Scientific publications - Institut du Cerveau

All publications can be found on NCBI – Pubmed

2018

ADAMSEN, D et al.	Autism spectrum disorder associated with low serotonin in CSF and mutations in the SLC29A4 plasma membrane monoamine transporter (PMAT) gene	Mol. Autism
AGUIAR, AS et al.	Effects of exercise on mitochondrial function, neuroplasticity and anxio-depressive behavior of mice	Neuroscience
AGUIAR, AS et al.	Six Weeks of Voluntary Exercise don”t Protect C57BL/6 Mice Against Neurotoxicity of MPTP and MPP+	Neurotox. Res.
ALCACER, C et al.	Mitogen- and stress-activated protein kinase 1 is required for specific signaling responses in dopamine-denervated mouse striatum, but is not necessary for L-DOPA-induced dyskinesia	Neurosci. Lett.
ALENTORN, A et al.	Clinical value of chromosome arms 19q and 11p losses in low-grade gliomas	Neuro-Oncology
ALLARD, J et al.	Immunohistochemical toolkit for tracking and quantifying xenotransplanted human stem cells	Regen. Med.
ALLENBACH, Y et al.	Anti-HMGCR Autoantibodies in European Patients With Autoimmune Necrotizing Myopathies Inconstant Exposure to Statin	Medicine (Baltimore)
ALLENBACH, Y et al.	Th1 Response and Systemic Treg Deficiency in Inclusion Body Myositis	PLoS One
ALONSO, I et al.	Hippocampal sclerosis affects fMR-adaptation of lyric and melodies in songs	Front. Hum. Neurosci.
AL-SARRAJ, S et al.	Mitochondrial abnormalities and low grade inflammation are present in the skeletal muscle of a minority of patients with amyotrophic lateral sclerosis; an observational myopathology study	Acta Neuropathol. Commun.
ALTWEGG-BOUSSAC, T et al.	Excitability and responsiveness of rat barrel cortex neurons in the presence and absence of spontaneous synaptic activity in vivo	J. Physiol.-London
ALVARADO-ROJAS, C et al.	Slow modulations of high-frequency activity (40-140 Hz) discriminate preictal changes in human focal epilepsy	Sci Rep
ALVES, S et al.	The autophagy/lysosome pathway is impaired in SCA7 patients and SCA7 knock-in mice	Acta Neuropathol.
AMEQRANE, I et al.	Implicit and Explicit Timing in Oculomotor Control	PLoS One
ANDO, K et al.	Vaccination with Sarkosyl Insoluble PHF-Tau Decrease Neurofibrillary Tangles Formation in Aged Tau Transgenic Mouse Model: A Pilot Study	J. Alzheimers Dis.
ANDRE-OBADIA, N et al.	French Guidelines on electroencephalogram	Neurophysiol. Clin.-Clin. Neurophysiol.
APPENZELLER, S et al.	De Novo Mutations in Synaptic Transmission Genes Including DNM1 Cause Epileptic Encephalopathies	Am. J. Hum. Genet.
ARNULF, I et al.	Will students pass a competitive exam that they failed in their dreams?	Conscious. Cogn.
ARNULF, I et al.	A Scale for Assessing the Severity of Arousal Disorders	Sleep
ASSOUAD, R et al.	Clinical and MRI characterization of MS patients with a pure and severe cognitive onset	Clin. Neurol. Neurosurg.
ASSOULINE, A et al.	Radiation Therapy for Hypersalivation: A Prospective Study in 50 Amyotrophic Lateral Sclerosis Patients	Int. J. Radiat. Oncol. Biol. Phys.
AUBART, M et al.	Early-Onset Osteoarthritis, Charcot-Marie-Tooth Like Neuropathy, Autoimmune Features, Multiple Arterial Aneurysms and Dissections: An Unrecognized and Life Threatening Condition	PLoS One
AVILA, CL et al.	Structural Characterization of Heparin-induced Glyceraldehyde-3-phosphate Dehydrogenase Protofibrils Preventing alpha- Synuclein Oligomeric Species Toxicity	J. Biol. Chem.
