Pages that link to "Q564414"
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The following pages link to Annals of Neurology (Q564414):
Displaying 50 items.
- REV756 (Q11833028) (← links)
- Environmental risk factors for multiple sclerosis. Part II: Noninfectious factors (Q22252931) (← links)
- Natural history of multiple sclerosis (Q22252934) (← links)
- Meta-analysis of early nonmotor features and risk factors for Parkinson disease (Q22252935) (← links)
- Assessment of current diagnostic criteria for Guillain-Barré syndrome (Q22252936) (← links)
- Environmental risk factors for multiple sclerosis. Part I: The role of infection (Q22252937) (← links)
- Diagnostic criteria for multiple sclerosis: 2005 revisions to the “McDonald Criteria” (Q22252938) (← links)
- Abnormal imitation-related cortical activation sequences in Asperger's syndrome (Q22252939) (← links)
- Interface between tauopathies and synucleinopathies: A tale of two proteins (Q22252940) (← links)
- APOE epsilon4 is not associated with Alzheimer's disease in elderly Nigerians (Q22252941) (← links)
- Recommended diagnostic criteria for multiple sclerosis: Guidelines from the international panel on the diagnosis of multiple sclerosis (Q22252943) (← links)
- An evidence-based causative classification system for acute ischemic stroke (Q22337438) (← links)
- Selective early cardiolipin peroxidation after traumatic brain injury: an oxidative lipidomics analysis (Q23913701) (← links)
- Does a defect of energy metabolism in the nerve fiber underlie axonal degeneration in polyneuropathies? (Q23919466) (← links)
- Confounding underlies the apparent month of birth effect in multiple sclerosis (Q24289541) (← links)
- Gain-of-function ADCY5 mutations in familial dyskinesia with facial myokymia (Q24293635) (← links)
- TMEM43 mutations in Emery-Dreifuss muscular dystrophy-related myopathy (Q24296250) (← links)
- Aprataxin, the causative protein for EAOH is a nuclear protein with a potential role as a DNA repair protein (Q24306836) (← links)
- A pilot proteomic study of amyloid precursor interactors in Alzheimer's disease (Q24310599) (← links)
- A nonsense mutation of the MASS1 gene in a family with febrile and afebrile seizures (Q24313526) (← links)
- A beta-subunit mutation in the acetylcholine receptor channel gate causes severe slow-channel syndrome (Q24317127) (← links)
- Machado-Joseph disease gene product is a cytoplasmic protein widely expressed in brain (Q24317460) (← links)
- Localization of LRRK2 to membranous and vesicular structures in mammalian brain (Q24318643) (← links)
- A mutation in sigma-1 receptor causes juvenile amyotrophic lateral sclerosis (Q24322790) (← links)
- Quinidine sulfate therapy for the slow-channel congenital myasthenic syndrome (Q24336166) (← links)
- Cloning and characterization of a Lambert-Eaton myasthenic syndrome antigen (Q24336405) (← links)
- The α2B-adrenergic receptor is mutant in cortical myoclonus and epilepsy (Q24338211) (← links)
- Rett syndrome: revised diagnostic criteria and nomenclature (Q24596295) (← links)
- Mutations in the autoregulatory domain of β-tubulin 4a cause hereditary dystonia (Q24605412) (← links)
- Diagnostic criteria for multiple sclerosis: 2010 revisions to the McDonald criteria (Q24605493) (← links)
- Solvent exposures and Parkinson disease risk in twins (Q24613285) (← links)
- A common polymorphism near PER1 and the timing of human behavioral rhythms (Q24630975) (← links)
- Days to criterion as an indicator of toxicity associated with human Alzheimer amyloid-beta oligomers (Q24633883) (← links)
- Anti-N-methyl-D-aspartate receptor (NMDAR) encephalitis in children and adolescents (Q24644532) (← links)
- A novel human disease with abnormal prion protein sensitive to protease (Q24648865) (← links)
- Cognition and anatomy in three variants of primary progressive aphasia (Q24650108) (← links)
- Paraneoplastic anti-N-methyl-D-aspartate receptor encephalitis associated with ovarian teratoma (Q24653500) (← links)
- Neuronal endoplasmic reticulum stress in axon injury and neurodegeneration (Q26826912) (← links)
- Mouse models of frontotemporal dementia (Q26829009) (← links)
- Pathogenic protein seeding in Alzheimer disease and other neurodegenerative disorders (Q26850298) (← links)
- Spinal muscular atrophy: development and implementation of potential treatments (Q26861377) (← links)
- Novel approaches and challenges to treatment of central nervous system viral infections (Q26862449) (← links)
- Training for a neurology career in a rare disease: The role of cyberconsults (Q26992032) (← links)
- Cell-surface central nervous system autoantibodies: clinical relevance and emerging paradigms (Q27006941) (← links)
- Comparative effectiveness and implementation research: directions for neurology (Q27010166) (← links)
- Zika virus: An emergent neuropathological agent (Q27010749) (← links)
- Hypomyelinating leukodystrophies: translational research progress and prospects (Q27012678) (← links)
- Abnormal synaptic Ca(2 ) homeostasis and morphology in cortical neurons of familial hemiplegic migraine type 1 mutant mice (Q27339873) (← links)
- Physiological consequences of abnormal connectivity in a developmental epilepsy (Q27340003) (← links)
- A large animal model of spinal muscular atrophy and correction of phenotype (Q27340106) (← links)