Professor of Neurology
Neurology
Dr. James F. Meschia, MD
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James Meschia works in the field of Neurology. He attended Johns Hopkins University School of Medicine. Johns Hopkins University School of Medicine is a top medical university. Johns Hopkins University School of Medicine is ranked 3 in research and 29 in primary care medicine Doctor James F. Meschia, MD is a published doctor and has 98 publications published. The lastest was: 'Long-Term Results of Stenting versus Endarterectomy for Carotid-Artery Stenosis.' James Meschia accepts Medicare payments and is listed with Medicare.gov.
Publications
- Multi-Center Study of Diffusion-Weighted Imaging in Coma After Cardiac Arrest.
- Genome-Wide Association Analysis of Young-Onset Stroke Identifies a Locus on Chromosome 10q25 Near HABP2.
- Long-Term Results of Stenting versus Endarterectomy for Carotid-Artery Stenosis.
- Heritability of young- and old-onset ischaemic stroke.
- Time From Symptoms to Carotid Endarterectomy or Stenting and Perioperative Risk.
- Genetic architecture of white matter hyperintensities differs in hypertensive and nonhypertensive ischemic stroke.
- Pathogenic Ischemic Stroke Phenotypes in the NINDS-Stroke Genetics Network.
- Common variation in PHACTR1 is associated with susceptibility to cervical Artery dissection.
- Agreement between TOAST and CCS ischemic stroke classification: The NINDS SiGN Study.
- Picking the Good Apples: Statistics Versus Good Judgment in Choosing Stent Operators for a Multicenter Clinical Trial.
- Mechanism of mesenchymal stem Cell-induced neuron recovery and anti-inflammation.
- Meta-analysis of Genome-wide Association Studies Identifies 1q22 as a Susceptibility Locus for IntraCerebral Hemorrhage.
- Rare coding variation in paraoxonase-1 is associated with ischemic stroke in the NHLBI Exome Sequencing Project.
- Early-Onset Stroke and Vasculopathy Associated with Mutations in ADA2.
- Asymptomatic Carotid stenosis: What we can learn from the next generation of randomized clinical trials.
- Nonconvulsive Status With Metronidazole.
- Stroke Genetics Network (SiGN) Study: Design and Rationale for a Genome-Wide Association Study of Ischemic Stroke Subtypes.
- Raising the red flag over white-matter changes.
- NINDS stroke genetics network (SiGN) experience with the causative classification System.
- Advances in stroke: genetics 2012.
- Burden of blood pressure-related alleles is associated with larger hematoma volume and worse outcome in intraCerebral hemorrhage.
- Shared associations of nonatherosclerotic, large-vessel, cerebrovascular arteriopathies: considering intracranial Aneurysms, cervical artery dissection, moyamoya disea...
- Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.
- Genetic variants associated with myocardial infarction in the PSMA6 gene and Chr9p21 are also associated with ischaemic stroke.
- Common Variants Within Oxidative Phosphorylation Genes Influence Risk of Ischemic Stroke and IntraCerebral Hemorrhage.
- Mutations in the colony stimulating factor 1 receptor (CSF1R) gene cause hereditary diffuse leukoencephalopathy with spheroids.
- Identifying a High Stroke Risk Subgroup in Individuals With Heart Failure.
- Stroke Genetics Update: 2011.
- Primary central Nervous system vasculitis presenting with intracranial hemorrhage.
- Clinical, Anatomic, and Procedural Durability of Carotid Revascularization.
- Self-Reported Atrial Fibrillation and Risk of Stroke in the Reasons for Geographic and Racial Differences in Stroke (REGARDS) Study.
- Low Medication Adherence and the Incidence of Stroke Symptoms Among Individuals With Hypertension: The REGARDS Study.
- Ataxin-2 repeat-length variation and neurodegeneration.
- Genetic susceptibility to ischemic stroke.
- Incidence of stroke symptoms among adults with chronic kidney Disease: results from the REasons for Geographic And Racial Differences in Stroke (REGARDS) study.
- The effect of survival bias on case-control genetic association studies of highly lethal Diseases.
- New information on the genetics of stroke.
- Advances in genetics 2010.
- Genomic risk profiling of ischemic stroke: results of an international genome-wide association meta-analysis.
- Acute ischemic stroke management: medical management.
- LRRK2 variation and Parkinson's Disease in African Americans.
- Mayo Acute Stroke Trial for Enhancing Recovery (MASTER) protocol.
- Behavioral symptoms in long-term survivors of ischemic stroke.
- Safety of recombinant activated factor VII in patients with warfarin-associated hemorrhages of the central Nervous system.
- Principal-component analysis for assessment of population stratification in mitochondrial medical genetics.
- Stroke genome-wide association studies: the large numbers imperative.
- Racial disparities in awareness and treatment of atrial fibrillation: the REasons for Geographic and Racial Differences in Stroke (REGARDS) study.
- The Carotid Revascularization Endarterectomy versus Stenting Trial: credentialing of interventionalists and final results of lead-in phase.
- Candidate gene polymorphisms for ischemic stroke.
