Dopamine Receptor D2 Gene Polymorphisms Are Associated in Taiwanese Children With Tourette Syndrome Fulltext Access 5 Pages 2005
Méningite récurrente aseptique associée à une cirrhose biliaire primitive Fulltext Access 5 Pages 2005
Leucoencéphalopathie multifocale progressive à BK virus chez un patient immunodéprimé par une corticothérapie Fulltext Access 5 Pages 2005
Severe fetal acidemia and subsequent neonatal encephalopathy in the larger premature infant Fulltext Access 5 Pages 2005
Maternal uniparental disomy chromosome 14: Case report and literature review Fulltext Access 5 Pages 2005
Dopamine Transporter in Attention-Deficit Hyperactivity Disorder Normalizes After Cessation of Methylphenidate Fulltext Access 5 Pages 2005
Extrapyramidal Parkinsonism Complicating Acute Organophosphate Insecticide Poisoning Fulltext Access 5 Pages 2005
Intrathecal Baclofen Overdose Followed by Withdrawal: Clinical and EEG Features Fulltext Access 5 Pages 2005
Cyclosporine in Chronic Inflammatory Demyelinating Polyradiculoneuropathy Fulltext Access 5 Pages 2005
Cytokines Involved in CNS Manifestations Caused by Mycoplasma pneumoniae Fulltext Access 5 Pages 2005
Epilepsia Partialis Continua: Acute Disseminated Encephalomyelitis or Rasmussen's Encephalitis? Fulltext Access 5 Pages 2005
Research in Geriatric Depression: A Model for Mental Health Research in the 21st Century? Fulltext Access 5 Pages 2005
Intensive Care Unit Management of Interventional Neuroradiology Patients Fulltext Access 5 Pages 2005
Aspartoacylase gene knockout results in severe vacuolation in the white matter and gray matter of the spinal cord in the mouse Fulltext Access 5 Pages 2005
D3 dopamine receptors do not regulate neurogenesis in the subventricular zone of adult mice Fulltext Access 5 Pages 2005
General-Medical Conditions in Older Patients With Serious Mental Illness Fulltext Access 5 Pages 2005
Cognitive, Behavioral, and Physiological Changes in Alzheimer Disease Patients as a Function of Incontinence Medications Fulltext Access 5 Pages 2005
Association of the Serotonin Transporter Gene-Linked Polymorphic Region (5-HTTLPR) Genotype With Depression in Elderly Persons After Hip Fracture Fulltext Access 5 Pages 2005
Caregiver Assessment of Patients' Depression in Alzheimer Disease: Longitudinal Analysis in a Drug Treatment Study Fulltext Access 5 Pages 2005
A Variant of the Sigma Receptor Type-1 Gene Is a Protective Factor for Alzheimer Disease Fulltext Access 5 Pages 2005
Visual outcome of blind eyes in pituitary apoplexy after transsphenoidal surgery: a series of 14 eyes Fulltext Access 5 Pages 2005
Meningeal melanocytoma of the posterior fossa: case report and literature review Fulltext Access 5 Pages 2005
Correspondence of microelectrode mapping with magnetic resonance imaging for subthalamic nucleus procedures Fulltext Access 5 Pages 2005
Sudden Unexpected Death in People with Epilepsy: A Pediatric Perspective Fulltext Access 5 Pages 2005
The Relationship Between Tourette Syndrome, Attention Deficit Hyperactivity Disorder, and Stimulant Medication: A Critical Review Fulltext Access 5 Pages 2005
Spinal cord injury induces early and persistent lesional P2X4 receptor expression Fulltext Access 5 Pages 2005
A whole brain MR spectroscopy study from patients with Alzheimer's disease and mild cognitive impairment Fulltext Access 5 Pages 2005
The neural correlates of understanding the other's distress: A positron emission tomography investigation of accurate empathy Fulltext Access 5 Pages 2005
Chemokine profile in the cerebrospinal fluid and serum of Vogt-Koyanagi-Harada disease Fulltext Access 5 Pages 2005
CTLA-4 gene polymorphism is not associated with conventional multiple sclerosis in Japanese Fulltext Access 5 Pages 2005
P/Q-type calcium channel antibodies, Lambert-Eaton myasthenic syndrome and survival in small cell lung cancer Fulltext Access 5 Pages 2005
Decreased frequency of intrathymic regulatory T cells in patients with myasthenia-associated thymoma Fulltext Access 5 Pages 2005
E-selectin A561C and G98T polymorphisms influence susceptibility and course of multiple sclerosis Fulltext Access 5 Pages 2005
