D. Hannequin

O. Martinaud, D. Hannequin, E. Gerardin, 2014, Archives of clinical neuropsychology : the official journal of the National Academy of Neuropsychologists.

Anatomy of executive deficit following ruptured anterior communicating artery aneurysm

O. Martinaud, D. Hannequin, O. Godefroy, 2009, European journal of neurology.

Cognitive inhibition impairments in presymptomatic C9orf72 carriers

B. Dubois, R. Levy, F. Pasquier, 2020, Journal of Neurology, Neurosurgery, and Psychiatry.

No replication of the association between the Nicastrin gene and familial early-onset Alzheimer's disease

B. Dubois, E. Génin, D. Campion, 2003, Neuroscience Letters.

Familial intracranial aneurysm, the relationship of the aortic diameter.

D. Hannequin, H. Cebula, L. Guyant‐Maréchal, 2015, Neuro-Chirurgie.

Movement disorders and Creutzfeldt-Jakob disease: a review.

D. Hannequin, D. Maltête, L. Guyant‐Maréchal, 2006, Parkinsonism & related disorders.

Genetically elevated high-density lipoprotein cholesterol through the cholesteryl ester transfer protein gene does not associate with risk of Alzheimer ' s disease

D. G. Clark, M. Fornage, A. Hofman, 2022 .

Picture written naming: Performance parallels and divergencies between aphasic patients and normal subjects

M. Metz-Lutz, D. Hannequin, D. Cardebat, 1997 .

XPR1 mutations are a rare cause of primary familial brain calcification

M. Sitbon, D. Campion, D. Hannequin, 2016, Journal of Neurology.

Plasma NfL levels and longitudinal change rates in C9orf72 and GRN-associated diseases: from tailored references to clinical applications

J. Pariente, R. Levy, F. Pasquier, 2021, Journal of Neurology Neurosurgery & Psychiatry.

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

J. Lambert, P. Amouyel, D. Campion, 2007, Neurology.

Pediatric cerebral aneurysms.

D. Hannequin, P. Toussaint, F. Proust, 2001, Journal of neurosurgery.

Frontal Assessment Battery is a marker of dorsolateral and medial frontal functions: A SPECT study in frontotemporal dementia

B. Dubois, D. Hannequin, G. Allali, 2008, Journal of the Neurological Sciences.

Mendelian randomization implies no direct causal association between leukocyte telomere length and amyotrophic lateral sclerosis

Nick C Fox, Alan J. Thomas, D. Hernandez, 2020, Scientific Reports.

Frontotemporal dementia phenotype associated with MAPT gene duplication.

D. Campion, D. Hannequin, O. Guillin, 2010, Journal of Alzheimer's disease : JAD.

Visual Agnosia and Posterior Cerebral Artery Infarcts: An Anatomical-Clinical Study

L. Cohen, O. Martinaud, D. Hannequin, 2012, PloS one.

Apolipoprotein E epsilon4 allele and familial aggregation of Alzheimer disease.

Y. Agid, B. Dubois, D. Campion, 1998, Archives of neurology.

SOD 1 , ANG , VAPB , TARDBP , and FUS mutations in familial Amyotrophic Lateral Sclerosis : genotype-phenotype correlations

V. Meininger, F. Salachas, D. Hannequin, 2017 .

SOD1, ANG, VAPB, TARDBP, and FUS mutations in familial amyotrophic lateral sclerosis: genotype–phenotype correlations

V. Meininger, F. Salachas, D. Hannequin, 2010, Journal of Medical Genetics.

TARDBP mutations in motoneuron disease with frontotemporal lobar degeneration

B. Dubois, V. Meininger, F. Salachas, 2009, Annals of neurology.

Definite behavioral variant of frontotemporal dementia with C9ORF72 expansions despite positive Alzheimer's disease cerebrospinal fluid biomarkers.

J. Pariente, F. Pasquier, D. Campion, 2012, Journal of Alzheimer's disease : JAD.

Meta-analysis of genetic association with diagnosed Alzheimer’s disease identifies novel risk loci and implicates Abeta, Tau, immunity and lipid processing

J. Gallacher, M. Fornage, I. Giegling, 2018, bioRxiv.

Brain Calcifications in Adult-Onset Genetic Leukoencephalopathies: A Review

D. Hannequin, P. Labauge, X. Ayrignac, 2017, JAMA neurology.

PDGFB Partial Deletion: a New, Rare Mechanism Causing Brain Calcification with Leukoencephalopathy

O. Martinaud, D. Campion, D. Hannequin, 2014, Journal of Molecular Neuroscience.

Biological effects of four PSEN1 gene mutations causing Alzheimer disease with spastic paraparesis and cotton wool plaques

C. Duyckaerts, D. Campion, D. Hannequin, 2006, Human mutation.

Submental sensitive transcutaneous electrical stimulation (SSTES) at home in neurogenic oropharyngeal dysphagia: a pilot study.

D. Hannequin, D. Maltête, A. Leroi, 2011, Annals of physical and rehabilitation medicine.

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

Y. Agid, B. Dubois, F. Pasquier, 1997, American journal of human genetics.

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

P. Bosco, Y. Kamatani, G. Spalletta, 2012, Molecular Psychiatry.

Erratum: Genome-wide haplotype association study identifies the FRMD4A gene as a risk locus for Alzheimer's disease (Molecular Psychiatry (2013) 18 (521) DOI: 10.1038/mp.2012.75))

P. Bosco, Y. Kamatani, G. Spalletta, 2013 .

[Autosomal dominant limb-girdle muscular dystrophy associated with conduction defects (LGMD1B): a description of 8 new families with the LMNA gene mutations].

D. Hannequin, A. Toutain, V. Drouin‐Garraud, 2005, Revue neurologique.

Impaired functional differentiation for categories of objects in the ventral visual stream: A case of developmental visual impairment

F. Ramus, L. Cohen, G. Dehaene-Lambertz, 2015, Neuropsychologia.

Effect of the Histone Deacetylase Inhibitor FRM-0334 on Progranulin Levels in Patients With Progranulin Gene Haploinsufficiency

G. Frisoni, B. Boeve, F. Pasquier, 2021, JAMA network open.

Causes of morbidity and mortality after ruptured aneurysm surgery in a series of 230 patients. The importance of control angiography.

