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Items: 48

1.

Acute hemichorea revealing atrial flutter.

Hebant B, Guyant-Marechal L, Maltête D, Lefaucheur R.

J Postgrad Med. 2018 Dec 27. doi: 10.4103/jpgm.JPGM_448_18. [Epub ahead of print]

2.

Hereditary neuropathy with liability to pressure palsies mimicking chronic inflammatory demyelinating polyneuropathy.

Özel G, Maisonobe T, Guyant-Maréchal L, Maltête D, Lefaucheur R.

Rev Neurol (Paris). 2018 Sep - Oct;174(7-8):575-577. doi: 10.1016/j.neurol.2017.11.012. Epub 2018 Jul 13. No abstract available.

PMID:
30017102
3.

Novel VCP mutations expand the mutational spectrum of frontotemporal dementia.

Saracino D, Clot F, Camuzat A, Anquetil V, Hannequin D, Guyant-Maréchal L, Didic M, Guillot-Noël L, Rinaldi D, Latouche M, Forlani S, Ghassab Y, Coppola C, Di Iorio G, David I; French research network on FTD/FTD-ALS, Le Guern E, Brice A, Le Ber I.

Neurobiol Aging. 2018 Dec;72:187.e11-187.e14. doi: 10.1016/j.neurobiolaging.2018.06.037. Epub 2018 Jun 30.

PMID:
30005904
4.

Morphological features in juvenile Huntington disease associated with cerebellar atrophy - magnetic resonance imaging morphometric analysis.

Hedjoudje A, Nicolas G, Goldenberg A, Vanhulle C, Dumant-Forrest C, Deverrière G, Treguier P, Michelet I, Guyant-Maréchal L, Devys D, Gerardin E, Dacher JN, Vivier PH.

Pediatr Radiol. 2018 Sep;48(10):1463-1471. doi: 10.1007/s00247-018-4167-z. Epub 2018 Jun 20.

PMID:
29926145
5.

Cardiac Abnormalities in Type 1 Facioscapulohumeral Muscular Dystrophy.

Labombarda F, Maurice M, Simon JP, Legallois D, Guyant-Maréchal L, Bedat-Millet AL, Merle P, Saloux E, Chapon F, Milliez P.

J Clin Neuromuscul Dis. 2017 Jun;18(4):199-206. doi: 10.1097/CND.0000000000000144.

PMID:
28538250
6.

17q21.31 duplication causes prominent tau-related dementia with increased MAPT expression.

Le Guennec K, Quenez O, Nicolas G, Wallon D, Rousseau S, Richard AC, Alexander J, Paschou P, Charbonnier C, Bellenguez C, Grenier-Boley B, Lechner D, Bihoreau MT, Olaso R, Boland A, Meyer V, Deleuze JF, Amouyel P, Munter HM, Bourque G, Lathrop M, Frebourg T, Redon R, Letenneur L, Dartigues JF, Martinaud O, Kalev O, Mehrabian S, Traykov L, Ströbel T, Le Ber I, Caroppo P, Epelbaum S, Jonveaux T, Pasquier F, Rollin-Sillaire A, Génin E, Guyant-Maréchal L, Kovacs GG, Lambert JC, Hannequin D, Campion D, Rovelet-Lecrux A.

Mol Psychiatry. 2017 Aug;22(8):1119-1125. doi: 10.1038/mp.2016.226. Epub 2016 Dec 13.

PMID:
27956742
7.

Tubular aggregate myopathy with features of Stormorken disease due to a new STIM1 mutation.

Noury JB, Böhm J, Peche GA, Guyant-Marechal L, Bedat-Millet AL, Chiche L, Carlier RY, Malfatti E, Romero NB, Stojkovic T.

Neuromuscul Disord. 2017 Jan;27(1):78-82. doi: 10.1016/j.nmd.2016.10.006. Epub 2016 Oct 14.

PMID:
27876257
8.

The wide POLG-related spectrum: An integrated view.

Béreau M, Anheim M, Echaniz-Laguna A, Magot A, Verny C, Goideau-Sevrain M, Barth M, Amati-Bonneau P, Allouche S, Ayrignac X, Bédat-Millet AL, Guyant-Maréchal L, Kuntzer T, Ochsner F, Petiot P, Vial C, Omer S, Sole G, Taieb G, Carvalho N, Tio G, Kremer S, Acquaviva-Bourdain C, de Camaret BM, Tranchant C.