AZUAR, C et al.	Testing the model of caudo-rostral organization of cognitive control in the human with frontal lesions	Neuroimage
BACHINSKI, LL et al.	Most expression and splicing changes in myotonic dystrophy type 1 and type 2 skeletal muscle are shared with other muscular dystrophies	Neuromusc. Disord.
BAHI-BUISSON, N et al.	The wide spectrum of tubulinopathies: what are the key features for the diagnosis?	Brain
BAIER, CJ et al.	Intrastriatal 6-OHDA Lesion Differentially Affects Dopaminergic Neurons in the Ventral Tegmental Area of Prenatally Stressed Rats	Neurotox. Res.
BAIZABAL-CARVALLO, JF et al.	Clinical Deterioration Following Middle Cerebral Artery Hemodynamic Changes after Intravenous Thrombolysis for Acute Ischemic Stroke	J. Stroke Cerebrovasc. Dis.
BANNWARTH, S et al.	A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvement	Brain
BARALLOBRE, MJ et al.	DYRK1A promotes dopaminergic neuron survival in the developing brain and in a mouse model of Parkinson”s disease	Cell Death Dis.
BARTOLOMEO, P et al.	The anatomy of cerebral achromatopsia: A reappraisal and comparison of two case reports	Cortex
BARTON, BR et al.	Comparison of the Movement Disorder Society Parkinson”s Disease Dementia Criteria With Neuropsychological Testing	Mov. Disord.
BATAIL, JM et al.	Use of very-high-dose olanzapine in treatment-resistant schizophrenia	Schizophr. Res.
BAULAC, M et al.	Long-term safety and efficacy of zonisamide versus carbamazepine monotherapy for treatment of partial seizures in adults with newly diagnosed epilepsy: Results of a phase III, randomized, double-blind study	Epilepsia
BAULAC, S et al.	Role of the phosphoinositide phosphatase FIG4 gene in familial epilepsy with polymicrogyria	Neurology
BAUMANN, CR et al.	Challenges in Diagnosing Narcolepsy without Cataplexy: A Consensus Statement	Sleep
BEILINA, A et al.	Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease.	Proc. Natl. Acad. Sci. U.S.A.
BELAID, H et al.	Sleep Disorders in Parkinsonian Macaques: Effects of L-Dopa Treatment and Pedunculopontine Nucleus Lesion	J. Neurosci.
BELL, J et al.	Towards a Polya-Carlson dichotomy for algebraic dynamics	Indag. Math.-New Ser.
BENZ-DE BRETAGNE, I et al.	Urinary coproporphyrin I/(I plus III) ratio as a surrogate for MRP2 or other transporter activities involved in methotrexate clearance	Br. J. Clin. Pharmacol.
BERG, D et al.	Time to redefine PD? Introductory statement of the MDS Task Force on the definition of Parkinson”s disease	Mov. Disord.
BERRIH-AKNIN, S et al.	Diagnostic and clinical classification of autoimmune myasthenia gravis	J. Autoimmun.
BERTOUX, M et al.	Behavioral variant frontotemporal dementia patients do not succumb to the Allais paradox	Front. Neurosci.
BERTOUX, M et al.	Two Distinct Amnesic Profiles in Behavioral Variant Frontotemporal Dementia	Biol. Psychiatry
BERTOUX, M et al.	Neural correlates of the mini-SEA (Social cognition and Emotional Assessment) in behavioral variant frontotemporal dementia	Brain Imaging Behav.
BESSON, P et al.	Structural connectivity differences in left and right temporal lobe epilepsy	Neuroimage
BISSERIEX, H et al.	Sexual Dysfunction Management and Expectations Assessment in Multiple Sclerosis-Female (SEA-MS-F): creation and validation of a specific questionnaire.	J Sex Med
BIZEC, CL et al.	No Mutation in the SLC2A3 Gene in Cohorts of GLUT1 Deficiency Syndrome-Like Patients Negative for SLC2A1 and in Patients with AHC Negative for ATP1A3.	JIMD Rep
BLASCO, H et al.	What are the applications of biomarkers in ALS today?	Presse Med.
