I. Coyle-gilchrist, K. Dick, K. Patterson, V. Rodríquez, P. Wehmann et al., Prevalence, characteristics, and survival of frontotemporal lobar degeneration syndromes, Neurology, vol.86, issue.18, pp.1736-1779, 2016.
DOI : 10.1212/WNL.0000000000002638

URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4854589

J. Whitwell and K. Josephs, Neuroimaging in frontotemporal lobar degeneration???predicting molecular pathology, Nature Reviews Neurology, vol.20, issue.3, pp.131-173, 2012.
DOI : 10.1523/JNEUROSCI.2160-09.2009

H. Morris, M. Khan, J. Janssen, J. Brown, J. Perez-tur et al., The Genetic and Pathological Classification of Familial Frontotemporal Dementia, Archives of Neurology, vol.58, issue.11, pp.1813-1819, 2001.
DOI : 10.1001/archneur.58.11.1813

A. Sieben, T. Van-langenhove, S. Engelborghs, J. Martin, P. Boon et al., The genetics and neuropathology of frontotemporal lobar degeneration, Acta Neuropathologica, vol.207, issue.1, pp.353-72, 2012.
DOI : 10.1084/jem.20091568

M. Dejesus-hernandez, I. Mackenzie, B. Boeve, A. Boxer, M. Baker et al., Expanded GGGGCC Hexanucleotide Repeat in Noncoding Region of C9ORF72 Causes Chromosome 9p-Linked FTD and ALS, Neuron, vol.72, issue.2, pp.245-56, 2011.
DOI : 10.1016/j.neuron.2011.09.011

M. Hutton, C. Lendon, P. Rizzu, M. Baker, S. Froelich et al., Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17, Nature, vol.393, issue.6686, pp.702-707, 1998.
DOI : 10.1038/31508

J. Rohrer, R. Guerreiro, J. Vandrovcova, J. Uphill, D. Reiman et al., The heritability and genetics of frontotemporal lobar degeneration, Neurology, vol.73, issue.18, pp.1451-1457, 2009.
DOI : 10.1212/WNL.0b013e3181bf997a

A. Ochs, D. Ross, M. Zannoni, T. Abildskov, and E. Bigler, Comparison of Automated Brain Volume Measures obtained with NeuroQuant?? and FreeSurfer, Journal of Neuroimaging, vol.44, issue.2, pp.721-728, 2015.
DOI : 10.1016/j.neuroimage.2008.10.037

K. Persson, G. Selbaek, A. Braekhus, M. Beyer, M. Barca et al., Fully automated structural MRI of the brain in clinical dementia workup, Acta Radiologica, vol.13, issue.6, 1987.
DOI : 10.3233/JAD-2010-100678

L. Souza, M. Chupin, M. Bertoux, S. Lehéricy, B. Dubois et al., Is hippocampal volume a good marker to differentiate Alzheimer's disease from frontotemporal dementia?, Alzheimer's & Dementia, vol.9, issue.4, pp.57-66, 2013.
DOI : 10.1016/j.jalz.2013.05.743

A. Du, N. Schuff, J. Kramer, H. Rosen, M. Gorno-tempini et al., Different regional patterns of cortical thinning in Alzheimer's disease and frontotemporal dementia, Brain, vol.130, issue.4
DOI : 10.1093/brain/awm016

Y. Zhang, M. Tartaglia, N. Schuff, G. Chiang, C. Ching et al., MRI signatures of brain macrostructural atrophy and microstructural degradation in frontotemporal lobar degeneration subtypes, J. Alzheimers Dis, vol.33, pp.431-444, 2013.

F. Agosta, S. Galantucci, G. Magnani, A. Marcone, D. Martinelli et al., MRI signatures of the frontotemporal lobar degeneration continuum, Human Brain Mapping, vol.60, issue.Pt. 2, 2015.
DOI : 10.1002/ana.20916

J. Rohrer, A. Isaacs, S. Mizielinska, S. Mead, T. Lashley et al., C9orf72 expansions in frontotemporal dementia and amyotrophic lateral sclerosis, The Lancet Neurology, vol.14, issue.3, pp.291-301, 2015.
DOI : 10.1016/S1474-4422(14)70233-9

J. Snowden, J. Adams, J. Harris, J. Thompson, S. Rollinson et al., Distinct clinical and pathological phenotypes in frontotemporal dementia associated with MAPT, PGRN and C9orf72 mutations, Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, vol.34, issue.7-8, pp.497-505, 2015.
DOI : 10.1093/hmg/ddl241

