Revue Neurologique

• Articles en prépublication
• • • Prise en charge de l’AVC en réanimation : mesures thérapeutiques générales. Recommandations formalisées d’experts
    • D. Pugin, F. Woimant
  • • Aspects cliniques et thérapeutiques des dystonies en Tunisie : étude prospective sur cinq ans
    • H. Benrhouma, I. Kraoua, H. Klaa, A. Rouissi, I. Turki, N. Gouider-Khouja
  • • Accident vasculaire cérébral : encore de nouvelles recommandations ?
    • P.-E. Bollaert, I. Vinatier
  • • Vascularite cérébrale à Toxocara canis révélée par des AVC itératifs
    • L.-D. Lompo, F.-K. Kamdem, E. Revenco, R. Allibert, E. Medeiros, F. Vuillier, T. Moulin
  • • Les nouvelles recommandations 2011 du National Institute on Aging et de l’Alzheimer’s Association sur le diagnostic de la maladie d’Alzheimer : stades précliniques, mild cognitive impairment et démence
    • B. Croisile, S. Auriacombe, F. Etcharry-Bouyx, M. Vercelletto
  • • Voir +

• Contenu(s) associé(s)
• • • Neurochirurgie
  • • Motricité cérébrale
  • • Pratique neurologique - FMC
  • • Neurophysiologie Clinique / Clinical Neurophysiology
  • • Neurologie
  • • NPG
  • • Médecine du Sommeil
  • • RADIOLOGIE ET IMAGERIE MÉDICALE : Musculosquelettique - Neurologique - Maxillofaciale

• Articles gratuits
• • • Prise en charge des biopsies musculaires et nerveuses. Recommandations formalisées d’experts sous l’égide de la Société française de neuropathologie, de la Société française de myologie et de l’Association française contre les myopathies
  • • Lissencéphalies : aspects cliniques et génétiques
    • A. Verloes, M. Elmaleh, M. Gonzales, A. Laquerrière, P. Gressens
  • • Recent developments in the management of peripheral neuropathy using skin biopsy
    • G Lauria
  • • Boundary caps: a gating function at the CNS/PNS interface and a source of pluripotent neural cells in the PNS
    • P Topilko, G Maro, P Charnay
  • • Parry-Romberg syndrome with dysphonia
    • MA Rafai, FZ Boulaajal, B El Moutawakil, M Bourezgui, M Sibai, M Mahtar, M Chekkouri, I Slassi
  • • Long-term efficiency of vagus nerve stimulation in non-surgical refractory epilepsies of adolescents and adults
    • A Montavont, G Demarquay, P Ryvlin, M Rabilloud, M Guénot, K Ostrowsky, J Isnard, C Fisher, F Mauguière
  • • Fragile X pre-mutation presenting with postural tremor and ataxia (FXTAS syndrome)
    • P Davous, R Juntas-Morales, C Dupel-Pottier, E Bertolle
  • • Polymyositis and cranial neuropathy
    • C Crinquette, J de Sèze, CA Maurage, D Launay, D Ferriby, S Delalande, E Hachulla, T Stojchovic, P Vermersch
  • • Acute myelitis and Lyme disease
    • F Blanc, S Froelich, F Vuillemet, S Carré, E Baldauf, S de Martino, B Jauliac, D Maîtrot, C Tranchant, J de Sèze
  • • Phenotype-genotype study of 154 French NF2 mutation carriers
    • L Demange, C de Montcuit, G Thomas, S Olschwang, R Huguenin
  • • Overview
  • • Patent foramen ovale and migraine
    • MG Bousser
  • • Multiple system atrophy: survival and prognostic factors in the MSA-Aquitaine cohort
    • E Krim, F Yekhlef, V Chrysostome, I Ghoraieb, F Tison
  • • Cerebral infarction related to intracranial radiation induced arteritis twenty years after cerebral radiation therapy
    • JP Ferroir, B Marro, Y Belkacem, B Stilhart, M Schlienger
  • • Status epilepticus and gatifloxacine
    • S Koussa, S Hage Chahine, A Zoghbi, P Yasbeck
