Topic: Adult

Journal: Neurology

Documents

A list of abstracts that contain a topic of "Adult" and a journal name of "Neurology".

• Family History of Stroke and Severity of Neurologic Deficit After Stroke.

  PMID: 17060565

• In Utero Antiepileptic Drug Exposure: Fetal Death and Malformations.

  PMID: 16894099

• Where is the "Straight Ahead" in Spatial Neglect?

  PMID: 17060587

• Limb-girdle Muscular Dystrophy in the Netherlands: Gene Defect Identified in Half the Families.

  PMID: 17562833

• Pediatric Multiple Sclerosis: a Short History of a Long Story.

  PMID: 17438236

• Surviving Glioblastoma for More Than 5 Years: the Patient's Perspective.

  PMID: 16434662

• Stiff Person Syndrome with Cerebellar Disease and High-titer Anti-gad Antibodies.

  PMID: 17000981

• Botulinum Toxin Injection for Congenital Muscular Torticollis Presenting in Children and Adults.

  PMID: 17000985

• Diagnostic Challenges in Facioscapulohumeral Muscular Dystrophy.

  PMID: 17060574

• Status Epilepticus: an Independent Outcome Predictor After Cerebral Anoxia.

  PMID: 17636063

• Predictors of Fitness to Drive in People with Parkinson Disease.

  PMID: 17909156

• Genetic Diagnosis in Lafora Disease: Genotype-phenotype Correlations and Diagnostic Pitfalls.

  PMID: 17389303

• Muscle Coenzyme Q10 Deficiencies in Ataxia with Oculomotor Apraxia 1.

  PMID: 17242337

• Preservation of Cognitive Function in Dystonia Treated by Pallidal Stimulation.

  PMID: 16717218

• A Genome-wide Scan and Hcrtr2 Candidate Gene Analysis in a European Cluster Headache Cohort.

  PMID: 16801656

• Proof of Genetic Heterogeneity in X-linked Charcot-marie-tooth Disease.

  PMID: 17159110

• Fmri Study of Episodic Memory in Relapsing-remitting Ms: Correlation with T2 Lesion Volume.

  PMID: 17101897

• Hyperacusis in Williams Syndrome: Characteristics and Associated Neuroaudiologic Abnormalities.

  PMID: 16476938

• Outcome and Effect of Pregnancy in Myotonic Dystrophy Type 2.

  PMID: 16505316

• Apoe-epsilon4 is Associated with Reduced Memory in Long-standing Intractable Temporal Lobe Epilepsy.

  PMID: 17283313

• Is Late-onset Multiple Sclerosis Associated with a Worse Outcome?

  PMID: 17000960

• Predictors of Hospital Length of Stay and Cost in Patients with Intracerebral Hemorrhage.

  PMID: 17030767

• A Secondary Progressive Clinical Course is Uncommon in Neuromyelitis Optica.

  PMID: 17310032

• A Door-to-door Survey of Intracranial Atherosclerosis in Liangbei County, China.

  PMID: 17548554

• Homonymous Hemianopias: Clinical-anatomic Correlations in 904 Cases.

  PMID: 16567710

• Delayed Orthostatic Hypotension: a Frequent Cause of Orthostatic Intolerance.

  PMID: 16832073

• Neurologic Prognosis and Withdrawal of Life Support After Resuscitation from Cardiac Arrest.

  PMID: 16832087

• Relapses and Subsequent Worsening of Disability in Relapsing-remitting Multiple Sclerosis.

  PMID: 16966541

• Recurrent Primary Thunderclap Headache and Benign Cns Angiopathy: Spectra of the Same Disorder?

  PMID: 17190937

• Physical Fitness and Lifetime Cognitive Change.

  PMID: 17030752

• Liver Test Abnormalities in Multiple Sclerosis: Findings from Placebo-treated Patients.

  PMID: 17030771

• Frequency of Lrrk2 Mutations in Early- and Late-onset Parkinson Disease.

  PMID: 17050822

• Incidence and Outcome of Cervical Artery Dissection: a Population-based Study.

  PMID: 17130413

• Minimum Incidence of Primary Cervical Dystonia in a Multiethnic Health Care Population.

  PMID: 17698789

• The Lrrk2 G2019s Mutation in Ashkenazi Jews with Parkinson Disease: is There a Gender Effect?

  PMID: 17938369

• Gamt Deficiency: Features, Treatment, and Outcome in an Inborn Error of Creatine Synthesis.

  PMID: 16855203

• Association Between Number of Siblings and Nervous System Tumors Suggests an Infectious Etiology.

  PMID: 17159104

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