C. Mahoney, L. Downey, G. Ridgway, J. Beck, S. Clegg et al., Longitudinal neuroimaging and neuropsychological profiles of frontotemporal dementia with C9ORF72 expansions, Alzheimer's Research & Therapy, vol.4, issue.5, p.41, 2012.
DOI : 10.1007/s00401-011-0907-y

J. Whitwell, B. Boeve, S. Weigand, M. Senjem, J. Gunter et al., Brain atrophy over time in genetic and sporadic frontotemporal dementia: a study of 198 serial magnetic resonance images, European Journal of Neurology, vol.73, issue.5, pp.745-52, 2015.
DOI : 10.1212/WNL.0b013e3181b9c8b9

F. Ameur, O. Colliot, P. Caroppo, S. Ströer, D. Dormont et al., mutations, Neurology Genetics, vol.2, issue.1, p.47, 2016.
DOI : 10.1212/NXG.0000000000000047

URL : https://hal.archives-ouvertes.fr/pasteur-00865888

B. Kelley, W. Haidar, B. Boeve, M. Baker, N. Graff-radford et al., Prominent phenotypic variability associated with mutations in Progranulin, Neurobiology of Aging, vol.30, issue.5, pp.739-51, 2009.
DOI : 10.1016/j.neurobiolaging.2007.08.022

URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3164546

J. Van-swieten and P. Heutink, Mutations in progranulin (GRN) within the spectrum of clinical and pathological phenotypes of frontotemporal dementia, The Lancet Neurology, vol.7, issue.10, pp.965-974, 2008.
DOI : 10.1016/S1474-4422(08)70194-7

J. Whitwell, C. Jack, B. Boeve, M. Senjem, M. Baker et al., Voxelbased morphometry patterns of atrophy in FTLD with mutations in MAPT or PGRN

J. Rohrer, G. Ridgway, M. Modat, S. Ourselin, S. Mead et al., Distinct profiles of brain atrophy in frontotemporal lobar degeneration caused by progranulin and tau mutations, NeuroImage, vol.53, issue.3, pp.1070-1076, 2010.
DOI : 10.1016/j.neuroimage.2009.12.088

M. Bozzali, V. Battistoni, E. Premi, A. Alberici, G. Giulietti et al., Structural brain signature of FTLD driven by granulin mutation, J. Alzheimers Dis, vol.33, pp.483-494, 2013.

C. Mahoney, L. Downey, G. Ridgway, J. Beck, S. Clegg et al., Longitudinal neuroimaging and neuropsychological profiles of frontotemporal dementia with C9ORF72 expansions, Alzheimer's Research & Therapy, vol.4, issue.5, p.41, 2012.
DOI : 10.1007/s00401-011-0907-y

P. Caroppo, L. Ber, I. Camuzat, A. Clot, F. Naccache et al., Extensive White Matter Involvement in Patients With Frontotemporal Lobar Degeneration, JAMA Neurology, vol.71, issue.12
DOI : 10.1001/jamaneurol.2014.1316

URL : https://hal.archives-ouvertes.fr/hal-01439037

B. Ghetti, S. Spina, J. Murrell, E. Huey, P. Pietrini et al., In vivo and Postmortem Clinicoanatomical Correlations in Frontotemporal Dementia and Parkinsonism Linked to Chromosome 17, Neurodegenerative Diseases, vol.5, issue.3-4, pp.215-222, 2008.
DOI : 10.1159/000113706

J. Whitwell, S. Weigand, B. Boeve, M. Senjem, J. Gunter et al., Neuroimaging signatures of frontotemporal dementia genetics: C9ORF72, tau, progranulin and sporadics, Brain, vol.135, issue.3, pp.794-806, 2012.
DOI : 10.1093/brain/aws001

J. Whitwell, K. Josephs, M. Rossor, J. Stevens, T. Revesz et al., Magnetic Resonance Imaging Signatures of Tissue Pathology in Frontotemporal Dementia, Archives of Neurology, vol.62, issue.9, pp.1402-1410, 2005.
DOI : 10.1001/archneur.62.9.1402

A. Frank, Z. Wszolek, C. Jack, and B. Boeve, Distinctive MRI findings in pallidopontonigral degeneration (PPND), Neurology, vol.68, issue.8, pp.620-621, 2007.
DOI : 10.1212/01.wnl.0000254614.39759.3d