  • • The predominance of myopathy as a cause of intensive care unit acquired paralysis: the diagnostic value of direct muscle stimulation
    • T Nordine, JP Lefaucheur
  • • Phenotypic aspects of FKRP-linked muscular dystrophy type 21 in a series of eleven patients
    • H Bourteel, T Stojkovic, JM Cuisset, CA Maurage, P Laforêt, P Richard, P Vermersch
  • • Wolfram’syndrome presenting as a cerebellar ataxia
    • S Mathis, V Paquis, V Mesnage, I Balaboï, R Gil, B Gilbert, JP Neau
  • • Bickerstaff’s syndrome presenting with coma, tetraplegia and blindness
    • G Fourcade, C Bengler, CH Campello, J Froger, J Pelissier, P Labauge
  • • Overview
  • • Genetic and clinical aspects of lissencephaly
    • A Verloes, M Elmaleh, M Gonzales, A Laquerrière, P Gressens
  • • Optic nerve sheath meningioma: the Lyon experience in twenty patients
    • S Mouton, C Tilikete, M Bernard, P Krolak-Salmon, A Vighetto
  • • Dilatation of the Virchow-Robin spaces (type III lacunae): clinical and radiological correlations
    • D Marnet, R Noudel, P Peruzzi, A Bazin, MH Bernard, B Scherpereel, M Pluot, P Rousseaux
  • • Clinical and therapeutic characteristics of late onset Rasmussen’s syndrome
    • V Jaillon-Rivière, S Dupont, F Bertran, V de la Sayette, F Beuvon, M Baulac, G Defer
  • • Experimental models of multiple sclerosis
    • H Lassmann
  • • Emerging therapies for MS
    • E Waubant
  • • Recent advances in the neuropathology of multiple sclerosis
    • C Stadelmann
  • • What’s new in multiple sclerosis genetics?
    • B Fontaine, G Sémana, F Clerget-Darpoux
  • • The neurophysiology of corticobasal degeneration
    • L Tyvaert, F Cassim, P Derambure, L Defebvre
  • • Childhood Ataxia with Central Nervous System Hypomyelination or Vanishing White Matter (CACH / VWM) syndrome and leucodystrophies related to EIF2B mutations (Orphanet)
    • P Labauge, A Fogli, F Niel, D Rodriguez, O Boesplug-Tanguy
  • • Sneddon’s syndrome: 15 cases studied with cerebral angiography
    • A Maamar, M Rahmani, S Aidi, M Benabdeljlil, R El Hassani My, M Jiddane, Ch Hicham, M El Alaoui-Faris
  • • The presentation of cerebral abscess and subdural empyema with symptomatic short-lasting unilateral neuralgiform headache attacks with conjunctival injection and tearing (SUNCT syndrome)
    • M El Amrani, JC Roger, P Fossati, J de Monredon, JP Serveaux
  • • Atteintes du système nerveux central et infection par le VIH-1
    • A. Moulignier
  • • Les lymphomes cérébraux primitifs associés au SIDA : aspects physiopathogéniques
    • S. Camilleri-Broët, M. Raphaël
  • • A nosology of the dementias; a neuropathologist’s viewpoint
    • C Duyckaerts
  • • Human memory and Alzheimer’disease
    • F Eustache, B Giffard, G Rauchs, G Chételat, P Piolino, B Desgranges
  • • Idiopathic acute transverse myelitis: application of new diagnostic criteria to 17 patients
    • C Lanctin, S Wiertlewski, C Moreau, C Verny, P Derkinderen, P Damier, F Dubas
  • • Finnish amyloid polyneuropathy in a French patient
    • F Contégal, S Bidot, C Thauvin, L Lévêque, P Soichot, P Gras, T Moreau, M Giroud
  • • Long-term outcome in patients with symptomatic low-grade oligodendrogliomas treated with cytotoxic agents
    • H Catenoix, J Honnorat, S Cartelat-Carel, F Chapuis, N Nighoghossian, P Trouillas
  • • Neurologic manifestations of type I Gaucher’s disease: is a revision of disease classification needed?