BLASCO, H et al.	Untargeted 1H-NMR metabolomics in CSF	Neurology
BLETON, JP et al.	Impaired Force Control in Writer”s Cramp Showing a Bilateral Deficit in Sensorimotor Integration	Mov. Disord.
BOCCARDI, M et al.	Establishing magnetic resonance images orientation for the EADC-ADNI manual hippocampal segmentation protocol.	J Neuroimaging
BOHM, J et al.	Clinical, histological and genetic characterisation of patients with tubular aggregate myopathy caused by mutations in STIM1	J. Med. Genet.
BOHM, J et al.	Adult-onset autosomal dominant centronuclear myopathy due to BIN1 mutations	Brain
BOILLOT, M et al.	Glutamatergic neuron-targeted loss of LGI1 epilepsy gene results in seizures	Brain
BONNET, C et al.	Eye Movements in Ephedrone-Induced Parkinsonism	PLoS One
BOTTHALI, F et al.	Anatomical Connections of the Visual Word Form Area	J. Neurosci.
BOUAFIA, A et al.	Axonal expression of sodium channels and neuropathology of the plaques in multiple sclerosis	Neuropathol. Appl. Neurobiol.
BOURLON, C et al.	Dual-tasking postural control in patients with right brain damage	Gait Posture
BOUTET, C et al.	Detection of volume loss in hippocampal layers in Alzheimer”s disease using 7 T MRI: A feasibility study	NeuroImage-Clin.
BOXER, AL et al.	Davunetide in patients with progressive supranuclear palsy: a randomised, double-blind, placebo-controlled phase 2/3 trial	Lancet Neurol.
BRANZOLI, F et al.	The interaction between apparent diffusion coefficients and transverse relaxation rates of human brain metabolites and water studied by diffusion- weighted spectroscopy at 7 T	NMR Biomed.
BRUNELIN, J et al.	The efficacy and safety of low frequency repetitive transcranial magnetic stimulation for treatment-resistant depression: the results from a large multicenter French RCT.	Brain Stimul
BRUNO, A et al.	Mutational analysis of primary central nervous system lymphoma	Oncotarget
BUHLMAN, L et al.	Functional interplay between Parkin and Drp1 in mitochondrial fission and clearance	Biochim. Biophys. Acta-Mol. Cell Res.
BUI, LC et al.	A high-performance liquid chromatography assay for Dyrk1a, a Down syndrome-associated kinase	Anal. Biochem.
CANAUD, G et al.	Inhibition of the mTORC Pathway in the Antiphospholipid Syndrome	N. Engl. J. Med.
CANO, SJ et al.	RASCH ANALYSIS OF CLINICAL OUTCOME MEASURES IN SPINAL MUSCULAR ATROPHY	Muscle Nerve
CAROPPO, P et al.	Extensive White Matter Involvement in Patients With Frontotemporal Lobar Degeneration Think Progranulin	JAMA Neurol.
CAROPPO, P et al.	DCTN1 Mutation Analysis in Families With Progressive Supranuclear Palsy-Like Phenotypes	JAMA Neurol.
CARVILL, GL et al.	GABRA1 and STXBP1: Novel genetic causes of Dravet syndrome	Neurology
CASTAGNETO-GISSEY, G et al.	Dynamic Granger-causal networks of electricity spot prices: A novel approach to market integration	Energy Econ.
CATTEAU, A et al.	A new sensitive PCR assay for one-step detection of 12 IDH1/2 mutations in glioma	Acta Neuropathol. Commun.
CAVEDO, E et al.	The Road Ahead to Cure Alzheimer’s Disease: Development of Biological Markers and Neuroimaging Methods for Prevention Trials Across all Stages and Target Populations.	J Prev Alzheimers Dis
CECCOM, J et al.	Reduced sphingosine kinase-1 and enhanced sphingosine 1-phosphate lyase expression demonstrate deregulated sphingosine 1-phosphate signaling in Alzheimer”s disease	Acta Neuropathol. Commun.