O. Dowd, S. Murray, B. Roberts, K. Cummins, G. Magennis et al., Pallidopontonigral degeneration: A deceptive familial tauopathy, Movement Disorders, vol.13, issue.7, pp.817-826, 2012.
DOI : 10.1016/j.parkreldis.2006.10.007

J. Snowden, Q. Hu, S. Rollinson, N. Halliwell, A. Robinson et al., The most common type of FTLD-FUS (aFTLD-U) is associated with a distinct clinical form of frontotemporal dementia but is not related to mutations in the FUS gene, Acta Neuropathologica, vol.115, issue.1
DOI : 10.1007/s00401-007-0329-z

S. Lee, W. Seeley, P. Poorzand, R. Rademakers, A. Karydas et al., Clinical characterization of bvFTD due to FUS neuropathology, Neurocase, vol.156, issue.4, pp.305-322, 2012.
DOI : 10.1093/brain/awn343

K. Josephs, J. Whitwell, J. Parisi, R. Petersen, B. Boeve et al., Caudate atrophy on MRI is a characteristic feature of FTLD-FUS, European Journal of Neurology, vol.29, issue.Pt 5, pp.969-75, 2010.
DOI : 10.1016/j.neurobiolaging.2007.04.027

J. Rohrer, T. Lashley, J. Schott, J. Warren, S. Mead et al., Clinical and neuroanatomical signatures of tissue pathology in frontotemporal lobar degeneration, Brain, vol.134, issue.9
DOI : 10.1093/brain/awr198

J. Whitwell, K. Josephs, M. Rossor, J. Stevens, T. Revesz et al., Magnetic Resonance Imaging Signatures of Tissue Pathology in Frontotemporal Dementia, Archives of Neurology, vol.62, issue.9, pp.1402-1408, 2005.
DOI : 10.1001/archneur.62.9.1402

J. Hodges, K. Patterson, S. Oxbury, and E. Funnell, Semantic dementia: progressive fluent aphasia with temporal lobe atrophy, Neurocase, vol.1, issue.1, pp.1783-806, 1992.
DOI : 10.1093/neucas/1.1.39-g

C. Mummery, K. Patterson, C. Price, J. Ashburner, R. Frackowiak et al., A voxel-based morphometry study of semantic dementia: Relationship between temporal lobe atrophy and semantic memory, Annals of Neurology, vol.94, issue.1, pp.36-45, 2000.
DOI : 10.1176/jnp.6.2.100

J. Hodges, K. Patterson, S. Oxbury, and E. Funnell, Semantic dementia: progressive fluent aphasia with temporal lobe atrophy, Neurocase, vol.1, issue.1, pp.1783-806, 1992.
DOI : 10.1093/neucas/1.1.39-g

M. Schroeter, K. Raczka, J. Neumann, Y. Von-cramon, and D. , Towards a nosology for frontotemporal lobar degenerations???A meta-analysis involving 267 subjects, NeuroImage, vol.36, issue.3, pp.497-510, 2007.
DOI : 10.1016/j.neuroimage.2007.03.024

R. Landin-romero, R. Tan, J. Hodges, and F. Kumfor, An update on semantic dementia: genetics, imaging, and pathology, Alzheimer's Research & Therapy, vol.65, issue.2, pp.2016-13195
DOI : 10.1001/archneurol.2007.34

URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5137205

F. Agosta, P. Ferraro, E. Canu, M. Copetti, S. Galantucci et al., Differentiation between Subtypes of Primary Progressive Aphasia by Using Cortical Thickness and Diffusion-Tensor MR Imaging Measures, Radiology, vol.276, issue.1, 2015.
DOI : 10.1148/radiol.15141869

L. Iaccarino, C. Crespi, P. Rosa, . Della, E. Catricalà et al., The Semantic Variant of Primary Progressive Aphasia: Clinical and Neuroimaging Evidence in Single Subjects, PLOS ONE, vol.8, issue.1, p.120197, 2015.
DOI : 10.1371/journal.pone.0120197.t005

S. Sajjadi, J. Acosta-cabronero, K. Patterson, L. Diaz-de-grenu, G. Williams et al., Diffusion tensor magnetic resonance imaging for single subject diagnosis in neurodegenerative diseases, Brain, vol.136, issue.7, pp.2253-61, 2013.
DOI : 10.1093/brain/awt118

J. Whitwell, R. Avula, M. Senjem, K. Kantarci, S. Weigand et al., Gray and white matter water diffusion in the syndromic variants of frontotemporal dementia, Neurology, vol.74, issue.16, pp.1279-87, 2010.
DOI : 10.1212/WNL.0b013e3181d9edde

F. Agosta and S. , Disruption of structural connectivity along the dorsal and ventral language pathways in patients with nonfluent and semantic variant primary progressive aphasia: A DT MRI study and a literature review, Brain and Language, vol.127, issue.2, 2013.
DOI : 10.1016/j.bandl.2013.06.003

. Atrophy, hypometabolism and white matter abnormalities in semantic dementia tell a coherent story, Brain J. Neurol, vol.134, pp.2025-2060, 2011.