    • P Chérin, F Sedel, C Mignot, M Schupbach, I Gourfinkel-An, M Verny, N Baumann
  • • Neurological involvement in Behçet’s disease: 154 cases from a cohort of 925 patients and a review of the literature
    • S Benamour, T Naji, FZ Alaoui, H El Kabli, S El Aidouni
  • • Treatment with intravenous rt-PA in a general hospital context: a review of the St Jean Hospital experience from Perpignan
    • D Sablot, JF Cassarini, A Akout, JM Benejean, F Leibinger, X Faillie, E Vidry, X Ayrignac, S Castro, L Sinaya, JL Bertrand, Y Garcia, B Arnoud, C Negre
  • • Neurosarcoidosis
    • C Chapelon-Abric
  • • The neurology of cerebral arteriovenous malformations
    • C Stapf
  • • Neuropsychology and magnetic resonance imaging in 5 patients after carbon monoxide poisoning
    • M Rahmani, M Bennani, M Benadbdeljlil, S Aidi, M Jiddanee, T Chkili, M El Alaoui Faris
  • • Adult onset nemaline myopathy presenting with respiratory insufficiency
    • P Befort, L Landreau, AM Pagès, O Jonquet, M Pagès
  • • Neurological aspects of Fabry’s disease
    • P Clavelou, G Besson, C Elziere, A Ferrier, JM Pinard, M Hermier, JY Artigou, DP Germain
  • • Neuroradiological criteria of remitting neuromyelitis optica
    • M Bonnan, S Olindo, A Signale, S Khaddam, D Caparros-Lefebvre, D Smadja, P Cabre
  • • The presentation of viral hepatitis C infection without cryoglobulinemia with a peripheral neuropathy. Five cases reports
    • MA Rafai, I Gam, H Fadel, K Hakim, B El Moutawakkil, A Bendahmane, N Kissani, R Alaoui, A Cherkaoui, I Slassi
  • • Turcot’s syndrome confirmed by molecular biological tests
    • S Jeannin, C Lebrun, F van den Boos, S Olschwang, V Bourg, M Frenay
  • • Bilateral idiopathic orbital myositis
    • N El Ouafi, MA Rafai, H Faddel, I Gam
  • • Chronic demyelinating polyneuropathy with cranial nerve involvement associated with anti-MAG/SGPS/SGPLG antibodies
    • A Drouet, C Caudie, JM Vallat, JH Ruel, D Felten, L Guilloton, P Giraud
  • • CADASIL with minimal symptoms after 60 years
    • A Mourad, M Levasseur, MG Bousser, H Chabriat
  • • Homocystinaemia with thrombophilic factors in unexplained decompression sickness
    • M Candito, E Candito, M Chatel, E van Obberghen, A Dunac
  • • Type I glutaric aciduria: an unrecognized cause of progressive dystonia
    • N Gouider-Khouja, I Ben Youssef-Turki
  • • Rapid sensory motor neuropathy after gastric restriction surgery
    • H Korri, A Awada, S Hadjj
  • • Devic’s neuromyelitis optica in Morocco. A study of 9-cases.
    • H El Otmani, MA Rafai, F Moutaouakil, B El Moutawakkil, FZ Boulaajaj, M Moudden, I Gam, I Slassi
  • • Validity of the five-word screening test for Alzheimer’s disease in a population based study.
    • P Cowppli-Bony, C Fabrigoule, L Letenneur, K Ritchie, A Alpérovitch, JF Dartigues, B Dubois
  • • Severe visual loss due to retinal artery occlusion associated with Susac’s syndrome: a case report.
    • B Bodaghi, B Wechsler, R Adam, D Galanaud, C Fardeau, T Papo, P LeHoang, JC Piette
  • • Acute motor axonopathy, enteroviruses and amyotrophic lateral sclerosis: is there a link?
  • • Lyme disease
    • C. Tranchant, J.-M. Warter
  • • Progressive supranuclear palsy: a study of clinical features, natural history and disability
    • F. Macia, G. Ballan, F. Yekhlef, O. Delmer, C. Vital, A. Lagueny, F. Tison
  • • Good outcome in a case of post-anoxic myoclonus (Lance-Adams syndrome)
    • L. Errguig, A. Benomar, W. Messouak, W. Regragui, M. Benabdejlil, M. Yahyaoui, T. Chkili
  • • Dystonia: Phenotypes and Genotypes
    • S. B. Bressman,
  • • What can we learn from animal models?
    • N.N. Byl
  • • Psychogenic Dystonia
    • T. Pringsheim, A. E Lang
  • • Problems of treating writer's cramp with botulinum toxin injections: results from 10 years experience.
    • M-H Marion, K. Afors, M.P. Sheehy
  • • Cerebellar mutism syndromes with subsequent dysarthria: a study of three children and a review of the literature
  • • Functional prognosis of paraplegia due to cord ischaemia: a retrospective study of 23 patients
  • • Neurological manifestations of leprosy
  • • Pathophysiology and therapy of L-Dopa induced dyskinesia.
