A Case of Partial 14q- with Facial Features of Holoprosencephaly and Hydranencephaly Fulltext Access 4 Pages 2007
Myofasciite à macrophages : maladie systémique ou tatouage post-vaccinal ? Fulltext Access 4 Pages 2007
Les maladies métaboliques héréditaires à l'âge adulte : le point de vue du pédiatre Fulltext Access 4 Pages 2007
Carbamazépine et clarithromycine : une interaction médicamenteuse cliniquement significative Fulltext Access 4 Pages 2007
Vers une nouvelle éthique de la relation médecin malade lors de l'annonce diagnostique de SLA ? Fulltext Access 4 Pages 2007
Neonatal Subependymal Giant Cell Astrocytoma: New Case and Review of Literature Fulltext Access 4 Pages 2007
A Stereotypic “Elbowing” Movement, a Possible New Primitive Reflex in Newborns Fulltext Access 4 Pages 2007
Neuroimage Findings in 2-Methyl-3-Hydroxybutyryl-CoA Dehydrogenase Deficiency Fulltext Access 4 Pages 2007
Ribosomal DNA Assay of Culture-Negative Streptococcus pneumoniae Meningitis Fulltext Access 4 Pages 2007
Neuropathie périphérique au cours du lupus érythémateux disséminé avec vascularite épineurale et anticorps antiphospholipides Fulltext Access 4 Pages 2007
3-Hydroxy-3-Methylglutaryl Coenzyme A Lyase Deficiency with Reversible White Matter Changes after Treatment Fulltext Access 4 Pages 2007
Spinal Intramedullary Abscess With an Epidermoid Secondary to a Dermal Sinus Fulltext Access 4 Pages 2007
Clinical Profile of Oxcarbazepine-Related Angioneurotic Edema: Case Report and Review Fulltext Access 4 Pages 2007
Serial Diffusion-Weighted MRI in Hemorrhagic Shock and Encephalopathy Syndrome Fulltext Access 4 Pages 2007
Early-Onset Ophthalmoplegia in Leigh-Like Syndrome Due to NDUFV1 Mutations Fulltext Access 4 Pages 2007
Human Herpesvirus 6 Encephalopathy Predominantly Affecting the Frontal Lobes Fulltext Access 4 Pages 2007
Nonclassic Neurologic Features in Cryopyrin-Associated Periodic Syndromes Fulltext Access 4 Pages 2007
Qu'attendre des nouvelles techniques IRM dans l'étude de la sclérose en plaques Fulltext Access 4 Pages 2007
Sleepiness in medical residents: Impact of mandated reduction in work hours Fulltext Access 4 Pages 2007
RLS-like symptoms: Differential diagnosis by history and clinical assessment Fulltext Access 4 Pages 2007
Paraplégie spastique familiale avec amyotrophie sévère des mains (syndrome de Silver?) Fulltext Access 4 Pages 2007
Réponses cérébrales à la stimulation laser en IRMf et réponses anticipatoires à cette même stimulation Fulltext Access 4 Pages 2007
Hypersignal T2 transitoire du splenium du corps calleux chez une patiente non épileptique Fulltext Access 4 Pages 2007
Exagération de symptômes mnésiques hors contexte médicolégal chez un patient atteint de sclérose en plaques Fulltext Access 4 Pages 2007
Sclérose en plaques : aspects cliniques, encéphalomyélites aiguës disséminées, neuromyélites optiques et variantes inflammatoires Fulltext Access 4 Pages 2007
Les neuropathies périphériques révélatrices de maladies métaboliques chez l'enfant Fulltext Access 4 Pages 2007
Les cellules des capsules frontières - une niche des cellules souches neurales dans le système nerveux péripherique Fulltext Access 4 Pages 2007
Syndrome cérébelleux isolé révélant un syndrome de Gougerot-Sjögren primaire Fulltext Access 4 Pages 2007
Neuropathie démyélinisante au cours d'un traitement par anti-TNF alpha et revue de la littérature Fulltext Access 4 Pages 2007
Nécrose laminaire corticale : aspects en imagerie par résonance magnétique et étude anatomoclinique Fulltext Access 4 Pages 2007
Infarctus cérébral complication de l'hémoglobinurie paroxystique nocturne Fulltext Access 4 Pages 2007
Serial casting of the ankles in Duchenne muscular dystrophy: can it be an alternative to surgery? Fulltext Access 4 Pages 2007