CHAUSSENOT, A et al.	Screening of CHCHD10 in a French cohort confirms the involvement of this gene in frontotemporal dementia with amyotrophic lateral sclerosis patients	Neurobiol. Aging
CHICA, AB et al.	Causal Contributions of the Left Frontal Eye Field to Conscious Perception	Cereb. Cortex
CHINOT, OL et al.	Bevacizumab plus Radiotherapy-Temozolomide for Newly Diagnosed Glioblastoma	N. Engl. J. Med.
CHUNG, SJ et al.	Alpha-Synuclein Repeat Variants and Survival in Parkinson”s Disease	Mov. Disord.
CLOT, F et al.	Partial deletions of the GRN gene are a cause of frontotemporal lobar degeneration	Neurogenetics
COBO-CALVO, A et al.	Etiologic Spectrum and Prognosis of Longitudinally Extensive Transverse Myelopathies	Eur. Neurol.
COEZ, A et al.	Brain voice processing with bilateral cochlear implants: a positron emission tomography study	Eur. Arch. Oto-Rhino-Laryn.
COHEN, M et al.	Switching From Natalizumab to Fingolimod in Multiple Sclerosis A French Prospective Study	JAMA Neurol.
COLLONGUES, N et al.	Characterization of neuromyelitis optica and neuromyelitis optica spectrum disorder patients with a late onset	Mult. Scler. J.
CORVOL, JC et al.	Behavioral addictions in Parkinson”s disease	Bull. Acad. Natl. Med.
COSENTINO, S et al.	Social cognition in Alzheimer”s disease: A separate construct contributing to dependence	Alzheimers. Dement.
CRISTANCHO-LACROIX, V et al.	A web-based program for informal caregivers of persons with Alzheimer’s disease: an iterative user-centered design.	JMIR Res Protoc
DAI, DL et al.	Liver disease in infancy caused by oxysterol 7 alpha-hydroxylase deficiency: successful treatment with chenodeoxycholic acid	J. Inherit. Metab. Dis.
DAMIANO, M et al.	Tissue- and Cell-Specific Mitochondrial Defect in Parkin-Deficient Mice	PLoS One
DAMOTTE, V et al.	A gene pathway analysis highlights the role of cellular adhesion molecules in multiple sclerosis susceptibility	Genes Immun.
DAOUD, H et al.	C9orf72 Repeat Expansions in Rapid Eye Movement Sleep Behaviour Disorder	Can. J. Neurol. Sci.
DAUNIZEAU, J et al.	VBA: A Probabilistic Treatment of Nonlinear Models for Neurobiological and Behavioural Data	PLoS Comput. Biol.
DAUPHINOT, L et al.	TRANSCRIPTOMIC APPROACH TO LESCH-NYHAN DISEASE	Nucleosides Nucleotides Nucleic Acids
DE LA TORRE, R et al.	Epigallocatechin-3-gallate, a DYRK1A inhibitor, rescues cognitive deficits in Down syndrome mouse models and in humans.	Mol Nutr Food Res
DE LAVAL, B et al.	Thrombopoietin promotes NHEJ DNA repair in hematopoietic stem cells through specific activation of Erk and NF-kappa B pathways and their target, IEX-1	Blood
DE SOUZA, LC et al.	Frontal lobe neurology and the creative mind	Front. Psychol.
DEBAS, K et al.	Off-line consolidation of motor sequence learning results in greater integration within a cortico-striatal functional network	Neuroimage
DEBETTE, S et al.	Familial occurrence and heritable connective tissue disorders in cervical artery dissection	Neurology
DEGOS, B et al.	POLG mutations associated with remitting/relapsing neurological events	J. Clin. Neurosci.
DEIVA, K et al.	Sudden and isolated Broca”s aphasia: A new clinical phenotype of anti NMDA receptor antibodies encephalitis in children	Eur. J. Paediatr. Neurol.
DEL GIUDICE, E et al.	CNS involvement in OFD1 syndrome: a clinical, molecular, and neuroimaging study	Orphanet J. Rare Dis.