    • A. Hadj Tahar, E. Bezard, R. Grondin, C.E. Gross, P.J. Bédard
  • • Choreo-acanthocytosis: report of a new family
    • D. Uzeno, J. P. Azulay, S. Attarian, A. Verschueren, J. Pouget
  • • Neurobrucellosis: clinical features and therapeutic responses in 15 patients
    • S. Koussa, A. Tohmé, E. Ghayad, R. Nasnas, K. El Kallab, R. Chemaly
  • • Myopathy-lipomatosis associated with a tRNA ^-lys A8344 mitochondrial DNA mutation
    • K. Auré, D. Sternberg, T. Maisonobe, S. Herson, C. Jardel, P. Blondy, A. Lombes, B. Laforêt
  • • Lessons from macrophagic myofasciitis: towards a definition of a vaccination adjuvant-related syndrome.
  • • Treatment of peripheral neuropathies with neurotrophic factors: animal models and clinical trials.
    • P.-F. Pradat
  • • (AFTER RSJF’s COMMENTS) The GEFS+ syndrome: phenotypic variations from newborns to adults in a large French family
    • F. Audic-Gérard, P. Szepetowski, P. Genton
  • • Importance of molecular genetic analysis of the PRNP gene in patients with cerebellar ataxia: a new case of fatal familial insomnia.
    • V. Marcaud, J.- L. Laplanche, B. Defontaines, P. Beaudry, A. Vital, D. Vincent, V. Sazdovitch, J.-J. Hauw, P. Jung, F. Vecchierrini, C.- F. Degos
  • • Plasticity of motor maps in primates: recent advances and therapeutic perspectives.
    • Y. Vandermeeren, E. Bastings, D. Good, E. Rouiller, E. Olivier
  • • Orbital myositis: a report of three cases with a study of clinical and radiological features of disease progression.
    • S. Attarian, C. Fernandez, J. Ph. Azoulay, J. Serratrice, J. F. Pellissier, J. Pouget
  • • Pontine infarction after a base of skull fracture.
    • O. Detante, F. Colle, P. Vu, P. Pradat-Diehl
  • • Cranial neuritis due to Lyme disease: MRI features after contrast enhancement.
    • M. Khalil, M. P. Boncoeur, F. Torny, L. Magy, P. Couratier
  • • At the interface between developmental and degenerative disease: Cerebellar disorders of infancy - a classification and practical approach to diagnosis.
  • • Melanocytic meningitis with a large congenital melanocytic naevus: neuro-cutaneous melanosis.
  • • Muscle granulomata: clinico-pathological correlations and immunohistochemistry in seven cases.
  • • Relapsing-remitting inflammatory disease of the central nervous system with normal MRI: multiple sclerosis or phenocopies in a series of 15 patients?
  • • Angelman?s syndrome: a clinical and genetic model
  • • Neurological disorders after eating fish, molluscs and shellfish
  • • Clinical and electrophysiological features of cortical tremor
  • • Neuropsychological and scintigraphic features of fronto-temporal dementia preceding amyotrophic lateral sclerosis.
  • • Dysembryoplastic neuroepithelial tumors
  • • Intravenous immunoglobulins for relapsing-remitting multiple sclerosis after failure of treatment with other immuno-modulators. An evaluation in 18 patients.
  • • Primary dural lymphoma: a report of two cases with a review of the literature.
  • • Two unusual complications of the Klippel-Trenaunay syndrome: a case of carpal tunnel syndrome one of cerebral venous thrombosis,
  • • Cellular aspects of neuroinflammation in Guillain-Barré syndrome (GBS): a key to a new therapeutic option?
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  • • Isolated pontine infarcts: vascular anatomy helps understand the clinical signs.
  • • Paraplegia due to an intracranial dural arterio-venous fistula draining around the spinal cord.
  • • Disorders of behaviour during REM sleep
  • • Natural history of patients surviving very severe strokes.
  • • Neurotoxicity of ethylene-bis-dithiocarbamates in humans
  • • A case-report of central nervous system involvement by hepatitis C
  • • Rapid-eye movement sleep disorders in Parkinson’s disease
  • • Argyrophilic inclusion body disease, a frequent and largely underestimated cause of dementia in the elderly.
  • • Vacuolar leucoencephalopathy induced by heroin: 4 cases
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  • • Genetics of epilepsy: current knowledge and perpectives.
  • • Critical illness neuropathy
  • • Characterization and discrimination of kinetic tremor in Parkinson’s disease
  • • Aneurysm of the anterior cerebral artery revealed by an isolated hemianopic scotoma.