D. Hannequin, F. Proust, O. Langlois, 1995, Stroke.

MEMENTO: A NATIONAL COHORT ON DETERMINANTS AND BIOMARKERS OF ALZHEIMER'S DISEASE AND ASSOCIATED DISORDERS

J. Pariente, O. Beauchet, F. Pasquier, 2014, Alzheimer's & Dementia.

Usefulness of transcranial color-coded sonography in the diagnosis of cerebral vasospasm.

D. Hannequin, F. Proust, J. Lestrat, 1999, Stroke.

Outcome in 43 patients with distal anterior cerebral artery aneurysms.

D. Hannequin, P. Toussaint, D. Le Gars, 1997, Stroke.

Tentorial edge traumatic aneurysm of the superior cerebellar artery. Case report.

D. Hannequin, A. Laquérriere, F. Proust, 1997, Journal of neurosurgery.

Extensive white matter involvement in patients with frontotemporal lobar degeneration: think progranulin.

L. Naccache, O. Colliot, F. Lamari, 2014, JAMA neurology.

Contribution of ATXN2 intermediary polyQ expansions in a spectrum of neurodegenerative disorders

A. Bonnet, F. Pasquier, S. Rivaud-Pechoux, 2014, Neurology.

TBK1 mutation frequencies in French frontotemporal dementia and amyotrophic lateral sclerosis cohorts

B. Dubois, R. Levy, F. Pasquier, 2015, Neurobiology of Aging.

SQSTM1 mutations in French patients with frontotemporal dementia or frontotemporal dementia with amyotrophic lateral sclerosis.

J. Hardy, R. Guerreiro, D. Campion, 2013, JAMA neurology.

Added value of 18F-florbetaben amyloid PET in the diagnostic workup of most complex patients with dementia in France: A naturalistic study

B. Dubois, J. Pariente, F. Pasquier, 2018, Alzheimer's & Dementia.

Comparison of Pittsburgh compound B and florbetapir in cross-sectional and longitudinal studies

Andrei G. Vlassenko, J. Morris, C. Jack, 2019, Alzheimer's & dementia.

Polymorphisms of insulin degrading enzyme gene are not associated with Alzheimer's disease

D. Campion, D. Hannequin, A. Brice, 2002, Neuroscience Letters.

Deletion of the progranulin gene in patients with frontotemporal lobar degeneration or Parkinson disease

F. Pasquier, J. Lambert, D. Campion, 2008, Neurobiology of Disease.

[Stiff-person syndrome and other neurological disorders associated with anti-GAD antibodies].

D. Hannequin, A. Bédat-Millet, J. Hijazi, 2010, La Revue de medecine interne.

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

D. Campion, D. Hannequin, A. Brice, 2005, Journal of Medical Genetics.

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

D. Campion, D. Hannequin, C. Boulay, 2007, Journal of Neurology, Neurosurgery, and Psychiatry.

Mutations other than null mutations producing a pathogenic loss of progranulin in frontotemporal dementia

K. Sleegers, C. van Broeckhoven, S. Engelborghs, 2007, Human mutation.

D. Hannequin, D. Wallon, E. Magnin, 2013, Journal of Alzheimer's disease : JAD.

Clozapine for the treatment of psychosis in Parkinson's disease: a review

D. Hannequin, P. Auzou, P. Augustin, 1996, Acta neurologica Scandinavica.

Segregation analysis of Alzheimer pedigrees: rare Mendelian dominant mutation(s) explain a minority of early-onset cases. French Alzheimer Collaborative Group.

Y. Agid, J. Mallet, D. Campion, 1996, American journal of medical genetics.

Identification of three novel mutations (E196K, V203I, E211Q) in the prion protein gene (PRNP) in inherited prion diseases with Creutzfeldt‐Jakob disease phenotype

J. Laplanche, D. Hannequin, P. Beaudry, 2000, Human mutation.

C9ORF72 repeat expansions in the frontotemporal dementias spectrum of diseases: a flow-chart for genetic testing.

B. Dubois, J. Pariente, M. Ruberg, 2013, Journal of Alzheimer's disease : JAD.

Worsening of psychotic symptoms by clozapine in Parkinson's disease

D. Hannequin, P. Auzou, I. Landrin, 1994, The Lancet.

Early Cognitive, Structural, and Microstructural Changes in Presymptomatic C9orf72 Carriers Younger Than 40 Years

B. Dubois, R. Levy, S. Durrleman, 2018, JAMA neurology.

INTRAFAMILIAL DIVERSITY OF PHENOTYPE ASSOCIATED WITH APP DUPLICATION

D. Campion, D. Hannequin, L. Rumbach, 2008, Neurology.

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

J. Hauw, O. Martinaud, D. Campion, 2005, Acta Neuropathologica.

No eVect of the á1-antichymotrypsin A allele in Alzheimer’s disease

Y. Agid, F. Pasquier, D. Campion, 1998 .

The NACP/synuclein gene: chromosomal assignment and screening for alterations in Alzheimer disease.

R. Heilig, D. Campion, D. Hannequin, 1995, Genomics.

An Autopsy Case of Amyotrophic Lateral Sclerosis with Waldenström Macroglobulinemia and Anti-MAG Gammopathy

F. Jardin, O. Martinaud, D. Hannequin, 2011, Case Reports in Neurology.

Plasma amyloid levels within the Alzheimer's process and correlations with central biomarkers

M. Chupin, J. Mangin, P. Robert, 2018, Alzheimer's & Dementia.

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

Miguel Ángel Martínez, Y. Agid, D. Campion, 1998, Journal of medical genetics.

Chromosome 9p-linked families with frontotemporal dementia associated with motor neuron disease

S. Heath, B. Dubois, C. Duyckaerts, 2009, Neurology.

Prosodic Aspects of Speech

Y. Joanette, D. Hannequin, P. Goulet, 1990 .

Dementia with prominent frontotemporal features associated with L113P presenilin 1 mutation

D. Campion, D. Hannequin, A. Brice, 2000, Neurology.

Mutations in the neuroserpin gene are rare in familial dementia

Y. Agid, B. Dubois, D. Hannequin, 2000 .

A case of logopenic primary progressive aphasia with C9ORF72 expansion and cortical florbetapir binding.