DEL ZOMPO, M et al.	Association study in three different populations between the GPR88 gene and major psychoses.	Mol Genet Genomic Med
DEL-BEL, E et al.	Counteraction by Nitric Oxide Synthase Inhibitor of Neurochemical Alterations of Dopaminergic System in 6-OHDA-Lesioned Rats Under L-DOPA Treatment	Neurotox. Res.
DELPLANQUE, J et al.	TMEM240 mutations cause spinocerebellar ataxia 21 with mental retardation and severe cognitive impairment	Brain
DEMAIN, A et al.	High-level gait and balance disorders in the elderly: a midbrain disease?	J. Neurol.
DESAMERICQ, G et al.	Effectiveness of Anti-Psychotics and Related Drugs in the Huntington French-Speaking Group Cohort	PLoS One
DESMAZIERES, A et al.	Differential Stability of PNS and CNS Nodal Complexes When Neuronal Neurofascin Is Lost	J. Neurosci.
DEVAINE, M et al.	The Social Bayesian Brain: Does Mentalizing Make a Difference When We Learn?	PLoS Comput. Biol.
DEVAINE, M et al.	Theory of Mind: Did Evolution Fool Us?	PLoS One
DEVIC, P et al.	Antibodies to clustered acetylcholine receptor: expanding the phenotype	Eur. J. Neurol.
DEVOS, D et al.	Targeting Chelatable Iron as a Therapeutic Modality in Parkinson”s Disease	Antioxid. Redox Signal.
DEVOS, D et al.	Dopa-decarboxylase gene polymorphisms affect the motor response to L-dopa in Parkinson”s disease	Parkinsonism Relat. Disord.
DI GREGORIO, E et al.	ELOVLS Mutations Cause Spinocerebellar Ataxia 38	Am. J. Hum. Genet.
DIACONESCU, AO et al.	Inferring on the Intentions of Others by Hierarchical Bayesian Learning	PLoS Comput. Biol.
DIEKSTRA, FP et al.	C9orf72 and UNC13A Are Shared Risk Loci for Amyotrophic Lateral Sclerosis and Frontotemporal Dementia: A Genome-Wide Meta-Analysis	Ann. Neurol.
DINKEL, J et al.	Long-Term White Matter Changes after Severe Traumatic Brain Injury: A 5-Year Prospective	Am. J. Neuroradiol.
DJAAFRI, I et al.	A novel tumor suppressor function of Kindlin-3 in solid cancer	Oncotarget
DJEMIE, T et al.	PRRT2 mutations: exploring the phenotypical boundaries	J. Neurol. Neurosurg. Psychiatry
DJENOUNE, L et al.	Investigation of spinal cerebrospinal fluid-contacting neurons expressing PKD2L1 evidence for a conserved system from fish to primates	Front. Neuroanat.
DOGAN, SA et al.	Tissue-Specific Loss of DARS2 Activates Stress Responses Independently of Respiratory Chain Deficiency in the Heart	Cell Metab.
DONDAINE, T et al.	Biases in facial and vocal emotion recognition in chronic schizophrenia	Front. Psychol.
DONG, J et al.	Susceptibility loci for pigmentation and melanoma in relation to Parkinson’s disease.	Neurobiol. Aging
DOR, T et al.	KIF1C mutations in two families with hereditary spastic paraparesis and cerebellar dysfunction	J. Med. Genet.
DORBOZ, I et al.	Severe dystonia, cerebellar atrophy, and cardiomyopathy likely caused by a missense mutation in TOR1AIP1	Orphanet J. Rare Dis.
DOSSI, E et al.	Multi-electrode Array Recordings of Human Epileptic Postoperative Cortical Tissue	J. Vis. Exp.
DROUOT, L et al.	Exploring necrotizing autoimmune myopathies with a novel immunoassay for anti-3-hydroxy-3-methyl-glutaryl-CoA reductase autoantibodies	Arthritis Res. Ther.
DU MONTCEL, ST et al.	Modulation of the age at onset in spinocerebellar ataxia by CAG tracts in various genes	Brain
DU MONTCEL, ST et al.	Prediction of the age at onset in spinocerebellar ataxia type 1, 2, 3 and 6	J. Med. Genet.
