Maladie d'Alzheimer et maladies apparentées

Publications

 

 2011
 2010
 2009
 2008
 2007
 2006

 2005
 2004
 2003
 2002
 2001
 2000

2011

  • Laure Saint-Aubert, Pierre Payoux, Didier Hannequin, Emmanuel J. Barbeau, Dominique Campion, Marie-Bernadette Delisle, Mathieu Tafani, Gérard Viallard, Patrice Péran, Michèle Puel, François Chollet, Jean-François Demonet, Jérémie Pariente. MR, 18F-FDG and 18F-AV45 PET correlate with AD PSEN1 original phenotype" Alzheimer Dis Assoc Disord. 2011 (in press).

  • Cousin E, Mace S, Rocher C, Dib C, Muzard G, Hannequin D, Pradier L, Deleuze JF, Genin E, Brice A, Campion D. No replication of genetic association between candidate polymorphisms and alzheimer's disease. Neurobiol Aging. 2011 Aug;32(8): 1443-51.

  • Jurici S, Laquerrière A, Bedat-Millet AL, Jardin F, Musset L, Vallat JM, Hannequin D, Martinaud O. An Autopsy Case of Amyotrophic Lateral Sclerosis with Waldenström Macroglobulinemia and Anti-MAG Gammopathy. Case Rep Neurol. 2011 Sep;3(3): 294-300.

  • Rovelet-Lecrux A, Legallic S, Wallon D, Flaman JM, Martinaud O, Bombois S,
    Rollin-Sillaire A, Michon A, Le Ber I, Pariente J, Puel M, Paquet C, Croisile B, Thomas-Antérion C, Vercelletto M, Lévy R, Frébourg T, Hannequin D, Campion D. A genome-wide study reveals rare CNVs exclusive to extreme phenotypes of Alzheimer disease. Eur J Hum Genet. 2011 Dec 14.

  • Saint-Aubert L, Planton M, Hannequin D, Albucher JF, Delisle MB, Payoux P,Hitzel A, Viallard G, Péran P, Campion D, Laquerrière A, Barbeau EJ, Puel M,Raposo N, Chollet F, Pariente J. Amyloid Imaging with AV45 (18F-florbetapir) in a cognitively Normal AβPP Duplication Carrier. J Alzheimers Dis. 2011 Dec 9.

  • Pottier C, Wallon D, Lecrux AR, Maltete D, Bombois S, Jurici S, Frebourg T, Hannequin D, Campion D. Amyloid-β Protein Precursor Gene Expression in Alzheimer's Disease and Other Conditions. J Alzheimers Dis. 2011 Nov 1.

  • Hannequin D, Wallon D, Martinaud O,  Maltete D, Campion D, Deramecourt V, Le Ber I. Nosologie des degenerescences lobaires frontotemporales. Rev Neurol, Pratique Neurologique.2011; 2: 53-63

  • Deramecourt V, Koric L, Hannequin D, Maisonobe T, Campion D, Sellal F. Troubles de la mémoire d'installation progressive chez un homme de 62 ans. Rev Neurol, Pratique Neurologique.2011; 2: 139-148.

  • Hainselin M, Quinette P, Desgranges B, Martinaud O, Hannequin D, de la Sayette V, Viader F, Eustache F. Can we remember future actions yet forget the last two minutes? Study in transient global amnesia. J Cogn Neurosci. 2011; Dec;23(12): 4138-49.

  • Hollingworth P, Harold D, Sims R, Gerrish A, Lambert JC, Carrasquillo MM, Abraham R, Hamshere ML, Pahwa JS, Moskvina V, Dowzell K, Jones N, Stretton A, Thomas C, Richards A, Ivanov D, Widdowson C, Chapman J, Lovestone S, Powell J, Proitsi P, Lupton MK, Brayne C, Rubinsztein DC, Gill M, Lawlor B, Lynch A, Brown KS, Passmore PA, Craig D, McGuinness B, Todd S, Holmes C, Mann D, Smith AD, Beaumont H, Warden D, Wilcock G, Love S, Kehoe PG, Hooper NM, Vardy ER, Hardy J, Mead S, Fox NC, Rossor M, Collinge J, Maier W, Jessen F, Ruther E, Schurmann B, Heun R, Kolsch H, van den Bussche H, Heuser I, Kornhuber J, Wiltfang J, Dichgans M, Frolich L, Hampel H, Gallacher J, Hull M, Rujescu D, Giegling I, Goate AM, Kauwe JS, Cruchaga C, Nowotny P, Morris JC, Mayo K, Sleegers K, Bettens K, Engelborghs S, De Deyn PP, Van Broeckhoven C, Livingston G, Bass NJ, Gurling H, McQuillin A, Gwilliam R, Deloukas P, Al-Chalabi A, Shaw CE, Tsolaki M, Singleton AB, Guerreiro R, Muhleisen TW, Nothen MM, Moebus S, Jockel KH, Klopp N, Wichmann HE, Pankratz VS, Sando SB, Aasly JO, Barcikowska M, Wszolek ZK, Dickson DW, Graff-Radford NR, Petersen RC, van Duijn CM, Breteler MM, Ikram MA, Destefano AL, Fitzpatrick AL, Lopez O, Launer LJ, Seshadri S, Berr C, Campion D, Epelbaum J, Dartigues JF, Tzourio C, Alperovitch A, Lathrop M, Feulner TM, Friedrich P, Riehle C, Krawczak M, Schreiber S, Mayhaus M, Nicolhaus S, Wagenpfeil S, Steinberg S, Stefansson H, Stefansson K, Snaedal J, Bjornsson S, Jonsson PV, Chouraki V, Genier-Boley B, Hiltunen M, Soininen H, Combarros O, Zelenika D, Delepine M, Bullido MJ, Pasquier F, Mateo I, Frank-Garcia A, Porcellini E, Hanon O, Coto E, Alvarez V, Bosco P, Siciliano G, Mancuso M, Panza F, Solfrizzi V, Nacmias B, Sorbi S, Bossu P, Piccardi P, Arosio B, Annoni G, Seripa D, Pilotto A, Scarpini E, Galimberti D, Brice A, Hannequin D, Licastro F, Jones L, Holmans PA, Jonsson T, Riemenschneider M, Morgan K, Younkin SG, Owen MJ, O'Donovan M, Amouyel P, Williams J. Common variants at abca7, ms4a6a/ms4a4e, epha1, cd33 and cd2ap are associated with alzheimer's disease. Nat Genet. 2011;43: 429-435