J Neurol Sci. 2016 Sep 15;368:70-6. doi: 10.1016/j.jns.2016.06.062. Epub 2016 Jun 29. No abstract available.

PMID:
27538604
9.

Clinical and electroencephalographic abnormalities during the full duration of a sporadic hemiplegic migraine attack.

Chastan N, Lebas A, Legoff F, Parain D, Guyant-Marechal L.

Neurophysiol Clin. 2016 Nov;46(4-5):307-311. doi: 10.1016/j.neucli.2016.03.004. Epub 2016 May 5.

PMID:
27155821
10.

Familial intracranial aneurysm, the relationship of the aortic diameter.

Verdure P, Gilard V, Guyant-Maréchal L, Belien J, Cebula H, Hannequin D, Dacher JN, Johannides R, Proust F.

Neurochirurgie. 2015 Dec;61(6):385-91. doi: 10.1016/j.neuchi.2015.08.001. Epub 2015 Nov 17.

PMID:
26597604
11.

Delayed-onset Friedreich's ataxia revisited.

Lecocq C, Charles P, Azulay JP, Meissner W, Rai M, N'Guyen K, Péréon Y, Fabre N, Robin E, Courtois S, Guyant-Maréchal L, Zagnoli F, Rudolf G, Renaud M, Sévin-Allouet M, Lesne F, Alaerts N, Goizet C, Calvas P, Eusebio A, Guissart C, Derkinderen P, Tison F, Brice A, Koenig M, Pandolfo M, Tranchant C, Dürr A, Anheim M.

Mov Disord. 2016 Jan;31(1):62-9. doi: 10.1002/mds.26382. Epub 2015 Sep 21.

PMID:
26388117
12.

New practical definitions for the diagnosis of autosomal recessive spastic ataxia of Charlevoix-Saguenay.

Pilliod J, Moutton S, Lavie J, Maurat E, Hubert C, Bellance N, Anheim M, Forlani S, Mochel F, N'Guyen K, Thauvin-Robinet C, Verny C, Milea D, Lesca G, Koenig M, Rodriguez D, Houcinat N, Van-Gils J, Durand CM, Guichet A, Barth M, Bonneau D, Convers P, Maillart E, Guyant-Marechal L, Hannequin D, Fromager G, Afenjar A, Chantot-Bastaraud S, Valence S, Charles P, Berquin P, Rooryck C, Bouron J, Brice A, Lacombe D, Rossignol R, Stevanin G, Benard G, Burglen L, Durr A, Goizet C, Coupry I.

Ann Neurol. 2015 Dec;78(6):871-86. doi: 10.1002/ana.24509. Epub 2015 Nov 14.

PMID:
26288984
13.

Screening of dementia genes by whole-exome sequencing in early-onset Alzheimer disease: input and lessons.

Nicolas G, Wallon D, Charbonnier C, Quenez O, Rousseau S, Richard AC, Rovelet-Lecrux A, Coutant S, Le Guennec K, Bacq D, Garnier JG, Olaso R, Boland A, Meyer V, Deleuze JF, Munter HM, Bourque G, Auld D, Montpetit A, Lathrop M, Guyant-Maréchal L, Martinaud O, Pariente J, Rollin-Sillaire A, Pasquier F, Le Ber I, Sarazin M, Croisile B, Boutoleau-Bretonnière C, Thomas-Antérion C, Paquet C, Sauvée M, Moreaud O, Gabelle A, Sellal F, Ceccaldi M, Chamard L, Blanc F, Frebourg T, Campion D, Hannequin D.

Eur J Hum Genet. 2016 May;24(5):710-6. doi: 10.1038/ejhg.2015.173. Epub 2015 Aug 5.

14.

Heterozygous HTRA1 mutations are associated with autosomal dominant cerebral small vessel disease.

Verdura E, Hervé D, Scharrer E, Amador Mdel M, Guyant-Maréchal L, Philippi A, Corlobé A, Bergametti F, Gazal S, Prieto-Morin C, Beaufort N, Le Bail B, Viakhireva I, Dichgans M, Chabriat H, Haffner C, Tournier-Lasserve E.

Brain. 2015 Aug;138(Pt 8):2347-58. doi: 10.1093/brain/awv155. Epub 2015 Jun 10.

PMID:
26063658
15.

Adult-onset genetic leukoencephalopathies: a MRI pattern-based approach in a comprehensive study of 154 patients.

