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Daneshyari Neurology Journas Latest Articles

Neurology Research Articles

A case of psychosis with temporal lobe epilepsy: SPECT changes with treatment
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Maladie de Gilles de la Tourette et troubles obsessionnels compulsifs
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Leukoencephalopathy around a tumor cyst following intracystic methotrexate injection
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Treatment of electrical status epilepticus during slow-wave sleep with high-dose corticosteroid
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Acute disseminated encephalomyelitis presenting with bilateral transient amaurosis
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Enigmatic osteomyelitis and bilateral upper limb palsy in a neonate
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Changes in cerebral glucose metabolism in newborn infants with cerebral infarction
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Brain glutamine by MRS in a patient with urea cycle disorder and coma
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Visual disturbance associated with postoperative cerebellar mutism
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Zonisamide monotherapy for epilepsy in children and young adults
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Fatal neurologic involvement in pediatric Wegener's granulomatosis
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Focal seizure and cerebral contrast retention after cardiac catheterization
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Severe lethal spinal muscular atrophy variant with arthrogryposis
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Complication neuroméningée d'une infection systémique à Candida albicans chez un prématuré
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Infant botulism, type F, presenting at 54 hours of life
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Intra-hospital lethality among infants with pyogenic meningitis
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Electroencephalographic patterns in unresponsive pediatric patients
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Neonatal Seizures and Familial Hypomagnesemia With Secondary Hypocalcemia
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Chorioamnionitis and Neonatal Encephalopathy in Term Infants With Fetal Acidemia: Histopathologic Correlations
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Infantile Myofibromatosis Presenting With Scalp Dermoid Cyst
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Successful Treatment of Epilepsy and Celiac Disease With a Gluten-Free Diet
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The Pharyngeal-Cervical-Brachial Form of Guillain-Barré Syndrome in Childhood
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Soluble Adhesion Molecules in Acute Disseminated Encephalomyelitis
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Clinical Heterogeneity in Familial Congenital Ptosis: Analysis of Fourteen Cases in One Family Over Five Generations
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A Female With Angelman Syndrome and Unusual Limb Deformities
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Syndrome de Gougerot-Sjögren et pupille tonique d'Adie
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Inhibition of P53-related apoptosis had no effect on PrPSc accumulation and prion disease incubation time
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Author Index for Volume 18
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An animal model of a spontaneously reversible obstructive sleep apnea syndrome in the monkey
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Volume Author Index
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Maladie de Creutzfeldt-Jakob génétique par mutation du codon 200
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Polyradiculonévrite inflammatoire démyélinisante chronique et atteinte du système nerveux autonome
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Baisse visuelle sévère liée à une occlusion artérielle rétinienne au cours du syndrome de Susac : à propos d'un cas
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Paralysie bilatérale du nerf moteur oculaire commun secondaire à une poussée de sclérose en plaques
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Forme de Heidenhain de la maladie de Creutzfeldt-Jakob
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Parésie trochléaire transitoire comme signe neurologique inaugural d'une panartérite noueuse
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Infarctus latéro-bulbaire sur dissection intracrânienne suivi d'une hémorragie sous-arachnoïdienne
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Syndrome choréo-athétosique révélant une maladie lupique associée à des anticorps antiphospholipides
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Basilar Meningitis Associated With Ethmoid and Sphenoid Cephaloceles
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La prise en charge des accidents vasculaires cérébraux en France
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Douleurs oro-faciales et céphalées secondaires
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Ophtalmoplégies douloureuses
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Traitement des céphalées trigémino-vasculaires : nouveautés et perspectives
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Trigeminal autonomic cephalalgias. Pathophysiology and classification
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Traitement médicamenteux de fond de la migraine
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Une mucormycose rhinocérébrale
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Tétraparésie aiguë d'origine cérébrale
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Syndrome de Miller-Fisher récidivant
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Accidents vasculaires cérébraux multiples et primo-infection varicelleuse chez un adulte
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Vasculite cérébrale secondaire à une infection à VZV
