, D, Dourlen, P, Grenier-Boley, B, Kamatani, Y, Delepine, B, Demiautte, F, Zelenika, D, Zommer, N, Hamdane, M, Bellenguez, C, Dartigues, J-F, Hauw, J-J, Letronne, F, Ayral, A-M, Sleegers, K, Schellens, A, Broeck, L V, Engelborghs, S, De Deyn, P P, Vandenberghe, R, O'Donovan, M, Owen, M, Epelbaum, J, Mercken, M, Karran, E, Bantscheff, M, Drewes, G, Joberty, G, Campion, D, Octave, J-N, Berr, C, Lathrop, M, Callaerts, P, Mann, D, Williams, J, Buée, L, Dewachter, I, Van Broeckhoven, C, Amouyel, P, Moechars, D, Dermaut, B, Lambert, J-C
Veröffentlicht 2013

Genome-wide haplotype association study identifies the FRMD4A gene as a risk locus for Alzheimer's disease

von Lambert, J-C, Grenier-Boley, B, Harold, D, Zelenika, D, Chouraki, V, Kamatani, Y, Sleegers, K, Ikram, M A, Hiltunen, M, Reitz, C, Mateo, I, Feulner, T, Bullido, M, Galimberti, D, Concari, L, Alvarez, V, Sims, R, Gerrish, A, Chapman, J, Deniz-Naranjo, C, Solfrizzi, V, Sorbi, S, Arosio, B, Spalletta, G, Siciliano, G, Epelbaum, J, Hannequin, D, Dartigues, J-F, Tzourio, C, Berr, C, Schrijvers, E M C, Rogers, R, Tosto, G, Pasquier, F, Bettens, K, Van Cauwenberghe, C, Fratiglioni, L, Graff, C, Delepine, M, Ferri, R, Reynolds, C A, Lannfelt, L, Ingelsson, M, Prince, J A, Chillotti, C, Pilotto, A, Seripa, D, Boland, A, Mancuso, M, Bossù, P, Annoni, G, Nacmias, B, Bosco, P, Panza, F, Sanchez-Garcia, F, Del Zompo, M, Coto, E, Owen, M, O'Donovan, M, Valdivieso, F, Caffara, P, Scarpini, E, Combarros, O, Buée, L, Campion, D, Soininen, H, Breteler, M, Riemenschneider, M, Van Broeckhoven, C, Alpérovitch, A, Lathrop, M, Trégouët, D-A, Williams, J, Amouyel, P
Veröffentlicht 2013

Genome-wide haplotype association study identifies the FRMD4A gene as a risk locus for Alzheimer's disease

von Lambert, J-C, Grenier-Boley, B, Harold, D, Zelenika, D, Chouraki, V, Kamatani, Y, Sleegers, K, Ikram, M A, Hiltunen, M, Reitz, C, Mateo, I, Feulner, T, Bullido, M, Galimberti, D, Concari, L, Alvarez, V, Sims, R, Gerrish, A, Chapman, J, Deniz-Naranjo, C, Solfrizzi, V, Sorbi, S, Arosio, B, Spalletta, G, Siciliano, G, Epelbaum, J, Hannequin, D, Dartigues, J-F, Tzourio, C, Berr, C, Schrijvers, E M C, Rogers, R, Tosto, G, Pasquier, F, Bettens, K, Van Cauwenberghe, C, Fratiglioni, L, Graff, C, Delepine, M, Ferri, R, Reynolds, C A, Lannfelt, L, Ingelsson, M, Prince, J A, Chillotti, C, Pilotto, A, Seripa, D, Boland, A, Mancuso, M, Bossù, P, Annoni, G, Nacmias, B, Bosco, P, Panza, F, Sanchez-Garcia, F, Zompo, M Del, Coto, E, Owen, M, O'Donovan, M, Valdivieso, F, Caffara, P, Scarpini, E, Combarros, O, Buée, L, Campion, D, Soininen, H, Breteler, M, Riemenschneider, M, Van Broeckhoven, C, Alpérovitch, A, Lathrop, M, Trégouët, D-A, Williams, J, Amouyel, P
Veröffentlicht 2013

A novel highly-penetrant form of obesity due to microdeletions on chromosome 16p11.2

von Walters, R. G., Jacquemont, S., Valsesia, A., de Smith, A. J., Martinet, D., Andersson, J., Falchi, M., Chen, F., Andrieux, J., Lobbens, S., Delobel, B., Stutzmann, F., Moustafa, J. S. El-Sayed, Chèvre, J.-C., Lecoeur, C., Vatin, V., Bouquillon, S., Buxton, J. L., Boute, O., Holder-Espinasse, M., Cuisset, J.-M., Lemaitre, M.-P., Ambresin, A.-E., Brioshi, A., Gaillard, M., Giusti, V., Fellmann, F., Ferrarini, A., Hadjikhani, N., Campion, D., Guilmatre, A., Goldenberg, A., Calmels, N., Mandel, J.-L., Le Caignec, C., David, A., Isidor, B., Cordier, M.-P., Dupuis-Girod, S., Labalme, A., Sanlaville, D., Béri-Deixheimer, M., Jonveaux, P., Leheup, B., Õunap, K., Bochukova, E. G., Henning, E., Keogh, J., Ellis, R. J., MacDermot, K. D., Vincent-Delorme, C., Plessis, G., Touraine, R., Philippe, A., Malan, V., Mathieu-Dramard, M., Chiesa, J., Blaumeiser, B., Kooy, R. F., Caiazzo, R., Pigeyre, M., Balkau, B., Sladek, R., Bergmann, S., Mooser, V., Waterworth, D., Reymond, A., Vollenweider, P., Waeber, G., Kurg, A., Palta, P., Esko, T., Metspalu, A., Nelis, M., Elliott, P., Hartikainen, A.-L., McCarthy, M. I., Peltonen, L., Carlsson, L., Jacobson, P., Sjöström, L., Huang, N., Hurles, M. E., O’Rahilly, S., Farooqi, I. S., Männik, K., Jarvelin, M.-R., Pattou, F., Meyre, D., Walley, A. J., Coin, L. J. M., Blakemore, A. I. F., Froguel, P., Beckmann, J. S.
Veröffentlicht 2010