F. Chollet, J. Pariente, D. Campion, 2014, Journal of Alzheimer's disease : JAD.

Author Correction: Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

Nick C Fox, Michelle K. Lupton, Charles C. White, 2019, Nature Genetics.

Identification of evolutionarily conserved gene networks mediating neurodegenerative dementia.

Nick C. Fox, Pietro Pietrini, Alexander Gerhard, 2018, Nature Medicine.

Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study

Kevin F. Bieniek, C. Geula, M. Mesulam, 2018, The Lancet Neurology.

hnRNPA2B1 and hnRNPA1 mutations are rare in patients with “multisystem proteinopathy” and frontotemporal lobar degeneration phenotypes

D. Hannequin, A. Brice, D. Wallon, 2014, Neurobiology of Aging.

Brain calcification process and phenotypes according to age and sex: Lessons from SLC20A2, PDGFB, and PDGFRB mutation carriers

D. Geschwind, G. Coppola, D. Campion, 2015, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Novel VCP mutations expand the mutational spectrum of frontotemporal dementia

D. Hannequin, M. Didic, S. Forlani, 2018, Neurobiology of Aging.

FUS mutations in frontotemporal lobar degeneration with amyotrophic lateral sclerosis.

B. Dubois, V. Meininger, F. Salachas, 2010, Journal of Alzheimer's disease : JAD.

Relations between C9orf72 expansion size in blood, age at onset, age at collection and transmission across generations in patients and presymptomatic carriers

S. Lehéricy, B. Dubois, J. Pariente, 2019, Neurobiology of Aging.

Oropharyngeal dysphagia in amyotrophic lateral sclerosis alters quality of life.

A. Cuvelier, D. Hannequin, E. Vérin, 2013, Journal of oral rehabilitation.

Clinical screening of oropharyngeal dysphagia in patients with ALS.

A. Cuvelier, D. Hannequin, E. Vérin, 2012, Annals of physical and rehabilitation medicine.

Plasma progranulin levels for frontotemporal dementia in clinical practice: a 10-year French experience

B. Dubois, J. Pariente, R. Levy, 2020, Neurobiology of Aging.

Mutation in the 3’untranslated region of APP as a genetic determinant of cerebral amyloid angiopathy

J. Dartigues, S. Hébert, J. Lambert, 2015, European Journal of Human Genetics.

Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia: An MRI Study of 16 French Cases

D. Hannequin, F. Etcharry-Bouyx, C. Marelli, 2018, American Journal of Neuroradiology.

Microangiopathy in primary familial brain calcification: Evidence from skin biopsies

D. Hannequin, A. Laquérriere, G. Nicolas, 2017, Neurology: Genetics.

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

P. Vermersch, M. Giroud, M. Clanet, 2015, Brain : a journal of neurology.

Hemidystonia as initial manifestation of sporadic Creutzfeldt–Jakob disease

D. Hannequin, A. Laquérriere, D. Maltête, 2006, European journal of neurology.

Implication of the immune system in Alzheimer's disease: evidence from genome-wide pathway analysis.

Simon Heath, Christophe Tzourio, Philippe Amouyel, 2010, Journal of Alzheimer's disease : JAD.

Severe Attacks of Familial Hemiplegic Migraine, Childhood Epilepsy and ATP1A2 Mutation

D. Hannequin, L. Guyant‐Maréchal, D. Parain, 2008, Cephalalgia : an international journal of headache.

Segregation of a missense mutation in the microtubule-associated protein tau gene with familial frontotemporal dementia and parkinsonism.

Y. Agid, B. Dubois, D. Campion, 1998, Human molecular genetics.

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

A. Durr, P. Convers, M. Koenig, 2015, Annals of neurology.

Recurrence of an early postzygotic rescue of an inherited unbalanced translocation resulting in mosaic segmental uniparental isodisomy of chromosome 11q in siblings

D. Hannequin, T. Frebourg, K. Cassinari, 2021, American journal of medical genetics. Part A.

An Acute Cerebellar Syndrome . Who Is Involved ?

D. Hannequin, D. Maltête, X. Monnet, 2016 .

Exacerbation of multiple sclerosis during therapy that included brain extracts

D. Hannequin, A. Coquerel, O. Lees, 1988, The Medical journal of Australia.

Picture Confrontation Oral Naming: Performance Differences between Aphasics and Normals

D. Hannequin, D. Cardebat, M. Metz-Lutz, 1996, Brain and Language.

Giant cervical epidural veins after lumbar puncture in a case of intracranial hypotension.

D. Hannequin, F. Douvrin, F. Clarot, 2000, AJNR. American journal of neuroradiology.

Relevance of Follow-Up in Patients with Core Clinical Criteria for Alzheimer Disease and Normal CSF Biomarkers.

F. Pasquier, L. Buée, S. Lehmann, 2018, Current Alzheimer Research.

Asessment of paraneoplastic limbic encephalitis in testicular cancer.

D. Hannequin, P. Grise, C. Pfister, 2003, Clinical oncology (Royal College of Radiologists (Great Britain)).

α2‐Macroglobulin gene and Alzheimer's disease: Confirmation of association by haplotypes analyses

Y. Agid, B. Dubois, D. Campion, 2000, Annals of neurology.

Seizures in dominantly inherited Alzheimer disease

J. Pariente, F. Pasquier, O. Martinaud, 2016, Neurology.

Biallelic MYORG mutation carriers exhibit primary brain calcification with a distinct phenotype.

L. Defebvre, M. Vidailhet, J. Pariente, 2019, Brain : a journal of neurology.

Neuroimaging Correlates of Frontotemporal Dementia Associated with SQSTM1 Mutations.

C. van Broeckhoven, D. Galimberti, D. Hannequin, 2016, Journal of Alzheimer's disease : JAD.

No association of apolipoprotein epsilon 4 allele with schizophrenia even in cognitively impaired patients

D. Campion, D. Hannequin, S. Dollfus, 1998, Schizophrenia Research.

The Neurobiological Basis of Time Estimation and Temporal Order

D. Hannequin, Robert Lalonde, R Lalonde, 1999, Reviews in the neurosciences.

Convergent genetic and expression data implicate immunity in Alzheimer's disease

J. Gallacher, K. Lunetta, M. Nalls, 2014, Alzheimer's & Dementia.

Association between the extended tau haplotype and frontotemporal dementia.