Hypokalaemic periodic paralysis due to the CACNA1S R1239H mutation in a large African family Fulltext Access 4 Pages 2007
A novel mutation in the mitochondrial DNA tRNA Leu (UUR) gene associated with late-onset ocular myopathy Fulltext Access 4 Pages 2007
The Hammersmith functional score correlates with the SMN2 copy number: A multicentric study Fulltext Access 4 Pages 2007
Mild ocular myopathy associated with a novel mutation in mitochondrial twinkle helicase Fulltext Access 4 Pages 2007
Amyotrophic lateral sclerosis with mutation of the Cu/Zn superoxide dismutase gene (SOD1) in a patient with Down syndrome Fulltext Access 4 Pages 2007
Delayed auditory processing underlying stimulus detection in Down syndrome Fulltext Access 4 Pages 2007
Detection and measurement of neurofibromatosis-1 mouse optic glioma in vivo Fulltext Access 4 Pages 2007
[123I]Epidepride binding to cerebellar dopamine D2/D3 receptors is displaceable: Implications for the use of cerebellum as a reference region Fulltext Access 4 Pages 2007
A review of micro- and macrovascular analyses in the assessment of tumor-associated vasculature as visualized by MR Fulltext Access 4 Pages 2007
Skeletal dysplasia presenting as a neuromuscular disorder – report of three children Fulltext Access 4 Pages 2007
Pharmacogenetics of MXA SNPs in interferon-β treated multiple sclerosis patients Fulltext Access 4 Pages 2007
Increased IL-13-producing T cells in ALS: Positive correlations with disease severity and progression rate Fulltext Access 4 Pages 2007
Genetic polymorphisms of macrophage-mediators in Guillain–Barré syndrome Fulltext Access 4 Pages 2007
Anti-heat shock protein 90β antibodies are detected in patients with multiple sclerosis during remission Fulltext Access 4 Pages 2007
Regulatory T cells in cerebrospinal fluid from Behçet's disease with neurological manifestations Fulltext Access 4 Pages 2007
Adenylate kinase 5 autoimmunity in treatment refractory limbic encephalitis Fulltext Access 4 Pages 2007
Transient Hypermetabolism of the Basal Ganglia Following Perinatal Hypoxia Fulltext Access 4 Pages 2007
Generalized Nonconvulsive Status Epilepticus in Symptomatic Partial Epilepsy Fulltext Access 4 Pages 2007
JC Virus Granule Cell Neuronopathy in a Child With CD40 Ligand Deficiency Fulltext Access 4 Pages 2007
Recurrent Spontaneous Spinal Epidural Hematoma in a Child: First Case Report Fulltext Access 4 Pages 2007
Elevated Thyroid Peroxidase Antibodies with Encephalopathy in MELAS Syndrome Fulltext Access 4 Pages 2007
Bilateral Periventricular Nodular Heterotopia with Amniotic Band Syndrome Fulltext Access 4 Pages 2007
The Spectrum of Polyneuropathies in Childhood Detected with Electromyography Fulltext Access 4 Pages 2007
Albinism and Developmental Delay: The Need to Test for 15q11-q13 Deletion Fulltext Access 4 Pages 2007
Unusual Focal Ictal Pattern in Children With Eyelid Myoclonia and Absences Fulltext Access 4 Pages 2007
Late-Onset Nonketotic Hyperglycinemia With Leukodystrophy and an Unusual Clinical Course Fulltext Access 4 Pages 2007
Pallidal Stimulation for Dystonia in Pantothenate Kinase-associated Neurodegeneration Fulltext Access 4 Pages 2007
Novel Mutation Confirms Seizure Locus SCN1A is Also Familial Hemiplegic Migraine Locus FHM3 Fulltext Access 4 Pages 2007
Neurologic Abnormalities in Patients with Adenosine Deaminase Deficiency Fulltext Access 4 Pages 2007
Concomitant Transverse Myelitis and Acute Motor Axonal Neuropathy in an Adolescent Fulltext Access 4 Pages 2007
Novel COLQ mutation 950delC in synaptic congenital myasthenic syndrome and symptomatic heterozygous relatives Fulltext Access 4 Pages 2007
Severe encephalomyopathy in a patient with homoplasmic A5814G point mutation in mitochondrial tRNACys gene Fulltext Access 4 Pages 2007