Impact of the Asp299Gly polymorphism in the toll-like receptor 4 (tlr-4) gene on disease course of multiple sclerosis Fulltext Access 5 Pages 2005
Evaluation of cerebrospinal fluid uPA, PAI-1, and soluble uPAR levels in HIV-infected patients Fulltext Access 5 Pages 2005
A novel technique to study the brain's response to pain: Proton magnetic resonance spectroscopy Fulltext Access 5 Pages 2005
Anti-brain but not celiac disease antibodies in Landau-Kleffner Syndrome and related epilepsies Fulltext Access 5 Pages 2005
Autocrine actions of macrophage-derived catecholamines on interleukin-1β Fulltext Access 5 Pages 2005
Increased levels of APRIL (A Proliferation-Inducing Ligand) mRNA in multiple sclerosis Fulltext Access 5 Pages 2005
TNF-related apoptosis inducing ligand (TRAIL) gene polymorphism in Japanese patients with multiple sclerosis Fulltext Access 5 Pages 2005
High dose methylprednisolone induces FcγRI on granulocytes in MS-patients Fulltext Access 5 Pages 2005
Lack of association with the CD28/CTLA4/ICOS gene region among Norwegian multiple sclerosis patients Fulltext Access 5 Pages 2005
In vivo detection of myelin proteins in cervical lymph nodes of MS patients using ultrasound-guided fine-needle aspiration cytology Fulltext Access 5 Pages 2005
BR serine/threonine kinase 2: A new autoantigen in paraneoplastic limbic encephalitis Fulltext Access 5 Pages 2005
The human PNMA family: Novel neuronal proteins implicated in paraneoplastic neurological disease Fulltext Access 5 Pages 2005
Depressor responses to L-proline microinjected into the rat ventrolateral medulla are mediated by ionotropic excitatory amino acid receptors Fulltext Access 5 Pages 2005
Deletion of the LMNA initiator codon leading to a neurogenic variant of autosomal dominant Emery-Dreifuss muscular dystrophy Fulltext Access 5 Pages 2005
A family with a novel frameshift mutation in the PMP22 gene (c.433_434insC) causing a phenotype of hereditary neuropathy with liability to pressure palsies Fulltext Access 5 Pages 2005
Comparison of different techniques for detecting 17p12 duplication in CMT1A Fulltext Access 5 Pages 2005
Recurrent somatic mosaicism for D4Z4 contractions in a family with facioscapulohumeral muscular dystrophy Fulltext Access 5 Pages 2005
129th ENMC International Workshop: Clinical Trials for Chronic Inflammatory Demyelinating Polyradiculoneuropathy and Multifocal Motor Neuropathy, 27th October 2004, Schiphol airport, The Netherlands Fulltext Access 5 Pages 2005
The genes encoding for D4Z4 binding proteins HMGB2, YY1, NCL, and MYOD1 are excluded as candidate genes for FSHD1B Fulltext Access 5 Pages 2005
A novel ANT1 gene mutation with probable germline mosaicism in autosomal dominant progressive external ophthalmoplegia Fulltext Access 5 Pages 2005
An autosomal recessive limb girdle muscular dystrophy (LGMD2) with mild mental retardation is allelic to Walker-Warburg syndrome (WWS) caused by a mutation in the POMT1 gene Fulltext Access 5 Pages 2005
Dilated cardiomyopathy may be an early sign of the C826A Fukutin-related protein mutation Fulltext Access 5 Pages 2005
A rapid PCR method for genotyping the Largemyd mouse, a model of glycosylation-deficient congenital muscular dystrophy Fulltext Access 5 Pages 2005
Evolution of microglial activation in patients after ischemic stroke: a [11C](R)-PK11195 PET study Fulltext Access 5 Pages 2005
The influence of sex differences and individual task performance on brain activation during planning Fulltext Access 5 Pages 2005
Dysfunctional supplementary motor area implication during attention and time estimation tasks in schizophrenia: a PET-O15 water study Fulltext Access 5 Pages 2005
Motion or activity: their role in intra- and inter-subject variation in fMRI Fulltext Access 5 Pages 2005
Ventricular enlargement in schizophrenia is associated with a genetic polymorphism at the interleukin-1 receptor antagonist gene Fulltext Access 5 Pages 2005
The missing link: analogous human and primate cortical gamma oscillations Fulltext Access 5 Pages 2005