  • Goumidi L, Flamant F, Lendon C, Galimberti D, Pasquier F, Scarpini E, Hannequin D, Campion D, Amouyel P, Lambert JC, Meirhaeghe A. Study of thyroid hormone receptor alpha gene polymorphisms on alzheimer's disease. Neurobiol Aging. 2011;32: 624-630

  • Genin E, Hannequin D, Wallon D, Sleegers K, Hiltunen M, Combarros O, Bullido MJ, Engelborghs S, De Deyn P, Berr C, Pasquier F, Dubois B, Tognoni G, Fievet N, Brouwers N, Bettens K, Arosio B, Coto E, Del Zompo M, Mateo I, Epelbaum J, Frank-Garcia A, Helisalmi S, Porcellini E, Pilotto A, Forti P, Ferri R, Scarpini E, Siciliano G, Solfrizzi V, Sorbi S, Spalletta G, Valdivieso F, Vepsalainen S, Alvarez V, Bosco P, Mancuso M, Panza F, Nacmias B, Bossu P, Hanon O, Piccardi P, Annoni G, Seripa D, Galimberti D, Licastro F, Soininen H, Dartigues JF, Kamboh MI, Van Broeckhoven C, Lambert JC, Amouyel P, Campion D. Apoe and alzheimer disease: A major gene with semi-dominant inheritance. Mol Psychiatry. 2011 Sep;16(9): 903-7.

  • Picard C, Pasquier F, Martinaud O, Hannequin D, Godefroy O. Early onset dementia: Characteristics in a large cohort from academic memory clinics. Alzheimer Dis Assoc Disord. 2011  Jul-Sep;25(3): 203-5.

  • Modzelewski R, Lepretre S, Martinaud O, Hannequin D, Hitzel A, Habert M-O, Tilly H, Vera P. Brain perfusion in adult patients with acute myeloblastic leukemia receiving cytosine arabinoside. Mol Imaging Biol 2011; 13 (4): 747-53.

  • Miguel L, Avequin T, Delarue M, Feuillette S, Frébourg T, Campion D, Lecourtois M. Accumulation of insoluble forms of FUS protein correlates with toxicity in Drosophila. Neurobiol Aging. 2011 Nov 23.

  • Miguel L, Frébourg T, Campion D, Lecourtois M. Both cytoplasmic and nuclear accumulations of the protein are neurotoxic in Drosophila models of TDP-43 proteinopathies. Neurobiol Dis. 2011 Feb;41(2): 398-406.

2010

  • Broustal O, Camuzat A, Guillot-Noel L, Guy N, Millecamps S, Deffond D, Lacomblez L, Golfier V, Hannequin D, Salachas F, Camu W, Didic M, Dubois B, Meininger V, Le Ber I, Brice A. Fus mutations in frontotemporal lobar degeneration with amyotrophic lateral sclerosis. J Alzheimers Dis. 2010: 22: 765-769.

  • Lambert JC, Sleegers K, Gonzalez-Perez A, Ingelsson M, Beecham GW, Hiltunen M, Combarros O, Bullido MJ, Brouwers N, Bettens K, Berr C, Pasquier F, Richard F, Dekosky ST, Hannequin D, Haines JL, Tognoni G, Fievet N, Dartigues JF, Tzourio C, Engelborghs S, Arosio B, Coto E, De Deyn P, Del Zompo M, Mateo I, Boada M, Antunez C, Lopez-Arrieta J, Epelbaum J, Schjeide BM, Frank-Garcia A, Giedraitis V, Helisalmi S, Porcellini E, Pilotto A, Forti P, Ferri R, Delepine M, Zelenika D, Lathrop M, Scarpini E, Siciliano G, Solfrizzi V, Sorbi S, Spalletta G, Ravaglia G, Valdivieso F, Vepsalainen S, Alvarez V, Bosco P, Mancuso M, Panza F, Nacmias B, Bossu P, Hanon O, Piccardi P, Annoni G, Mann D, Marambaud P, Seripa D, Galimberti D, Tanzi RE, Bertram L, Lendon C, Lannfelt L, Licastro F, Campion D, Pericak-Vance MA, Soininen H, Van Broeckhoven C, Alperovitch A, Ruiz A, Kamboh MI, Amouyel P. The calhm1 p86l polymorphism is a genetic modifier of age at onset in alzheimer's disease: A meta-analysis study. J Alzheimers Dis. 2010;22, 1: 247-55.