Ayrignac X, Carra-Dalliere C, Menjot de Champfleur N, Denier C, Aubourg P, Bellesme C, Castelnovo G, Pelletier J, Audoin B, Kaphan E, de Seze J, Collongues N, Blanc F, Chanson JB, Magnin E, Berger E, Vukusic S, Durand-Dubief F, Camdessanche JP, Cohen M, Lebrun-Frenay C, Brassat D, Clanet M, Vermersch P, Zephir H, Outteryck O, Wiertlewski S, Laplaud DA, Ouallet JC, Brochet B, Goizet C, Debouverie M, Pittion S, Edan G, Deburghgraeve V, Le Page E, Verny C, Amati-Bonneau P, Bonneau D, Hannequin D, Guyant-Maréchal L, Derache N, Defer GL, Moreau T, Giroud M, Guennoc AM, Clavelou P, Taithe F, Mathis S, Neau JP, Magy L, Devoize JL, Bataillard M, Masliah-Planchon J, Dorboz I, Tournier-Lasserve E, Levade T, Boespflug Tanguy O, Labauge P.

Brain. 2015 Feb;138(Pt 2):284-92. doi: 10.1093/brain/awu353. Epub 2014 Dec 19.

PMID:
25527826
16.

Phenotypic spectrum of probable and genetically-confirmed idiopathic basal ganglia calcification.

Nicolas G, Pottier C, Charbonnier C, Guyant-Maréchal L, Le Ber I, Pariente J, Labauge P, Ayrignac X, Defebvre L, Maltête D, Martinaud O, Lefaucheur R, Guillin O, Wallon D, Chaumette B, Rondepierre P, Derache N, Fromager G, Schaeffer S, Krystkowiak P, Verny C, Jurici S, Sauvée M, Vérin M, Lebouvier T, Rouaud O, Thauvin-Robinet C, Rousseau S, Rovelet-Lecrux A, Frebourg T, Campion D, Hannequin D; French IBGC Study Group.

Brain. 2013 Nov;136(Pt 11):3395-407. doi: 10.1093/brain/awt255. Epub 2013 Sep 24.

PMID:
24065723
17.

Mutation of the PDGFRB gene as a cause of idiopathic basal ganglia calcification.

Nicolas G, Pottier C, Maltête D, Coutant S, Rovelet-Lecrux A, Legallic S, Rousseau S, Vaschalde Y, Guyant-Maréchal L, Augustin J, Martinaud O, Defebvre L, Krystkowiak P, Pariente J, Clanet M, Labauge P, Ayrignac X, Lefaucheur R, Le Ber I, Frébourg T, Hannequin D, Campion D.

Neurology. 2013 Jan 8;80(2):181-7. doi: 10.1212/WNL.0b013e31827ccf34. Epub 2012 Dec 19.

PMID:
23255827
18.

PRRT2 mutations cause hemiplegic migraine.

Riant F, Roze E, Barbance C, Méneret A, Guyant-Maréchal L, Lucas C, Sabouraud P, Trébuchon A, Depienne C, Tournier-Lasserve E.

Neurology. 2012 Nov 20;79(21):2122-4. doi: 10.1212/WNL.0b013e3182752cb8. Epub 2012 Oct 17.

PMID:
23077016
19.

FXTAS: new insights and the need for revised diagnostic criteria.

Apartis E, Blancher A, Meissner WG, Guyant-Maréchal L, Maltête D, De Broucker T, Legrand AP, Bouzenada H, Thanh HT, Sallansonnet-Froment M, Wang A, Tison F, Roué-Jagot C, Sedel F, Charles P, Whalen S, Héron D, Thobois S, Poisson A, Lesca G, Ouvrard-Hernandez AM, Fraix V, Palfi S, Habert MO, Gaymard B, Dussaule JC, Pollak P, Vidailhet M, Durr A, Barbot JC, Gourlet V, Brice A, Anheim M.

Neurology. 2012 Oct 30;79(18):1898-907. doi: 10.1212/WNL.0b013e318271f7ff. Epub 2012 Oct 17.

PMID:
23077007
20.

Chorea in an 83-year-old woman: don't forget Huntington's disease.

Lefaucheur R, Guyant-Maréchal L, Wallon D, Nicolas G, Borden A, Maltête D, Tollard E.

J Am Geriatr Soc. 2012 May;60(5):983-4. doi: 10.1111/j.1532-5415.2012.03912.x. No abstract available.