DUBAL, S et al.	A PSYCHOPHYSICAL EXPLORATION OF THE PERCEPTION OF EMOTION FROM ABSTRACT ART	Empir. Stud. Arts
DUCRAY, F et al.	Seronegative paraneoplastic cerebellar degeneration: the PNS Euronetwork experience	Eur. J. Neurol.
DUITS, FH et al.	The cerebrospinal fluid \”Alzheimer profile\”: Easily said, but what does it mean?	Alzheimers. Dement.
DUMONT, M et al.	PGC-1 alpha overexpression exacerbates beta-amyloid and tau deposition in a transgenic mouse model of Alzheimer”s disease	Faseb J.
DUMONT, M et al.	[The development and benefits of working together in geriatric short stay units].	Soins Gerontol
DURRLEMAN, S et al.	Morphometry of anatomical shape complexes with dense deformations and sparse parameters	Neuroimage
ECHANIZ-LAGUNA, A et al.	Phenotypic spectrum and incidence of TRPV4 mutations in patients with inherited axonal neuropathy	Neurology
EL HALLANI, S et al.	Tumor and Endothelial Cell Hybrids Participate in Glioblastoma Vasculature	Biomed Res. Int.
EL MENDILI, MM et al.	Multi-Parametric Spinal Cord MRI as Potential Progression Marker in Amyotrophic Lateral Sclerosis	PLoS One
EL-BEHI, M et al.	Committed Tc17 cells are phenotypically and functionally resistant to the effects of IL-27	Eur. J. Immunol.
ESCOTT-PRICE, V et al.	Gene-Wide Analysis Detects Two New Susceptibility Genes for Alzheimer”s Disease	PLoS One
ESHAGHI, A et al.	Temporal and spatial evolution of grey matter atrophy in primary progressive multiple sclerosis	Neuroimage
ESTEVES, T et al.	Loss of Association of REEP2 with Membranes Leads to Hereditary Spastic Paraplegia	Am. J. Hum. Genet.
ETCHEVERRY, A et al.	DGKI Methylation Status Modulates the Prognostic Value of MGMT in Glioblastoma Patients Treated with Combined Radio-Chemotherapy with Temozolomide	PLoS One
EUGENE, E et al.	An organotypic brain slice preparation from adult patients with temporal lobe epilepsy	J. Neurosci. Methods
EVILA, A et al.	Atypical phenotypes in titinopathies explained by second titin mutations	Ann. Neurol.
EYMARD, B et al.	Congenital myasthenic syndromes ; French experience	Bull. Acad. Natl. Med.
EYMARD, B et al.	Myasthenia, from the internist”s point of view	Rev. Med. Interne
FACCHINETTI, P et al.	SET translocation is associated with increase in caspase cleaved amyloid precursor protein in CA1 of Alzheimer and Down syndrome patients	Neurobiol. Aging
FAHED, R et al.	Just a drop of cement: a case of cervical spine bone aneurysmal cyst successfully treated by percutaneous injection of a small amount of polymethyl-methacrylate cement.	BMJ Case Rep
FALLANI, FDV et al.	Nonparametric resampling of random walks for spectral network clustering	Phys. Rev. E
FERINI-STRAMBI, L et al.	Autonomic symptoms in idiopathic REM behavior disorder: a multicentre case-control study	J. Neurol.
FERRARI, R et al.	Frontotemporal dementia and its subtypes: a genome-wide association study	Lancet Neurol.
FERRY, A et al.	Advances in the understanding of skeletal muscle weakness in murine models of diseases affecting nerve-evoked muscle activity, motor neurons, synapses and myofibers	Neuromusc. Disord.
FIGARELLA-BRANGER, D et al.	Mitotic index, microvascular proliferation, and necrosis define 3 groups of 1p/19q codeleted anaplastic oligodendrogliomas associated with different genomic alterations	Neuro-Oncology
FISHBAUGH, J et al.	GEODESIC REGRESSION OF IMAGE AND SHAPE DATA FOR IMPROVED MODELING OF 4D TRAJECTORIES.	Proc IEEE Int Symp Biomed Imaging
FOGEL, SM et al.	fMRI and Sleep Correlates of the Age-Related Impairment in Motor Memory Consolidation	Hum. Brain Mapp.