  • Wallon D., Sommervogel C., Laquerrière A., Martinaud O., Lecourtois M., Hannequin D. La maladie des grains argyrophiles : composante synergique de la démence ? Rev Neurol (Paris). 2010;  4: 428-432.

  • Laumet G, Petitprez V, Sillaire A, Ayral AM, Hansmanel F, Chapuis J, Hannequin D, Pasquier F, Scarpini E, Galimberti D, Lendon C, Campion D, Amouyel P, Lambert JC. A study of the association between the adam12 and sh3pxd2a (sh3md1) genes and alzheimer's disease. Neurosci Lett. 2010;468: 1-2.

  • D. Wallon,1 L. Guyant-Maréchal,1,2 A. Laquerrière,3 R.A. Wevers,4 O. Martinaud,1 L. Kluijtmans,4 H.G. Yntema,5 P. Saugier-Veber,2 D. Hannequin,1,2 Clinical, imaging and neuropathological correlations in an unusual Cerebrotendinous Xanthomatosis case. Clinical Neuropathology

  • Rovelet-Lecrux A, Hannequin D, Guillin O, Legallic S, Jurici S, Wallon D, Frebourg T, Campion D. Frontotemporal dementia phenotype associated with mapt gene duplication. J Alzheimers Dis. 2010

  • Schoder D, Hannequin D, Martinaud O, Opolczynski G, Guyant-Marechal L, Le Ber I, Campion D. Morbid risk for schizophrenia in first-degree relatives of people with frontotemporal dementia. Br J Psychiatry. 2010;197:28-35

  • Millecamps S, Salachas F, Cazeneuve C, Gordon P, Bricka B, Camuzat A, Guillot-Noel L, Russaouen O, Bruneteau G, Pradat PF, Le Forestier N, Vandenberghe N, Danel-Brunaud V, Guy N, Thauvin-Robinet C, Lacomblez L, Couratier P, Hannequin D, Seilhean D, Le Ber I, Corcia P, Camu W, Brice A, Rouleau G, LeGuern E, Meininger V. Sod1, ang, vapb, tardbp, and fus mutations in familial amyotrophic lateral sclerosis: Genotype-phenotype correlations. J Med Genet. 2010;47:554-560

  • Hansmannel F, Sillaire A, Kamboh MI, Lendon C, Pasquier F, Hannequin D, Laumet G, Mounier A, Ayral AM, Dekosky ST, Hauw JJ, Berr C, Mann D, Amouyel P, Campion D, Lambert JC. Is the urea cycle involved in alzheimer's disease? J Alzheimers Dis. 2010;

  • Laumet G, Chouraki V, Grenier-Boley B, Legry V, Heath S, Zelenika D, Fievet N, Hannequin D, Delepine M, Pasquier F, Hanon O, Brice A, Epelbaum J, Berr C, Dartigues JF, Tzourio C, Campion D, Lathrop M, Bertram L, Amouyel P, Lambert JC. Systematic analysis of candidate genes for alzheimer's disease in a french, genome-wide association study. J Alzheimers Dis. 2010;20:1181-1188

  • Lambert JC, Grenier-Boley B, Chouraki V, Heath S, Zelenika D, Fievet N, Hannequin D, Pasquier F, Hanon O, Brice A, Epelbaum J, Berr C, Dartigues JF, Tzourio C, Campion D, Lathrop M, Amouyel P. Implication of the immune system in alzheimer's disease: Evidence from genome-wide pathway analysis. J Alzheimers Dis. 2010;20:1107-1118

  • Feuillette S, Deramecourt V, Laquerriere A, Duyckaerts C, Delisle MB, Maurage CA, Blum D, Buée L, Frébourg T, Campion D, Lecourtois M. Filamin-A and Myosin VI colocalize with fibrillary Tau protein in Alzheimer's disease and FTDP-17 brains. Brain Res. 2010 Jul 23;1345:182-9.

  • Feuillette S, Miguel L, Frébourg T, Campion D, Lecourtois M. Drosophila models of human tauopathies indicate that Tau protein toxicity in vivo is mediated by soluble cytosolic phosphorylated forms of the protein. J Neurochem. 2010 May;113(4):895-903.

  • Genome-wide analysis of genetic loci associated with Alzheimer disease. Seshadri S, Fitzpatrick AL, Ikram MA, DeStefano AL, Gudnason V, Boada M, Bis JC, Smith AV, Carassquillo MM, Lambert JC, Harold D, Schrijvers EM, Ramirez-Lorca R, Debette S, Longstreth WT Jr, Janssens AC, Pankratz VS, Dartigues JF, Hollingworth P, Aspelund T, Hernandez I, Beiser A, Kuller LH, Koudstaal PJ, Dickson DW, Tzourio C, Abraham R, Antunez C, Du Y, Rotter JI, Aulchenko YS, Harris TB, Petersen RC, Berr C, Owen MJ, Lopez-Arrieta J, Varadarajan BN, Becker JT, Rivadeneira F, Nalls MA, Graff-Radford NR, Campion D, Auerbach S, Rice K, Hofman A, Jonsson PV, Schmidt H, Lathrop M, Mosley TH, Au R, Psaty BM, Uitterlinden AG, Farrer LA, Lumley T, Ruiz A, Williams J, Amouyel P, Younkin SG, Wolf PA, Launer LJ, Lopez OL, van Duijn CM, Breteler MM; CHARGE Consortium; GERAD1 Consortium; EADI1 Consortium.JAMA. 2010 May 12;303(18):1832-40.