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Acknowledgement of Referees for 2004
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Visualization of temporal increase in compound nerve action magnetic fields in the human median nerve during ischemia
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Author Index for Volume 25
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Author Index for Volume 24
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Reduced neuronal activity in the V5 complex underlies smooth-pursuit deficit in schizophrenia: evidence from an fMRI study
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Author Index for Volume 26
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Imaging the visual autokinetic illusion with fMRI
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The role of complement in myasthenia gravis: serological evidence of complement consumption in vivo
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Antibodies against OspA epitopes of Borrelia burgdorferi cross-react with neural tissue
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Oligoclonal IgG bands in Japanese patients with multiple sclerosis. A comparative study between isoelectric focusing with IgG immunofixation and high-resolution agarose gel electrophoresis
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Effects of phospholipids on antiganglioside antibody reactivity in GBS
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Subject index of volume 165
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Lymphocyte subsets, TNFα and interleukin-4 levels in treated and untreated subacute sclerosing panencephalitis patients
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Complex fMRI analysis with unrestricted phase is equivalent to a magnitude-only model
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Subject index of volume 162
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Modulation of prolactin expression in human T lymphocytes by cytokines
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Subject index of volume 160
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Subject index of volume 167
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Lower brain-derived neurotrophic factor in serum of relapsing remitting MS: Reversal by glatiramer acetate
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Subject index of volume 166
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PSGL-1 is not required for development of experimental autoimmune encephalomyelitis
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Hyaluronate receptor (CD44) and integrin α4 (CD49d) are up-regulated on T cells during MS relapses
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Subject Index
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Role of interleukin 4 in Spanish multiple sclerosis patients
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Subject index of volume 169
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Increased muscle nucleoside levels associated with a novel frameshift mutation in the thymidine phosphorylase gene in a Spanish patient with MNGIE
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Early-Onset Ataxia With Oculomotor Apraxia With a Novel APTX Mutation
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Limb Preference in Children with Obstetric Brachial Plexus Palsy
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EEG Evaluation of Fixation-Off Sensitivity in Eyelid Myoclonia With Absences
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Incomplete Alpha Coma Pattern in a Child
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Epilepsy and Intrathecal Baclofen Therapy in Children With Cerebral Palsy
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Migraine and Recurrent Epistaxis in Children
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CNS Siderosis and Dandy-Walker Variant After Neonatal Alloimmune Thrombocytopenia
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Neurologic Complications Associated With Respiratory Syncytial Virus
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Novel mutations in the thymidine kinase 2 gene (TK2) associated with fatal mitochondrial myopathy and mitochondrial DNA depletion
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Antisense oligonucleotides in the treatment of Duchenne muscular dystrophy: Where are we now?
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Transforming growth factor-β enhances connective tissue growth factor expression in L6 rat skeletal myotubes
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ADAM12 overexpression does not improve outcome in mice with laminin α2-deficient muscular dystrophy
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Intraosseous lipoma of the body of the sphenoid bone
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Novel EGR2 mutation R359Q is associated with CMT type 1 and progressive scoliosis
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Marked phenotypic variation in a family with a new myelin protein zero mutation
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Keyword Index
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Major myofibrillar changes in early onset myopathy due to de novo heterozygous missense mutation in lamin A/C gene
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α-Dystroglycan, the usual suspect?
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Commentary from the Editor
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Clinical features and neurophysiological follow-up in a case of Brown-Vialetto-Van Laere syndrome
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Two patients with 'Dropped head syndrome' due to mutations in LMNA or SEPN1 genes
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Peripheral nerve lesions associated with a dominant missense mutation, E33D, of the lamin A/C gene
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Early onset myopathy with a novel mutation in the Selenoprotein N gene (SEPN1)
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A full-size MRI-compatible keyboard response system
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