B. Dubois, D. Campion, D. Hannequin, 2002, Archives of neurology.

A Polymorphism in CALHM1 Influences Ca2+ Homeostasis, Aβ Levels, and Alzheimer's Disease Risk

F. Pasquier, D. Mann, J. Lambert, 2008, Cell.

De novo deleterious genetic variations target a biological network centered on Aβ peptide in early-onset Alzheimer disease

D. Campion, D. Hannequin, D. Wallon, 2015, Molecular Psychiatry.

Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

Nick C Fox, Michelle K. Lupton, Charles C. White, 2019, Nature Genetics.

Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases.

Michelle K. Lupton, D. Geschwind, J. Haines, 2012, Human molecular genetics.

Mutations of the presenilin I gene in families with early-onset Alzheimer's disease.

B. Dubois, D. Campion, D. Hannequin, 1995, Human molecular genetics.

Mutations in the gene encoding PDGF-B cause brain calcifications in humans and mice

D. Geschwind, P. Svenningsson, A. Aguzzi, 2013, Nature Genetics.

Primary brain calcification: an international study reporting novel variants and associated phenotypes

D. Geschwind, M. Vidailhet, D. Galasko, 2018, European Journal of Human Genetics.

Primary brain calcification: an international study reporting novel variants and associated phenotypes

D. Geschwind, M. Vidailhet, D. Galasko, 2018, European Journal of Human Genetics.

Mutations in XPR1 cause primary familial brain calcification associated with altered phosphate export

D. Geschwind, P. Svenningsson, J. Pariente, 2015, Nature Genetics.

PDGFB Partial Deletion: a New, Rare Mechanism Causing Brain Calcification with Leukoencephalopathy

O. Martinaud, D. Campion, D. Hannequin, 2014, Journal of Molecular Neuroscience.

A de novo nonsense PDGFB mutation causing idiopathic basal ganglia calcification with laryngeal dystonia

Y. Béjot, M. Giroud, D. Campion, 2014, European Journal of Human Genetics.

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

L. Defebvre, J. Pariente, M. Vérin, 2013, Brain : a journal of neurology.

[Alzheimer's disease cerebro-spinal fluid biomarkers: A clinical research tool sometimes useful in daily clinical practice of memory clinics for the diagnosis of complex cases].

F. Pasquier, S. Lehmann, J. Laplanche, 2017, La Revue de medecine interne.

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

M Mancuso, R Ferri, P. Bosco, 2012, Molecular Psychiatry.

REEP1 mutations in SPG31: Frequency, mutational spectrum, and potential association with mitochondrial morpho‐functional dysfunction

A. Durr, D. Hannequin, S. Forlani, 2011, Human mutation.

Mutations in SPG11 are frequent in autosomal recessive spastic paraplegia with thin corpus callosum, cognitive decline and lower motor neuron degeneration.

F. Pasquier, A. Durr, D. Hannequin, 2008, Brain : a journal of neurology.

A trial of gantenerumab or solanezumab in dominantly inherited Alzheimer’s disease

A. Fagan, M. Mintun, J. Morris, 2021, Nature Medicine.

Phenotype associated with APP duplication in five families.

Florence Pasquier, Didier Hannequin, Thierry Frebourg, 2006, Brain : a journal of neurology.

Gene Expression Imputation Across Multiple Tissue Types Provides Insight Into the Genetic Architecture of Frontotemporal Dementia and Its Clinical Subtypes

Nick C Fox, Alan J. Thomas, D. Hernandez, 2021, Biological Psychiatry.

Causative Mutations and Genetic Risk Factors in Sporadic Early Onset Alzheimer's Disease Before 51 Years.

J. Pariente, F. Pasquier, O. Martinaud, 2019, Journal of Alzheimer's disease : JAD.

Alzheimer's disease and other dementias

D. Campion, D. Hannequin, A. Brice, 2006 .

ALZH EIMER ’ S DISEASE AND OTHER

D. Campion, D. Hannequin, A. Brice, 2006 .

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

A. Montpetit, G. Bourque, J. Pariente, 2015, European Journal of Human Genetics.

Efficacy of Exome-Targeted Capture Sequencing to Detect Mutations in Known Cerebellar Ataxia Genes

A. Singleton, M. Vidailhet, A. Durr, 2018, JAMA neurology.

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

R Redon, R. Redon, M. Bihoreau, 2017, Molecular Psychiatry.

Involvement of hyperprolinemia in cognitive and psychiatric features of the 22q11 deletion syndrome.

T. van Amelsvoort, D. Campion, D. Hannequin, 2007, Human molecular genetics.

Index of authors

D. Hannequin, A. Fourcin, 1963, Parasitology.

The CALHM1 P86L polymorphism is a genetic modifier of age at onset in Alzheimer's disease: a meta-analysis study.

P. Bosco, J. Haines, M. Pericak-Vance, 2010, Journal of Alzheimer's disease : JAD.

ABCA7 rare variants and Alzheimer disease risk

R. Redon, G. Bourque, E. Génin, 2016, Neurology.

Identification of partial SLC20A2 deletions in primary brain calcification using whole-exome sequencing

M. Vérin, D. Campion, D. Hannequin, 2016, European Journal of Human Genetics.

SORL1 rare variants: a major risk factor for familial early-onset Alzheimer’s disease

R. Redon, G. Bourque, E. Génin, 2016, Molecular Psychiatry.

[Myasthenic syndrome induced by lithium].

D. Hannequin, P. Auzou, C. Ozsancak, 2000, Presse medicale.

Utility of CSF biomarkers in psychiatric disorders: a national multicentre prospective study

F. Pasquier, P. Robert, F. Bellivier, 2016, Alzheimer's Research & Therapy.

A panel study on patients with dominant cerebellar ataxia highlights the frequency of channelopathies

A. Durr, D. Hannequin, A. Brice, 2017, Brain : a journal of neurology.

Spastic paraplegia due to SPAST mutations is modified by the underlying mutation and sex

S. Tezenas du Montcel, C. Duyckaerts, A. Durr, 2018, Brain : a journal of neurology.

Esophageal Manometry in Patients with Unilateral Hemispheric Cerebrovascular Accidents or Idiopathic Parkinsonism

D. Hannequin, F. Beuret-Blanquart, B. Mihout, 1991 .

Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS

E. Haan, P. Pietrini, R. Petersen, 2017, Scientific Reports.

D. Hernandez, M. Nalls, L. Ferrucci, 2017, bioRxiv.

Biallelic Loss of Function of SORL1 in an Early Onset Alzheimer's Disease Patient.