FOGH, I et al.	A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis	Hum. Mol. Genet.
FONOV, VS et al.	Framework for integrated MRI average of the spinal cord white and gray matter: The MNI-Poly-AMU template	Neuroimage
FONTAINE, B et al.	Emergence of band-pass filtering through adaptive spiking in the owl”s cochlear nucleus	J. Neurophysiol.
FONTAINE, B et al.	Spike-Threshold Adaptation Predicted by Membrane Potential Dynamics In Vivo	PLoS Comput. Biol.
FORKEL, SJ et al.	Anatomical predictors of aphasia recovery: a tractography study of bilateral perisylvian language networks	Brain
FORKEL, SJ et al.	The anatomy of fronto-occipital connections from early blunt dissections to contemporary tractography	Cortex
FOURNIER, E et al.	Channels: a new way to revisit pathology	Bull. Acad. Natl. Med.
FRAIDAKIS, MJ et al.	Phenotypic diversity associated with the MT-TV gene m.1644G > A mutation, a matter of quantity	Mitochondrion
FRAUSCHER, B et al.	Comorbidity and medication in REM sleep behavior disorder A multicenter case-control study	Neurology
FRETON, M et al.	The dark side of self-focus: brain activity during self-focus in low and high brooders	Soc. Cogn. Affect. Neurosci.
FRETON, M et al.	The eye of the self: precuneus volume and visual perspective during autobiographical memory retrieval	Brain Struct. Funct.
FRIED, PJ et al.	Causal evidence supporting functional dissociation of verbal and spatial working memory in the human dorsolateral prefrontal cortex	Eur. J. Neurosci.
FURBY, A et al.	Heterozygous CLCN1 mutations can modulate phenotype in sodium channel myotonia	Neuromusc. Disord.
GALLAGHER, MD et al.	TMEM106B is a genetic modifier of frontotemporal lobar degeneration with C9orf72 hexanucleotide repeat expansions	Acta Neuropathol.
GARGIULO, M et al.	Anticipating disability. The psychological risks of genetic testing	Esprit
GASNAULT, J et al.	Efficacy of recombinant human interleukin 7 in a patient with severe lymphopenia-related progressive multifocal leukoencephalopathy.	Open Forum Infect Dis
GAUDIN, M et al.	Ultra performance liquid chromatography – mass spectrometry studies of formalin-induced alterations of human brain lipidome	J. Mass Spectrom.
GERI, G et al.	Central nervous system angiitis: a series of 31 patients	Clin. Rheumatol.
GHOSHAL, A et al.	Unilateral whisker trimming in newborn rats alters neuronal coincident discharge among mature barrel cortex neurons	J. Neurophysiol.
GILLET, E et al.	TP53 and p53 statuses and their clinical impact in diffuse low grade gliomas	J. Neuro-Oncol.
GOETZ, JG et al.	Endothelial Cilia Mediate Low Flow Sensing during Zebrafish Vascular Development	Cell Reports
GORIS, A et al.	No evidence for shared genetic basis of common variants in multiple sclerosis and amyotrophic lateral sclerosis	Hum. Mol. Genet.
GRIMALDI-BENSOUDA, L et al.	Autoimmune disorders and quadrivalent human papillomavirus vaccination of young female subjects	J. Intern. Med.
GU, Y et al.	Change in Body Mass Index Before and After Alzheimer”s Disease Onset	Curr. Alzheimer Res.
GUIBAL, P et al.	Simultaneous Determination of All Forms of Biopterin and Neopterin in Cerebrospinal Fluid	ACS Chem. Neurosci.
HABETS, EJJ et al.	Health-related quality of life and cognitive functioning in longterm anaplastic oligodendroglioma and oligoastrocytoma survivors	J. Neuro-Oncol.
HAIK, S et al.	Doxycycline in Creutzfeldt-Jakob disease: a phase 2, randomised, double-blind, placebo-controlled trial	Lancet Neurol.