PMID:
22587859
21.

Factors influencing disease progression in autosomal dominant cerebellar ataxia and spastic paraplegia.

Tezenas du Montcel S, Charles P, Goizet C, Marelli C, Ribai P, Vincitorio C, Anheim M, Guyant-Maréchal L, Le Bayon A, Vandenberghe N, Tchikviladzé M, Devos D, Le Ber I, N'Guyen K, Cazeneuve C, Tallaksen C, Brice A, Durr A.

Arch Neurol. 2012 Apr;69(4):500-8. doi: 10.1001/archneurol.2011.2713.

PMID:
22491195
22.

The French series of autosomal dominant early onset Alzheimer's disease cases: mutation spectrum and cerebrospinal fluid biomarkers.

Wallon D, Rousseau S, Rovelet-Lecrux A, Quillard-Muraine M, Guyant-Maréchal L, Martinaud O, Pariente J, Puel M, Rollin-Sillaire A, Pasquier F, Le Ber I, Sarazin M, Croisile B, Boutoleau-Bretonnière C, Thomas-Antérion C, Paquet C, Moreaud O, Gabelle A, Sellal F, Sauvée M, Laquerrière A, Duyckaerts C, Delisle MB, Streichenberger N, Lannes B, Frebourg T, Hannequin D, Campion D; collaborators of GMAJ project.

J Alzheimers Dis. 2012;30(4):847-56. doi: 10.3233/JAD-2012-120172.

PMID:
22475797
23.

[Stroke and cornea verticillata revealing Fabry's disease in a female].

Fetter D, Bagan-Triquenot A, Guegan-Massardier E, Guyant-Marechal L, Tollard E, Bekri S, Hannequin D.

Rev Neurol (Paris). 2012 Feb;168(2):181-6. doi: 10.1016/j.neurol.2011.03.013. Epub 2011 Oct 26. French.

PMID:
22033111
24.

Singular DYT6 phenotypes in association with new THAP1 frameshift mutations.

Blanchard A, Roubertie A, Simonetta-Moreau M, Ea V, Coquart C, Frederic MY, Gallouedec G, Adenis JP, Benatru I, Borg M, Burbaud P, Calvas P, Cif L, Damier P, Destee A, Faivre L, Guyant-Marechal L, Janik P, Janoura S, Kreisler A, Lusakowska A, Odent S, Potulska-Chromik A, Rudzińska M, Thobois S, Vuillaume I, Tranchant C, Tuffery-Giraud S, Coubes P, Sablonnière B, Claustres M, Collod-Béroud G.

Mov Disord. 2011 Aug 1;26(9):1775-7. doi: 10.1002/mds.23641. Epub 2011 Apr 25. No abstract available.

PMID:
21520283
25.

Juvenile Huntington disease in an 18-month-old boy revealed by global developmental delay and reduced cerebellar volume.

Nicolas G, Devys D, Goldenberg A, Maltête D, Hervé C, Hannequin D, Guyant-Maréchal L.

Am J Med Genet A. 2011 Apr;155A(4):815-8. doi: 10.1002/ajmg.a.33911. Epub 2011 Mar 15.

PMID:
21412977
26.

Quantitative assessment of the evolution of cerebellar signs in spinocerebellar ataxias.

Chan E, Charles P, Ribai P, Goizet C, Marelli C, Vincitorio CM, Le Bayon A, Guyant-Maréchal L, Vandenberghe N, Anheim M, Devos D, Freeman L, Le Ber I, N'Guyen K, Tchikviladzé M, Labauge P, Hannequin D, Brice A, Durr A, du Montcel ST.

Mov Disord. 2011 Feb 15;26(3):534-8. doi: 10.1002/mds.23531. Epub 2011 Feb 1.

PMID:
21287600
27.

Clinical imaging and neuropathological correlations in an unusual case of cerebrotendinous xanthomatosis.

Wallon D, Guyant-Maréchal L, Laquerrière A, Wevers RA, Martinaud O, Kluijtmans LA, Yntema HG, Saugier-Veber P, Hannequin D.

Clin Neuropathol. 2010 Nov-Dec;29(6):361-4.

PMID:
21073839
28.

Morbid risk for schizophrenia in first-degree relatives of people with frontotemporal dementia.

Schoder D, Hannequin D, Martinaud O, Opolczynski G, Guyant-Maréchal L, Le Ber I, Campion D.