D. Campion, D. Hannequin, D. Wallon, 2018, Journal of Alzheimer's disease : JAD.

Cardiac conduction alterations in a French family with amyloidosis of the finnish type with the p.Asp187Tyr mutation in the GSN gene

N. Chastan, D. Hannequin, T. Frebourg, 2006, Muscle & nerve.

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

P. Bosco, Y. Kamatani, G. Spalletta, 2012, Molecular Psychiatry.

PNPLA 6 seed analysis in more than 500 exomes of index patients with ataxia , hereditary spastic paraplegia and Charcot – Marie – Tooth disease

T. Strom, S. Züchner, H. Prokisch, 2014 .

PNPLA6 mutations cause Boucher-Neuhauser and Gordon Holmes syndromes as part of a broad neurodegenerative spectrum.

T. Strom, S. Züchner, H. Prokisch, 2014, Brain : a journal of neurology.

Frontotemporal dementia and its subtypes: a genome-wide association study

Alexander Gerhard, Adrian Danek, Luigi Ferrucci, 2014, The Lancet Neurology.

Somatic variants in autosomal dominant genes are a rare cause of sporadic Alzheimer’s disease

A. Hoischen, J. Attems, J. Veltman, 2018, Alzheimer's & Dementia.

Unusual cerebrotendinous xanthomatosis with fronto‐temporal dementia phenotype

D. Campion, D. Hannequin, R. Wevers, 2005, American journal of medical genetics. Part A.

Treatment of anterior communicating artery aneurysms: complementary aspects of microsurgical and endovascular procedures.

D. Hannequin, E. Gerardin, F. Proust, 2003, Journal of neurosurgery.

Amyloid-β protein precursor gene expression in alzheimer's disease and other conditions.

D. Campion, D. Hannequin, S. Bombois, 2012, Journal of Alzheimer's disease : JAD.

Superior interhemispheric approach for midline meningioma from the anterior cranial base.

D. Hannequin, E. Gerardin, S. Derrey, 2011, Neuro-Chirurgie.

Neurosurgeons Involved in the Treatment of Retinoblastoma

D. Hannequin, P. Macpherson, A. Rabinstein, 2010 .

Validation of the superior interhemispheric approach for tuberculum sellae meningioma: clinical article.

Hélène Castel, Didier Hannequin, D. Hannequin, 2012, Journal of neurosurgery.

Is the Saitohin gene involved in neurodegenerative diseases?

B. Dubois, D. Campion, D. Hannequin, 2002, Annals of neurology.

Differential Diagnosis of Dementia with High Levels of Cerebrospinal Fluid Tau Protein.

F. Pasquier, O. Martinaud, J. Laplanche, 2016, Journal of Alzheimer's disease : JAD.

Dementia in middle-aged patients with schizophrenia.

O. Martinaud, D. Campion, D. Hannequin, 2014, Journal of Alzheimer's disease : JAD.

Development of a Model for Study of the Antiedematous Properties of Ginkgo Biloba Extract

D. Hannequin, Y. Vaschalde, A. Thibert, 1988 .

Apolipoprotein E ϵ4 Allele and Familial Aggregation of Alzheimer Disease

Y. Agid, B. Dubois, D. Campion, 1998 .

Evidence for apolipoprotein E epsilon 4 association in early-onset Alzheimer's patients with late-onset relatives.

Y. Agid, A. Delacourte, D. Campion, 1995, American journal of medical genetics.

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

D. Hannequin, D. Maltête, L. Guyant‐Maréchal, 2011, American journal of medical genetics. Part A.

Psychosis revealing familial idiopathic basal ganglia calcification.

D. Hannequin, O. Guillin, R. Lefaucheur, 2013, General hospital psychiatry.

[Stroke and iridodonesis revealing a homocystinuria caused by a compound heterozygous mutation of cystathionine beta-synthase].

D. Hannequin, O. Genevois, R. Lefaucheur, 2008, Revue neurologique.

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

Miguel Ángel Martínez, Y Agid, Y. Agid, 1997, American journal of human genetics.

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

O. Martinaud, D. Campion, D. Hannequin, 2010, British Journal of Psychiatry.

Brain Perfusion in Adult Patients with Acute Myeloblastic Leukemia before and after Cytosine Arabinoside

O. Martinaud, D. Hannequin, R. Modzelewski, 2011, Molecular Imaging and Biology.

[Cortico-basal degeneration].

D. Hannequin, P. Auzou, C. Ozsancak, 1999, Revue neurologique.

Epsilon sarcoglycan mutations and phenotype in French patients with myoclonic syndromes

M. Vidailhet, S. Tezenas du Montcel, J. Houeto, 2005, Journal of Medical Genetics.

Severe myoclonus‐dystonia syndrome associated with a novel epsilon‐sarcoglycan gene truncating mutation

D. Campion, D. Hannequin, T. Frebourg, 2003, American Journal of Medical Genetics Part B: Neuropsychiatric Genetics.

Shared genetic contribution to ischemic stroke and Alzheimer's disease

Nick C Fox, C. Sudlow, J. Gallacher, 2016, Annals of neurology.

[Stress-induced pituitary apoplexy in 2 phases].

D. Hannequin, M. Tadié, F. Proust, 1995, Neuro-Chirurgie.

Long-term follow-up of acute partial transverse myelitis.

P. Vermersch, D. Hannequin, S. Debette, 2012, Archives of neurology.

Anorectal manometric anomalies in seven patients with frontal lobe brain damage

D. Hannequin, J. Weber, T. Delangre, 1990, Digestive Diseases and Sciences.

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

J. Pariente, F. Pasquier, C. Duyckaerts, 2012, Journal of Alzheimer's disease : JAD.

Is the urea cycle involved in Alzheimer's disease?

S. DeKosky, F. Pasquier, J. Hauw, 2010, Journal of Alzheimer's Disease.

Who needs cerebrospinal biomarkers? A national survey in clinical practice.