S. Brambati, S. Amici, C. Racine, J. Neuhaus, Z. Miller et al., Longitudinal gray matter contraction in three variants of primary progressive aphasia: A tenser-based morphometry study, NeuroImage: Clinical, vol.8, pp.345-55, 2015.
DOI : 10.1016/j.nicl.2015.01.011

F. Agosta, E. Scola, E. Canu, A. Marcone, G. Magnani et al., White Matter Damage in Frontotemporal Lobar Degeneration Spectrum, Cerebral Cortex, vol.22, issue.12, pp.2705-2719, 2012.
DOI : 10.1093/cercor/bhr288

J. Rohrer, J. Warren, M. Modat, G. Ridgway, A. Douiri et al., Patterns of cortical thinning in the language variants of frontotemporal lobar degeneration, Neurology, vol.72, issue.18, pp.1562-1571, 2009.
DOI : 10.1212/WNL.0b013e3181a4124e

S. Galantucci, M. Tartaglia, S. Wilson, M. Henry, M. Filippi et al., White matter damage in primary progressive aphasias: a diffusion tensor tractography study, Brain, vol.134, issue.10
DOI : 10.1093/brain/awr099

URL : http://doi.org/10.1093/brain/awr099

N. Kato, K. Arai, and T. Hattori, Study of the rostral midbrain atrophy in progressive supranuclear palsy, Journal of the Neurological Sciences, vol.210, issue.1-2, pp.57-60, 2003.
DOI : 10.1016/S0022-510X(03)00014-5

M. Adachi, T. Kawanami, H. Ohshima, Y. Sugai, and T. Hosoya, Morning Glory Sign: A Particular MR Finding in Progressive Supranuclear Palsy, Magnetic Resonance in Medical Sciences, vol.3, issue.3
DOI : 10.2463/mrms.3.125

A. Quattrone, G. Nicoletti, D. Messina, F. Fera, F. Condino et al., MR Imaging Index for Differentiation of Progressive Supranuclear Palsy from Parkinson Disease and the Parkinson Variant of Multiple System Atrophy, Radiology, vol.246, issue.1, pp.214-235, 2008.
DOI : 10.1148/radiol.2453061703

M. Mascalchi, A. Vella, and R. Ceravolo, Movement disorders: role of imaging in diagnosis, J

A. Righini, A. Antonini, D. Notaris, R. Bianchini, E. Meucci et al., MR imaging of the superior profile of the midbrain: differential diagnosis between progressive supranuclear palsy and Parkinson disease, AJNR Am. J. Neuroradiol, vol.25, pp.927-959, 2004.

T. Hanihara, N. Amano, T. Takahashi, Y. Itoh, and S. Yagishita, Hypertrophy of the Inferior Olivary Nucleus in Patients with Progressive Supranuclear Palsy, European Neurology, vol.39, issue.2, pp.97-102, 1998.
DOI : 10.1159/000007915

O. Katsuse and D. Dickson, Inferior olivary hypertrophy is uncommon in progressive supranuclear palsy, Acta Neuropathologica, vol.108, issue.2, pp.143-149, 2004.
DOI : 10.1007/s00401-004-0878-3

M. Tir, C. Delmaire, P. Besson, and L. Defebvre, The value of novel MRI techniques in

N. Upadhyay, A. Suppa, M. Piattella, D. Stasio, F. Petsas et al., Gray and white matter structural changes in corticobasal syndrome, Neurobiology of Aging, vol.37, pp.82-90, 2016.
DOI : 10.1016/j.neurobiolaging.2015.10.011

N. Kouri, J. Whitwell, K. Josephs, R. Rademakers, and D. Dickson, Corticobasal degeneration: a pathologically distinct 4R tauopathy, Nature Reviews Neurology, vol.24, issue.5, pp.263-72, 2011.
DOI : 10.1002/humu.20086