2009

  • Hansmannel F, Lendon C, Pasquier F, Dumont J, Hannequin D, Chapuis J, Laumet G, Ayral AM, Galimberti D, Scarpini E, Campion D, Amouyel P, Lambert JC. Is the ornithine transcarbamylase gene a genetic determinant of Alzheimer's disease ? Neurosci Lett. 2009; 449, 76-80

  • Finch N, Baker M, Crook R, Swanson K, Kuntz K, Surtees R, Bisceglio G, Rovelet-Lecrux A, Boeve B, Petersen RC, Dickson DW, Younkin SG, Deramecourt V, Crook J, Graff-Radford NR, Rademakers R. Plasma progranulin levels predict progranulin mutation status in frontotemporal dementia patients and asymptomatic family members. Brain. 2009 Mar; 132(Pt 3) : 583-91.

  • Guyant-Marechal L, Campion D, Hannequin D. Génétique de la maladie d'Alzheimer: Formes autosomiques dominantes. Rev Neurol (Paris). 2009 Mar; 165(3) : 223-31.

  • Lechowski L, Benoit M, Chassagne P, Vedel I, Tortrat D, Teillet L, Vellas B. Persistent apathy in Alzheimer's disease as an independent factor of rapid functional decline: the REAL longitudinal cohort study. Int J Geriatr Psychiatry. 2009 Apr;24(4):341-6.

  • Wallon D., Sommervogel C., Laquerrière A., Martinaud O., Lecourtois M., Hannequin D. La maladie des grains argyrophiles : composante synergique de la démence ? Rev Neurol (Paris). 2010; 4 : 428-432

  • Martinaud O, Gaillard MJ, Opolcinski G, Hannequin D. Category-specific effect in Alzheimer's disease. Dement Geriatr Cogn Disord. 2009; 28(5) : 413-8.

  • Cousin E, Mace S, Rocher C, Dib C, Muzard G, Hannequin D, Pradier L, Deleuze JF, Genin E, Brice A, Campion D. No replication of genetic association between candidate polymorphisms and alzheimer's disease. Neurobiol Aging. 2009

  • Laumet G, Petitprez V, Sillaire A, Ayral AM, Hansmanel F, Chapuis J, Hannequin D, Pasquier F, Scarpini E, Galimberti D, Lendon C, Campion D, Amouyel P, Lambert JC. A study of the association between the adam12 and sh3pxd2a (sh3md1) genes and alzheimer's disease. Neurosci Lett. 2009

  • Lambert JC, Heath S, Even G, Campion D, Sleegers K, Hiltunen M, Combarros O, Zelenika D, Bullido MJ, Tavernier B, Letenneur L, Bettens K, Berr C, Pasquier F, Fievet N, Barberger-Gateau P, Engelborghs S, De Deyn P, Mateo I, Franck A, Helisalmi S, Porcellini E, Hanon O, de Pancorbo MM, Lendon C, Dufouil C, Jaillard C, Leveillard T, Alvarez V, Bosco P, Mancuso M, Panza F, Nacmias B, Bossu P, Piccardi P, Annoni G, Seripa D, Galimberti D, Hannequin D, Licastro F, Soininen H, Ritchie K, Blanche H, Dartigues JF, Tzourio C, Gut I, Van Broeckhoven C, Alperovitch A, Lathrop M, Amouyel P. Genome-wide association study identifies variants at clu and cr1 associated with alzheimer's disease. Nat Genet. 2009

  • Hannequin D., Guyant-Maréchal L., Le Ber I., Wallon D., Campion D., Sedel F. Démences du sujet jeune : démarche diagnostique. Rev Neurol (Paris). 2009; 165 Spec No 2; 87-96

  • Goumidi L, Flamant F, Lendon C, Galimberti D, Pasquier F, Scarpini E, Hannequin D, Campion D, Amouyel P, Lambert JC, Meirhaeghe A. Study of thyroid hormone receptor alpha gene polymorphisms on Alzheimer's disease. Neurobiol Aging. 2010 (sous presse)

  • Le Ber I, Camuzat A, Berger E, Hannequin D, Laquerriere A, Golfier V, Seilhean D, Viennet G, Couratier P, Verpillat P, Heath S, Camu W, Martinaud O, Lacomblez L, Vercelletto M, Salachas F, Sellal F, Didic M, Thomas-Anterion C, Puel M, Michel BF, Besse C, Duyckaerts C, Meininger V, Campion D, Dubois B, Brice A. Chromosome 9p-linked families with frontotemporal dementia associated with motor neuron disease. Neurology. 2009;72:1669-1676

  • Benajiba L, Le Ber I, Camuzat A, Lacoste M, Thomas-Anterion C, Couratier P, Legallic S, Salachas F, Hannequin D, Decousus M, Lacomblez L, Guedj E, Golfier V, Camu W, Dubois B, Campion D, Meininger V, Brice A. TARDBP mutations in motoneuron disease with frontotemporal lobar degeneration. Ann Neurol. 2009;65:470-473

  • Rovelet-Lecrux A, Lecourtois M, Thomas-Anterion C, Le Ber I, Brice A, Frebourg T, Hannequin D, Campion D. Partial deletion of the MAPT gene: A novel mechanism of FTDP-17. Hum Mutat. 2009,30;4:591-602

  • Thery-Langlois C, Amosse C, Lefaucheur R, Bioux S, Gerardin E, Hannequin D, Martinaud O. Une lectrice aphasique. Rev Neurol (Paris). 2009;165(6-7):601-4.