F. Pasquier, P. Robert, D. Hannequin, 2014, Journal of Alzheimer's disease : JAD.

Impact of cerebro-spinal fluid biomarkers of Alzheimer’s disease in clinical practice: a multicentric study

F. Pasquier, P. Robert, V. Sayette, 2013, Journal of Neurology.

TREM2 R47H variant as a risk factor for early-onset Alzheimer's disease.

D. Campion, D. Hannequin, D. Wallon, 2013, Journal of Alzheimer's disease : JAD.

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

Miguel Ángel Martínez, Y. Agid, B. Dubois, 1996, Journal of medical genetics.

A study of the association between the ADAM12 and SH3PXD2A (SH3MD1) genes and Alzheimer's disease

F. Pasquier, J. Lambert, P. Amouyel, 2010, Neuroscience Letters.

A large pedigree with early-onset Alzheimer's disease

Y. Agid, B. Dubois, J. Mallet, 1995, Neurology.

Just do it! How performing an action enhances remembering in transient global amnesia

Francis Eustache, Béatrice Desgranges, Fausto Viader, 2014, Cortex.

Can We Remember Future Actions yet Forget the Last Two Minutes? Study in Transient Global Amnesia

Francis Eustache, Béatrice Desgranges, Fausto Viader, 2011, Journal of Cognitive Neuroscience.

Apolipoprotein E gene in frontotemporal dementia: an association study and meta-analysis

B. Dubois, D. Campion, D. Hannequin, 2002, European Journal of Human Genetics.

Genetic analysis of inherited leukodystrophies: genotype-phenotype correlations in the CSF1R gene.

Nick C Fox, J. Hardy, M. Rossor, 2013, JAMA neurology.

Lateral Temporal Lobe: An Early Imaging Marker of the Presymptomatic GRN Disease?

Stanley Durrleman, Habib Benali, Olivier Colliot, 2015, Journal of Alzheimer's disease : JAD.

No replication of genetic association between candidate polymorphisms and Alzheimer's disease

E. Génin, C. Dib, D. Campion, 2011, Neurobiology of Aging.

A genome-wide study reveals rare CNVs exclusive to extreme phenotypes of Alzheimer disease

Claire Paquet, Jérémie Pariente, Bernard Croisile, 2011, European Journal of Human Genetics.

Amyloid imaging with AV45 ((18)F-florbetapir) in a cognitively normal AβPP duplication carrier.

F. Chollet, J. Pariente, J. Albucher, 2012, Journal of Alzheimer's disease : JAD.

Association study of the NEDD9 gene with the risk of developing Alzheimer's and Parkinson's disease.

F. Pasquier, J. Lambert, P. Amouyel, 2008, Human molecular genetics.

Association study of the GAB2 gene with the risk of developing Alzheimer's disease

F. Pasquier, J. Lambert, P. Amouyel, 2008, Neurobiology of Disease.

A diagnostic scale for Alzheimer’s disease based on cerebrospinal fluid biomarker profiles

F. Pasquier, S. Lehmann, J. Touchon, 2014, Alzheimer's Research & Therapy.

Measurement of Voice Onset Time in Dysarthric Patients: Methodological Considerations

Didier Hannequin, D. Hannequin, P. Auzou, 2000, Folia Phoniatrica et Logopaedica.

Early verbal fluency decline after STN implantation: Is it a cognitive microlesion effect?

N. Chastan, O. Martinaud, D. Hannequin, 2012, Journal of the Neurological Sciences.

Primary Progressive Aphasia in the Network of French Alzheimer Plan Memory Centers.

F. Pasquier, P. Robert, J. Démonet, 2016, Journal of Alzheimer's disease : JAD.

[Clinical assessment of dysarthria: presentation and validation of a method].

F. Eustache, D. Hannequin, P. Auzou, 1998, Revue neurologique.

Early Onset Dementia: Characteristics in a Large Cohort From Academic Memory Clinics

F. Pasquier, O. Martinaud, D. Hannequin, 2011, Alzheimer disease and associated disorders.

Use of haplotype information to test involvement of the LRP gene in Alzheimer's disease in the French population

Y. Agid, B. Dubois, D. Campion, 2001, European Journal of Human Genetics.

Tangier disease phenotype diversity in dizygous twin sisters.

D. Hannequin, L. Guyant‐Maréchal, R. Bittar, 2010, Revue neurologique.

Atlastin1 mutations are frequent in young-onset autosomal dominant spastic paraplegia.

M. Ruberg, D. Hannequin, A. Dürr, 2004, Archives of neurology.

Phenotype variability in progranulin mutation carriers: a clinical, neuropsychological, imaging and genetic study.

Eric Guedj, Valérie Hahn-Barma, Marie-Odile Habert, 2008, Brain : a journal of neurology.

Valosin-containing protein gene mutations

C. Duyckaerts, D. Campion, D. Hannequin, 2006, Neurology.

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

D. Hannequin, D. Wallon, A. Laquérriere, 2010, Clinical neuropathology.

A non-DM1, non-DM2 multisystem myotonic disorder with frontotemporal dementia: phenotype and suggestive mapping of the DM3 locus to chromosome 15q21-24.

A. Delacourte, C. Duyckaerts, D. Campion, 2004, Brain : a journal of neurology.

A non-DM 1 , non-DM 2 multisystem myotonic disorder with frontotemporal dementia : phenotype and suggestive mapping of the DM 3 locus to chromosome 15 q 21-24

A. Delacourte, C. Duyckaerts, D. Campion, 2004 .

Progranulin null mutations in both sporadic and familial frontotemporal dementia

B. Dubois, C. Duyckaerts, C. van Broeckhoven, 2007, Human mutation.

Association study of the NEDD 9 gene with the risk of developing Alzheimer ’ s and Parkinson ’ s disease

F. Pasquier, J. Lambert, P. Amouyel, 2008 .

Identification of evolutionarily conserved gene networks mediating neurodegenerative dementia.

Nick C Fox, Alan J. Thomas, D. Hernandez, 2018, Nature Medicine.