Br J Psychiatry. 2010 Jul;197(1):28-35. doi: 10.1192/bjp.bp.109.068981.

PMID:
20592430
29.

Whatever the disease duration, stimulation of the subthalamic nucleus improves Parkin disease.

Lefaucheur R, Derrey S, Guyant-Maréchal L, Chastan N, Maltête D.

Parkinsonism Relat Disord. 2010 Aug;16(7):482-3. doi: 10.1016/j.parkreldis.2010.04.013. Epub 2010 May 20. No abstract available.

PMID:
20493755
30.

Tangier disease phenotype diversity in dizygous twin sisters.

Pichit P, Quillard M, Couvert P, Sénant J, Carrié A, Bittar R, Hannequin D, Guyant-Maréchal L.

Rev Neurol (Paris). 2010 May;166(5):534-7. doi: 10.1016/j.neurol.2009.12.001. Epub 2010 Jan 12.

PMID:
20070997
31.

SPG15 is the second most common cause of hereditary spastic paraplegia with thin corpus callosum.

Goizet C, Boukhris A, Maltete D, Guyant-Maréchal L, Truchetto J, Mundwiller E, Hanein S, Jonveaux P, Roelens F, Loureiro J, Godet E, Forlani S, Melki J, Auer-Grumbach M, Fernandez JC, Martin-Hardy P, Sibon I, Sole G, Orignac I, Mhiri C, Coutinho P, Durr A, Brice A, Stevanin G.

Neurology. 2009 Oct 6;73(14):1111-9. doi: 10.1212/WNL.0b013e3181bacf59.

PMID:
19805727
32.

[Insanity in the young: diagnostic course].

Hannequin D, Guyant-Maréchal L, Le Ber I, Wallon D, Campion D, Sedel F.

Rev Neurol (Paris). 2009 Apr;165 Spec No 2:F87-96. Review. French. No abstract available.

PMID:
19593863
33.

CYP7B1 mutations in pure and complex forms of hereditary spastic paraplegia type 5.

Goizet C, Boukhris A, Durr A, Beetz C, Truchetto J, Tesson C, Tsaousidou M, Forlani S, Guyant-Maréchal L, Fontaine B, Guimarães J, Isidor B, Chazouillères O, Wendum D, Grid D, Chevy F, Chinnery PF, Coutinho P, Azulay JP, Feki I, Mochel F, Wolf C, Mhiri C, Crosby A, Brice A, Stevanin G.

Brain. 2009 Jun;132(Pt 6):1589-600. doi: 10.1093/brain/awp073. Epub 2009 May 12.

PMID:
19439420
34.

[Alzheimer disease: autosomal dominant forms].

Guyant-Maréchal L, Campion D, Hannequin D.

Rev Neurol (Paris). 2009 Mar;165(3):223-31. doi: 10.1016/j.neurol.2008.10.019. Epub 2008 Dec 10. French.

PMID:
19081588
35.

[Multiple cervical arterial dissections in two brothers: fibro-muscular dysplasia or connective tissue disease?].

Verdure P, Triquenot-Bagan A, Perdu J, Gerardin E, Laquerriere A, Hannequin D, Guyant-Marechal L.

Rev Neurol (Paris). 2008 Sep;164 Spec No 3:F211-5. doi: 10.1016/S0035-3787(08)74101-8. French. No abstract available.

PMID:
18992581
36.

Nephroangiosclerosis in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: is NOTCH3 mutation the common culprit?

Guerrot D, François A, Boffa JJ, Boulos N, Hanoy M, Legallicier B, Triquenot-Bagan A, Guyant-Marechal L, Laquerriere A, Freguin-Bouilland C, Ronco P, Godin M.

Am J Kidney Dis. 2008 Aug;52(2):340-5. doi: 10.1053/j.ajkd.2008.04.017. Epub 2008 Jun 24.

PMID:
18572291
37.

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.

Cephalalgia. 2008 Jul;28(7):774-7. doi: 10.1111/j.1468-2982.2008.01603.x. Epub 2008 May 21.

PMID:
18498390
38.

Composite cerebellar functional severity score: validation of a quantitative score of cerebellar impairment.

du Montcel ST, Charles P, Ribai P, Goizet C, Le Bayon A, Labauge P, Guyant-Maréchal L, Forlani S, Jauffret C, Vandenberghe N, N'guyen K, Le Ber I, Devos D, Vincitorio CM, Manto MU, Tison F, Hannequin D, Ruberg M, Brice A, Durr A.