  • Guyant-Marechal L, Campion D, Hannequin D. Génétique de la maladie d'Alzheimer: Formes autosomiques dominantes. Rev Neurol (Paris). 2009; 165(3):223-31

2008

  • Guyant-Maréchal I, Berger E, Laquerriere A, Rovelet-Lecrux A, Viennet G, Frebourg T, Rumbach L, Campion D, Hannequin D. Intrafamilial diversity of phenotype associated with app duplication. Neurology. 2008;71:1925-1926

  • Andrieu S, Ousset PJ, Coley N, Ouzid M, Mathiex-Fortunet H, Vellas B et coll. Guidage study: A 5-year double blind, randomised trial of egb 761 for the prevention of alzheimer's disease in elderly subjects with memory complaints. I. Rationale, design and baseline data. Curr Alzheimer Res. 2008;5:406-415

  • Guedj E, Allali G, Goetz C, Le Ber I, Volteau M, Lacomblez L, Vera P, Hitzel A, Hannequin D, Decousus M, Thomas-Anterion C, Magne C, Vercelletto M, Bernard AM, Didic M, Lotterie JA, Puel M, Brice A, Habert MO, Dubois B. Frontal assessment battery is a marker of dorsolateral and medial frontal functions: A spect study in frontotemporal dementia. J Neurol Sci. 2008;273:84-87

  • Aziz NA, van der Burg JM, Landwehrmeyer GB, Brundin P, Stijnen T, EHDI Group, Roos RA  Weight loss in Huntington disease increases with higher CAG repeat number. Neurology. 2008 Nov 4;71(19):1506-13.

  • Lechowski L, Benoit M, Chassagne P, Vedel I, Tortrat D, Teillet L, Vellas B. Persistent apathy in Alzheimer's disease as an independent factor of rapid functional decline: the REAL longitudinal cohort study. Int J Geriatr Psychiatry. 2008 Sep 23.

  • Chassagne P, Idrissi-Kassimy F, Rigal O. [Comorbidity and dementia] Psychol Neuropsychiatr Vieil. 2008 Mar;6(1):43-8. Review. French.

  • Lechowski L, de Stampa M, Denis B, Tortrat D, Chassagne P, Robert P, Teillet L, Vellas B. Patterns of loss of abilities in instrumental activities of daily living in Alzheimer's disease: the REAL cohort study. Dement Geriatr Cogn Disord. 2008;25(1):46-53. Epub 2007 Nov 20.

  • Modzelewski R, de la Rue T, Janvresse E, Hitzel A, Menard JF, Manrique A, Gardin I, Gerardin E, Hannequin D, Vera P. Development and validation of the random walk algorithm: Application to the classification of diffuse heterogeneity in brain SPECT perfusion images. J Comput Assist Tomogr. 2008;32:651-659

  • Chapuis J, Moisan F, Mellick G, Elbaz A, Pasquier F, Hannequin D, Lendon C, Campion D,Amouyel P, Lambert JC. Association study of the NEDD9 gene with the risk of developing Alzheimer's and Parkinson's disease. Hum Mol Genet. 2008; 177:2863-2867

  • Dreses-Werringloer U, Lambert JC, Vingtdeux V, Zhao H, Vais H, Siebert A, Jain A, Koppel J, Rovelet-Lecrux A, Hannequin D, Pasquier F, Galimberti D, Scarpini E, Mann D, Lendon C, Campion D, Amouyel P, Davies P, Foskett JK, Campagne F, Marambaud P. A polymorphism in CALHM1 influences ca2+ homeostasis, abeta levels, and Alzheimer's disease risk. Cell. 2008;133:1149-1161

  • Rovelet-Lecrux A, Deramecourt V, Legallic S, Maurage CA, Le Ber I, Brice A, Lambert JC, Frebourg T, Hannequin D, Pasquier F, Campion D. Deletion of the progranulin gene in patients with frontotemporal lobar degeneration or parkinson disease. Neurobiol Dis. 2008;31(1):41-45

  • Chapuis J, Hannequin D, Pasquier F, Bentham P, Brice A, Leber I, Frebourg T, Deleuze JF, Cousin E, Thaker U, Amouyel P, Mann D, Lendon C, Campion D, Lambert JC. Association study of the gab2 gene with the risk of developing alzheimer's disease. Neurobiol Dis. 2008;30:103-6   

  • Le Ber I, Camuzat A, Hannequin D, Pasquier F, Guedj E, Rovelet-Lecrux A, Hahn-Barma V, van der Zee J, Clot F, Bakchine S, Puel M, Ghanim M, Lacomblez L, Mikol J, Deramecourt V, Lejeune P, de la Sayette V, Belliard S, Vercelletto M, Meyrignac C, Broeckhoven CV, Lambert JC, Verpillat P, Campion D, Habert MO, Dubois B, Brice A. Phenotype variability in progranulin mutation carriers: A clinical, neuropsychological, imaging and genetic study. Brain. 2008; 131:732-46

2007

  • Rovelet-Lecrux A, Frebourg T, Tuominen H, Majamaa K, Campion D, Remes AM. APP locus duplication in a Finnish family with dementia and intracerebral haemorrhage. J Neurol Neurosurg Psychiatry. 2007 Oct;78(10):1158-9.