Quantitative assessment of the evolution of cerebellar signs in spinocerebellar ataxias

A. Durr, D. Hannequin, P. Ribai, 2011, Movement disorders : official journal of the Movement Disorder Society.

Low Prevalence and Clinical Effect of Vascular Risk Factors in Early-Onset Alzheimer’s Disease

B. Dubois, F. Pasquier, F. Lebert, 2017, Journal of Alzheimer's disease : JAD.

A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers

Nick C Fox, Alan J. Thomas, D. Hernandez, 2018, Brain : a journal of neurology.

Penetrance estimation of Alzheimer disease in SORL1 loss-of-function variant carriers using a family-based strategy and stratification by APOE genotypes

Nick C Fox, W. M. van der Flier, A. Uitterlinden, 2022, Genome Medicine.

A novel presenilin 1 mutation resulting in familial Alzheimer's disease with an onset age of 29 years.

Y. Agid, M. Baulac, C. Duyckaerts, 1996, Neuroreport.

How many patients are eligible for disease-modifying treatment in Alzheimer’s disease? A French national observational study over 5 years

B. Dubois, F. Pasquier, P. Robert, 2019, BMJ Open.

Right ventral frontal hypometabolism and abnormal sense of self in a case of disproportionate retrograde amnesia

B. Desgranges, F. Eustache, D. Hannequin, 2005, Cognitive neuropsychology.

Overall mutational spectrum of SLC20A2, PDGFB and PDGFRB in idiopathic basal ganglia calcification

F. Durif, D. Campion, D. Hannequin, 2014, neurogenetics.

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

M. Ruberg, A. Durr, D. Hannequin, 2008, Brain : a journal of neurology.

APP Mutations in Cerebral Amyloid Angiopathy with or without Cortical Calcifications: Report of Three Families and a Literature Review.

M. Frosch, D. Campion, D. Hannequin, 2017, Journal of Alzheimer's disease : JAD.

Evidence of bilateral temporal lobe involvement in primary progressive aphasia: a SPECT study.

D. Hannequin, A. Hitzel, S. Bakchine, 2003, Journal of nuclear medicine : official publication, Society of Nuclear Medicine.

Nucleus Basalis of Meynert Stimulation for Lewy Body Dementia

L. Defebvre, K. Dujardin, M. Welter, 2020, Neurology.

Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment

S. Klebe, C. Duyckaerts, C. van Broeckhoven, 2020, Genetics in Medicine.

Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment

S. Klebe, C. Duyckaerts, C. van Broeckhoven, 2020, Genetics in Medicine.

Midsagittal MR measurements of the corpus callosum in healthy subjects and diseased patients: a prospective survey.

D. Hannequin, J. Laissy, D Hannequin, 1993, AJNR. American journal of neuroradiology.

Dysarthria and orofacial apraxia in corticobasal degeneration

D. Hannequin, P. Auzou, C. Özsancak, 2000, Movement disorders : official journal of the Movement Disorder Society.

Microsubthalamotomy effect at day 3: Screening for determinants

Didier Hannequin, Nathalie Chastan, N. Chastan, 2009, Movement disorders : official journal of the Movement Disorder Society.

Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS

Nick C Fox, D. Hernandez, M. Nalls, 2017, Scientific Reports.

Clinical and neuropathological diversity of tauopathy in MAPT duplication carriers

C. Duyckaerts, M. Sarazin, D. Campion, 2021, Acta Neuropathologica.

Quality of life and brain damage after microsurgical clip occlusion or endovascular coil embolization for ruptured anterior communicating artery aneurysms: neuropsychological assessment.

Olivier Langlois, Olivier Martinaud, Didier Hannequin, 2009, Journal of neurosurgery.

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

Y. Agid, B. Dubois, F. Pasquier, 1997 .

Calculation and number processing in mild Alzheimer's disease.

F. Pasquier, D. Hannequin, A. Agniel, 1995, Journal of clinical and experimental neuropsychology.

Characteristics of familial aggregation in early-onset Alzheimer's disease: evidence of subgroups.

B. Dubois, D. Campion, D. Hannequin, 1995, American journal of medical genetics.

Marchiafava-Bignami disease

D. Hannequin, T. Delangre, E. Clavier, 1986, Neuroradiology.

Does amnesia specifically predict Alzheimer’s pathology? A neuropathological study

B. Dubois, F. Pasquier, F. Lebert, 2020, Neurobiology of Aging.

BRAIN SPECT PERFUSION OF FRONTOTEMPORAL DEMENTIA ASSOCIATED WITH MOTOR NEURON DISEASE

B. Dubois, V. Meininger, F. Salachas, 2007, Neurology.

Partial deletion of the MAPT gene: A novel mechanism of FTDP‐17

D. Campion, D. Hannequin, A. Brice, 2009, Human mutation.

Exploring the diagnosis delay and ALS functional impairment at diagnosis as relevant criteria for clinical trial enrolment*

F. Viader, D. Hannequin, P. Preux, 2017, Amyotrophic lateral sclerosis & frontotemporal degeneration.

Factors influencing the age at onset in familial frontotemporal lobar dementia

J. Pariente, E. Génin, F. Pasquier, 2017, Neurology: Genetics.

A risk for early-onset Alzheimer's disease associated with the APBB1 gene (FE65) intron 13 polymorphism

Jean-François Deleuze, Bruno Dubois, Didier Hannequin, 2003, Neuroscience Letters.

What is the clinical impact of cerebrospinal fluid biomarkers on final diagnosis and management in patients with mild cognitive impairment in clinical practice? Results from a nation-wide prospective survey in France

F. Pasquier, P. Robert, V. de la Sayette, 2019, BMJ Open.

NEUROMYELITIS OPTICA WITH VERY LATE ONSET

D. Hannequin, P. Ahtoy, D. Maltête, 2011, Journal of the American Geriatrics Society.

Clozapine in Parkinson's disease

D. Hannequin, P. Auzou, N. Moore, 1995, The Lancet.

PET Correlate With AD PSEN1 Original Phenotype

F. Chollet, J. Pariente, E. Barbeau, 2013 .

MR, (18)F-FDG, and (18)F-AV45 PET correlate with AD PSEN1 original phenotype.