Brain. 2008 May;131(Pt 5):1352-61. doi: 10.1093/brain/awn059. Epub 2008 Mar 31.

PMID:
18378516
39.

Myoclonus-dystonia: clinical and electrophysiologic pattern related to SGCE mutations.

Roze E, Apartis E, Clot F, Dorison N, Thobois S, Guyant-Marechal L, Tranchant C, Damier P, Doummar D, Bahi-Buisson N, André-Obadia N, Maltete D, Echaniz-Laguna A, Pereon Y, Beaugendre Y, Dupont S, De Greslan T, Jedynak CP, Ponsot G, Dussaule JC, Brice A, Dürr A, Vidailhet M.

Neurology. 2008 Mar 25;70(13):1010-6. doi: 10.1212/01.wnl.0000297516.98574.c0.

PMID:
18362280
40.

Variations in the APP gene promoter region and risk of Alzheimer disease.

Guyant-Maréchal L, Rovelet-Lecrux A, Goumidi L, Cousin E, Hannequin D, Raux G, Penet C, Ricard S, Macé S, Amouyel P, Deleuze JF, Frebourg T, Brice A, Lambert JC, Campion D.

Neurology. 2007 Feb 27;68(9):684-7.

PMID:
17325276
41.

Phenotype associated with APP duplication in five families.

Cabrejo L, Guyant-Maréchal L, Laquerrière A, Vercelletto M, De la Fournière F, Thomas-Antérion C, Verny C, Letournel F, Pasquier F, Vital A, Checler F, Frebourg T, Campion D, Hannequin D.

Brain. 2006 Nov;129(Pt 11):2966-76. Epub 2006 Sep 7.

PMID:
16959815
42.

Hemidystonia as initial manifestation of sporadic Creutzfeldt-Jakob disease.

Maltête D, Guyant-Maréchal L, Gérardin E, Laquerrière A, Martinaud O, Mihout B, Hannequin D.

Eur J Neurol. 2006 Jun;13(6):667-8. No abstract available.

PMID:
16796596
43.

Valosin-containing protein gene mutations: clinical and neuropathologic features.

Guyant-Maréchal L, Laquerrière A, Duyckaerts C, Dumanchin C, Bou J, Dugny F, Le Ber I, Frébourg T, Hannequin D, Campion D.

Neurology. 2006 Aug 22;67(4):644-51. Epub 2006 Jun 21.

PMID:
16790606
44.

Movement disorders and Creutzfeldt-Jakob disease: a review.

Maltête D, Guyant-Maréchal L, Mihout B, Hannequin D.

Parkinsonism Relat Disord. 2006 Mar;12(2):65-71. Epub 2005 Dec 20. Review.

PMID:
16364674
45.

Unusual cerebrotendinous xanthomatosis with fronto-temporal dementia phenotype.

Guyant-Maréchal L, Verrips A, Girard C, Wevers RA, Zijlstra F, Sistermans E, Vera P, Campion D, Hannequin D.

Am J Med Genet A. 2005 Dec 1;139A(2):114-7.

PMID:
16278884
46.

Epsilon sarcoglycan mutations and phenotype in French patients with myoclonic syndromes.

Tezenas du Montcel S, Clot F, Vidailhet M, Roze E, Damier P, Jedynak CP, Camuzat A, Lagueny A, Vercueil L, Doummar D, Guyant-Maréchal L, Houeto JL, Ponsot G, Thobois S, Cournelle MA, Durr A, Durif F, Echenne B, Hannequin D, Tranchant C, Brice A; French Dystonia Network.

J Med Genet. 2006 May;43(5):394-400. Epub 2005 Oct 14.

47.

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

Raux G, Guyant-Maréchal L, Martin C, Bou J, Penet C, Brice A, Hannequin D, Frebourg T, Campion D.

J Med Genet. 2005 Oct;42(10):793-5. Epub 2005 Jul 20.

48.

Frontotemporal dementia, motor neuron disease and tauopathy: clinical and neuropathological study in a family.

Martinaud O, Laquerrière A, Guyant-Maréchal L, Ahtoy P, Vera P, Sergeant N, Camuzat A, Bourgeois P, Hauw JJ, Campion D, Hannequin D.

Acta Neuropathol. 2005 Jul;110(1):84-92. Epub 2005 Jun 17.

PMID:
15965697

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