  • Anheim M, Hannequin D, Boulay C, Martin C, Campion D, Tranchant C.  Ataxic variant of Alzheimer's disease caused by Pro117Ala PSEN1 mutation. JNNP.2007;78, 1414-1415

  • Guedj E, Le Ber I, Lacomblez L, Dubois B, Verpillat P, Mira D, Salachas F, Véra P, Hannequin D, Lotterie J-A. L, Puel M, Decousus M, Thomas-Antérion C, Magne C, Vercelletto M, Bernard A-M., Golfier V, Pasquier J, Michel B, Namer I, Sellal F, Bochet J, Volteau M, Brice A, Meininger V, Habert MO. Brain SPECT perfusion of frontotemporal dementia associated with motor neuron disease. Neurology.2007;69:488-490

  • Van der Zee J, Le Ber I, Maurer-Stroh S, Engelborghs S, Gijselinck I, Camuzat A, Brouwers N, Vandenberghe R, Hannequin D, Sleegers K, Dermaut B, Santens P, Martin J-J, Campion D, De Pooter T, Peeters K, Mattheijssens M, Lacomblez L, Van den Broeck M, Vercelletto M, De Dyn P, Schymkowitz J, Rousseau F, Brice A, Cruts M, Van Broeckhoven C. Mutations other than null mutations producing a pathological loss of progranulin in frontotemporal dementia. Hum Mutat. 2007;28(4): 416- 429

  • Le Ber I, Van der Zee J, Hannequin D, Gijselinck I, Campion D, Puel M, A. L, De Pooter T, Camuzat A, Van den Broeck M, Dubois B, Sellal F, Lacomblez L, Vercelletto M, Thomas Anterion C, Michel BF, Golfier V, Didic M, Salachas F, Duyckaerts C, Cruts M, Verpillat P, Van Broeckhoven C, Brice A. Progranulin null mutations in both sporadic and familial frontotemporal dementia. Hum Mutat. 2007;28(9):846-855

  • Belmin J, Pariel-Madjlessi S, Surun P, Bentot C, Feteanu D, Lefebvre des Noettes V, Onen F, Drunat O, Trivalle C, Chassagne P, Golmard JL. The cognitive disorders examination (Codex) is a reliable 3-minute test for detection of dementia in the elderly (validation study on 323 subjects). Presse Med. 2007 Apr 11

  • Guyant-Maréchal L, Rovelet-Lecrux A, Goumidi L, Cousin E, Hannequin D, Raux G, Penet C, Ricard S, Mace S, Amouyel P, Deleuze JF, Frebourg T, Brice A, Lambert J, Campion D. Variations in the APP gene promoter region and risk to Alzheimer's disease. Neurology. 2007 68(9):684-7.

  • Blard O, Feuillette S, Bou J, Chaumette B, Frebourg T, Campion D, Lecourtois M. Cytoskeleton proteins are modulators of mutant tau-induced neurodegeneration in drosophila. Hum Mol Genet. 2007 Feb 19

2006

  • Kadri N, Chassagne P, Benichou J, Hellot MF, Delangre T, Derambure V, Druesne L,Bentot C, Bercoff E. The value of clinical characteristics from a standard questionnaire to discriminate cardiac from neurological syncope in the elderly. J Nutr Health Aging. 2006 Nov-Dec;10(6):546-53.

  • Chassagne P, Druesne L, Capet C, Menard JF, Bercoff E. Clinical presentation of hypernatremia in elderly patients: a case control study. J Am Geriatr Soc. 2006 Aug;54(8):1225-30.

  • Blard O, Frebourg T, Campion D, Lecourtois M. Inhibition of proteasome and Shaggy/Glycogen synthase kinase-3beta kinase prevents clearance of phosphorylated tau in Drosophila. J Neurosci Res. 2006 Oct;84(5):1107-15.

  • Doucet J, Kalimoutou S, Chedru C, Remy E, Cabrejo L, Meliot C, Chassagne P. Les prescriptions des anticholinestérasiques sont-elles adaptées aux maladies et traitements  associés dans la maladie d'Alzheimer ? Therapie. 2006 Jan-Feb;61(1):23-7.

  • Le Ber I, Guedj E, Gabelle A, Verpillat P, Volteau M, Thomas Anterion C, Decousus M, Hannequin D, Vera P, Lacomblez L, Camuzat A, Didic M, Puel M, Lotterie J, Golfier V, Bernard A, Vercelletto M, Magne C, Sellal F, Namer I, Michel BF, Pasquier J, Salachas F, Bochet J, Brice A, Habert M, Dubois B. Demographic, neurological, behavioural characteristics and brain perfusion spect in frontal variant of frontotemporal dementia. Brain. 2006; 129;11:3051-3065

  • Dumanchin C, Tournier I, Martin C, Didic M, Belliard S, Carlander B, Rouhart F, Duyckaerts C, Pellissier JF, Latouche JB, Hannequin D., Frebourg T, Tosi M, Campion D. Biological effects of four PSEN1 gene mutations causing Alzheimer disease with spastic paraparesis and cotton wool plaques. Hum Mutat. 2006;27:1063-1073

  • Campion D, Hannequin D. La duplication du gène APP, cause de maladie d'Alzheimer associée à une importante angiopathie amyloïde. Med Sci (Paris). 2006;22:468-469

  • Cabrejo L, Guyant-Marechal L, Laquerriere A, Vercelletto M, De La Fourniere F, Thomas-Anterion C, Verny C, Letournel F, Pasquier F, Vital A, Checler F, Frebourg T, Campion D, Hannequin D. Phenotype associated with APP duplication in five families. Brain. 2006;129;11:2966-2976

  • Cabrejo L, Chassagne P, Doucet J, Laquerriere A, Puech N, Hannequin D. Angiopathie amyloïde cérébrale sporadique: Revue. Revue Neurologique. 2006;162:11:1059-1067

  • Pitrou, Mélanie Drouet, Joël Ladner, Yves Moynot, Pierre Czernichow (2006). Maladie d'Alzheimer,profil et besoins des aidants professionnels. Soins Gérontologie, 59, Mai Juin.