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  • • 5: 555-564
  • • Sub-cortico-frontal encephalopathy with choreic movements related to recombinant interferon-alpha-2b.
  • • 5: 579-588
  • • Slow channel syndrome due to a chromosomal translocation between 2q31 and 9p27.
  • • OVERVIEW
  • • Psychoses in epilepsy
  • • Encephalopathy associated with severe bacterial infections: presuppurative encephalitis” or toxi-infectious disorder”?
  • • Necrosis of a pituitary adenoma and ischaemic stroke
  • • Bilateral phrenic paralysis, dysautonomia and restrictive cardiomyopathy in a patient with POEMS syndrome
  • • OVERVIEW
  • • Pathophysiology of cardiovascular risk in the sleep-apnea syndrome (SAS)
  • • Chronic inflammatory demyelinating polyradiculoneuropathy with hypertrophy of the spinal roots, brachial plexus and cranial nerves.
  • • Recurrent idiopathic stupor: is there a role for exogenous and endogenous benzodiazepines?
  • • Hemi-megalencephaly: a misleading EEG
  • • Long-term treatment of Alzheimer’s disease. Follow-up of 255 patients treated with tacrine for 4 years.
  • • Non-ketotic hyperglycaemia presenting with hemichorea and hemiballismus.
  • • Rapidly evolving diabetic mononeuritis multiplex. Favourable outcome after immunosupressive treatment.
  • • Evaluation and management of non traumatic intra-cerebral hemorrhage.
  • • Management of newly diagnosed seizures: a French experience.
  • • Idiopathic SUNCT syndrome: two new French cases.
  • • Identification of variables associated with time of hospital admission after ischaemic stroke: a study of a rural population.
  • • Susac’s syndrome in a 35 year-old man.
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  • • Chronic inflammatory demyelinating polyradiculopathy (CIDP) in patients with solid organ transplantation: a clinical, neurophysiological, and neuropathological study of 4 cases.
    • A Echaniz-Laguna, M Anheim, P Wolf, R Kessler, G Massard, M Mohr, B Moulin, L Braun-Parvez, D Jaeck, C Tranchant
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• Articles les plus vus
• • • Dilatation des espaces périvasculaires de Virchow-Robin (Lacunes de type III) : corrélations radio-cliniques
    • D. Marnet, R. Noudel, P. Peruzzi, A. Bazin, M.H. Bernard, B. Scherpereel, M. Pluot, P. Rousseaux
  • • Coma, tétraplégie flasque et cécité révélant un syndrome de Bickerstaff
    • G. Fourcade, C. Bengler, C.H. Campello, J. Froger, J. Pelissier, P. Labauge
  • • Anticorps dans la myasthénie
    • B. Eymard
  • • Explorations de la fonction musculaire par spectrométrie et imagerie de résonance magnétique
    • D. Bendahan, J.P. Mattei, S. Guis, G. Kozak-Ribbens, P.J. Cozzone
  • • Les nouvelles recommandations 2011 du National Institute on Aging et de l’Alzheimer’s Association sur le diagnostic de la maladie d’Alzheimer : stades précliniques, mild cognitive impairment et démence
    • B. Croisile, S. Auriacombe, F. Etcharry-Bouyx, M. Vercelletto
  • • Syndrome de Susac : étude de cinq cas
    • E. Maillart, R. Deschamps, A. Moulignier, C. Vignal-Clermont, M. Obadia, Y. Le Mer, L. Laloum, O. Gout
  • • Troubles neuropsychiatriques révélateurs de la maladie de Horton, à propos d’un cas
    • L. Koric, O. Felician, J. Gallard, G. Gautier, M. Ceccaldi
  • • Testing musculaire manuel et quantifié dans les maladies neuromusculaires. Comment assurer la qualité des mesures de force dans les protocoles cliniques ?
    • J.Y. Hogrel, G. Ollivier, C. Desnuelle
  • • Le cortex préfrontal : compositeur et chef d’orchestre des comportements volontaires
    • R. Levy, E. Volle
  • • P3-38 Le ratio Tau/Ab42 dans le LCR différencie la MA de la DFT avec une spécificité élevée
    • L. De Souza, F. Lamari, C. Jardel, M. Sarazin, B. Dubois
  • Voir +
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Vol 168 - N° 5 - mai 2012

© Elsevier Masson SAS