F. Chollet, J. Pariente, E. Barbeau, 2013, Alzheimer disease and associated disorders.

No e V ect of the á 1-antichymotrypsin A allele in Alzheimer ’ s disease

Y. Agid, B. Dubois, F. Pasquier, 1998 .

Phenotype and imaging features associated with APP duplications

J. Pariente, C. Duyckaerts, D. Campion, 2023, Alzheimer's Research & Therapy.

APOE promoter polymorphisms do not confer independent risk for Alzheimer's disease in a French population

D. Campion, D. Hannequin, A. Brice, 2000, European Journal of Human Genetics.

Cognitive impairment after cerebral venous thrombosis: a two-center study

O. Martinaud, D. Hannequin, D. Wallon, 2013, Journal of Neurology.

Systematic analysis of candidate genes for Alzheimer's disease in a French, genome-wide association study.

S. Heath, F. Pasquier, J. Dartigues, 2010, Journal of Alzheimer's disease : JAD.

Alleviation of off-period dystonia in Parkinson disease by a microlesion following subthalamic implantation.

N. Chastan, D. Hannequin, D. Maltête, 2010, Journal of neurosurgery.

Common variants at ABCA 7 , MS 4 A 6 A / MS 4 A 4 E , EPHA 1 , CD 33 and CD 2 AP are associated with Alzheimer ’ s disease

Nick C Fox, John X. Morris, Thomas W. Mühleisen, 2011 .

CXCR4 involvement in neurodegenerative diseases

O. Andreassen, G. Schellenberg, A. Dale, 2017, bioRxiv.

[Speech therapy of dysarthria in Parkinson's disease].

D. Hannequin, P. Auzou, C. Ozsancak, 2003, Presse medicale.

Diversity of patterns of improvement in confrontation naming rehabilitation: some tentative hypotheses.

G Deloche, M. Metz-Lutz, D. Hannequin, 1997, Journal of communication disorders.

[Semiology of language].

Olivier Martinaud, Didier Hannequin, O. Martinaud, 2003, La Revue du praticien.

[EEG recordings during episodes of palinacousis and palinopsia].

D. Hannequin, P. Auzou, D. Parain, 1997, Revue neurologique.

[Palinacousis with hemianacusia caused by left temporal lesion].

D. Hannequin, P. Auzou, P. Augustin, 1995, Revue neurologique.

Relevant Category-Specific Effect on Naming in Alzheimer’s Disease

O. Martinaud, D. Hannequin, G. Opolczynski, 2009, Dementia and Geriatric Cognitive Disorders.

Apolipoprotein E (cid:101) 4 Allele and Familial Aggregation of Alzheimer Disease

Y. Agid, B. Dubois, D. Campion, 2000 .

Microsubthalamotomy: An immediate predictor of long‐term subthalamic stimulation efficacy in Parkinson disease

Didier Hannequin, Nathalie Chastan, N. Chastan, 2008, Movement disorders : official journal of the Movement Disorder Society.

[Alzheimer's disease cerebro-spinal fluid biomarkers: A clinical research tool sometimes useful in daily clinical practice of memory clinics for the diagnosis of complex cases].

F. Pasquier, S. Lehmann, J. Laplanche, 2017, La Revue de medecine interne.

Detailed neuropsychological evaluation in a patient with Floating Harbor syndrome

D. Hannequin, V. Cormier-Daire, A. Goldenberg, 2012, Journal of clinical and experimental neuropsychology.

A Diagnosis of Idiopathic Basal Ganglia Calcification in an 82‐Year‐Old Man

O. Martinaud, D. Campion, D. Hannequin, 2013, Journal of the American Geriatrics Society.

Study of thyroid hormone receptor alpha gene polymorphisms on Alzheimer's disease

F. Pasquier, J. Lambert, P. Amouyel, 2011, Neurobiology of Aging.

Genetic variation across RNA metabolism and cell death gene networks is implicated in the semantic variant of primary progressive aphasia

P. Pietrini, R. Desikan, J. Trojanowski, 2019, Scientific Reports.

Is the ornithine transcarbamylase gene a genetic determinant of Alzheimer’s disease?

F. Pasquier, J. Lambert, P. Amouyel, 2009, Neuroscience Letters.

Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

Genetic, Nick C Fox, Michelle K. Lupton, 2019, Nature Genetics.

Impaired functional differentiation for categories of objects in the ventral visual stream: A case of developmental visual impairment

F. Ramus, L. Cohen, G. Dehaene-Lambertz, 2015, Neuropsychologia.

Can We Remember Future Actions yet Forget the Last Two Minutes? Study in Transient Global Amnesia

O. Martinaud, B. Desgranges, F. Viader, 2011, Journal of Cognitive Neuroscience.

Written sentence comprehension and agrammatism: Diversity of deficits and strategies

Jean-Luc Nespoulous, Gérard Deloche, Didier Hannequin, 1989, Journal of Neurolinguistics.

Extensive white matter involvement in patients with frontotemporal lobar degeneration: think progranulin.

L. Naccache, O. Colliot, F. Lamari, 2014, JAMA neurology.

Deletion of the progranulin gene in patients with frontotemporal lobar degeneration or Parkinson disease

F. Pasquier, J. Lambert, D. Campion, 2008, Neurobiology of Disease.

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

A. Durr, P. Convers, M. Koenig, 2015, Annals of neurology.

Relations between C9orf72 expansion size in blood, age at onset, age at collection and transmission across generations in patients and presymptomatic carriers

S. Lehéricy, B. Dubois, J. Pariente, 2019, Neurobiology of Aging.

Age and Sex

Miguel Ángel Martínez, D. Campion, D. Hannequin, 2006 .

PHASE 2A RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED TRIAL OF THE HISTONE DEACETYLASE INHIBITOR (HDACI), FRM-0334, IN ASYMPTOMATIC CARRIERS OF, OR PATIENTS WITH FRONTOTEMPORAL LOBAR DEGENERATION (FTLD) DUE TO, PROGRANULIN GENE MUTATIONS

G. Frisoni, B. Boeve, F. Pasquier, 2019, Alzheimer's & Dementia.

The effects of age, educational background and sex on confrontation naming in normals; principles for testing naming ability

Dominique Cardebat, Gérard Deloche, I. Ferrand, 1991 .

Is the urea cycle involved in Alzheimer's disease?

S. DeKosky, D. Mann, P. Amouyel, 2010, Journal of Alzheimer's disease : JAD.

[Saccadic latencies and unilateral spatial neglect caused by parietal lesions].

D. Hannequin, P. Auzou, P. Augustin, 1996, Revue neurologique.