  • Guyant-Marechal L, Laquerriere A, Duyckaerts C, Dumanchin C, Bou J, Dugny F, Le Ber I, Frebourg T, Hannequin D, Campion D. Valosin-containing protein gene mutations: clinical and neuropathologic features. Neurology. 2006 Aug 22;67(4):644-51.

  • Blard O, Frebourg T, Campion D, Lecourtois M. Inhibition of proteasome and Shaggy/Glycogen synthase kinase-3beta kinase prevents clearance of phosphorylated tau in Drosophila. J Neurosci Res. 2006 Jul 28;

  • Rovelet-Lecrux A, Hannequin D, Raux G, Le Meur N, Laquerriere A, Vital A, Dumanchin C, Feuillette S, Brice A, Vercelletto M, Dubas F, Frebourg T, Campion D. App locus duplication causes autosomal dominant early-onset alzheimer disease with cerebral amyloid angiopathy. Nat Genet. 2006;38:24-26

  • Maltete D, Guyant-Marechal L, Mihout B, Hannequin D. Movement disorders and Creutzfeldt-Jakob disease: A review. Parkinsonism Relat Disord. 2006 Mar;12(2):65-71.

  • Maltete D, Guyant-Maréchal L, Gérardin E, Laquerriere A, Martinaud O, Mihout B, Hannequin D. Hemidystonia as initial manifestation of sporadic Creutzfeldt-jakob disease. European Journal of Neurology. 2006 Jun;13(6):667-8

2005

  • Chassagne P, Druesne L, Bentot C, Kadri N.
    La confusion mentale du patient âgé. Presse Med. 2005 Jul 2;34(12):863-8.

  • Martinaud O, Laquerriere A, Guyant-Marechal L, Ahtoy P, Vera P, Sergeant N, Camuzat A, Bourgeois P, Hauw JJ, Campion D, Hannequin D. Frontotemporal dementia, motor neuron disease and tauopathy: Clinical and neuropathological study in a family. Acta Neuropathol (Berl). 2005;110:84-92

  • Raux G, Guyant-Marechal L, Martin C, Bou J, Penet C, Brice A, Hannequin D, Frebourg T, Campion D. Molecular diagnosis of autosomal dominant early onset alzheimer's disease: An update. J Med Genet. 2005;42:793-795

  • Piolino P, Hannequin D, Desgranges B, Girard C, Beaunieux H, Giffard B, Lebreton K, Eustache F. Right ventral frontal hypometabolism and abnormal sense of self in a case of disproportionate retrograde amnesia. Cognitive Neuropsychology. 2005;22:1005-1034

  • Guyant-Marechal L, Verrips A, Girard C, Wevers RA, Zijlstra F, Sistermans E, Vera P, Campion D, Hannequin D. Unusual cerebrotendinous xanthomatosis with fronto-temporal dementia phenotype. Am J Med Genet A. 2005;139A:114-117

  • Chetelat G, Eustache F, Viader F, De La Sayette V, Pelerin A, Mezenge F, Hannequin D, Dupuy B, Baron JC, Desgranges B. Fdg-pet measurement is more accurate than neuropsychological assessments to predict global cognitive deterioration in patients with mild cognitive impairment. Neurocase. 2005;11:14-25

  • Feuillette S, Blard O, Lecourtois M, Frebourg T, Campion D, Dumanchin C. Tau is not normally degraded by the proteasome. J Neurosci Res. 2005 May 1;80(3):400-5.

  • Mace S, Cousin E, Ricard S, Genin E, Spanakis E, Lafargue-Soubigou C, Genin B, Fournel R, Roche S, Haussy G, Massey F, Soubigou S, Brefort G, Benoit P, Brice A, Campion D, Hollis M, Pradier L, Benavides J, Deleuze JF. ABCA2 is a strong genetic risk factor for early-onset Alzheimer's disease.
    Neurobiol Dis. 2005 Feb;18(1):119-25.

2004

  • Le Ber I, Martinez M, Campion D, Laquerriere A, Betard C, Bassez G, Girard C, Saugier-Veber P, Raux G, Sergeant N, Magnier P, Maisonobe T, Eymard B, Duyckaerts C, Delacourte A, Frebourg T, Hannequin D. A non-dm1, non-dm2 multisystem myotonic disorder with frontotemporal dementia: Phenotype and suggestive mapping of the dm3 locus to chromosome 15q21-24. Brain. 2004;127:1979-1992

2003

  • Soriani-Lefevre MH, Hannequin D, Bakchine S, Menard JF, Manrique A, Hitzel A, Kotzki PO, Boudousq V, Vera P. Evidence of bilateral temporal lobe involvement in primary progressive aphasia: A spect study. J Nucl Med. 2003;44:1013-1022

  • Marechal L, Campion D, Hannequin D. Formes familiales de la maladie d'alzheimer. Presse Med. 2003;32:756-763