- Pharmacogenetics and stroke.
- Whole genome approaches in ischemic stroke.
- Genetics of ischemic stroke: inheritance of a sporadic disorder.
- Camera in the emergency department: the evolution of stroke telemedicine.
- Primary central Nervous system vasculitis: comparison of patients with and without cerebral amyloid angiopathy.
- Decoding cryptogenic cardioembolism.
- Proband race/ethnicity affects pedigree completion rate in a genetic study of ischemic stroke.
- Angiography-negative primary central Nervous system vasculitis: a syndrome involving small cerebral vessels.
- Evaluation of subclinical cerebral injury and neuropsychologic function in patients undergoing Carotid endarterectomy.
- Heterogeneity of Moyamoya Disease: after a decade of linkage, is there new hope for a gene?
- Structural genomic variation in ischemic stroke.
- Efficacy of tumor necrosis factor alpha blockade in primary central Nervous system vasculitis resistant to immunosuppressive treatment.
- Primary central Nervous system vasculitis with prominent leptomeningeal enhancement: a subset with a benign outcome.
- Computer-assisted volumetric analysis compared with ABC/2 method for assessing warfarin-related intracranial Hemorrhage volumes.
- Ethics consultations and patients with neurological Diseases.
- Primary central Nervous system vasculitis: analysis of 101 patients.
- Fragile vessels: handle with care.
- Stroke symptoms in individuals reporting no prior stroke or transient ischemic attack are associated with a decrease in indices of mental and physical functioning.
- Sex differences in stroke evaluations in the Ischemic Stroke Genetics Study.
- Brain injury after cardiopulmonary arrest and its assessment with diffusion-weighted magnetic resonance imaging.
- Diagnosis and invasive management of Carotid atherosclerotic stenosis.
- Choice of neuroimaging in perioperative acute stroke management.
- High prevalence of stroke symptoms among persons without a diagnosis of stroke or transient ischemic attack in a general population: the REasons for Geographic And Rac...
- Lessons from adult stroke trials.
- Spanish cross-cultural adaptation and validation of the National Institutes of Health Stroke Scale.
- The Siblings With Ischemic Stroke Study (SWISS): a progress report.
- Ischemic stroke as a complex genetic disorder.
- Genetics of vascular cognitive impairment: the opportunity and the challenges.
- Defining stroke risks in sickle Cell anemia.
- Genetics of cerebrovascular Disorders.
- Recombinant factor VIIa for rapid reversal of warfarin anticoagulation in acute intracranial Hemorrhage.
- Clinically translated ischemic stroke genomics.
- Not so accidental outcomes following Cerebrovascular accidents.
- New advances in identifying genetic anomalies in stroke-prone probands.
- Characteristics of 100 consecutive patients presenting with orthostatic hypotension.
- Editorial comment--Vascular thickness and calcification as markers of atherosclerotic burden.
- Willingness of ischemic stroke patients to donate DNA for genetic research: a Systematic review.
- Familial Clustering of stroke according to proband age at onset of presenting ischemic stroke.
- Familial hypercholesterolemia: stroke and the broader perspective.
- Addressing the heterogeneity of the ischemic stroke phenotype in human genetics research.
- Planning genetic studies and human stroke: sample size estimates based on family history data.
- Subtyping in ischemic stroke genetic research.
- Thrombolytic treatment of acute ischemic stroke.
- Paraneoplastic chorea associated with CRMP-5 neuronal antibody and lung carcinoma.
- Thrombolysis for acute ischemic stroke: future directions.
- Contrasting the neurologic complications of cardiac transplantation in adults and children.
- Management of Vascular Risk Factors in the Carotid Revascularization Endarterectomy Versus Stenting Trial (CREST).
- Association of the APOE, MTHFR and ACE Genes Polymorphisms and Stroke in Zambian Patients.
Schools
Johns Hopkins University School Of Medicine
University Of Colorado Hospital
Barnes Jewish Hospital
Indiana Hospital
Procedures Preformed
- EEG (Electroencephalogram)
- EMG (Electromyography)
- Vascular Transcatheter Embolization
Conditions Treated
- Alzheimer's Disease
- Anterior Horn Disease
- Ataxia
- Autonomic Disorders
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Doctors Specialties
- Vascular Neurology
- Neurology
Accepted Insurances
Education
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Washington University - Barnes-Jewish Hospital -
University of Colorado -
Johns Hopkins University School of Medicine
Hospital
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Mayo Clinic - Jacksonville, Florida
Drug Facts
| NPI NUMBER | 1912996364 | |
| NPPES Provider LastName | MESCHIA | |
| NPPES Provider FirstName | JAMES | |
| NPPES Provider ZIPCode | 322241865 | |
| NPPES Provider State | FL | |
| Specialty Description | Neurology | |
| Total Claim Count | 67.0 | |
| Distinct Opioid Count | 1.0 | |
| Opioid Claim Count | 13.0 | |
| Percent Opioid Claims | 19.4 |
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1912996364 |
| Last Name Of The Provider | MESCHIA |
| First Name Of The Provider | JAMES |
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