Scientific publications

Find here all the scientific publications of the ICM research.
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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.

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