  • Portet F, Dauvilliers Y, Campion D, Raux G, Hauw JJ, Lyon-Caen O, Camu W, Touchon J. Very early onset AD with a de novo mutation in the presenilin 1 gene (Met 233 Leu). Neurology. 2003 Oct 28;61(8):1136-7

  • Cousin E, Hannequin D, Ricard S, Mace S, Genin E, Chansac C, Brice A, Dubois B, Frebourg T, Mercken L, Benavides J, Pradier L, Campion D, Deleuze JF. A risk for early-onset alzheimer's disease associated with the apbb1 gene (fe65) intron 13 polymorphism. Neurosci Lett. 2003;342:5-8

  • Cousin E, Hannequin D, Mace S, Dubois B, Ricard S, Genin E, Brun C, Chansac C, Pradier L, Frebourg T, Brice A, Campion D, Deleuze JF. No replication of the association between the nicastrin gene and familial early-onset alzheimer's disease. Neurosci Lett. 2003;353:153-155

  • Chetelat G, Desgranges B, de la Sayette V, Viader F, Berkouk K, Landeau B, Lalevee C, Le Doze F, Dupuy B, Hannequin D, Baron JC, Eustache F. Dissociating atrophy and hypometabolism impact on episodic memory in mild cognitive impairment. Brain. 2003;126:1955-1967

  • Myriam Coue-touflet, Pascale Denis, Fabienne Marc, Brigitte Sergent-Salle. Préface : Yves Moynot. (2003). Lhôpital de jour,un lieu pour comprendre et soigner la maladie démentielle.

2002

  • Verpillat P, Ricard S, Hannequin D, Dubois B, Bou J, Camuzat A, Pradier L, Frebourg T, Brice A, Clerget-Darpoux F, Deleuze JF, Campion D. Is the saitohin gene involved in neurodegenerative diseases ? Ann Neurol. 2002;52:829-832

  • Verpillat P, Camuzat A, Hannequin D, Thomas-Anterion C, Puel M, Belliard S, Dubois B, Didic M, Michel BF, Lacomblez L, Moreaud O, Sellal F, Golfier V, Campion D, Clerget-Darpoux F, Brice A. Association between the extended tau haplotype and frontotemporal dementia. Arch Neurol. 2002;59:935-939

  • Verpillat P, Camuzat A, Hannequin D, Thomas-Anterion C, Puel M, Belliard S, Dubois B, Didic M, Lacomblez L, Moreaud O, Golfier V, Campion D, Brice A, Clerget-Darpoux F. Apolipoprotein e gene in frontotemporal dementia: An association study and meta-analysis. Eur J Hum Genet. 2002;10:399-405

  • Boussaha M, Hannequin D, Verpillat P, Brice A, Frebourg T, Campion D. Polymorphisms of insulin degrading enzyme gene are not associated with alzheimer's disease. Neurosci Lett. 2002;329:121-123

2001

  • Verpillat P, Bouley S, Campion D, Hannequin D, Dubois B, Belliard S, Puel M, Thomas-Anterion C, Agid Y, Brice A, Clerget-Darpoux F. Use of haplotype information to test involvement of the lrp gene in alzheimer's disease in the french population. Eur J Hum Genet. 2001;9:464-468

  • Martinaud O, Hannequin D. Deux échelles de confusion. Rev Neurol (Paris). 2001;157:708-712

  • Hannequin D, Campion D. Les formes autosomiques dominantes de la maladie d'Alzheimer: Du genotype au phénotype. Rev Neurol (Paris). 2001;157:384-392

2000

  • Verpillat P, Bouley S, Hannequin D, Belliard S, Puel M, Thomas-Anterion C, Dubois B, Agid Y, Campion D, Clerget-Darpoux F, Brice A. Alpha2-macroglobulin gene and alzheimer's disease: Confirmation of association by haplotypes analyses. Ann Neurol. 2000;48:400-402

  • Raux G, Gantier R, Thomas-Anterion C, Boulliat J, Verpillat P, Hannequin D, Brice A, Frebourg T, Campion D. Dementia with prominent frontotemporal features associated with l113p presenilin 1 mutation. Neurology. 2000;55:1577-1578

  • Peoc'h K, Manivet P, Beaudry P, Attane F, Besson G, Hannequin D, Delasnerie-Laupretre N, Laplanche JL. Identification of three novel mutations (e196k, v203i, e211q) in the prion protein gene (prnp) in inherited prion diseases with creutzfeldt-jakob disease phenotype. Hum Mutat. 2000;15:482

  • Ozsancak C, Auzou P, Hannequin D. Dysarthria and orofacial apraxia in corticobasal degeneration. Mov Disord. 2000;15:905-910

  • Martinaud O, Hannequin D. Etats confusionnels et agitation. Rev Prat. 2000;50:1994-1998

  • Eustache F, Piolino P, Desgranges B, Guillery B, Gaillard MJ, Hannequin D. L'évaluation de la mémoire du passé lointain et des connaissances sémantiques. Rev Neurol (Paris). 2000;156:739-757

  • Camuzat A, Verpillat P, Dubois B, Penet C, Agid Y, Brice A, Moreaud O, Puel M, Clerget-Darpoux F, Kinter J, Kozlov S, Berger P, Sonderegger P, Raux G, Campion D, Hannequin D, Frebourg T. Mutations in the neurosperpin gene are rare  in familial alzheimer dementia. Annals of Neurology. 2000;47:688