HALLIEZ, S et al.	Accelerated, Spleen-Based Titration of Variant Creutzfeldt-Jakob Disease Infectivity in Transgenic Mice Expressing Human Prion Protein with Sensitivity Comparable to That of Survival Time Bioassay	J. Virol.
HAMMOND, TR et al.	Astrocyte-Derived Endothelin-1 Inhibits Remyelination through Notch Activation	Neuron
HANNAOUI, S et al.	Cycline Efficacy on the Propagation of Human Prions in Primary Cultured Neurons is Strain-Specific	J. Infect. Dis.
HECKMAN, MG et al.	Protective effect of LRRK2 p.R1398H on risk of Parkinson’s disease is independent of MAPT and SNCA variants.	Neurobiol. Aging
HERON, D et al.	GIS modelling in support of earthquake-induced rockfall and cliff collapse risk assessment in the Port Hills, Christchurch	J. Spat. Sci.
HOANG-XUAN, K et al.	[Brain metastases: first, don’t give up!].	Rev Prat
HORELLOU, S et al.	Adaptive and non-adaptive changes in activity-deprived presynaptic terminals	Eur. J. Neurosci.
HUGUET, G et al.	Heterogeneous Pattern of Selective Pressure for PRRT2 in Human Populations, but No Association with Autism Spectrum Disorders	PLoS One
INOCENTE, CO et al.	Quality of Life in Children with Narcolepsy	CNS Neurosci. Ther.
INOCENTE, CO et al.	Depressive feelings in children with narcolepsy	Sleep Med.
JANEL, N et al.	Plasma DYRK1A as a novel risk factor for Alzheimer”s disease	Transl. Psychiatr.
JESSEN, F et al.	A conceptual framework for research on subjective cognitive decline in preclinical Alzheimer”s disease	Alzheimers. Dement.
JONES, R et al.	The potential of composite cognitive scores for tracking progression in Huntington’s disease.	J Huntingtons Dis
KADAR, H et al.	MALDI Mass Spectrometry Imaging of 1-Methyl-4-phenylpyridinium (MPP+) in Mouse Brain	Neurotox. Res.
KARAYANNIS, T et al.	Cntnap4 differentially contributes to GABAergic and dopaminergic synaptic transmission	Nature
KAS, A et al.	Feeling unreal: a functional imaging study in patients with Kleine-Levin syndrome	Brain
KEBIR, O et al.	Family-based association study of common variants, raremutation study and epistatic interaction detection in HDAC genes in schizophrenia	Schizophr. Res.
KEREVER, A et al.	Perlecan is required for FGF-2 signaling in the neural stem cell niche	Stem Cell Res.
KHAN, AO et al.	Ophthalmic features of PLA2G6-related paediatric neurodegeneration with brain iron accumulation	Br. J. Ophthalmol.
KILIMANN, I et al.	Subregional basal forebrain atrophy in Alzheimer’s disease: a multicenter study.	J. Alzheimers Dis.
KING, JR et al.	Two Distinct Dynamic Modes Subtend the Detection of Unexpected Sounds	PLoS One
KISHORE, A et al.	Age-related decline in the responsiveness of motor cortex to plastic forces reverses with levodopa or cerebellar stimulation	Neurobiol. Aging
KISHORE, A et al.	Cerebellar Sensory Processing Alterations Impact Motor Cortical Plasticity in Parkinson”s Disease: Clues from Dyskinetic Patients	Cereb. Cortex
KLJAJEVIC, V et al.	The epsilon 4 genotype of apolipoprotein E and white matter integrity in Alzheimer”s disease	Alzheimers. Dement.
KLOMJAI, W et al.	Changes in spinal inhibitory networks induced by furosemide in humans	J. Physiol.-London
KOSTRO, D et al.	Correction of inter-scanner and within-subject variance in structural MRI based automated diagnosing	Neuroimage
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2017

AABOUD, M et al.	Measurement of the W+ W- production cross section in pp collisions at a centre-of-mass energy of root s=13 TeV with the ATLAS experiment	Phys. Lett. B
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